Structure of PDB 2dab Chain B Binding Site BS01
Receptor Information
>2dab Chain B (length=282) Species:
72579
(Bacillus sp. YM-1) [
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GYTLWNDQIVKDEEVKIDKEDRGYQFGDGVYEVVKVYNGEMFTVNEHIDR
LYASAEKIRITIPYTKDKFHQLLHELVEKNELNTGHIYFQVTRGTSPRAH
QFPENTVKPVIIGYTKENPRPLENLEKGVKATFVEDIRWLRCDIKSLNLL
GAVLAKQEAHEKGCYEAILHRNNTVTEGSSSNVFGIKDGILYTHPANNMI
AKGITRDVVIACANEINMPVKEIPFTTHEALKMDELFVTSTTSEITPVIE
IDGKLIRDGKVGEWTRKLQKQFETKIPKPLHI
Ligand information
Ligand ID
PLP
InChI
InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(C=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C=O)O
ACDLabs 10.04
O=P(O)(O)OCc1cnc(c(O)c1C=O)C
Formula
C8 H10 N O6 P
Name
PYRIDOXAL-5'-PHOSPHATE;
VITAMIN B6 Phosphate
ChEMBL
CHEMBL82202
DrugBank
DB00114
ZINC
ZINC000001532514
PDB chain
2dab Chain B Residue 285 [
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Receptor-Ligand Complex Structure
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PDB
2dab
Crystal structures of L201A mutant of D-amino acid aminotransferase at 2.0 A resolution: implication of the structural role of Leu201 in transamination.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Y31 R50 K145 E177 S181 G203 I204 T205 T241
Binding residue
(residue number reindexed from 1)
Y31 R50 K145 E177 S181 G203 I204 T205 T241
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y31 V33 K145 E177 A201
Catalytic site (residue number reindexed from 1)
Y31 V33 K145 E177 A201
Enzyme Commision number
2.6.1.21
: D-amino-acid transaminase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
GO:0047810
D-alanine-2-oxoglutarate aminotransferase activity
Biological Process
GO:0019478
D-amino acid catabolic process
GO:0019752
carboxylic acid metabolic process
GO:0046394
carboxylic acid biosynthetic process
GO:0046416
D-amino acid metabolic process
GO:0046437
D-amino acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2dab
,
PDBe:2dab
,
PDBj:2dab
PDBsum
2dab
PubMed
9749913
UniProt
P19938
|DAAA_BACYM D-alanine aminotransferase (Gene Name=dat)
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