Structure of PDB 5w8l Chain D Binding Site BS01
Receptor Information
>5w8l Chain D (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
5w8l Chain D Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5w8l
Discovery and Optimization of Potent, Cell-Active Pyrazole-Based Inhibitors of Lactate Dehydrogenase (LDH).
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
G28 V30 D51 V52 I53 T94 A95 G96 R98 I115 I119 V135 N137 L164 H192 I251
Binding residue
(residue number reindexed from 1)
G28 V30 D51 V52 I53 T94 A95 G96 R98 I115 I119 V135 N137 L164 H192 I251
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R105 D165 R168 H192
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:5w8l
,
PDBe:5w8l
,
PDBj:5w8l
PDBsum
5w8l
PubMed
29120638
UniProt
P00338
|LDHA_HUMAN L-lactate dehydrogenase A chain (Gene Name=LDHA)
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