Structure of PDB 4e5n Chain A Binding Site BS01
Receptor Information
>4e5n Chain A (length=329) Species:
316
(Stutzerimonas stutzeri) [
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MLPKLVITHRVHEEILQLLAPHCELITNQTDSTLTREEILRRCRDAQAMM
AFMPDRVDADFLQACPELRVIGCALKGFDNFDVDACTARGVWLTFVPDLL
TVPTAELAIGLAVGLGRHLRAADAFVRSGKFRGWQPRFYGTGLDNATVGF
LGMGAIGLAMADRLQGWGATLQYHEAKALDTQTEQRLGLRQVACSELFAS
SDFILLALPLNADTLHLVNAELLALVRPGALLVNPCRGSVVDEAAVLAAL
ERGQLGGYAADVFEMEDWARADRPQQIDPALLAHPNTLFTPHIGSAVRAV
RLEIERCAAQNILQALAGERPINAVNRLP
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
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)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)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)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]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)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
4e5n Chain A Residue 800 [
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Receptor-Ligand Complex Structure
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PDB
4e5n
Crystal structures of phosphite dehydrogenase provide insights into nicotinamide cofactor regeneration.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
K76 L100 L151 G152 G154 A155 I156 E175 A176 L208 P209 P235 C236 R237 H292
Binding residue
(residue number reindexed from 1)
K76 L100 L151 G152 G154 A155 I156 E175 A176 L208 P209 P235 C236 R237 H292
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L100 R237 D261 E266 H292
Catalytic site (residue number reindexed from 1)
L100 R237 D261 E266 H292
Enzyme Commision number
1.20.1.1
: phosphonate dehydrogenase.
Gene Ontology
Molecular Function
GO:0008465
hydroxypyruvate reductase (NADH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0030267
glyoxylate reductase (NADPH) activity
GO:0050609
phosphonate dehydrogenase activity
GO:0051287
NAD binding
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:4e5n
,
PDBe:4e5n
,
PDBj:4e5n
PDBsum
4e5n
PubMed
22564171
UniProt
O69054
|PTXD_STUST Phosphonate dehydrogenase (Gene Name=ptxD)
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