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TargetPhospho-N-acetylmuramoyl-pentapeptide-transferase
LigandBDBM50386967
Substrate/Competitorn/a
Meas. Tech.ChEMBL_827497 (CHEMBL2051354)
IC50 8900±n/a nM
Citation Okamoto, KSakagami, MFeng, FTakahashi, FUotani, KTogame, HTakemoto, HIchikawa, SMatsuda, A Synthesis of pacidamycin analogues via an Ugi-multicomponent reaction. Bioorg Med Chem Lett22:4810-5 (2012) [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_STAAU | mraY
Type:PROTEIN
Mol. Mass.:35238.55
Organism:Staphylococcus aureus (strain MRSA252)
Description:ChEMBL_827497
Residue:321
Sequence:
MIFVYALLALVITFVLVPVLIPTLKRMKFGQSIREEGPQSHMKKTGTPTMGGLTFLLSIV
ITSLVAIIFVDQANPIILLLFVTIGFGLIGFIDDYIIVVKKNNQGLTSKQKFLAQIGIAI
IFFVLSNVFHLVNFSTSIHIPFTNVAIPLSFAYVIFIVFWQVGFSNAVNLTDGLDGLATG
LSIIGFTMYAIMSFVLGETAIGIFCIIMLFALLGFLPYNINPAKVFMGDTGSLALGGIFA
TISIMLNQELSLIFIGLVFVIETLSVMLQVASFKLTGKRIFKMSPIHHHFELIGWSEWKV
VTVFWAVGLISGLIGLWIGVH
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50386967
n/a
NameBDBM50386967
Synonyms:CHEMBL2048832
TypeSmall organic molecule
Emp. Form.C40H48N10O13
Mol. Mass.876.8683
SMILESC[C@H](NC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O)C(=O)N[C@H]([C@H](C)N(C)C(=O)[C@@H](Cc1cccc(O)c1)NC(=O)CN)C(=O)N\C=C1/O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O |r|
Structure
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