Cathelineau L, Briand P, Petit F, Nuyts J P, Farriaux J P, Kamoun P P
Biochim Biophys Acta. 1980 Jul 10;614(1):40-5. doi: 10.1016/0005-2744(80)90165-5.
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.
在一名患有鸟氨酸氨甲酰基转移酶(氨甲酰磷酸:L-鸟氨酸氨甲酰基转移酶,EC 2.1.3.3)缺乏症的患者中发现了一种新的人类酶变体。这种突变酶的亲和力降低,鸟氨酸的Km值异常(在所有pH值下均比对照大3至5倍)。最大反应速度(V)随pH值变化,与正常酶相同,但得到的S形曲线(V对pH)向碱性pH值偏移。功能性催化基团的pK为8.3,而对照酶为6.65。在其最适pH值下,突变酶的V大于正常酶的V。已经描述了其他对鸟氨酸具有异常亲和力的突变酶蛋白。它们都与本文报道的不同。