Structure of PDB 2vss Chain F Binding Site BS01
Receptor Information
>2vss Chain F (length=246) Species:
294
(Pseudomonas fluorescens) [
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TYEGRWKTVKVEIEDGIAFVILNRPERRNAMSPTLNREMIDVLETLEQDP
AAGVLVLTGAGEAWTAGMDLKEYFREVDAGPEILQEKIRREASQWQWKLL
RMYAKPTIAMVNGWCFGGGFSPLVACDLAICADEATFGLSEINWGIPPGN
LVSKAMADTVGHRQSLYYIMTGKTFGGQKAAEMGLVNESVPLAQLREVTI
ELARNLLEKNPVVLRAAKHGFKRCRELTWEQNEDYLYAKLDQSRLL
Ligand information
Ligand ID
ACO
InChI
InChI=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
InChIKey
ZSLZBFCDCINBPY-ZSJPKINUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
CACTVS 3.341
CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
ACDLabs 10.04
O=C(SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O)C
CACTVS 3.341
CC(=O)SCCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C23 H38 N7 O17 P3 S
Name
ACETYL COENZYME *A
ChEMBL
CHEMBL1230809
DrugBank
ZINC
ZINC000008551095
PDB chain
2vss Chain F Residue 1249 [
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Receptor-Ligand Complex Structure
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PDB
2vss
A Ternary Complex of Hydroxycinnamoyl-Coa Hydratase-Lyase (Hchl) with Acetyl-Coa and Vanillin Gives Insights Into Substrate Specificity and Mechanism.
Resolution
2.22 Å
Binding residue
(original residue number in PDB)
E28 R29 R30 A32 A68 M70 D71 L72 F76 W116 F118 S142
Binding residue
(residue number reindexed from 1)
E26 R27 R28 A30 A66 M68 D69 L70 F74 W114 F116 S140
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M70 Y75 D80 R92 Q96 G120 S123 S142 E143 I148 P150 G151 Y239
Catalytic site (residue number reindexed from 1)
M68 Y73 D78 R90 Q94 G118 S121 S140 E141 I146 P148 G149 Y237
Enzyme Commision number
4.1.2.61
: feruloyl-CoA hydratase/lyase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0050547
feruloyl-CoA hydratase/lyase activity
Biological Process
GO:0008300
isoprenoid catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2vss
,
PDBe:2vss
,
PDBj:2vss
PDBsum
2vss
PubMed
18479250
UniProt
O69762
|HCHL_PSEFL Hydroxycinnamoyl-CoA hydratase-lyase
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