Structure of PDB 6sch Chain B Binding Site BS01
Receptor Information
>6sch Chain B (length=352) Species:
1520
(Clostridium beijerinckii) [
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MKGFAMLGINKLGWIEKERPVAGSYDAIVRPLAVSPCTSDIHTVFEGALG
DRKNMILGHEAVGEVVEVGSEVKDFKPGDRVIVPCTTPDWRSLEVQAGFQ
QHSNGMLAGWKFSNFKDGVFGEYFHVNDADMNLAILPKDMPLENAVMITD
MMTTGFHGAELADIQMGSSVVVIGIGAVGLMGIAGAKLRGAGRIIGVDYR
PICVEAAKFYGATDILNPKNGHIVDQVMKLTNGKGVDRVIMAGGGSETLS
QAVSMVKPGGIISNINYHGSGDALLIPRVEWGCGMAHKTIKGGLCPGGRL
RAEMLRDMVVYNRVDLSKLVTHVYHGFDHIEEALLLMKDKPKDLIKAVVI
LH
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
6sch Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6sch
Versatile selective evolutionary pressure using synthetic defect in universal metabolism.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
T38 S39 H42 H59 D150 T154 G176 A177 V178 D198 Y199 R200 A242 G244 N266 Y267
Binding residue
(residue number reindexed from 1)
T38 S39 H42 H59 D150 T154 G176 A177 V178 D198 Y199 R200 A242 G244 N266 Y267
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
C37 S39 H42 H59 D150
Catalytic site (residue number reindexed from 1)
C37 S39 H42 H59 D150
Enzyme Commision number
1.1.1.80
: isopropanol dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050009
isopropanol dehydrogenase (NADP+) activity
View graph for
Molecular Function
External links
PDB
RCSB:6sch
,
PDBe:6sch
,
PDBj:6sch
PDBsum
6sch
PubMed
34824282
UniProt
P25984
|ADH_CLOBE NADP-dependent isopropanol dehydrogenase (Gene Name=adh)
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