CINXE.COM
KEGG PATHWAY: rn01057
<!doctype html> <html><head> <title>KEGG PATHWAY: rn01057</title> <link type="text/css" rel="stylesheet" href="/css/gn2.css?1739824121"> <link type="text/css" rel="stylesheet" href="/css/bget.css?1739824121"> <meta name="viewport" content="width=device-width, initial-scale=1.0"> <link type="text/css" rel="stylesheet" href="/css/bgetm.css?1739824121" media="only screen and (max-width: 768px)"> <style>.kcfd{display:none;}</style> <script> <!-- var getElementsByClassName = document.getElementsByClassName ? function (cl){ return document.getElementsByClassName(cl); } : function (cl){ var elms = []; var objs = document.getElementsByTagName('*'); for(var i=0;i<objs.length;i++){ var obj = objs[i]; if(obj.className == cl){ elms.push(obj); } } return elms; }; function toggleField(clk,cl,show,hide){ var objs = getElementsByClassName(cl); for(var i=0;i<objs.length;i++){ var obj = objs[i]; if(!obj.style.display||obj.style.display == 'none'){ obj.style.display = 'block'; clk.innerHTML = ' « '+hide; } else{ obj.style.display = 'none'; clk.innerHTML = ' » '+show; } } } function toggleData(bobj,e){ var id = bobj.id.replace(/[^0-9]/g,''); var dt = document.getElementById('kcfd'+id); e.preventDefault(); if(!dt.style.display||dt.style.display == 'none'){ document.getElementById('kcfb'+id).innerHTML = 'Hide'; dt.style.display = 'block'; } else{ document.getElementById('kcfb'+id).innerHTML = 'Show'; dt.style.display = 'none'; } } function btn(bobj,img) { bobj.src = "/Fig/bget/button_" + img + ".gif"; } function btn_e(e) { e = e || event; var obj = e.target; var img = e.target.src; var img_base = img.replace(/\\/g,'/').replace(/(b|bd|bh)\.gif$/,''); if(e.type == 'mousedown'||e.type == 'touchstart'){ obj.src = img_base +'bd.gif'; } else if(e.type == 'mouseover'){ obj.src = img_base +'bh.gif'; } else if(e.type == 'mouseup'||e.type == 'touchend'){ obj.src = img_base +'b.gif'; } else if(e.type == 'mouseout'){ obj.src = img_base +'b.gif'; } } function init(){ for(var i=1;i<=1;i++){ if(document.getElementById('kcfb'+i)){ document.getElementById('kcfb'+i).onclick = function(e){toggleData(this,e);}; } } } function Link_XtrctSeq2(form) { var dna_from; var dna_to; var dna_len; var plus_up = Number(form.XtrctSeq_UP.value) ; var plus_down = Number(form.XtrctSeq_DOWN.value); var vector = Number(form.VECTOR.value); var org = form.ORG.value; var chr = form.CHR.value; var kid = form.KEGGID.value; var url; if (plus_up == 0 && plus_down == 0) { url = "/entry/-f+-n+n+" + kid; } else { if (vector == 1) { dna_from = Number(form.FROM.value) - plus_up; dna_to = Number(form.TO.value) + plus_down; } else { dna_from = Number(form.FROM.value) - plus_down; dna_to = Number(form.TO.value) + plus_up; } url = "/dbget-bin/cut_sequence_genes.pl?FROM=" + dna_from + "&TO=" + dna_to +"&VECTOR=" + vector + "&ORG=" + org; if (chr) url += "&CHR=" + chr; } //window.open( url, "_self" ); location.href = url; } function go_taxonomy(form,params){ for(var key in params){ if(form[key]){ form.setAttribute(key,params[key]); } else{ var obj = document.createElement('input'); obj.setAttribute('type','hidden'); obj.setAttribute('name',key); obj.setAttribute('value',params[key]); form.appendChild(obj); } } form.submit(); } window.onload=function(){window.focus();init();}; //---> </script> </head> <body> <div> <table border=0 cellpadding=0 cellspacing=0><tr><td> <table border=0 cellpadding=0 cellspacing=0 width="650"><tr><td width=70><a href="/kegg/kegg2.html"><img align="middle" alt="KEGG" border=0 src="/Fig/bget/kegg3.gif"></a></td><td> </td><td><a name="pathway:rn01057"></a><font class="title3">PATHWAY: rn01057</font></td><td class="tar vbot"><button class="btn" onclick="javascript:void(window.open('/kegg/document/help_bget_pathway.html','KEGG_Help','toolbar=no,location=no,directories=no,width=720,height=640,resizable=yes,scrollbars=yes'));return false;">Help</button></td></tr></table><form method="post" action="/entry/" enctype="application/x-www-form-urlencoded" id="form1" name="form1"></form><table class="w1" width="650"> <tr> <td class="fr3 w1"> <table width="650" class="w2"> <tr><th class="th30 deft tal vmid"><span class="nowrap">Entry</span></th> <td class="td30 defd"><table class="w1" width="100%"><tr><td class="tal pd0"><code><span class="nowrap">rn01057 Pathway <br> </span></code></td></tr></table></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Name</span></th> <td class="td31 defd"><div class="cel">Biosynthesis of type II polyketide products</div></td></tr> <tr><th class="th30 deft tal vtop"><span class="nowrap">Class</span></th> <td class="td30 defd"><div class="cel">Metabolism; Metabolism of terpenoids and polyketides<br> </div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Pathway map</span></th> <td class="td31 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/rn01057">rn01057</a> </span></td><td>Biosynthesis of type II polyketide products</td></tr></table><center><a href="/pathway/rn01057"><img src="/kegg/misc/thumbnail/map01057.gif" alt="rn01057" style="border-style:none;"></a></center><br><button class="btn" onclick="location.href='https://www.kegg.jp/kegg-bin/view_ortholog_table?map=01057';return false;">Ortholog table</button></td></tr> <tr><th class="th30 deft tal vtop"><span class="nowrap">Module</span></th> <td class="td30 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00779">M00779</a> </span></td><td>Dihydrokalafungin biosynthesis, octaketide => dihydrokalafungin [PATH:<a href="/pathway/rn01057+M00779">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00780">M00780</a> </span></td><td>Tetracycline/oxytetracycline biosynthesis, pretetramide => tetracycline/oxytetracycline [PATH:<a href="/pathway/rn01057+M00780">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00781">M00781</a> </span></td><td>Nogalavinone/aklavinone biosynthesis, deoxynogalonate/deoxyaklanonate => nogalavinone/aklavinone [PATH:<a href="/pathway/rn01057+M00781">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00782">M00782</a> </span></td><td>Mithramycin biosynthesis, 4-demethylpremithramycinone => mithramycin [PATH:<a href="/pathway/rn01057+M00782">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00783">M00783</a> </span></td><td>Tetracenomycin C/8-demethyltetracenomycin C biosynthesis, tetracenomycin F2 => tetracenomycin C/8-demethyltetracenomycin C [PATH:<a href="/pathway/rn01057+M00783">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00784">M00784</a> </span></td><td>Elloramycin biosynthesis, 8-demethyltetracenomycin C => elloramycin A [PATH:<a href="/pathway/rn01057+M00784">rn01057</a>]</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00823">M00823</a> </span></td><td>Chlortetracycline biosynthesis, pretetramide => chlortetracycline [PATH:<a href="/pathway/rn01057+M00823">rn01057</a>]</td></tr></table></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reaction</span></th> <td class="td31 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R04060">R04060</a> </span></td><td>anhydrotetracycline,NADPH:oxygen oxidoreductase (6-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R05459">R05459</a> </span></td><td>tetracycline:coenzyme-F420 oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R05462">R05462</a> </span></td><td>4-hydroxy-6-methylpretetramide,NADPH:oxygen oxidoreductase (12a-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R05463">R05463</a> </span></td><td>6-methylpretetramide,NADPH:oxygen oxidoreductase (4-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R05705">R05705</a> </span></td><td>FMNH2:NAD+ oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06650">R06650</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06651">R06651</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06652">R06652</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06653">R06653</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06654">R06654</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06655">R06655</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06656">R06656</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06659">R06659</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06660">R06660</a> </span></td><td>dTDP-D-olivose:compound-100-1 O-beta-D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06661">R06661</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06662">R06662</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06664">R06664</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06665">R06665</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06666">R06666</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06667">R06667</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06668">R06668</a> </span></td><td>dTDP-D-olivose:urdamycin-G D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06670">R06670</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06671">R06671</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06672">R06672</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06673">R06673</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06674">R06674</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06675">R06675</a> </span></td><td>S-adenosyl-L-methionine:nogalonic-acid O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06676">R06676</a> </span></td><td>auraviketone lyase (decyclizing)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06677">R06677</a> </span></td><td>auramycinone:NADP+ 7-oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06678">R06678</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06679">R06679</a> </span></td><td>12-deoxyaklanonic-acid:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06680">R06680</a> </span></td><td>S-adenosyl-L-methionine:aklanonate O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06681">R06681</a> </span></td><td>aklaviketone lyase (ring-opening)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06682">R06682</a> </span></td><td>aklavinone:NADP+ 7-oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06683">R06683</a> </span></td><td>aklavinone,NADPH:oxygen oxidoreductase (12-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06684">R06684</a> </span></td><td>dTDP-beta-L-daunosamine:epsilon-rhodomycinone beta-L-daunosaminyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06685">R06685</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06686">R06686</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06687">R06687</a> </span></td><td>S-adenosyl-L-methionine:13-deoxycarminomycin 4-O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06688">R06688</a> </span></td><td>13-deoxydaunorubicin,NADPH:oxygen oxidoreductase (13-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06689">R06689</a> </span></td><td>13-dihydrodaunorubicin,NADPH:oxygen oxidoreductase (13-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06690">R06690</a> </span></td><td>daunorubicin,NADPH:oxygen oxidoreductase (hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06691">R06691</a> </span></td><td>13-deoxycarminomycin,NADPH:oxygen oxidoreductase (13-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06692">R06692</a> </span></td><td>13-dihydrocarminomycin,NADPH:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06693">R06693</a> </span></td><td>S-adenosyl-L-methionine:carminomycin 4-O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06694">R06694</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06695">R06695</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06696">R06696</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06698">R06698</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06699">R06699</a> </span></td><td>tetracenomycin-F2 hydro-lyase (tetracenomycin-F1-forming)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06700">R06700</a> </span></td><td>tetracenomycin-F1:oxygen C5-monooxygenase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06701">R06701</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06702">R06702</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06703">R06703</a> </span></td><td>S-adenosyl-L-methionine:tetracenomycin-E O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06704">R06704</a> </span></td><td>tetracenomycin-A2,NADPH:oxygen oxidoreductase (tetracenomycin-C-forming)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06706">R06706</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06707">R06707</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06709">R06709</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06710">R06710</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06711">R06711</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06713">R06713</a> </span></td><td>S-adenosyl-L-methionine:tetracenomycin-B3 O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06714">R06714</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06715">R06715</a> </span></td><td>S-adenosyl-L-methionine:4-demethylpremithramycinone O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06716">R06716</a> </span></td><td>dTDP-D-olivose:premithramycinone D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06717">R06717</a> </span></td><td>dTDP-D-oliose:premithramycin-A1 D-oliosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06718">R06718</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R06719">R06719</a> </span></td><td>S-adenosyl-L-methionine:premithramycin-A3' C-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09188">R09188</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09189">R09189</a> </span></td><td>S-adenosyl-L-methionine:pretetramid C-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09190">R09190</a> </span></td><td>6-methylpretetramide,NADPH:oxygen oxidoreductase (4,12a-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09191">R09191</a> </span></td><td>S-adenosyl-L-methionine:4-amino-anhydrotetracycline N-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09192">R09192</a> </span></td><td>oxytetracycline:coenzyme-F420 oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09196">R09196</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09197">R09197</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09198">R09198</a> </span></td><td>5a,11a-dehydrotetracycline,NADPH:oxygen oxidoreductase (5-hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09305">R09305</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09306">R09306</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09307">R09307</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09308">R09308</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09309">R09309</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09310">R09310</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09311">R09311</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09312">R09312</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09313">R09313</a> </span></td><td>dihydrokalafungin-dihydroquinone,FMNH2:oxygen oxidoreductase (hydroxylating)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09314">R09314</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09325">R09325</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09326">R09326</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09327">R09327</a> </span></td><td>deoxynogalonate:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09328">R09328</a> </span></td><td>nogalaviketone lyase (ring-opening)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09329">R09329</a> </span></td><td>nogalavinone:NADP+ 7-oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09330">R09330</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09331">R09331</a> </span></td><td>dTDP-beta-L-rhodosamine:aklavinone 7-alpha-L-rhodosaminyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09332">R09332</a> </span></td><td>dTDP-2-deoxy-beta-L-fucose:aclacinomycin-T 2-deoxy-alpha-L-fucosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09333">R09333</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09334">R09334</a> </span></td><td>aclacinomycin N:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09335">R09335</a> </span></td><td>aclacinomycin A:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09336">R09336</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09337">R09337</a> </span></td><td>epsilon-rhodomycin-T acylhydrolase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09338">R09338</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09340">R09340</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09341">R09341</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09342">R09342</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09343">R09343</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09344">R09344</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09345">R09345</a> </span></td><td>dTDP-D-olivose:UWM6 9-C-beta-D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09346">R09346</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09347">R09347</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09348">R09348</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09349">R09349</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09350">R09350</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09351">R09351</a> </span></td><td>dTDP-D-olivose:premithramycin-A3 D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09352">R09352</a> </span></td><td>dTDP-D-olivose:3A-deolivosylpremithramycin-B D-olivosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09353">R09353</a> </span></td><td>premithramycin-B,NADPH:oxygen oxidoreductase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09354">R09354</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09355">R09355</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09357">R09357</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09360">R09360</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09361">R09361</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R09362">R09362</a> </span></td><td> </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10545">R10545</a> </span></td><td>aclacinomycin T acylhydrolase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10954">R10954</a> </span></td><td>tetracenomycin-B2,NADPH:oxygen oxidoreductase (8-demethyltetracenomycin-C-forming)</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10955">R10955</a> </span></td><td>dTDP-beta-L-rhamnose:8-demethyltetracenomycin-C alpha-L-rhamnosyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10956">R10956</a> </span></td><td>S-adenosyl-L-methionine:8-demethyl-8-alpha-L-rhamnosyltetracenomycin-C 2'-O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10957">R10957</a> </span></td><td>S-adenosyl-L-methionine:8-demethyl-8-(2-methoxy-alpha-L-rhamnosyl)tetracenomycin-C 3'-O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10958">R10958</a> </span></td><td>S-adenosyl-L-methionine:8-demethyl-8-(2,3-di-O-methoxy-alpha-L-rhamnosyl)tetracenomycin-C 4'-O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R10959">R10959</a> </span></td><td>S-adenosyl-L-methionine:8-demethyl-8-(2,3,4-tri-O-methyl-alpha-L-rhamnosyl)tetracenomycin-C O-methyltransferase</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/R11478">R11478</a> </span></td><td>tetracycline:FADH2 oxidoreductase (7-halogenating)</td></tr></table></td></tr> <tr><th class="th30 deft tal vtop"><span class="nowrap">Compound</span></th> <td class="td30 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C00061">C00061</a> </span></td><td>FMN</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C01661">C01661</a> </span></td><td>Doxorubicin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C01847">C01847</a> </span></td><td>Reduced FMN</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C01907">C01907</a> </span></td><td>Daunorubicin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C02811">C02811</a> </span></td><td>Anhydrotetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C03206">C03206</a> </span></td><td>5a,11a-Dehydrotetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06570">C06570</a> </span></td><td>Tetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06571">C06571</a> </span></td><td>Chlortetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06624">C06624</a> </span></td><td>Oxytetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06627">C06627</a> </span></td><td>4-Keto-anhydrotetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06628">C06628</a> </span></td><td>4-Hydroxy-6-methylpretetramide</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06629">C06629</a> </span></td><td>6-Methylpretetramide</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06654">C06654</a> </span></td><td>4-Amino-anhydrotetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06691">C06691</a> </span></td><td>Actinorhodin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06799">C06799</a> </span></td><td>Granaticin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C06801">C06801</a> </span></td><td>Tetracenomycin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12366">C12366</a> </span></td><td>Tetracenomycin F2</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12367">C12367</a> </span></td><td>Tetracenomycin F1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12368">C12368</a> </span></td><td>Tetracenomycin D3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12369">C12369</a> </span></td><td>Tetracenomycin B3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12370">C12370</a> </span></td><td>Tetracenomycin E</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12371">C12371</a> </span></td><td>Tetracenomycin A2</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12373">C12373</a> </span></td><td>Tetracenomycin F1 methylester</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12374">C12374</a> </span></td><td>Decarboxytetracenomycin F1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12375">C12375</a> </span></td><td>Tetracenomycin D3 methylester</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12376">C12376</a> </span></td><td>Tetracenomycin D1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12377">C12377</a> </span></td><td>Tetracenomycin B1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12378">C12378</a> </span></td><td>Tetracenomycin B2</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12379">C12379</a> </span></td><td>8-Demethyltetracenomycin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12380">C12380</a> </span></td><td>Tetracenomycin X</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12381">C12381</a> </span></td><td>Elloramycin A</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12382">C12382</a> </span></td><td>4-Demethylpremithramycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12383">C12383</a> </span></td><td>Premithramycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12384">C12384</a> </span></td><td>Premithramycin A1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12385">C12385</a> </span></td><td>Premithramycin A2'</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12386">C12386</a> </span></td><td>Premithramycin A3'</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12387">C12387</a> </span></td><td>Premithramycin A3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12388">C12388</a> </span></td><td>Premithramycin B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12389">C12389</a> </span></td><td>Mithramycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12390">C12390</a> </span></td><td>Dehydrorabelomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12391">C12391</a> </span></td><td>Kinobscurinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12392">C12392</a> </span></td><td>Stealthin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12393">C12393</a> </span></td><td>Prekinamycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12394">C12394</a> </span></td><td>Kinamycin D</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12395">C12395</a> </span></td><td>Jadomycin B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12396">C12396</a> </span></td><td>Tetrangomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12397">C12397</a> </span></td><td>Tetrangulol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12398">C12398</a> </span></td><td>8-O-Methyltetrangulol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12399">C12399</a> </span></td><td>19-Hydroxytetrangulol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12400">C12400</a> </span></td><td>19-Hydroxy-8-O-methyltetrangulol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12401">C12401</a> </span></td><td>PD116740</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12402">C12402</a> </span></td><td>Rabelomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12404">C12404</a> </span></td><td>Urdamycinone B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12405">C12405</a> </span></td><td>100-1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12406">C12406</a> </span></td><td>Urdamycin B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12407">C12407</a> </span></td><td>104-2</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12408">C12408</a> </span></td><td>100-2</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12409">C12409</a> </span></td><td>124-1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12410">C12410</a> </span></td><td>Urdamycinone F</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12411">C12411</a> </span></td><td>Urdamycin F</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12412">C12412</a> </span></td><td>Aquayamycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12413">C12413</a> </span></td><td>Urdamycin A</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12414">C12414</a> </span></td><td>Urdamycin G</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12415">C12415</a> </span></td><td>Methyl nogalonate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12416">C12416</a> </span></td><td>Nogalonate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12417">C12417</a> </span></td><td>Auraviketone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12418">C12418</a> </span></td><td>Dihydro-NAME</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12419">C12419</a> </span></td><td>Auramycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12420">C12420</a> </span></td><td>12-Deoxyaklanonic acid</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12421">C12421</a> </span></td><td>Aklanonate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12422">C12422</a> </span></td><td>Methyl aklanonate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12423">C12423</a> </span></td><td>Aklaviketone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12424">C12424</a> </span></td><td>Aklavinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12425">C12425</a> </span></td><td>epsilon-Rhodomycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12426">C12426</a> </span></td><td>Rhodomycin D</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12427">C12427</a> </span></td><td>10-Carboxy-13-deoxycarminomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12428">C12428</a> </span></td><td>13-Deoxycarminomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12429">C12429</a> </span></td><td>13-Deoxydaunorubicin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12430">C12430</a> </span></td><td>13-Dihydrodaunorubicin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12431">C12431</a> </span></td><td>13-Dihydrocarminomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12432">C12432</a> </span></td><td>Carminomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12433">C12433</a> </span></td><td>(13S)-13-Dihydrodaunorubicin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12434">C12434</a> </span></td><td>(S)-DNPA</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12435">C12435</a> </span></td><td>6-Deoxydihydrokalafungin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12436">C12436</a> </span></td><td>Dihydrokalafungin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12437">C12437</a> </span></td><td>Medermycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C12451">C12451</a> </span></td><td>Fridamycin E</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18293">C18293</a> </span></td><td>Nonaketamide monocyclic intermediate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18294">C18294</a> </span></td><td>Nonaketamide tricyclic intermediate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18295">C18295</a> </span></td><td>Pretetramid</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18296">C18296</a> </span></td><td>5a,11a-Dehydrooxytetracycline</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18329">C18329</a> </span></td><td>7,9,12-Octaketide intermediate 3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18332">C18332</a> </span></td><td>7,9,12-Decaketide intermediate 3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18335">C18335</a> </span></td><td>7,9,12-Decaketide intermediate 6</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18336">C18336</a> </span></td><td>7,12-Decaketide intermediate 1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18337">C18337</a> </span></td><td>9,14-Decaketide intermediate 1</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18353">C18353</a> </span></td><td>Octaketide bicyclic intermediate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18354">C18354</a> </span></td><td>(S)-Chiral alcohol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18355">C18355</a> </span></td><td>(R)-Chiral alcohol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18356">C18356</a> </span></td><td>(S)-Hemiketal</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18357">C18357</a> </span></td><td>(R)-Hemiketal</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18358">C18358</a> </span></td><td>DHKred-OH</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18359">C18359</a> </span></td><td>Dihydrogranaticin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18360">C18360</a> </span></td><td>Dihydrokalafungin dihydroquinone form</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18629">C18629</a> </span></td><td>Deoxynogalonate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18630">C18630</a> </span></td><td>Nogalaviketone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18631">C18631</a> </span></td><td>Nogalavinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18632">C18632</a> </span></td><td>1-OH-Nogalamycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18633">C18633</a> </span></td><td>Nogalamycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18634">C18634</a> </span></td><td>Aclacinomycin T</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18635">C18635</a> </span></td><td>Aclacinomycin S</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18637">C18637</a> </span></td><td>Aclacinomycin N</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18638">C18638</a> </span></td><td>Aclacinomycin A</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18639">C18639</a> </span></td><td>Aclacinomycin Y</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18640">C18640</a> </span></td><td>epsilon-Rhodomycin T</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18641">C18641</a> </span></td><td>15-Demethoxy-epsilon-rhodomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18642">C18642</a> </span></td><td>beta-Rhodomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18678">C18678</a> </span></td><td>UWM6</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18679">C18679</a> </span></td><td>2,3-Dehydro-UWM6</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18680">C18680</a> </span></td><td>Jadomycin A</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18681">C18681</a> </span></td><td>C1'-C9-Glycosylated UWM6</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18682">C18682</a> </span></td><td>11-Deoxylandomycinone</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18683">C18683</a> </span></td><td>Landomycin H</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18684">C18684</a> </span></td><td>Landomycin D</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18685">C18685</a> </span></td><td>Landomycin E</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18709">C18709</a> </span></td><td>Decaketide tricyclic intermediate</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18710">C18710</a> </span></td><td>3A-Deolivosylpremithramycin B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18711">C18711</a> </span></td><td>Mithramycin DK</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18778">C18778</a> </span></td><td>8-D-Olivosyl-landomycin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18822">C18822</a> </span></td><td>Landomycin A</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18823">C18823</a> </span></td><td>Landomycin B</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18824">C18824</a> </span></td><td>Landomycin J</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C18835">C18835</a> </span></td><td>(R)-DNPA</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C20689">C20689</a> </span></td><td>15-Demethylaclacinomycin T</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C20974">C20974</a> </span></td><td>8-Demethyl-8-alpha-L-rhamnosyltetracenomycin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C20975">C20975</a> </span></td><td>8-Demethyl-8-(2-O-methyl-alpha-L-rhamnosyl)tetracenomycin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C20976">C20976</a> </span></td><td>8-Demethyl-8-(2,3-di-O-methyl-alpha-L-rhamnosyl)tetracenomycin C</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/C20977">C20977</a> </span></td><td>8-Demethyl-8-(2,3,4-tri-O-methyl-alpha-L-rhamnosyl)tetracenomycin C</td></tr></table></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17227452">17227452</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Taguchi T, Okamoto S, Lezhava A, Li A, Ochi K, Ebizuka Y, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Possible involvement of ActVI-ORFA in transcriptional regulation of actVI tailoring-step genes for actinorhodin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">FEMS Microbiol Lett 269:234-9 (2007)<br>DOI:<a href="https://doi.org/10.1111/j.1574-6968.2007.00627.x">10.1111/j.1574-6968.2007.00627.x</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12855716">12855716</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ichinose K, Ozawa M, Itou K, Kunieda K, Ebizuka Y</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Cloning, sequencing and heterologous expression of the medermycin biosynthetic gene cluster of Streptomyces sp. AM-7161: towards comparative analysis of the benzoisochromanequinone gene clusters.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Microbiology 149:1633-45 (2003)<br>DOI:<a href="https://doi.org/10.1099/mic.0.26310-0">10.1099/mic.0.26310-0</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/16169737">16169737</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Li A, Itoh T, Taguchi T, Xiang T, Ebizuka Y, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Functional studies on a ketoreductase gene from Streptomyces sp. AM-7161 to control the stereochemistry in medermycin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Bioorg Med Chem 13:6856-63 (2005)<br>DOI:<a href="https://doi.org/10.1016/j.bmc.2005.07.060">10.1016/j.bmc.2005.07.060</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/9831526">9831526</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ichinose K, Bedford DJ, Tornus D, Bechthold A, Bibb MJ, Revill WP, Floss HG, Hopwood DA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The granaticin biosynthetic gene cluster of Streptomyces violaceoruber Tu22: sequence analysis and expression in a heterologous host.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 5:647-59 (1998)<br>DOI:<a href="https://doi.org/10.1016/S1074-5521(98)90292-7">10.1016/S1074-5521(98)90292-7</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11851466">11851466</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Hopwood DA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Genetic Contributions to Understanding Polyketide Synthases.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Rev 97:2465-2498 (1997)<br>DOI:<a href="https://doi.org/10.1021/cr960034i">10.1021/cr960034i</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/7929165">7929165</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Fernandez-Moreno MA, Martinez E, Caballero JL, Ichinose K, Hopwood DA, Malpartida F</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">DNA sequence and functions of the actVI region of the actinorhodin biosynthetic gene cluster of Streptomyces coelicolor A3(2).</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 269:24854-63 (1994)</div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17579485">17579485</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Itoh T, Taguchi T, Kimberley MR, Booker-Milburn KI, Stephenson GR, Ebizuka Y, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Actinorhodin biosynthesis: structural requirements for post-PKS tailoring intermediates revealed by functional analysis of ActVI-ORF1 reductase.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 46:8181-8 (2007)<br>DOI:<a href="https://doi.org/10.1021/bi700190p">10.1021/bi700190p</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11325954">11325954</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ichinose K, Taguchi T, Bedford DJ, Ebizuka Y, Hopwood DA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Functional complementation of pyran ring formation in actinorhodin biosynthesis in Streptomyces coelicolor A3(2) by ketoreductase genes for granaticin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 183:3247-50 (2001)<br>DOI:<a href="https://doi.org/10.1128/JB.183.10.3247-3250.2001">10.1128/JB.183.10.3247-3250.2001</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11707113">11707113</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Taguchi T, Ebizuka Y, Hopwood DA, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">A new mode of stereochemical control revealed by analysis of the biosynthesis of dihydrogranaticin in Streptomyces violaceoruber Tu22.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Am Chem Soc 123:11376-80 (2001)<br>DOI:<a href="https://doi.org/10.1021/ja015981+">10.1021/ja015981+</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15498668">15498668</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Taguchi T, Kunieda K, Takeda-Shitaka M, Takaya D, Kawano N, Kimberley MR, Booker-Milburn KI, Stephenson GR, Umeyama H, Ebizuka Y, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Remarkably different structures and reaction mechanisms of ketoreductases for the opposite stereochemical control in the biosynthesis of BIQ antibiotics.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Bioorg Med Chem 12:5917-27 (2004)<br>DOI:<a href="https://doi.org/10.1016/j.bmc.2004.08.026">10.1016/j.bmc.2004.08.026</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/19246012">19246012</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Okamoto S, Taguchi T, Ochi K, Ichinose K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Biosynthesis of actinorhodin and related antibiotics: discovery of alternative routes for quinone formation encoded in the act gene cluster.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 16:226-36 (2009)<br>DOI:<a href="https://doi.org/10.1016/j.chembiol.2009.01.015">10.1016/j.chembiol.2009.01.015</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/18245777">18245777</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Valton J, Mathevon C, Fontecave M, Niviere V, Ballou DP</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Mechanism and regulation of the Two-component FMN-dependent monooxygenase ActVA-ActVB from Streptomyces coelicolor.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 283:10287-96 (2008)<br>DOI:<a href="https://doi.org/10.1074/jbc.M709730200">10.1074/jbc.M709730200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/16267053">16267053</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Valton J, Fontecave M, Douki T, Kendrew SG, Niviere V</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">An aromatic hydroxylation reaction catalyzed by a two-component FMN-dependent Monooxygenase. The ActVA-ActVB system from Streptomyces coelicolor.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 281:27-35 (2006)<br>DOI:<a href="https://doi.org/10.1074/jbc.M506146200">10.1074/jbc.M506146200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15297451">15297451</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Valton J, Filisetti L, Fontecave M, Niviere V</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">A two-component flavin-dependent monooxygenase involved in actinorhodin biosynthesis in Streptomyces coelicolor.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 279:44362-9 (2004)<br>DOI:<a href="https://doi.org/10.1074/jbc.M407722200">10.1074/jbc.M407722200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20193654">20193654</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ellis HR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The FMN-dependent two-component monooxygenase systems.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Arch Biochem Biophys 497:1-12 (2010)<br>DOI:<a href="https://doi.org/10.1016/j.abb.2010.02.007">10.1016/j.abb.2010.02.007</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12417584">12417584</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Filisetti L, Fontecave M, Niviere V</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Mechanism and substrate specificity of the flavin reductase ActVB from Streptomyces coelicolor.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 278:296-303 (2003)<br>DOI:<a href="https://doi.org/10.1074/jbc.M209689200">10.1074/jbc.M209689200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/9209048">9209048</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Kendrew SG, Hopwood DA, Marsh EN</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Identification of a monooxygenase from Streptomyces coelicolor A3(2) involved in biosynthesis of actinorhodin: purification and characterization of the recombinant enzyme.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 179:4305-10 (1997)<br>DOI:<a href="https://doi.org/10.1128/JB.179.13.4305-4310.1997">10.1128/JB.179.13.4305-4310.1997</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12514126">12514126</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Sciara G, Kendrew SG, Miele AE, Marsh NG, Federici L, Malatesta F, Schimperna G, Savino C, Vallone B</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The structure of ActVA-Orf6, a novel type of monooxygenase involved in actinorhodin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">EMBO J 22:205-15 (2003)<br>DOI:<a href="https://doi.org/10.1093/emboj/cdg031">10.1093/emboj/cdg031</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20157809">20157809</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Fetzner S, Steiner RA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Cofactor-independent oxidases and oxygenases.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Appl Microbiol Biotechnol 86:791-804 (2010)<br>DOI:<a href="https://doi.org/10.1007/s00253-010-2455-0">10.1007/s00253-010-2455-0</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Krohn K (ed).</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Anthracycline Chemistry and Biology I : Biological Occurence and Biosynthesis, Synthesis and Chemistry</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Topics in Current Chemistry 282 (2008)</div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11683270">11683270</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Torkkell S, Kunnari T, Palmu K, Mantsala P, Hakala J, Ylihonko K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The entire nogalamycin biosynthetic gene cluster of Streptomyces nogalater: characterization of a 20-kb DNA region and generation of hybrid structures.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Mol Genet Genomics 266:276-88 (2001)<br>DOI:<a href="https://doi.org/10.1007/s004380100554">10.1007/s004380100554</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20052967">20052967</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Grocholski T, Koskiniemi H, Lindqvist Y, Mantsala P, Niemi J, Schneider G</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Crystal structure of the cofactor-independent monooxygenase SnoaB from Streptomyces nogalater: implications for the reaction mechanism.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 49:934-44 (2010)<br>DOI:<a href="https://doi.org/10.1021/bi901985b">10.1021/bi901985b</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/19255477">19255477</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Koskiniemi H, Grocholski T, Schneider G, Niemi J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Expression, purification and crystallization of the cofactor-independent monooxygenase SnoaB from the nogalamycin biosynthetic pathway.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Acta Crystallogr Sect F Struct Biol Cryst Commun 65:256-9 (2009)<br>DOI:<a href="https://doi.org/10.1107/S1744309109001389">10.1107/S1744309109001389</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12399480">12399480</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Chung JY, Fujii I, Harada S, Sankawa U, Ebizuka Y</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Expression, purification, and characterization of AknX anthrone oxygenase, which is involved in aklavinone biosynthesis in Streptomyces galilaeus.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 184:6115-22 (2002)<br>DOI:<a href="https://doi.org/10.1128/JB.184.22.6115-6122.2002">10.1128/JB.184.22.6115-6122.2002</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/7836284">7836284</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Dickens ML, Ye J, Strohl WR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Analysis of clustered genes encoding both early and late steps in daunomycin biosynthesis by Streptomyces sp. strain C5.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 177:536-43 (1995)<br>DOI:<a href="https://doi.org/10.1128/JB.177.3.536-543.1995">10.1128/JB.177.3.536-543.1995</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/10639368">10639368</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Torkkell S, Kunnari T, Palmu K, Hakala J, Mantsala P, Ylihonko K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Identification of a cyclase gene dictating the C-9 stereochemistry of anthracyclines from Streptomyces nogalater.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Antimicrob Agents Chemother 44:396-9 (2000)<br>DOI:<a href="https://doi.org/10.1128/AAC.44.2.396-399.2000">10.1128/AAC.44.2.396-399.2000</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15071504">15071504</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Sultana A, Kallio P, Jansson A, Wang JS, Niemi J, Mantsala P, Schneider G</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Structure of the polyketide cyclase SnoaL reveals a novel mechanism for enzymatic aldol condensation.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">EMBO J 23:1911-21 (2004)<br>DOI:<a href="https://doi.org/10.1038/sj.emboj.7600201">10.1038/sj.emboj.7600201</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/16414075">16414075</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Kallio P, Sultana A, Niemi J, Mantsala P, Schneider G</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Crystal structure of the polyketide cyclase AknH with bound substrate and product analogue: implications for catalytic mechanism and product stereoselectivity.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Mol Biol 357:210-20 (2006)<br>DOI:<a href="https://doi.org/10.1016/j.jmb.2005.12.064">10.1016/j.jmb.2005.12.064</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/8655529">8655529</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Dickens ML, Ye J, Strohl WR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Cloning, sequencing, and analysis of aklaviketone reductase from Streptomyces sp. strain C5.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 178:3384-8 (1996)<br>DOI:<a href="https://doi.org/10.1128/JB.178.11.3384-3388.1996">10.1128/JB.178.11.3384-3388.1996</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17685523">17685523</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Leimkuhler C, Fridman M, Lupoli T, Walker S, Walsh CT, Kahne D</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Characterization of rhodosaminyl transfer by the AknS/AknT glycosylation complex and its use in reconstituting the biosynthetic pathway of aclacinomycin A.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Am Chem Soc 129:10546-50 (2007)<br>DOI:<a href="https://doi.org/10.1021/ja072909o">10.1021/ja072909o</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15911373">15911373</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lu W, Leimkuhler C, Gatto GJ Jr, Kruger RG, Oberthur M, Kahne D, Walsh CT</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">AknT is an activating protein for the glycosyltransferase AknS in L-aminodeoxysugar transfer to the aglycone of aclacinomycin A.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 12:527-34 (2005)<br>DOI:<a href="https://doi.org/10.1016/j.chembiol.2005.02.016">10.1016/j.chembiol.2005.02.016</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15078101">15078101</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lu W, Leimkuhler C, Oberthur M, Kahne D, Walsh CT</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">AknK is an L-2-deoxyfucosyltransferase in the biosynthesis of the anthracycline aclacinomycin A.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 43:4548-58 (2004)<br>DOI:<a href="https://doi.org/10.1021/bi035945i">10.1021/bi035945i</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17395717">17395717</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Alexeev I, Sultana A, Mantsala P, Niemi J, Schneider G</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Aclacinomycin oxidoreductase (AknOx) from the biosynthetic pathway of the antibiotic aclacinomycin is an unusual flavoenzyme with a dual active site.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Proc Natl Acad Sci U S A 104:6170-5 (2007)<br>DOI:<a href="https://doi.org/10.1073/pnas.0700579104">10.1073/pnas.0700579104</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/19744497">19744497</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lindqvist Y, Koskiniemi H, Jansson A, Sandalova T, Schnell R, Liu Z, Mantsala P, Niemi J, Schneider G</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Structural basis for substrate recognition and specificity in aklavinone-11-hydroxylase from rhodomycin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Mol Biol 393:966-77 (2009)<br>DOI:<a href="https://doi.org/10.1016/j.jmb.2009.09.003">10.1016/j.jmb.2009.09.003</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20116225">20116225</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Malla S, Niraula NP, Singh B, Liou K, Sohng JK</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Limitations in doxorubicin production from Streptomyces peucetius.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Microbiol Res 165:427-35 (2010)<br>DOI:<a href="https://doi.org/10.1016/j.micres.2009.11.006">10.1016/j.micres.2009.11.006</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/7592454">7592454</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Otten SL, Liu X, Ferguson J, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Cloning and characterization of the Streptomyces peucetius dnrQS genes encoding a daunosamine biosynthesis enzyme and a glycosyl transferase involved in daunorubicin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 177:6688-92 (1995)<br>DOI:<a href="https://doi.org/10.1128/JB.177.22.6688-6692.1995">10.1128/JB.177.22.6688-6692.1995</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/19619853">19619853</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Malla S, Niraula NP, Liou K, Sohng JK</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Enhancement of doxorubicin production by expression of structural sugar biosynthesis and glycosyltransferase genes in Streptomyces peucetius.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biosci Bioeng 108:92-8 (2009)<br>DOI:<a href="https://doi.org/10.1016/j.jbiosc.2009.03.002">10.1016/j.jbiosc.2009.03.002</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/9098063">9098063</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Dickens ML, Priestley ND, Strohl WR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">In vivo and in vitro bioconversion of epsilon-rhodomycinone glycoside to doxorubicin: functions of DauP, DauK, and DoxA.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 179:2641-50 (1997)<br>DOI:<a href="https://doi.org/10.1128/JB.179.8.2641-2650.1997">10.1128/JB.179.8.2641-2650.1997</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/9864344">9864344</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lomovskaya N, Otten SL, Doi-Katayama Y, Fonstein L, Liu XC, Takatsu T, Inventi-Solari A, Filippini S, Torti F, Colombo AL, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Doxorubicin overproduction in Streptomyces peucetius: cloning and characterization of the dnrU ketoreductase and dnrV genes and the doxA cytochrome P-450 hydroxylase gene.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 181:305-18 (1999)<br>DOI:<a href="https://doi.org/10.1128/JB.181.1.305-318.1999">10.1128/JB.181.1.305-318.1999</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15548527">15548527</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Jansson A, Koskiniemi H, Erola A, Wang J, Mantsala P, Schneider G, Niemi J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Aclacinomycin 10-hydroxylase is a novel substrate-assisted hydroxylase requiring S-adenosyl-L-methionine as cofactor.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 280:3636-44 (2005)<br>DOI:<a href="https://doi.org/10.1074/jbc.M412095200">10.1074/jbc.M412095200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11520231">11520231</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Wohlert SE, Wendt-Pienkowski E, Bao W, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Production of aromatic minimal polyketides by the daunorubicin polyketide synthase genes reveals the incompatibility of the heterologous DpsY and JadI cyclases.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Nat Prod 64:1077-80 (2001)<br>DOI:<a href="https://doi.org/10.1021/np010067f">10.1021/np010067f</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20358042">20358042</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Zhou H, Li Y, Tang Y</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Cyclization of aromatic polyketides from bacteria and fungi.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Nat Prod Rep 27:839-68 (2010)<br>DOI:<a href="https://doi.org/10.1039/b911518h">10.1039/b911518h</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17268612">17268612</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Hertweck C, Luzhetskyy A, Rebets Y, Bechthold A</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Type II polyketide synthases: gaining a deeper insight into enzymatic teamwork.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Nat Prod Rep 24:162-90 (2007)<br>DOI:<a href="https://doi.org/10.1039/b507395m">10.1039/b507395m</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/20422670">20422670</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Chen Y, Fan K, He Y, Xu X, Peng Y, Yu T, Jia C, Yang K</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Characterization of JadH as an FAD- and NAD(P)H-dependent bifunctional hydroxylase/dehydrase in jadomycin biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chembiochem 11:1055-60 (2010)<br>DOI:<a href="https://doi.org/10.1002/cbic.201000178">10.1002/cbic.201000178</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15776503">15776503</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Rix U, Wang C, Chen Y, Lipata FM, Remsing Rix LL, Greenwell LM, Vining LC, Yang K, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The oxidative ring cleavage in jadomycin biosynthesis: a multistep oxygenation cascade in a biosynthetic black box.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chembiochem 6:838-45 (2005)<br>DOI:<a href="https://doi.org/10.1002/cbic.200400395">10.1002/cbic.200400395</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15817470">15817470</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Chen YH, Wang CC, Greenwell L, Rix U, Hoffmeister D, Vining LC, Rohr J, Yang KQ</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Functional analyses of oxygenases in jadomycin biosynthesis and identification of JadH as a bifunctional oxygenase/dehydrase.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 280:22508-14 (2005)<br>DOI:<a href="https://doi.org/10.1074/jbc.M414229200">10.1074/jbc.M414229200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17570722">17570722</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Borissow CN, Graham CL, Syvitski RT, Reid TR, Blay J, Jakeman DL</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Stereochemical integrity of oxazolone ring-containing jadomycins.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chembiochem 8:1198-203 (2007)<br>DOI:<a href="https://doi.org/10.1002/cbic.200700204">10.1002/cbic.200700204</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17640665">17640665</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Mittler M, Bechthold A, Schulz GE</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Structure and action of the C-C bond-forming glycosyltransferase UrdGT2 involved in the biosynthesis of the antibiotic urdamycin.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Mol Biol 372:67-76 (2007)<br>DOI:<a href="https://doi.org/10.1016/j.jmb.2007.06.005">10.1016/j.jmb.2007.06.005</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/10662691">10662691</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Trefzer A, Hoffmeister D, Kunzel E, Stockert S, Weitnauer G, Westrich L, Rix U, Fuchser J, Bindseil KU, Rohr J, Bechthold A</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Function of glycosyltransferase genes involved in urdamycin A biosynthesis.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 7:133-42 (2000)<br>DOI:<a href="https://doi.org/10.1016/S1074-5521(00)00079-X">10.1016/S1074-5521(00)00079-X</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11410375">11410375</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Hoffmeister D, Ichinose K, Bechthold A</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Two sequence elements of glycosyltransferases involved in urdamycin biosynthesis are responsible for substrate specificity and enzymatic activity.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 8:557-67 (2001)<br>DOI:<a href="https://doi.org/10.1016/S1074-5521(01)00039-4">10.1016/S1074-5521(01)00039-4</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Rohr J, Schonewolf M, Udvarnoki G, Eckardt K, Schumann G, Wagner C, Beale JM, Sorey SD.</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Investigations on the biosynthesis of the angucycline group antibiotics aquayamycin and the urdamycins A and B. Results from the structural analysis of novel blocked mutant products.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Org Chem 58:2547-51 (1993)<br>DOI:<a href="https://doi.org/10.1021/jo00061a032">10.1021/jo00061a032</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15651811">15651811</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Zhu L, Ostash B, Rix U, Nur-E-Alam M, Mayers A, Luzhetskyy A, Mendez C, Salas JA, Bechthold A, Fedorenko V, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Identification of the function of gene lndM2 encoding a bifunctional oxygenase-reductase involved in the biosynthesis of the antitumor antibiotic landomycin E by Streptomyces globisporus 1912 supports the originally assigned structure for landomycinone.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Org Chem 70:631-8 (2005)<br>DOI:<a href="https://doi.org/10.1021/jo0483623">10.1021/jo0483623</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17061307">17061307</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Baig I, Kharel M, Kobylyanskyy A, Zhu L, Rebets Y, Ostash B, Luzhetskyy A, Bechthold A, Fedorenko VA, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">On the acceptor substrate of C-glycosyltransferase UrdGT2: three prejadomycin C-Glycosides from an engineered mutant of Streptomyces globisporus 1912 DeltalndE(urdGT2).</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Angew Chem Int Ed Engl 45:7842-6 (2006)<br>DOI:<a href="https://doi.org/10.1002/anie.200603176">10.1002/anie.200603176</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15123249">15123249</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ostash B, Rix U, Rix LL, Liu T, Lombo F, Luzhetskyy A, Gromyko O, Wang C, Brana AF, Mendez C, Salas JA, Fedorenko V, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Generation of new landomycins by combinatorial biosynthetic manipulation of the LndGT4 gene of the landomycin E cluster in S. globisporus.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Biol 11:547-55 (2004)<br>DOI:<a href="https://doi.org/10.1016/j.chembiol.2004.03.011">10.1016/j.chembiol.2004.03.011</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/17013601">17013601</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lombo F, Menendez N, Salas JA, Mendez C</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The aureolic acid family of antitumor compounds: structure, mode of action, biosynthesis, and novel derivatives.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Appl Microbiol Biotechnol 73:1-14 (2006)<br>DOI:<a href="https://doi.org/10.1007/s00253-006-0511-6">10.1007/s00253-006-0511-6</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12022840">12022840</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Trefzer A, Blanco G, Remsing L, Kunzel E, Rix U, Lipata F, Brana AF, Mendez C, Rohr J, Bechthold A, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Rationally designed glycosylated premithramycins: hybrid aromatic polyketides using genes from three different biosynthetic pathways.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Am Chem Soc 124:6056-62 (2002)<br>DOI:<a href="https://doi.org/10.1021/ja017385l">10.1021/ja017385l</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/10652287">10652287</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Lozano MJ, Remsing LL, Quiros LM, Brana AF, Fernandez E, Sanchez C, Mendez C, Rohr J, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Characterization of two polyketide methyltransferases involved in the biosynthesis of the antitumor drug mithramycin by Streptomyces argillaceus.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 275:3065-74 (2000)<br>DOI:<a href="https://doi.org/10.1074/jbc.275.5.3065">10.1074/jbc.275.5.3065</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/10660060">10660060</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Blanco G, Fernandez E, Fernandez MJ, Brana AF, Weissbach U, Kunzel E, Rohr J, Mendez C, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Characterization of two glycosyltransferases involved in early glycosylation steps during biosynthesis of the antitumor polyketide mithramycin by Streptomyces argillaceus.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Mol Gen Genet 262:991-1000 (2000)<br>DOI:<a href="https://doi.org/10.1007/PL00008667">10.1007/PL00008667</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/15712316">15712316</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Nur-e-Alam M, Mendez C, Salas JA, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Elucidation of the glycosylation sequence of mithramycin biosynthesis: isolation of 3A-deolivosylpremithramycin B and its conversion to premithramycin B by glycosyltransferase MtmGII.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chembiochem 6:632-6 (2005)<br>DOI:<a href="https://doi.org/10.1002/cbic.200400309">10.1002/cbic.200400309</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/9733697">9733697</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Fernandez E, Weissbach U, Sanchez Reillo C, Brana AF, Mendez C, Rohr J, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Identification of two genes from Streptomyces argillaceus encoding glycosyltransferases involved in transfer of a disaccharide during biosynthesis of the antitumor drug mithramycin.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 180:4929-37 (1998)<br>DOI:<a href="https://doi.org/10.1128/JB.180.18.4929-4937.1998">10.1128/JB.180.18.4929-4937.1998</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/19364090">19364090</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Beam MP, Bosserman MA, Noinaj N, Wehenkel M, Rohr J</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Crystal structure of Baeyer-Villiger monooxygenase MtmOIV, the key enzyme of the mithramycin biosynthetic pathway .</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 48:4476-87 (2009)<br>DOI:<a href="https://doi.org/10.1021/bi8023509">10.1021/bi8023509</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/16511225">16511225</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Wang C, Gibson M, Rohr J, Oliveira MA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Crystallization and X-ray diffraction properties of Baeyer-Villiger monooxygenase MtmOIV from the mithramycin biosynthetic pathway in Streptomyces argillaceus.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Acta Crystallogr Sect F Struct Biol Cryst Commun 61:1023-6 (2005)<br>DOI:<a href="https://doi.org/10.1107/S1744309105033221">10.1107/S1744309105033221</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/12813091">12813091</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Rodriguez D, Quiros LM, Brana AF, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Purification and characterization of a monooxygenase involved in the biosynthetic pathway of the antitumor drug mithramycin.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 185:3962-5 (2003)<br>DOI:<a href="https://doi.org/10.1128/JB.185.13.3962-3965.2003">10.1128/JB.185.13.3962-3965.2003</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11851469">11851469</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Biosynthetic Studies of Daunorubicin and Tetracenomycin C.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Chem Rev 97:2525-2536 (1997)<br>DOI:<a href="https://doi.org/10.1021/cr960022x">10.1021/cr960022x</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/8244926">8244926</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Summers RG, Wendt-Pienkowski E, Motamedi H, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">The tcmVI region of the tetracenomycin C biosynthetic gene cluster of Streptomyces glaucescens encodes the tetracenomycin F1 monooxygenase, tetracenomycin F2 cyclase, and, most likely, a second cyclase.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 175:7571-80 (1993)<br>DOI:<a href="https://doi.org/10.1128/JB.175.23.7571-7580.1993">10.1128/JB.175.23.7571-7580.1993</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/8218177">8218177</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Shen B, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Tetracenomycin F2 cyclase: intramolecular aldol condensation in the biosynthesis of tetracenomycin C in Streptomyces glaucescens.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 32:11149-54 (1993)<br>DOI:<a href="https://doi.org/10.1021/bi00092a026">10.1021/bi00092a026</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/8329392">8329392</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Shen B, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Tetracenomycin F1 monooxygenase: oxidation of a naphthacenone to a naphthacenequinone in the biosynthesis of tetracenomycin C in Streptomyces glaucescens.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Biochemistry 32:6656-63 (1993)<br>DOI:<a href="https://doi.org/10.1021/bi00077a019">10.1021/bi00077a019</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/1548230">1548230</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Summers RG, Wendt-Pienkowski E, Motamedi H, Hutchinson CR</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Nucleotide sequence of the tcmII-tcmIV region of the tetracenomycin C biosynthetic gene cluster of Streptomyces glaucescens and evidence that the tcmN gene encodes a multifunctional cyclase-dehydratase-O-methyl transferase.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Bacteriol 174:1810-20 (1992)<br>DOI:<a href="https://doi.org/10.1128/JB.174.6.1810-1820.1992">10.1128/JB.174.6.1810-1820.1992</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/18388203">18388203</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ames BD, Korman TP, Zhang W, Smith P, Vu T, Tang Y, Tsai SC</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Crystal structure and functional analysis of tetracenomycin ARO/CYC: implications for cyclization specificity of aromatic polyketides.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Proc Natl Acad Sci U S A 105:5349-54 (2008)<br>DOI:<a href="https://doi.org/10.1073/pnas.0709223105">10.1073/pnas.0709223105</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11009387">11009387</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Rafanan ER Jr, Hutchinson CR, Shen B</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Triple hydroxylation of tetracenomycin A2 to tetracenomycin C involving two molecules of O(2) and one molecule of H(2)O.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Org Lett 2:3225-7 (2000)<br>DOI:<a href="https://doi.org/10.1021/ol0002267">10.1021/ol0002267</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/18310024">18310024</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Ramos A, Lombo F, Brana AF, Rohr J, Mendez C, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Biosynthesis of elloramycin in Streptomyces olivaceus requires glycosylation by enzymes encoded outside the aglycon cluster.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">Microbiology 154:781-8 (2008)<br>DOI:<a href="https://doi.org/10.1099/mic.0.2007/014035-0">10.1099/mic.0.2007/014035-0</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Reference</span></th> <td class="td31 defd"><div class="cel">PMID:<a href="https://www.ncbi.nlm.nih.gov/pubmed/11376004">11376004</a></div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Authors</span></th> <td class="td30 repd"><div class="cel">Patallo EP, Blanco G, Fischer C, Brana AF, Rohr J, Mendez C, Salas JA</div></td></tr> <tr><th class="th31 rept tal vtop"><span class="nowrap"> Title</span></th> <td class="td31 repd"><div class="cel">Deoxysugar methylation during biosynthesis of the antitumor polyketide elloramycin by Streptomyces olivaceus. Characterization of three methyltransferase genes.</div></td></tr> <tr><th class="th30 rept tal vtop"><span class="nowrap"> Journal</span></th> <td class="td30 repd"><div class="cel">J Biol Chem 276:18765-74 (2001)<br>DOI:<a href="https://doi.org/10.1074/jbc.M101225200">10.1074/jbc.M101225200</a></div></td></tr> <tr><th class="th31 deft tal vtop"><span class="nowrap">Related<br>pathway</span></th> <td class="td31 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/rn00253">rn00253</a> </span></td><td>Tetracycline biosynthesis</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/rn01056">rn01056</a> </span></td><td>Biosynthesis of type II polyketide backbone</td></tr></table></td></tr> <tr><th class="th30 deft tal vtop"><span class="nowrap">KO pathway</span></th> <td class="td30 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/entry/ko01057">ko01057</a> </span></td><td> </td></tr></table></td></tr> <tr><th class="th31 deft tal vmid"><span class="nowrap">LinkDB</span></th> <td class="td31 defd"><button class="btn" onclick="location.href='https://www.genome.jp/dbget-bin/get_linkdb?pathway+rn01057';return false;">All DBs</button></td></tr> </table></td></tr></table> <br></td></tr></table> <a href="/dbget/">DBGET</a> integrated database retrieval system</div> </body> </html>