Structure of PDB 6ke3 Chain A Binding Site BS01
Receptor Information
>6ke3 Chain A (length=335) Species:
9606
(Homo sapiens) [
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GVQTVTLIPGDGIGPEISAAVMKIFDAAKAPIQWEERNVTAIQGPGGKWM
IPSEAKESMDKNKMGLKGPLKTPIAAGHPSMNLLLRKTFDLYANVRPCVS
IEGYKTPYTDVNIVTIRENTEGEYSGIEHVIVDGVVQSIKLITEGASKRI
AEFAFEYARNNHRSNVTAVHKANIMRMSDGLFLQKCREVAESCKDIKFNE
MYLDTVCLNMVQDPSQFDVLVMPNLYGDILSDLCAGLIGGLGVTPSGNIG
ANGVAIFESVHGTAPDIAGKDMANPTALLLSAVMMLRHMGLFDHAARIEA
ACFATIKDGKSLTKDLGGNAKCSDFTEEICRRVKD
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
6ke3 Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6ke3
Molecular basis for the function of the alpha beta heterodimer of human NAD-dependent isocitrate dehydrogenase.
Resolution
3.307 Å
Binding residue
(original residue number in PDB)
N84 L243 H263 G264 T265 A266 D268 I269
Binding residue
(residue number reindexed from 1)
N82 L241 H261 G262 T263 A264 D266 I267
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
Y126 K173 D206 D230
Catalytic site (residue number reindexed from 1)
Y124 K171 D204 D228
Enzyme Commision number
1.1.1.41
: isocitrate dehydrogenase (NAD(+)).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004449
isocitrate dehydrogenase (NAD+) 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:0046872
metal ion binding
GO:0051287
NAD binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006099
tricarboxylic acid cycle
GO:0006102
isocitrate metabolic process
Cellular Component
GO:0005634
nucleus
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0045242
isocitrate dehydrogenase complex (NAD+)
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6ke3
,
PDBe:6ke3
,
PDBj:6ke3
PDBsum
6ke3
PubMed
31515270
UniProt
P50213
|IDH3A_HUMAN Isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial (Gene Name=IDH3A)
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