Structure of PDB 4pze Chain C Binding Site BS02
Receptor Information
>4pze Chain C (length=283) Species:
381666
(Cupriavidus necator H16) [
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SIRTVGIVGAGTMGNGIAQACAVVGLNVVMVDISDAAVQKGVATVASSLD
RLIKKEKLTEADKASALARIKGSTSYDDLKATDIVIEAATENYDLKVKIL
KQIDGIVGENVIIASNTSSISITKLAAVTSRADRFIGMHFFNPVPVMALV
ELIRGLQTSDTTHAAVEALSKQLGKYPITVKNSPGFVVNRILCPMINEAF
CVLGEGLASPEEIDEGMKLGCNHPIGPLALADMIGLDTMLAVMEVLYTEF
ADPKYRPAMLMREMVAAGYLGRKTGRGVYVYSK
Ligand information
Ligand ID
CAA
InChI
InChI=1S/C25H40N7O18P3S/c1-13(33)8-16(35)54-7-6-27-15(34)4-5-28-23(38)20(37)25(2,3)10-47-53(44,45)50-52(42,43)46-9-14-19(49-51(39,40)41)18(36)24(48-14)32-12-31-17-21(26)29-11-30-22(17)32/h11-12,14,18-20,24,36-37H,4-10H2,1-3H3,(H,27,34)(H,28,38)(H,42,43)(H,44,45)(H2,26,29,30)(H2,39,40,41)/t14-,18-,19-,20+,24-/m1/s1
InChIKey
OJFDKHTZOUZBOS-CITAKDKDSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(=O)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
CACTVS 3.341
CC(=O)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)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
OpenEye OEToolkits 1.5.0
CC(=O)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
ACDLabs 10.04
O=C(C)CC(=O)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
Formula
C25 H40 N7 O18 P3 S
Name
ACETOACETYL-COENZYME A
ChEMBL
DrugBank
DB03059
ZINC
ZINC000096014521
PDB chain
4pze Chain C Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4pze
Crystal structure and biochemical properties of the (S)-3-hydroxybutyryl-CoA dehydrogenase PaaH1 from Ralstonia eutropha
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
K56 S119 H140 F142 N143 M148 N190 I226 I235
Binding residue
(residue number reindexed from 1)
K55 S118 H139 F141 N142 M147 N189 I225 I234
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
S119 H140 E152 N190
Catalytic site (residue number reindexed from 1)
S118 H139 E151 N189
Enzyme Commision number
1.1.1.35
: 3-hydroxyacyl-CoA dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003857
3-hydroxyacyl-CoA dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0070403
NAD+ binding
Biological Process
GO:0006631
fatty acid metabolic process
GO:0009056
catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4pze
,
PDBe:4pze
,
PDBj:4pze
PDBsum
4pze
PubMed
24792376
UniProt
Q0KEY8
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