Reaction Details Report a problem with these data
Target
Oxa40
Ligand
BDBM92463
Substrate
BDBM92465
Meas. Tech.
Competitive Inhibition Assay
Ki
3.2e+3± 3e+2 nM
Citation
 Verma, V; Testero, SA; Amini, K; Wei, W; Liu, J; Balachandran, N; Monoharan, T; Stynes, S; Kotra, LP; Golemi-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:
BDBM92463
Synonyms:
Imipenem
Type:
Small organic molecule
Emp. Form.:
C12H19N3O4S
Mol. Mass.:
301.362
SMILES:
C[C@@H](O)[C@@H]1[C@H]2CC(SCCN=CN)[C@@H](N2C1=O)C(O)=O |r,w:11.11|
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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