Reaction Details |
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Target | Bacterial leucyl aminopeptidase |
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Ligand | BDBM23971 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_989563 (CHEMBL2444619) |
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Ki | 1.6±n/a nM |
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Citation | Al-Lakkis-Wehbe, M; Chaillou, B; Defoin, A; Albrecht, S; Tarnus, C Synthesis of amino-hydroxy-benzocycloheptenones as potent, selective, non-peptidic dinuclear zinc metalloaminopeptidase inhibitors. Bioorg Med Chem21:6447-55 (2013) [PubMed] Article |
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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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BDBM23971 |
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n/a |
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Name | BDBM23971 |
Synonyms: | (2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanoic acid | Bestatin | CHEMBL29292 | Ubenimex |
Type | Small organic molecule |
Emp. Form. | C16H24N2O4 |
Mol. Mass. | 308.3728 |
SMILES | CC(C)C[C@H](NC(=O)[C@@H](O)[C@H](N)Cc1ccccc1)C(O)=O |
Structure |
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