The crystal structure of methenyltetrahydromethanopterin cyclohydrolase from Methanobrevibacter ruminantium

Proteins. 2013 Nov;81(11):2064-70. doi: 10.1002/prot.24372. Epub 2013 Aug 23.

Abstract

Methenyltetrahydromethanopterin cyclohydrolase (Mch) is involved in the methanogenesis pathway of archaea as a C1 unit carrier where N(5) -formyl-tetrahydromethanopterin is converted to methenyl-tetrahydromethanopterin. Mch from Methanobrevibacter ruminantium was cloned, purified, crystallized and its crystal structure solved at 1.37 Å resolution. A biologically active trimer, the enzyme is composed of two domains including an N-terminal domain of six α-helices encompassing a series of four β-sheets and a predominantly anti-parallel β-sheet at the C-terminus flanked on one side by α-helices. Sequence and structural alignments have helped identify residues involved in substrate binding and trimer formation.

Keywords: archaea; autotroph; coenzyme synthesis; cyclohydrolase; methanogenesis; trimer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminohydrolases / chemistry*
  • Archaeal Proteins / chemistry
  • Crystallography, X-Ray
  • Methanobrevibacter / enzymology*

Substances

  • Archaeal Proteins
  • Aminohydrolases
  • methenyltetrahydromethanopterin cyclohydrolase