Structure of PDB 2coj Chain B Binding Site BS01
Receptor Information
>2coj Chain B (length=358) Species:
9606
(Homo sapiens) [
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TFKAKDLIVTPATILKEKPDPNNLVFGTVFTDHMLTVEWSSEFGWEKPHI
KPLQNLSLHPGSSALHYAVELFEGLKAFRGVDNKIRLFQPNLNMDRMYRS
AVRATLPVFDKEELLECIQQLVKLDQEWVPYSTSASLYIRPTFIGTEPSL
GVKKPTKALLFVLLSPVGPYFFNPVSLWANPKYVRAWKGGTGDCKMGGNY
GSSLFAQCEAVDNGCQQVLWLYGEDHQITEVGTMNLFLYWINEDGEEELA
TPPLDGIILPGVTRRCILDLAHQWGEFKVSERYLTMDDLTTALEGNRVRE
MFGSGTACVVCPVSDILYKGETIHIPTMENGPKLASRILSKLTDIQYGRE
ERDWTIVL
Ligand information
Ligand ID
GBN
InChI
InChI=1S/C9H17NO2/c10-7-9(6-8(11)12)4-2-1-3-5-9/h1-7,10H2,(H,11,12)
InChIKey
UGJMXCAKCUNAIE-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1CCC(CC1)(CC(=O)O)CN
CACTVS 3.341
NCC1(CCCCC1)CC(O)=O
ACDLabs 10.04
O=C(O)CC1(CN)CCCCC1
Formula
C9 H17 N O2
Name
[1-(AMINOMETHYL)CYCLOHEXYL]ACETIC ACID;
GABAPENTIN
ChEMBL
CHEMBL940
DrugBank
DB00996
ZINC
ZINC000000004949
PDB chain
2coj Chain A Residue 420 [
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Receptor-Ligand Complex Structure
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PDB
2coj
Structural determinants for branched-chain aminotransferase isozyme-specific inhibition by the anticonvulsant drug gabapentin
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
Y90 V175
Binding residue
(residue number reindexed from 1)
Y67 V152
Annotation score
1
Binding affinity
MOAD
: Ki=1.3mM
Enzymatic activity
Catalytic site (original residue number in PDB)
K222
Catalytic site (residue number reindexed from 1)
K195
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: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:0000082
G1/S transition of mitotic cell cycle
GO:0006629
lipid metabolic process
GO:0008652
amino acid biosynthetic process
GO:0009081
branched-chain amino acid metabolic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009098
L-leucine biosynthetic process
GO:0009099
L-valine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2coj
,
PDBe:2coj
,
PDBj:2coj
PDBsum
2coj
PubMed
16141215
UniProt
P54687
|BCAT1_HUMAN Branched-chain-amino-acid aminotransferase, cytosolic (Gene Name=BCAT1)
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