Structure of PDB 8xd0 Chain A Binding Site BS01
Receptor Information
>8xd0 Chain A (length=417) Species:
49899
(Thermococcus profundus) [
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EIDPFEMAVKQLERAAQYMDISEEALEWLKKPMRIVEVSVPIEMDDGSVK
VFTGFRVQHNWARGPTKGGIRWHPAETLSTVKALATWMTWKVAVVDLPYG
GGKGGIIVNPKELSEREQERLARAYIRAVYDVIGPWTDIPAPDVYTNPKI
MGWMMDEYETIMRRKGPAFGVITGKPLSIGGSLGRGTATAQGAIFTIREA
AKALGIDLKGKKIAVQGYGNAGYYTAKLAKEQLGMTVVAVSDSRGGIYNP
DGLDPDEVLKWKREHGSVKDFPGATNITNEELLELEVDVLAPAAIEEVIT
EKNADNIKAKIVAEVANGPVTPEADDILREKGILQIPDFLCNAGGVTVSY
FEWVQNINGYYWTEEEVREKLDKKMTKAFWEVYNTHKDKNIHMRDAAYVV
AVSRVYQAMKDRGWVKK
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/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/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
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)OP(=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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
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)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
8xd0 Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
8xd0
CryoEM-sampling of metastable conformations appearing in cofactor-ligand association and catalysis of glutamate dehydrogenase
Resolution
2.83 Å
Binding residue
(original residue number in PDB)
T191 Q218 Y220 G221 N222 D244 S245 K264 N281 A296 I297 N344
Binding residue
(residue number reindexed from 1)
T189 Q216 Y218 G219 N220 D242 S243 K262 N279 A294 I295 N342
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.4.1.3
: glutamate dehydrogenase [NAD(P)(+)].
Gene Ontology
Molecular Function
GO:0004352
glutamate dehydrogenase (NAD+) activity
GO:0004353
glutamate dehydrogenase [NAD(P)+] activity
GO:0004354
glutamate dehydrogenase (NADP+) activity
GO:0016491
oxidoreductase activity
GO:0016639
oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor
Biological Process
GO:0006520
amino acid metabolic process
GO:0006538
glutamate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:8xd0
,
PDBe:8xd0
,
PDBj:8xd0
PDBsum
8xd0
PubMed
38750092
UniProt
O74024
|DHE3_THEPR Glutamate dehydrogenase (Gene Name=gdhA)
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