Target
Oxa40
Ligand
BDBM92464
Substrate
BDBM92465
Meas. Tech.
Competitive Inhibition Assay
Ki
7.8e+4± 2e+3 nM
Citation
 Verma, VTestero, SAAmini, KWei, WLiu, JBalachandran, NMonoharan, TStynes, SKotra, LPGolemi-Kotra, D Hydrolytic mechanism of OXA-58 enzyme, a carbapenem-hydrolyzing class D β-lactamase from Acinetobacter baumannii. J Biol Chem 286:37292-303 (2011) [PubMed]  Article 
Target
Name:
Oxa40
Synonyms:
Beta-lactamase | Class D β-lactamase (OXA-24)
Type:
Enzyme
Mol. Mass.:
30946.50
Organism:
Acinetobacter baumannii
Description:
Q8RLA6
Residue:
275
Sequence:
MKKFILPIFSISILVSLSACSSIKTKSEDNFHISSQQHEKAIKSYFDEAQTQGVIIIKEGKNLSTYGNALARANKEYVPASTFKMLNALIGLENHKATTNEIFKWDGKKRTYPMWEKDMTLGEAMALSAVPVYQELARRTGLELMQKEVKRVNFGNTNIGTQVDNFWLVGPLKITPVQEVNFADDLAHNRLPFKLETQEEVKKMLLIKEVNGSKIYAKSGWGMGVTPQVGWLTGWVEQANGKKIPFSLNLEMKEGMSGSIRNEITYKSLENLGII
  
Inhibitor
Name:
BDBM92464
Synonyms:
Carbenicillin
Type:
Small organic molecule
Emp. Form.:
C17H18N2O6S
Mol. Mass.:
378.4
SMILES:
CC1(C)S[C@@H]2[C@H](NC(=O)[C@@H](C(O)=O)c3ccccc3)C(=O)N2[C@H]1C(O)=O
Structure:
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Substrate
Name:
BDBM92465
Synonyms:
Nitrocefin
Type:
Small organic molecule
Emp. Form.:
C13H14N2O4S2
Mol. Mass.:
326.391
SMILES:
OC(=O)C1=N[C@H](SCC1)[C@H](NC(=O)Cc1cccs1)C=O |t:3|
Structure:
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