Ontology highlight
ABSTRACT:
SUBMITTER: Oza JP
PROVIDER: S-EPMC3324563 | biostudies-literature | 2012 Mar
REPOSITORIES: biostudies-literature
Oza Javin P JP Sowers Kevin R KR Perona John J JJ
Biochemistry 20120313 12
Hydrogenotrophic methanogens possessing the hydrogen-dependent dehydrogenase Hmd also encode paralogs of this protein whose function is poorly understood. Here we present biochemical evidence that the two inactive Hmd paralogs of Methanocaldococcus jannaschii, HmdII and HmdIII, form binary and ternary complexes with several components of the protein translation apparatus. HmdII and HmdIII, but not the active dehydrogenase Hmd, bind with micromolar binding affinities to a number of tRNAs and form ...[more]