Structure of PDB 3wby Chain A Binding Site BS01
Receptor Information
>3wby Chain A (length=271) Species:
290633
(Gluconobacter oxydans 621H) [
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EAQTVISFHDGHTMPQIGLGVWETPPDETAEVVKEAVKLGYRSVATARLY
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
3wby Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
3wby
Crystal structure of Gox0644 D53A mutant in complex with NADPH
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
E31 W113 W191 R192 P193 L194 K196 L200 K234 S235 R240 E243 N244 A272
Binding residue
(residue number reindexed from 1)
E23 W105 W183 R184 P185 L186 K188 L192 K226 S227 R232 E235 N236 A264
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
A53 Y58 K79 H112
Catalytic site (residue number reindexed from 1)
A45 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:3wby
,
PDBe:3wby
,
PDBj:3wby
PDBsum
3wby
PubMed
UniProt
Q5FT75
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