Structure of PDB 2d1y Chain C Binding Site BS01
Receptor Information
>2d1y Chain C (length=248) Species:
274
(Thermus thermophilus) [
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GLFAGKGVLVTGGARGIGRAIAQAFAREGALVALCDLRPEGKEVAEAIGG
AFFQVDLEDERERVRFVEEAAYALGRVDVLVNNAAIAAPGSALTVRLPEW
RRVLEVNLTAPMHLSALAAREMRKVGGGAIVNVASVQGLFAEQENAAYNA
SKGGLVNLTRSLALDLAPLRIRVNAVAPGAIATEAVLEAIALSPDPERTR
RDWEDLHALRRLGKPEEVAEAVLFLASEKASFITGAILPVDGGMTASF
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
2d1y Chain C Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
2d1y
Biochemical and structural characterization of a short-chain dehydrogenase/reductase of Thermus thermophilus HB8: a hyperthermostable aldose-1-dehydrogenase with broad substrate specificity.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
G13 R16 I18 D37 L38 R39 V56 D57 L58 N84 A85 A86 I87 V134 S136 Y149 K153 P179 G180 A181 I182 T184 V187
Binding residue
(residue number reindexed from 1)
G12 R15 I17 D36 L37 R38 V55 D56 L57 N83 A84 A85 I86 V133 S135 Y148 K152 P178 G179 A180 I181 T183 V186
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G17 S136 N146 Y149 K153
Catalytic site (residue number reindexed from 1)
G16 S135 N145 Y148 K152
Enzyme Commision number
?
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:2d1y
,
PDBe:2d1y
,
PDBj:2d1y
PDBsum
2d1y
PubMed
18926808
UniProt
Q5SLC4
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