Structure of PDB 1hyg Chain A Binding Site BS01
Receptor Information
>1hyg Chain A (length=313) Species:
2190
(Methanocaldococcus jannaschii) [
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MKVTIIGASGRVGSATALLLAKEPFMKDLVLIGREHSINKLEGLREDIYD
ALAGTRSDANIYVESDENLRIIDESDVVIITSGVPRKEGMSRMDLAKTNA
KIVGKYAKKIAEICDTKIFVITNPVDVMTYKALVDSKFERNQVFGLGTHL
DSLRFKVAIAKFFGVHIDEVRTRIIGEHGDSMVPLLSATSIGGIPIQKFE
RFKELPIDEIIEDVKTKGEQIIRLKGGSEFGPAAAILNVVRCIVNNEKRL
LTLSAYVDGEFDGIRDVCIGVPVKIGRDGIEEVVSIELDKDEIIAFRKSA
EIIKKYCEEVKNL
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
1hyg Chain A Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
1hyg
Crystal structure of the MJ0490 gene product of the hyperthermophilic archaebacterium Methanococcus jannaschii, a novel member of the lactate/malate family of dehydrogenases
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
G7 S9 G10 R11 R34 S37 T81 G83 T122 N123 G227 S228
Binding residue
(residue number reindexed from 1)
G7 S9 G10 R11 R34 S37 T81 G83 T122 N123 G227 S228
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R92 D151 R154 H178
Catalytic site (residue number reindexed from 1)
R92 D151 R154 H178
Enzyme Commision number
1.1.1.375
: L-2-hydroxycarboxylate dehydrogenase [NAD(P)(+)].
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004459
L-lactate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0102443
L-2-hydroxycarboxylate dehydrogenase (NAD+) activity
Biological Process
GO:0006089
lactate metabolic process
GO:0006090
pyruvate metabolic process
GO:0006099
tricarboxylic acid cycle
GO:0019752
carboxylic acid metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1hyg
,
PDBe:1hyg
,
PDBj:1hyg
PDBsum
1hyg
PubMed
11292347
UniProt
Q60176
|MDH_METJA L-2-hydroxycarboxylate dehydrogenase (NAD(P)(+)) (Gene Name=mdh)
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