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Substrate Report for: Acetyl-CoA

Name Class
Acetyl-CoATypeCoA
Aminopurin
Other_Name (5)
Chemical_NomenclatureS-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] ethanethioate
FormulaC23H38N7O17P3S
MW809.57
PaperNazi_2005_Biochemistry_44_13560
Lejon_2008_J.Mol.Biol_377_935
Fiebig_2020_Nat.Commun_11_4723
Structure6YUS
2VAT
CommentAcetyl CoA participates in the biosynthesis of fatty acids and sterols, in the oxidation of fatty acids and in the metabolism of many amino acids. Acetyl-CoA also acts as a biological acetylating agent
Gene_locuscepac-cefg
neime-r0tza2
CID444493
FamilyHomoserine_transacetylase
AlphaBeta_hydrolase
InChIKeyZSLZBFCDCINBPY-ZSJPKINUSA-N
CanonicalSMILESCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)(O)O)O
InChIInChI=1S/C23H38N7O17P3S/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38)/t13-,16-,17-,18+,22-/m1/s1
WikipediaAcetyl-CoA

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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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