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TargetPhospho-N-acetylmuramoyl-pentapeptide-transferase
LigandBDBM50318263
Substrate/Competitorn/a
Meas. Tech.ChEMBL_629295 (CHEMBL1103975)
IC50 75000±n/a nM
Citation Ii, KIchikawa, SAl-Dabbagh, BBouhss, AMatsuda, A Function-oriented synthesis of simplified caprazamycins: discovery of oxazolidine-containing uridine derivatives as antibacterial agents against drug-resistant bacteria. J Med Chem53:3793-813 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phospho-N-acetylmuramoyl-pentapeptide-transferase
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:
MLEQVILFTILMGFLISVLLSPILIPFLRRLKFGQSIREEGPKSHQKKSGTPTMGGVMII
LSIIVTTIVMTQKFSEISPEMVLLLFVTLGYGLLGFLDDYIKVVMKRNLGLTSKQKLIGQ
IIIAVVFYAVYHYYNFATDIRIPGTDLSFDLGWAYFILVLFMLVGGSNAVNLTDGLDGLL
SGTAAIAFGAFAILAWNQSQYDVAIFSVAVVGAVLGFLVFNAHPAKVFMGDTGSLALGGA
IVTIAILTKLEILLVIIGGVFVIETLSVILQVISFKTTGKRIFKMSPLHHHYELVGWSEW
RVVVTFWAAGLLLAVLGIYIEVWL
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50318263
n/a
NameBDBM50318263
Synonyms:5-O-(5-Amino-5-deoxy-beta-D-ribofuranosyl)-6-deoxy-1-6-(4-octylphenylureido)(uracil-1-yl)-beta-D-glycero-L-talo-heptofuranuronicAcid Trifluoroacetic Salt | CHEMBL1095320
TypeSmall organic molecule
Emp. Form.C31H45N5O12
Mol. Mass.679.7153
SMILESCCCCCCCCc1ccc(NC(=O)N[C@@H]([C@H](O[C@@H]2O[C@H](CN)[C@@H](O)[C@H]2O)[C@@H]2O[C@H]([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)C(O)=O)cc1 |r|
Structure
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