Reaction Details |
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Target | 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase |
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Ligand | BDBM50136925 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_103130 (CHEMBL712301) |
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Ki | 4000±n/a nM |
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Citation | Li, X; Chu, S; Feher, VA; Khalili, M; Nie, Z; Margosiak, S; Nikulin, V; Levin, J; Sprankle, KG; Tedder, ME; Almassy, R; Appelt, K; Yager, KM Structure-based design, synthesis, and antimicrobial activity of indazole-derived SAH/MTA nucleosidase inhibitors. J Med Chem46:5663-73 (2003) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase |
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Name: | 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase |
Synonyms: | 5 -methylthioadenosine nucleosidase | 5'-methylthioadenosine nucleosidase | 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase | 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) | MTA/SAH nucleosidase | MTAN | MTNN_ECOLI | Methylthioadenosine Nucleosidase(MTAN) | P46 | S-adenosylhomocysteine nucleosidase | mtn | mtnN | pfs | yadA |
Type: | Enzyme |
Mol. Mass.: | 24347.14 |
Organism: | Escherichia coli (strain K12) |
Description: | P0AF12 |
Residue: | 232 |
Sequence: | MKIGIIGAMEEEVTLLRDKIENRQTISLGGCEIYTGQLNGTEVALLKSGIGKVAAALGAT
LLLEHCKPDVIINTGSAGGLAPTLKVGDIVVSDEARYHDADVTAFGYEYGQLPGCPAGFK
ADDKLIAAAEACIAELNLNAVRGLIVSGDAFINGSVGLAKIRHNFPQAIAVEMEATAIAH
VCHNFNVPFVVVRAISDVADQQSHLSFDEFLAVAAKQSSLMVESLVQKLAHG
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BDBM50136925 |
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n/a |
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Name | BDBM50136925 |
Synonyms: | 4-Chloro-N-(3-methyl-1H-indazol-5-yl)-benzenesulfonamide | CHEMBL152399 |
Type | Small organic molecule |
Emp. Form. | C14H12ClN3O2S |
Mol. Mass. | 321.782 |
SMILES | Cc1n[nH]c2ccc(NS(=O)(=O)c3ccc(Cl)cc3)cc12 |
Structure |
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