Structure of PDB 1zgd Chain B Binding Site BS01
Receptor Information
>1zgd Chain B (length=308) Species:
3879
(Medicago sativa) [
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EIPTKVLTNTSSQLKMPVVGMGSAPDFTCKKDTKDAIIEAIKQGYRHFDT
AAAYGSEQALGEALKEAIELGLVTRDDLFVTSKLWVTENHPHLVIPALQK
SLKTLQLDYLDLYLIHWPLSSQPGKFSFPIDVADLLPFDVKGVWESMEES
LKLGLTKAIGVSNFSVKKLENLLSVATVLPAVNQVEMNLAWQQKKLREFC
NAHGIVLTAFSPVRKGASRGPNEVMENDMLKEIADAHGKSVAQISLRWLY
EQGVTFVPKSYDKERMNQNLRIFDWSLTKEDHEKIAQIKQNRLIPGPTKP
GLNDLYDD
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/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/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[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)c1ccc[n+](c1)[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
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
1zgd Chain B Residue 1755 [
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Receptor-Ligand Complex Structure
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PDB
1zgd
Structural elucidation of chalcone reductase and implications for deoxychalcone biosynthesis
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
G26 S27 A28 D30 D53 Y58 K87 H120 Q188 F214 S215 P216 V217 K219 G220 A246 P262 K263 S264 R269 N273
Binding residue
(residue number reindexed from 1)
G22 S23 A24 D26 D49 Y54 K83 H116 Q184 F210 S211 P212 V213 K215 G216 A242 P258 K259 S260 R265 N269
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D53 Y58 K87 H120
Catalytic site (residue number reindexed from 1)
D49 Y54 K83 H116
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004032
aldose reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:1zgd
,
PDBe:1zgd
,
PDBj:1zgd
PDBsum
1zgd
PubMed
15970585
UniProt
Q40309
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