Structure of PDB 3wbw Chain A Binding Site BS01
Receptor Information
>3wbw Chain A (length=271) Species:
290633
(Gluconobacter oxydans 621H) [
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EAQTVISFHDGHTMPQIGLGVWETPPDETAEVVKEAVKLGYRSVDTARLY
KNEEGVGKGLEDHPEIFLTTKLWNDEQGYDSTLRAYEESARLLRRPVLDL
YLIHWPMPAQGQYVETWKALVELKKSGRVKSIGVSNFESEHLERIMDATG
VVPVVNQIELHPDFQQRALREFHEKHNIRTESWRPLGKGRVLSDERIGKI
AEKHSRTPAQVVIRWHLQNGLIVIPKSVNPKRLAENLDVFGFVLDADDMQ
AIEQMDRKDGRMGADPNTAKF
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
3wbw Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
3wbw
Crystal structure of Gox0644 in complex with NADPH
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
G28 H112 N144 W191 R192 P193 L194 L200 A217 K234 S235 V236 R240 E243 N244
Binding residue
(residue number reindexed from 1)
G20 H104 N136 W183 R184 P185 L186 L192 A209 K226 S227 V228 R232 E235 N236
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D53 Y58 K79 H112
Catalytic site (residue number reindexed from 1)
D45 Y50 K71 H104
Enzyme Commision number
1.1.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0050580
2,5-didehydrogluconate reductase activity
View graph for
Molecular Function
External links
PDB
RCSB:3wbw
,
PDBe:3wbw
,
PDBj:3wbw
PDBsum
3wbw
PubMed
UniProt
Q5FT75
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