Structure of PDB 4n5m Chain B Binding Site BS01
Receptor Information
>4n5m Chain B (length=246) Species:
381666
(Cupriavidus necator H16) [
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MTQRIAYVTGGMGGIGTAICQRLAKDGFRVVAGCGPNSPRREKWLEQQKA
LGFDFIASEGNVADWDSTKTAFDKVKSEVGEVDVLINNAGITRDVVFRKM
TRADWDAVIDTNLTSLFNVTKQVIDGMADRGWGRIVNISSVNGQKGQFGQ
TNYSTAKAGLHGFTMALAQEVATKGVTVNTVSPGYIATDMVKAIRQDVLD
KIVATIPVKRLGLPEEIASICAWLSSEESGFSTGADFSLNGGLHMG
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
4n5m Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4n5m
Crystal structure of (R)-3-hydroxybutyryl-CoA dehydrogenase PhaB from Ralstonia eutropha
Resolution
1.34 Å
Binding residue
(original residue number in PDB)
D94 Q147 F148 Q150 Y153 Y185 M190 V191 I194 R195
Binding residue
(residue number reindexed from 1)
D94 Q147 F148 Q150 Y153 Y185 M190 V191 I194 R195
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N112 S140 Y153 K157
Catalytic site (residue number reindexed from 1)
N112 S140 Y153 K157
Enzyme Commision number
1.1.1.36
: acetoacetyl-CoA reductase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0018454
acetoacetyl-CoA reductase activity
Biological Process
GO:0042619
poly-hydroxybutyrate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4n5m
,
PDBe:4n5m
,
PDBj:4n5m
PDBsum
4n5m
PubMed
24211201
UniProt
P14697
|PHAB_CUPNH Acetoacetyl-CoA reductase (Gene Name=phaB)
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