Reaction Details |
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Target | Phospho-N-acetylmuramoyl-pentapeptide-transferase |
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Ligand | BDBM50221506 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_208265 (CHEMBL813225) |
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IC50 | 182±n/a nM |
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Citation | Hotoda, H; Daigo, M; Furukawa, M; Murayama, K; Hasegawa, CA; Kaneko, M; Muramatsu, Y; Ishii, MM; Miyakoshi, S; Takatsu, T; Inukai, M; Kakuta, M; Abe, T; Fukuoka, T; Utsui, Y; Ohya, S Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: acylated derivatives of capuramycin-related compounds. Bioorg Med Chem Lett13:2833-6 (2003) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Phospho-N-acetylmuramoyl-pentapeptide-transferase |
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Name: | Phospho-N-acetylmuramoyl-pentapeptide-transferase |
Synonyms: | MRAY_ECOLI | Phospho-N-acetylmuramoyl-pentapeptide-transferase/UDP-N-acetylglucosamine--N-acetylmuramyl-(pentapeptide) pyrophosphoryl-undecaprenol N-acetylglucosamine transferase | mraY | murX |
Type: | PROTEIN |
Mol. Mass.: | 39889.38 |
Organism: | Escherichia coli (strain K12) |
Description: | ChEMBL_1454117 |
Residue: | 360 |
Sequence: | MLVWLAEHLVKYYSGFNVFSYLTFRAIVSLLTALFISLWMGPRMIAHLQKLSFGQVVRND
GPESHFSKRGTPTMGGIMILTAIVISVLLWAYPSNPYVWCVLVVLVGYGVIGFVDDYRKV
VRKDTKGLIARWKYFWMSVIALGVAFALYLAGKDTPATQLVVPFFKDVMPQLGLFYILLA
YFVIVGTGNAVNLTDGLDGLAIMPTVFVAGGFALVAWATGNMNFASYLHIPYLRHAGELV
IVCTAIVGAGLGFLWFNTYPAQVFMGDVGSLALGGALGIIAVLLRQEFLLVIMGGVFVVE
TLSVILQVGSFKLRGQRIFRMAPIHHHYELKGWPEPRVIVRFWIISLMLVLIGLATLKVR
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BDBM50221506 |
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n/a |
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Name | BDBM50221506 |
Synonyms: | CHEMBL428285 |
Type | Small organic molecule |
Emp. Form. | C31H45N5O14 |
Mol. Mass. | 711.7141 |
SMILES | [H][C@@]1(O[C@H]([C@H](OC(=O)OCCCCCC)[C@@H]1OC)n1ccc(=O)[nH]c1=O)[C@@H](O[C@H]1OC(=C[C@H](O)[C@@H]1O)C(=O)N[C@H]1CCC[C@@H](C)NC1=O)C(N)=O |c:32| |
Structure |
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