Structure of PDB 3qwb Chain D Binding Site BS01
Receptor Information
>3qwb Chain D (length=330) Species:
559292
(Saccharomyces cerevisiae S288C) [
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IPEQQKVILIDEIGGYDVIKYEDYPVPSISEEELLIKNKYTGVNYIESYF
RKGIYPCEKPYVLGREASGTVVAKGKGVTNFEVGDQVAYISNSTFAQYSK
ISSQGPVMKLPKGTSDEELKLYAAGLLQVLTALSFTNEAYHVKKGDYVLL
FAAAGGVGLILNQLLKMKGAHTIAVASTDEKLKIAKEYGAEYLINASKED
ILRQVLKFTNGKGVDASFDSVGKDTFEISLAALKRKGVFVSFGNASGLIP
PFSITRLSPKNITLVRPQLYGYIADPEEWKYYSDEFFGLVNSKKLNIKIY
KTYPLRDYRTAAADIESRKTVGKLVLEIPQ
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
3qwb Chain D Residue 335 [
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Receptor-Ligand Complex Structure
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PDB
3qwb
Structural insights into the cofactor-assisted substrate recognition of yeast quinone oxidoreductase Zta1
Resolution
1.59 Å
Binding residue
(original residue number in PDB)
Y49 Y53 Q132 T135 F139 A156 G159 G160 V161 A180 S181 K185 S224 V225 F246 A249 Q272 R322
Binding residue
(residue number reindexed from 1)
Y45 Y49 Q128 T131 F135 A152 G155 G156 V157 A176 S177 K181 S220 V221 F242 A245 Q268 R318
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N48 Y49 I50 Y53 R69 E70
Catalytic site (residue number reindexed from 1)
N44 Y45 I46 Y49 R65 E66
Enzyme Commision number
1.6.5.5
: NADPH:quinone reductase.
Gene Ontology
Molecular Function
GO:0003960
NADPH:quinone reductase activity
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0032440
2-alkenal reductase [NAD(P)+] activity
GO:0035925
mRNA 3'-UTR AU-rich region binding
GO:0070402
NADPH binding
Biological Process
GO:0034599
cellular response to oxidative stress
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3qwb
,
PDBe:3qwb
,
PDBj:3qwb
PDBsum
3qwb
PubMed
21820057
UniProt
P38230
|QOR_YEAST Probable quinone oxidoreductase (Gene Name=ZTA1)
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