Structure of PDB 5vt6 Chain C Binding Site BS01
Receptor Information
>5vt6 Chain C (length=240) Species:
320372
(Burkholderia pseudomallei 1710b) [
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KRVAFVTGGMGGLGAAISRRLHDAGMAVAVSHSERNDHVSTWLMHERDAG
RDFKAYAVDVADFESCERCAEKVLADFGKVDVLINNAGITRDATFMKMTK
GDWDAVMRTDLDAMFNVTKQFIAGMVERRFGRIVNIGSVNGSRGAFGQAN
YASAKAGIHGFTKTLALETAKRGITVNTVSPGYLATVPQDVLEAKILPQI
PVGRLGRPDEVAALIAFLCSDDAGFVTGADLAINGGMHMS
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
5vt6 Chain C Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5vt6
Crystal structure of Acetoacetyl-CoA Reductase from Burkholderia pseudomallei 1710b complexed with NADP
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
G11 G14 G15 L16 H35 S36 N39 V61 D62 V63 N89 A90 G91 I92 I139 Y154 K158 P184 Y186 L187
Binding residue
(residue number reindexed from 1)
G8 G11 G12 L13 H32 S33 N36 V58 D59 V60 N86 A87 G88 I89 I136 Y151 K155 P181 Y183 L184
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G15 D105 S141 Y154 K158
Catalytic site (residue number reindexed from 1)
G12 D102 S138 Y151 K155
Enzyme Commision number
1.1.1.36
: acetoacetyl-CoA reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0018454
acetoacetyl-CoA reductase activity
Biological Process
GO:0042619
poly-hydroxybutyrate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5vt6
,
PDBe:5vt6
,
PDBj:5vt6
PDBsum
5vt6
PubMed
UniProt
Q3JJT1
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