Structure of PDB 2hdk Chain B Binding Site BS01
Receptor Information
>2hdk Chain B (length=363) Species:
9606
(Homo sapiens) [
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SSFKAADLQLEMTQKPHKKPGPGEPLVFGKTFTDHMLMVEWNDKGWGQPR
IQPFQNLTLHPASSSLHYSLQLFEGMKAFKGKDQQVRLFRPWLNMDRMLR
SAMRLCLPSFDKLELLECIRRLIEVDKDWVPDAAGTSLYVRPVLIGNEPS
LGVSQPRRALLFVILCPVGAYFPGGSVTPVSLLADPAFIRAWVGGVGNYK
LGGNYGPTVLVQQEALKRGCEQVLWLYGPDHQLTEVGTMNIFVYWTHEDG
VLELVTPPLNGVILPGVVRQSLLDMAQTWGEFRVVERTITMKQLLRALEE
GRVREVFGSGTAAQVAPVHRILYKDRNLHIPTMENGPELILRFQKELKEI
QYGIRAHEWMFPV
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
2hdk Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2hdk
Human Mitochondrial Branched Chain Aminotransferase Isozyme: STRUCTURAL ROLE OF THE CXXC CENTER IN CATALYSIS.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
R599 K702 Y707 E737 T740 L766 G768 V769 V770 G812 T813
Binding residue
(residue number reindexed from 1)
R97 K200 Y205 E235 T238 L264 G266 V267 V268 G310 T311
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K702
Catalytic site (residue number reindexed from 1)
K200
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:0005515
protein binding
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:0006549
isoleucine metabolic process
GO:0006550
isoleucine catabolic process
GO:0006551
L-leucine metabolic process
GO:0006573
valine metabolic process
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:0009083
branched-chain amino acid catabolic process
GO:0009098
L-leucine biosynthetic process
GO:0009099
L-valine biosynthetic process
GO:0010817
regulation of hormone levels
GO:1990830
cellular response to leukemia inhibitory factor
Cellular Component
GO:0005654
nucleoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2hdk
,
PDBe:2hdk
,
PDBj:2hdk
PDBsum
2hdk
PubMed
17050531
UniProt
O15382
|BCAT2_HUMAN Branched-chain-amino-acid aminotransferase, mitochondrial (Gene Name=BCAT2)
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