Role of catalytic residues in enzymatic mechanisms of homologous ketosteroid isomerases

Biochemistry. 2000 Nov 14;39(45):13891-6. doi: 10.1021/bi001629h.

Abstract

Ketosteroid isomerase (KSI) is one of the most proficient enzymes catalyzing an allylic isomerization reaction at a diffusion-controlled rate. In this study of KSI, we have detailed the structures of its active site, the role of various catalytic residues, and have explained the origin of the its fast reactivity by carrying out a detailed investigation of the enzymatic reaction mechanism. This investigation included the X-ray determination of 15 crystal structures of two homologous enzymes in free and complexed states (with inhibitors) and extensive ab initio calculations of the interactions between the active sites and the reaction intermediates. The catalytic residues, through short strong hydrogen bonds, play the role of charge buffer to stabilize the negative charge built up on the intermediates in the course of the reaction. The hydrogen bond distances in the intermediate analogues are found to be about 0.2 A shorter in the product analogues both experimentally and theoretically.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspartic Acid
  • Binding Sites
  • Catalysis
  • Catalytic Domain*
  • Comamonas testosteroni / enzymology
  • Crystallography, X-Ray
  • Hydrogen Bonding
  • Pseudomonas putida / enzymology
  • Sequence Homology, Amino Acid*
  • Steroid Isomerases / chemistry*
  • Tyrosine / chemistry

Substances

  • Aspartic Acid
  • Tyrosine
  • Steroid Isomerases
  • steroid delta-isomerase

Associated data

  • PDB/1QJG