Structure of PDB 2pb2 Chain A Binding Site BS01
Receptor Information
>2pb2 Chain A (length=378) Species:
99287
(Salmonella enterica subsp. enterica serovar Typhimurium str. LT2) [
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ADFIPVKGKGSRVWDQQGKEYIDFAGGIAVTALGHCHPALVEALKSQGET
LWHTSNVFTNEPALRLGRKLIDATFAERVLFMNSGTEANETAFKLARHYA
CVRHSPFKTKIIAFHNAFHGRSLFTVSVGGQPKYSDGFGPKPADIIHVPF
NDLHAVKAVMDDHTCAVVVEPIQGEGGVQAATPEFLKGLRDLCDEHQALL
VFDEVQCGMGRTGDLFAYMHYGVTPDILTSAKALGGGFPVSAMLTTQEIA
SAFHGSTYGGNPLACAVAGAAFDIINTPEVLQGIHTKRQQFVQHLQAIDE
QFDIFSDIRGMGLLIGAELKPKYKGRARDFLYAGAEAGVMVLNAGADVMR
FAPSLVVEEADIHEGMQRFAQAVGKVVA
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
2pb2 Chain A Residue 1555 [
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Receptor-Ligand Complex Structure
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PDB
2pb2
Structure of biosynthetic N-acetylornithine aminotransferase from Salmonella typhimurium: Studies on substrate specificity and inhibitor binding
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
G108 T109 N112 F141 H142 D226 V228 Q229 K255
Binding residue
(residue number reindexed from 1)
G85 T86 N89 F118 H119 D203 V205 Q206 K232
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F141 E193 D226 Q229 K255 T284 R377
Catalytic site (residue number reindexed from 1)
F118 E170 D203 Q206 K232 T257 R350
Enzyme Commision number
2.6.1.11
: acetylornithine transaminase.
2.6.1.17
: succinyldiaminopimelate transaminase.
Gene Ontology
Molecular Function
GO:0003992
N2-acetyl-L-ornithine:2-oxoglutarate 5-aminotransferase activity
GO:0008483
transaminase activity
GO:0009016
succinyldiaminopimelate transaminase activity
GO:0030170
pyridoxal phosphate binding
GO:0042802
identical protein binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006525
arginine metabolic process
GO:0006526
L-arginine biosynthetic process
GO:0009085
lysine biosynthetic process
GO:0009089
lysine biosynthetic process via diaminopimelate
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Cellular Component
External links
PDB
RCSB:2pb2
,
PDBe:2pb2
,
PDBj:2pb2
PDBsum
2pb2
PubMed
17680699
UniProt
P40732
|ARGD_SALTY Acetylornithine/succinyldiaminopimelate aminotransferase (Gene Name=argD)
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