Literature DB >> 7397202

Kinetic analysis of a new human ornithine carbamoyltransferase variant.

L Cathelineau, P Briand, F Petit, J P Nuyts, J P Farriaux, P P Kamoun.   

Abstract

A new human enzymatic variant was found in a patient with ornithine carbamoyltransferase (carbamoylphosphate:L-ornithine carbamoyltransferase, EC 2.1.3.3) deficiency. This mutant enzyme has decreased affinity, with an abnormal Km value for ornithine (3-5-times greater than control at all pH values). The maximal velocity (V) varied with pH as a normal enzyme but the sigmoid curve obtained (V vs. pH) is shifted towards alkaline pH values. The pK of the functional catalytic group is 8.3 instead of 6.65 of a control enzyme. At its optimum pH the V of the mutant enzyme is greater than the V of the normal enzyme. Other mutant enzyme proteins with abnormal affinity for ornithine have already been described. They all are different from the reported here.

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Year:  1980        PMID: 7397202     DOI: 10.1016/0005-2744(80)90165-5

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  Molecular basis of ornithine transcarbamylase deficiency lacking enzyme protein.

Authors:  T Saheki; Y Imamura; I Inoue; S Miura; M Mori; A Ohtake; M Tatibana; N Katsumata; T Ohno
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

2.  The molecular basis of ornithine transcarbamylase deficiency: modelling the human enzyme and the effects of mutations.

Authors:  M Tuchman; H Morizono; O Reish; X Yuan; N M Allewell
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

  2 in total

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