Role of tryptophan hydroxylase Phe313 in determining substrate specificity

被引:18
作者
Daubner, SC
Moran, GR
Fitzpatrick, PF [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
关键词
tyrosine hydroxylase; tryptophan hydroxylase; substrate specificity; kinetics; mutagenesis; active site;
D O I
10.1006/bbrc.2002.6719
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The active site residue phenylalanine 313 is conserved in the sequences of all known tryptophan hydroxylases. The tryptophan hydroxylase F313W mutant protein no longer shows a preference for tryptophan over phenylalanine as a substrate, consistent with a role of this residue in substrate specificity. A tryptophan residue occupies the homologous position in tyrosine hydroxylase. The tyrosine hydroxylase W372F mutant enzyme does not show an increased preference for tryptophan over tyrosine or phenylalanine, so that this residue cannot be considered the dominant factor in substrate specificity in this family of enzymes. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:639 / 641
页数:3
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