Literature DB >> 41713

Proton-nuclear-magnetic-resonance/pH-titration studies of the histidines of pancreatic phospholipase A2.

A Aguiar, G H De Haas, E H Jansen, A J Slotboom, R J Williams.   

Abstract

The study by means of 1H nuclear magnetic resonance (NMR) of the histidines of phospholipase A2 isolated from porcine, bovine and equine pancreas is reported. Assignment of the histidine resonances was achieved by comparison of different enzymes and the use of paramagnetic probes. pH titration curves for various histidyl resonances were obtained and compared in the presence and absence of calcium. Calcium is shown to lower the pKa of the active site histidine. The NMR results are compared with the known X-ray three-dimensional structure for the bovine enzyme.

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Year:  1979        PMID: 41713     DOI: 10.1111/j.1432-1033.1979.tb04196.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  2 in total

Review 1.  Paramagnetic Chemical Probes for Studying Biological Macromolecules.

Authors:  Qing Miao; Christoph Nitsche; Henry Orton; Mark Overhand; Gottfried Otting; Marcellus Ubbink
Journal:  Chem Rev       Date:  2022-01-27       Impact factor: 72.087

2.  Structure and function of the catalytic site mutant Asp 99 Asn of phospholipase A2: absence of the conserved structural water.

Authors:  A Kumar; C Sekharudu; B Ramakrishnan; C M Dupureur; H Zhu; M D Tsai; M Sundaralingam
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

  2 in total

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