Structure of PDB 4okn Chain G Binding Site BS01
Receptor Information
>4okn Chain G (length=331) Species:
9606
(Homo sapiens) [
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ATLKDQLIYNLLKEEQTPQNKITVVGVGAVGMACAISILMKDLADELALV
DVIEDKLKGEMMDLQHGSLFLRTPKIVSGKDYNVTANSKLVIITAGARQQ
EGESRLNLVQRNVNIFKFIIPNVVKYSPNCKLLIVSNPVDILTYVAWKIS
GFPKNRVIGSGCNLDSARFRYLMGERLGVHPLSCHGWVLGEHGDSSVPVW
SGMNVAGVSLKTLHPDLGTDKDKEQWKEVHKQVVESAYEVIKLKGYTSWA
IGLSVADLAESIMKNLRRVHPVSTMIKGLYGIKDDVFLSVPCILGQNGIS
DLVKVTLTSEEEARLKKSADTLWGIQKELQF
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
4okn Chain G Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4okn
Structures of lactate dehydrogenase A (LDHA) in apo, ternary and inhibitor-bound forms.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
G29 A30 V31 D52 V53 K57 T95 A96 G97 A98 R99 V136 N138 H193 T248 I252
Binding residue
(residue number reindexed from 1)
G28 A29 V30 D51 V52 K56 T94 A95 G96 A97 R98 V135 N137 H192 T247 I251
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R106 D166 R169 H193
Catalytic site (residue number reindexed from 1)
R105 D165 R168 H192
Enzyme Commision number
1.1.1.27
: L-lactate dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004459
L-lactate dehydrogenase activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042802
identical protein binding
GO:0045296
cadherin binding
Biological Process
GO:0006089
lactate metabolic process
GO:0006090
pyruvate metabolic process
GO:0006096
glycolytic process
GO:0019752
carboxylic acid metabolic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0016020
membrane
GO:0070062
extracellular exosome
GO:1990204
oxidoreductase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4okn
,
PDBe:4okn
,
PDBj:4okn
PDBsum
4okn
PubMed
25664730
UniProt
P00338
|LDHA_HUMAN L-lactate dehydrogenase A chain (Gene Name=LDHA)
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