FEBS Letters · 1994 · 152 citations · 24 references
Life SciencesBiochemistryMicrobiologyEnzymologyProtein BiochemistryProteomicsCatalytic MechanismsEnzyme DiscoveryEnzyme InhibitionEnzyme KineticsEnzyme-substrate RecognitionMicrobial ProteomicsCis-trans Peptide IsomerizationEnzyme ActivityEscherichia ColiIsomerase DiscoveryMass Spectrometry ProteomicsMolecular Mass DeterminationPeptidase ActivitySubsite Specificity
A novel peptidyl-prolyl cis/trans isomerase was isolated from Escherichia coli cell extract and characterized partially. Determination of the molecular mass by electrospray mass spectrometry indicated a protein of 10102 +/- 2 Da, smaller than cyclophilins or FK 506 binding proteins currently known. The specificity constant kcat/Km determined with Succinyl-Ala-Xaa-Pro-Phe-4-nitroanilide (Xaa = Leu) had a value comparable to those from cyclophilins from the same organism. However, the pattern of subsite specificity (Xaa = Gly, Ala, Val, Ile, Leu, Phe, Trp, His, Lys and Glu) was reminiscent of FK506 binding peptidyl-prolyl cis/trans isomerases. The enzyme activity was not inhibited by cyclosporin A or FK506 at inhibitor concentrations of < 5 microM, concentrations that affect most bacterial peptidyl-prolyl cis/trans isomerases. Computer-assisted analysis of 21 amino acid residues of the N-terminus determined by Edman degradation revealed no homology to known peptidyl-prolyl cis/trans isomerases.
24
Catalysis of protein folding by prolyl isomerase
Kurt Lang, Franz X. Schmid, Gunter Fischer · Nature · 1987 · 493 citations