Reaction Details
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Phospho-N-acetylmuramoyl-pentapeptide-transferase
Ligand
BDBM50318255
Substrate
n/a
Meas. Tech.
ChEMBL_629295 (CHEMBL1103975)
IC50
980000±n/a nM
Citation
Ii, K; Ichikawa, S; Al-Dabbagh, B; Bouhss, A; Matsuda, A Function-oriented synthesis of simplified caprazamycins: discovery of oxazolidine-containing uridine derivatives as antibacterial agents against drug-resistant bacteria. J Med Chem 53:3793-813 (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:
BDBM50318255
Synonyms:
(2R,4S,5S)-Methyl-2-Aminomethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylate hydrochloride salt | CHEMBL1095324
Type:
Small organic molecule
Emp. Form.:
C30H50N4O9
Mol. Mass.:
610.7394
SMILES:
CCCCCCCCCCCCCCCC(=O)N1[C@@H](CN)O[C@H]([C@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)[C@H]1C(=O)OC |r|
Structure:
