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KEGG COMPOUND: C09813
<!doctype html> <html><head> <title>KEGG COMPOUND: C09813</title> <link type="text/css" rel="stylesheet" href="/css/gn2.css?1744318561"> <link type="text/css" rel="stylesheet" href="/css/bget.css?1744318561"> <meta name="viewport" content="width=device-width, initial-scale=1.0"> <link type="text/css" rel="stylesheet" href="/css/bgetm.css?1744318561" 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; 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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/kegg2.gif"></a></td><td> </td><td><a name="compound:C09813"></a><font class="title2">COMPOUND: C09813</font></td><td class="tar vbot"><button class="btn" onclick="javascript:void(window.open('/kegg/document/help_bget_compound.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="fr2 w1"> <table width="650" class="w2"> <tr><th class="th20 deft tal vmid"><span class="nowrap">Entry</span></th> <td class="td20 defd"><table class="w1" width="100%"><tr><td class="tal pd0"><code><span class="nowrap">C09813 Compound <br> </span></code></td></tr></table></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Name</span></th> <td class="td21 defd"><div class="cel"><div class="cel">2-Oxocyclohexane-1-carbonyl-CoA;<br> 2-Ketocyclohexane-1-carboxyl-CoA<br> </div></div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Formula</span></th> <td class="td20 defd"><div class="cel">C28H44N7O18P3S<br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Exact mass</span></th> <td class="td21 defd"><div class="cel">891.1676<br> </div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Mol weight</span></th> <td class="td20 defd"><div class="cel">891.67<br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Structure</span></th> <td class="td21 defd"><a href="/Fig/compound/C09813.gif"><img name="img0" src="/Fig/compound/C09813.gif" style="max-width:600px" border=0></a><br> <button class="btn" onclick="location.href='/entry/-f+m+C09813';return false;">Mol file</button><button class="btn" onclick="location.href='/entry/-f+k+C09813';return false;">KCF file</button><button class="btn" onclick="location.href='/tools-bin/strsearch_view?ENTRY=C09813&PROGRAM=simcomp&DATABASE=compound';return false;">DB search</button></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Reaction</span></th> <td class="td20 defd"><div class="cel"><a href="/entry/R05582">R05582</a> <a href="/entry/R05592">R05592</a><br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Pathway</span></th> <td class="td21 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00362+C09813">map00362</a> </span></td><td>Benzoate degradation</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01100+C09813">map01100</a> </span></td><td>Metabolic pathways</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01120+C09813">map01120</a> </span></td><td>Microbial metabolism in diverse environments</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01220+C09813">map01220</a> </span></td><td>Degradation of aromatic compounds</td></tr></table></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Module</span></th> <td class="td20 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00540+C09813">M00540</a> </span></td><td>Benzoate degradation, cyclohexanecarboxylic acid =>pimeloyl-CoA</td></tr></table></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Enzyme</span></th> <td class="td21 defd"><div class="cel">1.1.1.- 3.1.2.-<br> </div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Brite</span></th> <td class="td20 defd"><div class="cel"><span class="nowrap">Lipids [BR:<a href="/brite/br08002+C09813">br08002</a>]<br> FA Fatty acyls<br> FA07 Fatty esters<br> FA0705 Fatty acyl CoAs<br> C09813 2-Oxocyclohexane-1-carbonyl-CoA<br> </span></div><button class="btn" onclick="location.href='/kegg-bin/search_brite?option=-a&search_string=C09813';return false;">BRITE hierarchy</button></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Other DBs</span></th> <td class="td21 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">PubChem: </span></td><td><a href="https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?sid=12001">12001</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">ChEBI: </span></td><td><a href="https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:27664">27664</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">LIPIDMAPS: </span></td><td><a href="http://www.lipidmaps.org/data/LMSDRecord.php?LMID=LMFA07050193">LMFA07050193</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">NIKKAJI: </span></td><td><a href="https://jglobal.jst.go.jp/en/redirect?Nikkaji_No=J2.771.174J">J2.771.174J</a></td></tr></table></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">KCF data</span></th> <td class="td20 defd"><button class="btn" id="kcfb1">Show</button><div class="kcfd" id="kcfd1"><br>ATOM 57<br> 1 S2a S 12.2500 -20.3000<br> 2 C1b C 13.4400 -19.6000<br> 3 C1b C 14.7000 -20.3000<br> 4 N1b N 15.8900 -19.6000<br> 5 C5a C 17.0800 -20.3000<br> 6 C1b C 18.3400 -19.6000<br> 7 C1b C 19.5300 -20.3000<br> 8 N1b N 20.7200 -19.6000<br> 9 C5a C 21.9800 -20.3000<br> 10 C1c C 23.1700 -19.6000<br> 11 C1d C 24.3600 -20.3000<br> 12 C1b C 25.5500 -19.6000<br> 13 O2b O 26.8100 -20.3000<br> 14 O5a O 17.0800 -21.7000<br> 15 O5a O 21.9800 -21.7000<br> 16 O1a O 23.1700 -18.2000<br> 17 C1a C 24.3600 -18.9000<br> 18 C1a C 24.3600 -21.7000<br> 19 P1b P 28.2100 -20.3000<br> 20 O1c O 29.6100 -20.3000<br> 21 O1c O 28.2100 -21.7000<br> 22 C1y C 21.7000 -15.3300<br> 23 C1y C 23.1000 -15.3300<br> 24 C1y C 23.5200 -14.0000<br> 25 O2x O 22.4000 -13.1600<br> 26 C1y C 21.2800 -14.0000<br> 27 C1b C 24.8500 -13.5800<br> 28 O1a O 20.8600 -16.4500<br> 29 O2b O 23.9400 -16.4500<br> 30 P1b P 25.3400 -16.4500<br> 31 O1c O 25.3400 -15.0500<br> 32 O1c O 26.7400 -16.4500<br> 33 O1c O 25.3400 -17.8500<br> 34 C8y C 17.1500 -12.1800<br> 35 C8y C 17.1500 -13.5800<br> 36 N4y N 19.6000 -13.5800<br> 37 C8x C 19.6000 -12.1800<br> 38 N5x N 18.3400 -11.4800<br> 39 C8y C 15.9600 -11.4800<br> 40 N5x N 14.7000 -12.1800<br> 41 C8x C 14.7000 -13.5800<br> 42 N5x N 15.9600 -14.2800<br> 43 N1a N 15.9600 -10.0800<br> 44 O2b O 26.8100 -14.0000<br> 45 P1b P 28.2100 -14.0000<br> 46 O1c O 28.2100 -12.6000<br> 47 O1c O 29.6100 -14.0000<br> 48 O2c O 28.2100 -17.2200<br> 49 C5a C 11.1300 -19.6700<br> 50 C1y C 10.0100 -20.3000<br> 51 O5a O 11.1300 -18.3400<br> 52 C5x C 8.8900 -19.6700<br> 53 C1x C 10.0100 -21.5600<br> 54 C1x C 7.7000 -20.3000<br> 55 O5x O 8.8900 -18.3400<br> 56 C1x C 8.8900 -22.2600<br> 57 C1x C 7.7000 -21.6300<br> BOND 60<br> 1 1 2 1<br> 2 2 3 1<br> 3 3 4 1<br> 4 4 5 1<br> 5 5 6 1<br> 6 6 7 1<br> 7 7 8 1<br> 8 8 9 1<br> 9 9 10 1<br> 10 10 11 1<br> 11 11 12 1<br> 12 12 13 1<br> 13 5 14 2<br> 14 9 15 2<br> 15 10 16 1 #Down<br> 16 11 17 1<br> 17 11 18 1<br> 18 13 19 1<br> 19 19 20 2<br> 20 19 21 1<br> 21 22 23 1<br> 22 23 24 1<br> 23 24 25 1<br> 24 25 26 1<br> 25 22 26 1<br> 26 24 27 1 #Down<br> 27 22 28 1 #Up<br> 28 23 29 1 #Up<br> 29 29 30 1<br> 30 30 31 1<br> 31 30 32 1<br> 32 30 33 2<br> 33 34 35 2<br> 34 35 36 1<br> 35 36 37 1<br> 36 37 38 2<br> 37 34 38 1<br> 38 34 39 1<br> 39 39 40 2<br> 40 40 41 1<br> 41 41 42 2<br> 42 35 42 1<br> 43 39 43 1<br> 44 26 36 1 #Down<br> 45 27 44 1<br> 46 44 45 1<br> 47 45 46 1<br> 48 45 47 2<br> 49 45 48 1<br> 50 19 48 1<br> 51 1 49 1<br> 52 49 50 1<br> 53 49 51 2<br> 54 50 52 1<br> 55 50 53 1<br> 56 52 54 1<br> 57 52 55 2<br> 58 53 56 1<br> 59 54 57 1<br> 60 56 57 1<br> </div></td></tr> </table></td></tr></table> <br><span style="font-size:12px"><a href="/entry/cpd_ja:C09813">» Japanese version</a></span><br><br></td><td class="vtop"><div class="aw" style="margin-top:46px;"><div class="fm at th20"> All links </div> <div class="fm"><pre class="fm" style="margin-left:1em"> <span style="color:#006"><a href="/dbget-bin/get_linkdb?-t+6+cpd:C09813">Chemical substance (4)</a></span> <a href="/dbget-bin/get_linkdb?-t+pubchem+cpd:C09813">PubChem (1)</a> <a href="/dbget-bin/get_linkdb?-t+chebi+cpd:C09813">ChEBI (1)</a> <a href="/dbget-bin/get_linkdb?-t+lipidmaps+cpd:C09813">LIPIDMAPS (1)</a> <a href="/dbget-bin/get_linkdb?-t+nikkaji+cpd:C09813">NIKKAJI (1)</a> <a href="/dbget-bin/get_linkdb?-t+alldb+cpd:C09813">All databases (4)</a> <br><a href="/dbget-bin/get_linkdb?-N+cpd:C09813">Download RDF</a> </pre> </div></div> </td></tr></table> <a href="/dbget/">DBGET</a> integrated database retrieval system</div> </body> </html>