Structure of PDB 4nu5 Chain A Binding Site BS01
Receptor Information
>4nu5 Chain A (length=328) Species:
316
(Stutzerimonas stutzeri) [
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LPKLVITHRVHEEILQLLAPHCELITNQTDSTLTREEILRRCRDAQAMMA
FMPDRVDADFLQACPELRVIGCALKGFDNFDVDACTARGVWLTFVPDLLT
VPTAELAIGLAVGLGRHLRAADAFVRSGKFRGWQPRFYGTGLDNATVGFL
GMGAIGLAMADRLQGWGATLQYHAAKALDTQTEQRLGLRQVACSELFASS
DFILLALPLNADTLHLVNAELLALVRPGALLVNPCRGSVVDEAAVLAALE
RGQLGGYAADVFEMEDWARADRPQQIDPALLAHPNTLFTPHIGSAVRAVA
LEIERCAAQNILQALAGERPINAVNRLP
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
4nu5 Chain A Residue 800 [
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Receptor-Ligand Complex Structure
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PDB
4nu5
Chemical rescue and inhibition studies to determine the role of arg301 in phosphite dehydrogenase.
Resolution
2.35 Å
Binding residue
(original residue number in PDB)
K76 G77 L100 T104 G152 M153 G154 A155 I156 A175 A176 A207 L208 P209 T214 P235 C236 R237
Binding residue
(residue number reindexed from 1)
K75 G76 L99 T103 G151 M152 G153 A154 I155 A174 A175 A206 L207 P208 T213 P234 C235 R236
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L100 R237 D261 E266 H292
Catalytic site (residue number reindexed from 1)
L99 R236 D260 E265 H291
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:4nu5
,
PDBe:4nu5
,
PDBj:4nu5
PDBsum
4nu5
PubMed
24498026
UniProt
O69054
|PTXD_STUST Phosphonate dehydrogenase (Gene Name=ptxD)
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