Title : Inactivation of carboxypeptidase Y by mutational removal of the putative essential histidyl residue - Bech_1989_Carlsberg.Res.Commun_54_165 |
Author(s) : Bech LM , Breddam K |
Ref : Carlsberg Res Commun , 54 :165 , 1989 |
Abstract :
Carboxypeptidase Y is a serine carboxypeptidase assumed to contain a catalytic triad similar to the serine endopeptidases. On the basis of the homology between various serine carboxypeptidases His-397 is suspected to be part of the catalytic triad. To test this it was exchanged with Ala and Arg by site-directed mutagenesis of the cloned PRC1 gene. The catalytic efficiency of the mutant enzymes were reduced by a factor of 2 X 10(4) and 7 X 10(2), respectively, confirming the key role of His-397 in catalysis. Treatment of Ala-397-CPD-Y with Hg++ or CNBr, hence modifying Cys-341 located in the vicinity of the active site abolished the residual activity of the enzyme, indicating an additional involvement of this residue in catalysis. |
PubMedSearch : Bech_1989_Carlsberg.Res.Commun_54_165 |
PubMedID: 2639680 |
Gene_locus related to this paper: yeast-cbpy1 |
Gene_locus | yeast-cbpy1 |
Bech LM, Breddam K (1989)
Inactivation of carboxypeptidase Y by mutational removal of the putative essential histidyl residue
Carlsberg Res Commun
54 :165
Bech LM, Breddam K (1989)
Carlsberg Res Commun
54 :165