Reaction Details |
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Target | Bacterial leucyl aminopeptidase |
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Ligand | BDBM50129202 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_98920 |
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Ki | 350±n/a nM |
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Citation | Stoermer, D; Liu, Q; Hall, MR; Flanary, JM; Thomas, AG; Rojas, C; Slusher, BS; Tsukamoto, T Synthesis and biological evaluation of hydroxamate-Based inhibitors of glutamate carboxypeptidase II. Bioorg Med Chem Lett13:2097-100 (2003) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Bacterial leucyl aminopeptidase |
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Name: | Bacterial leucyl aminopeptidase |
Synonyms: | AMPX_VIBPR | Bacterial leucyl aminopeptidase precursor |
Type: | PROTEIN |
Mol. Mass.: | 54213.72 |
Organism: | Vibrio proteolyticus |
Description: | ChEMBL_1507540 |
Residue: | 504 |
Sequence: | MKYTKTLLAMVLSATFCQAYAEDKVWISIGADANQTVMKSGAESILPNSVASSGQVWVGQ
VDVAQLAELSHNMHEEHNRCGGYMVHPSAQSAMAASAMPTTLASFVMPPITQQATVTAWL
PQVDASQITGTISSLESFTNRFYTTTSGAQASDWIASEWQALSASLPNASVKQVSHSGYN
QKSVVMTITGSEAPDEWIVIGGHLDSTIGSHTNEQSVAPGADDDASGIAAVTEVIRVLSE
NNFQPKRSIAFMAYAAEEVGLRGSQDLANQYKSEGKNVVSALQLDMTNYKGSAQDVVFIT
DYTDSNFTQYLTQLMDEYLPSLTYGFDTCGYACSDHASWHNAGYPAAMPFESKFNDYNPR
IHTTQDTLANSDPTGSHAKKFTQLGLAYAIEMGSATGDTPTPGNQLEDGVPVTDLSGSRG
SNVWYTFELETQKNLQITTSGGYGDLDLYVKFGSKASKQNWDCRPYLSGNNEVCTFNNAS
PGTYSVMLTGYSNYSGASLKASTF
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BDBM50129202 |
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n/a |
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Name | BDBM50129202 |
Synonyms: | (S)-2-Amino-4-methyl-pentanoic acid hydroxyamide | (S)-2-amino-N-hydroxy-4-methylpentanamide | CHEMBL303296 | L-LEUCYL-HYDROXYLAMINE |
Type | Small organic molecule |
Emp. Form. | C6H14N2O2 |
Mol. Mass. | 146.1876 |
SMILES | CC(C)C[C@H](N)C(=O)NO |
Structure |
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