Structure of PDB 1ynq Chain B Binding Site BS02
Receptor Information
>1ynq Chain B (length=298) Species:
272558
(Halalkalibacterium halodurans C-125) [
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HMKKRQLGTSDLHVSELGFGCMSLGTDETKARRIMDEVLELGINYLDTAD
LYNQGLNEQFVGKALKGRRQDIILATKVGNRFEQGKEGWWWDPSKAYIKE
AVKDSLRRLQTDYIDLYQLHGGTIDDPIDETIEAFEELKQEGVIRYYGIS
SIRPNVIKEYLKRSNIVSIMMQYSILDRRPEEWFPLIQEHGVSVVVRGPV
ARGLLSRRPLPEGEGYLNYRYDELKLLRESLPTDRPLHELALQYCLAHDV
VATVAAGASSIDQVKANVQAVEATPLTAEERQHIQKLAKAAVYEQHRE
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
1ynq Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1ynq
High-resolution Crystal Structure of AKR11C1 from Bacillus halodurans: An NADPH-dependent 4-Hydroxy-2,3-trans-nonenal Reductase
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
G19 C20 M21 S22 D46 Y51 K76 S149 M169 R196 G197 P198 V199 R201 S205 R207 A254 A255 G256 S258 Q262 N266
Binding residue
(residue number reindexed from 1)
G20 C21 M22 S23 D47 Y52 K77 S150 M170 R197 G198 P199 V200 R202 S206 R208 A255 A256 G257 S259 Q263 N267
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D46 Y51 K85 H119
Catalytic site (residue number reindexed from 1)
D47 Y52 K86 H120
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:1ynq
,
PDBe:1ynq
,
PDBj:1ynq
PDBsum
1ynq
PubMed
16242712
UniProt
Q9KE47
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