Baker R T, Varshavsky A
Division of Biology, California Institute of Technology, Pasadena 91125, USA.
J Biol Chem. 1995 May 19;270(20):12065-74. doi: 10.1074/jbc.270.20.12065.
The N-end rule relates the in vivo half-life of a protein to the identity of its N-terminal residue. Tertiary destabilizing N-terminal residues asparagine and glutamine function through their conversion, by enzymatic deamidation, into the secondary destabilizing residues aspartate and glutamate, whose activity requires their enzymatic conjugation to arginine, one of the primary destabilizing residues. We isolated a Saccharomyces cerevisiae gene, termed NTA1, that encodes an amidase (Nt-amidase) specific for N-terminal asparagine and glutamine. Alterations at the putative active-site cysteine of the 52-kDa Nt-amidase inactivate the enzyme. Null nta1 mutants are viable but unable to degrade N-end rule substrates that bear N-terminal asparagine or glutamine. The effects of overexpressing Nt-amidase and other components of the N-end rule pathway suggest interactions between these components and the existence of a multienzyme targeting complex.
N端规则将蛋白质在体内的半衰期与其N端残基的性质联系起来。三级不稳定的N端残基天冬酰胺和谷氨酰胺通过酶促脱酰胺作用转化为二级不稳定残基天冬氨酸和谷氨酸来发挥作用,而后者的活性需要它们与一级不稳定残基之一的精氨酸进行酶促缀合。我们分离出了一个酿酒酵母基因,命名为NTA1,它编码一种对N端天冬酰胺和谷氨酰胺具有特异性的酰胺酶(Nt-酰胺酶)。52 kDa的Nt-酰胺酶假定活性位点的半胱氨酸发生改变会使该酶失活。nta1基因缺失的突变体是有活力的,但无法降解带有N端天冬酰胺或谷氨酰胺的N端规则底物。过表达Nt-酰胺酶和N端规则途径的其他组分的影响表明这些组分之间存在相互作用,并且存在一种多酶靶向复合物。