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TargetPBP2A
LigandBDBM50217404
Substrate/Competitorn/a
Meas. Tech.ChEBML_153664
IC50 1.4±n/a nM
Citation Wilkening, RRRatcliffe, RWWildonger, KJCama, LDDykstra, KDDiNinno, FPBlizzard, TAHammond, MLHeck, JVDorso, KLSt Rose, EKohler, JHammond, GG Synthesis and activity of 2-(sulfonamido)methyl-carbapenems: discovery of a novel, anti-MRSA 1,8-naphthosultam pharmacophore. Bioorg Med Chem Lett9:673-8 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
PBP2A
Name:PBP2A
Synonyms:MecA PBP2' (penicillin binding protein 2') | PBP2A | Penicillin-binding protein | mecA
Type:PROTEIN
Mol. Mass.:76283.66
Organism:Staphylococcus aureus
Description:ChEMBL_105733
Residue:668
Sequence:
MKKIKIVPLILIVVVVGFGIYFYASKDKEINNTIDAIEDKNFKQVYKDSSYISKSDNGEV
EMTERPIKIYNSLGVKDINIQDRKIKKVSKNKKRVDAQYKIKTNYGNIDRNVQFNFVKED
GMWKLDWDHSVIIPGMQKDQSIHIENLKSERGKILDRNNVELANTGTHMRLGIVPKNVSK
KDYKAIAKELSISEDYINNKWIKIGYKMIPSFHFKTVKKMDEYLSDFAKKFHLTTNETES
RNYPLEKATSHLLGYVGPINSEELKQKEYKGYKDDAVIGKKGLEKLYDKKLQHEDGYRVT
IVDDNSNTIAHTLIEKKKKDGKDIQLTIDAKVQKSIYNNMKNDYGSGTAIHPQTGELLAL
VSTPSYDVYPFMYGMSNEEYNKLTEDKKEPLLNKFQITTSPGSTQKILTAMIGLNNKTLD
DKTSYKIDGKGWQKDKSWGGYNVTRYEVVNGNIDLKQAIESSDNIFFARVALELGSKKFE
KGMKKLGVGEDIPSDYPFYNAQISNKNLDNEILLADSGYGQGEILINPVQILSIYSALEN
NGNINAPHLLKDTKNKVWKKNIISKENINLLNDGMQQVVNKTHKEDIYRSYANLIGKSGT
AELKMKQGESGRQIGWFISYDKDNPNMMMAINVKDVQDKGMASYNAKISGKVYDELYENG
NKKYDIDE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50217404
n/a
NameBDBM50217404
Synonyms:CHEMBL348278
TypeSmall organic molecule
Emp. Form.C23H19N2NaO6
Mol. Mass.442.3965
SMILES[Na+].[H][C@]12[C@@H](C)C(CN3C(=O)c4cccc5cccc(C3=O)c45)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C([O-])=O |c:23|
Structure
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