Structure of PDB 3dtg Chain A Binding Site BS02
Receptor Information
>3dtg Chain A (length=363) Species:
1772
(Mycolicibacterium smegmatis) [
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LEFTVSANTNPATDAVRESILANPGFGKYYTDHMVSIDYTVDEGWHNAQV
IPYGPIQLDPSAIVLHYGQEIFEGLKAYRWADGSIVSFRPEANAARLQSS
ARRLAIPELPEEVFIESLRQLIAVDEKWVPPAGGEESLYLRPFVIATEPG
LGVRPSNEYRYLLIASPAGAYFKGGIKPVSVWLSHEYVRASPGGTGAAKF
GGNYAASLLAQAQAAEMGCDQVVWLDAIERRYVEEMGGMNLFFVFGSGGS
ARLVTPELSGSLLPGITRDSLLQLATDAGFAVEERKIDVDEWQKKAGAGE
ITEVFACGTAAVITPVSHVKHHDGEFTIADGQPGEITMALRDTLTGIQRG
TFADTHGWMARLN
Ligand information
Ligand ID
OBZ
InChI
InChI=1S/C7H9NO/c8-9-6-7-4-2-1-3-5-7/h1-5H,6,8H2
InChIKey
XYEOALKITRFCJJ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1ccc(cc1)CON
CACTVS 3.341
NOCc1ccccc1
ACDLabs 10.04
[(aminooxy)methyl]benzene
Formula
C7 H9 N O
Name
O-benzylhydroxylamine
ChEMBL
CHEMBL443652
DrugBank
ZINC
ZINC000000155377
PDB chain
3dtg Chain A Residue 371 [
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Receptor-Ligand Complex Structure
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PDB
3dtg
Structural analysis of mycobacterial branched chain aminotransferase - implications for inhibitor design
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
F77 Y176 Y209
Binding residue
(residue number reindexed from 1)
F72 Y171 Y204
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K204
Catalytic site (residue number reindexed from 1)
K199
Enzyme Commision number
2.6.1.42
: branched-chain-amino-acid transaminase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004084
branched-chain-amino-acid transaminase activity
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
GO:0052654
L-leucine-2-oxoglutarate transaminase activity
GO:0052655
L-valine-2-oxoglutarate transaminase activity
GO:0052656
L-isoleucine-2-oxoglutarate transaminase activity
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009081
branched-chain amino acid metabolic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009098
L-leucine biosynthetic process
GO:0009099
L-valine biosynthetic process
GO:0018272
protein-pyridoxal-5-phosphate linkage via peptidyl-N6-pyridoxal phosphate-L-lysine
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Molecular Function
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Biological Process
External links
PDB
RCSB:3dtg
,
PDBe:3dtg
,
PDBj:3dtg
PDBsum
3dtg
PubMed
UniProt
A0R066
|ILVE_MYCS2 Branched-chain-amino-acid aminotransferase (Gene Name=ilvE)
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