Reaction Details
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Phospho-N-acetylmuramoyl-pentapeptide-transferase
Ligand
BDBM50343932
Substrate
n/a
Meas. Tech.
ChEMBL_748572 (CHEMBL1780425)
IC50
5000±n/a nM
Citation
Tanino, T; Ichikawa, S; Al-Dabbagh, B; Bouhss, A; Oyama, H; Matsuda, A Synthesis and Biological Evaluation of Muraymycin Analogues Active against Anti-Drug-Resistant Bacteria. ACS Med Chem Lett 1:258-262 (2010) [PubMed] Article More Info.:
Target
Name:
Phospho-N-acetylmuramoyl-pentapeptide-transferase
Synonyms:
MRAY_BACSU | mraY
Type:
PROTEIN
Mol. Mass.:
35531.14
Organism:
Bacillus subtilis
Description:
ChEMBL_796247
Residue:
324
Sequence:
MLEQVILFTILMGFLISVLLSPILIPFLRRLKFGQSIREEGPKSHQKKSGTPTMGGVMIILSIIVTTIVMTQKFSEISPEMVLLLFVTLGYGLLGFLDDYIKVVMKRNLGLTSKQKLIGQIIIAVVFYAVYHYYNFATDIRIPGTDLSFDLGWAYFILVLFMLVGGSNAVNLTDGLDGLLSGTAAIAFGAFAILAWNQSQYDVAIFSVAVVGAVLGFLVFNAHPAKVFMGDTGSLALGGAIVTIAILTKLEILLVIIGGVFVIETLSVILQVISFKTTGKRIFKMSPLHHHYELVGWSEWRVVVTFWAAGLLLAVLGIYIEVWL
Inhibitor
Name:
BDBM50343932
Synonyms:
5-O-(5-Amino-5-deoxy-beta-D-ribofuranosyl)-6-deoxy-6-dodecylamino-1-(uracil-1-yl)-beta-D-glycero-L-talo-heptofuranuronic acid | CHEMBL1780207
Type:
Small organic molecule
Emp. Form.:
C28H48N4O11
Mol. Mass.:
616.7009
SMILES:
CCCCCCCCCCCCN[C@@H]([C@H](O[C@@H]1O[C@H](CN)[C@@H](O)[C@H]1O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O)C(O)=O |r|
Structure:
