Structure of PDB 1zem Chain F Binding Site BS01
Receptor Information
>1zem Chain F (length=260) Species:
442
(Gluconobacter oxydans) [
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KKFNGKVCLVTGAGGNIGLATALRLAEEGTAIALLDMNREALEKAEASVR
EKGVEARSYVCDVTSEEAVIGTVDSVVRDFGKIDFLFNNAGYQGAFAPVQ
DYPSDDFARVLTINVTGAFHVLKAVSRQMITQNYGRIVNTASMAGVKGPP
NMAAYGTSKGAIIALTETAALDLAPYNIRVNAISPGYMGPGFMWERQVEL
QAKVGSQYFSTDPKVVAQQMIGSVPMRRYGDINEIPGVVAFLLGDDSSFM
TGVNLPIAGG
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
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)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)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)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]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)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
1zem Chain F Residue 7263 [
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Receptor-Ligand Complex Structure
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PDB
1zem
Structure-guided engineering of xylitol dehydrogenase cosubstrate specificity.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G14 G17 N18 I19 D38 M39 C63 D64 V65 N91 A92 T142 S144 Y157 K161 P187 M190
Binding residue
(residue number reindexed from 1)
G12 G15 N16 I17 D36 M37 C61 D62 V63 N89 A90 T140 S142 Y155 K159 P185 M188
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N18 S144 Y157 K161 D214
Catalytic site (residue number reindexed from 1)
N16 S142 Y155 K159 D212
Enzyme Commision number
1.1.1.9
: D-xylulose reductase.
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
View graph for
Molecular Function
External links
PDB
RCSB:1zem
,
PDBe:1zem
,
PDBj:1zem
PDBsum
1zem
PubMed
16531240
UniProt
Q8GR61
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