Reaction Details |
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Target | 4-aminobutyrate aminotransferase, mitochondrial |
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Ligand | BDBM50376755 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_477747 (CHEMBL939957) |
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IC50 | >5000000±n/a nM |
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Citation | Clift, MD; Silverman, RB Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase. Bioorg Med Chem Lett18:3122-5 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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4-aminobutyrate aminotransferase, mitochondrial |
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Name: | 4-aminobutyrate aminotransferase, mitochondrial |
Synonyms: | (S)-3-amino-2-methylpropionate transaminase | 4-aminobutyrate aminotransferase, mitochondrial | ABAT | GABA aminotransferase | GABA transaminase | GABA-AT | GABA-T | GABAT | GABT_HUMAN | Gamma-amino-N-butyrate transaminase | L-AIBAT |
Type: | PROTEIN |
Mol. Mass.: | 56449.39 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1459248 |
Residue: | 500 |
Sequence: | MASMLLAQRLACSFQHSYRLLVPGSRHISQAAAKVDVEFDYDGPLMKTEVPGPRSQELMK
QLNIIQNAEAVHFFCNYEESRGNYLVDVDGNRMLDLYSQISSVPIGYSHPALLKLIQQPQ
NASMFVNRPALGILPPENFVEKLRQSLLSVAPKGMSQLITMACGSCSNENALKTIFMWYR
SKERGQRGFSQEELETCMINQAPGCPDYSILSFMGAFHGRTMGCLATTHSKAIHKIDIPS
FDWPIAPFPRLKYPLEEFVKENQQEEARCLEEVEDLIVKYRKKKKTVAGIIVEPIQSEGG
DNHASDDFFRKLRDIARKHGCAFLVDEVQTGGGCTGKFWAHEHWGLDDPADVMTFSKKMM
TGGFFHKEEFRPNAPYRIFNTWLGDPSKNLLLAEVINIIKREDLLNNAAHAGKALLTGLL
DLQARYPQFISRVRGRGTFCSFDTPDDSIRNKLILIARNKGVVLGGCGDKSIRFRPTLVF
RDHHAHLFLNIFSDILADFK
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BDBM50376755 |
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n/a |
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Name | BDBM50376755 |
Synonyms: | CHEMBL535643 |
Type | Small organic molecule |
Emp. Form. | C9H11NO2 |
Mol. Mass. | 165.1891 |
SMILES | NCc1cccc(CC(O)=O)c1 |
Structure |
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