| Literature DB >> 27192667 |
Sunghark Kwon1, Yuichi Nishitani1, Satoshi Watanabe2, Yoshinori Hirao3, Tadayuki Imanaka4, Tamotsu Kanai3,5, Haruyuki Atomi3,5, Kunio Miki1,5.
Abstract
A [NiFe] hydrogenase maturation protease HybD from Thermococcus kodakarensis KOD1 (TkHybD) is involved in the cleavage of the C-terminal residues of [NiFe] hydrogenase large subunits by Ni recognition. Here, we report the crystal structure of TkHybD at 1.82 Å resolution to better understand this process. TkHybD exhibits an α/β/α sandwich fold with conserved residues responsible for the Ni recognition. Comparisons of TkHybD with homologous proteins also reveal that they share a common overall architecture, suggesting that they have similar catalytic functions. Our results including metal binding site prediction provide insight into the substrate recognition and catalysis mechanism of TkHybD. Proteins 2016; 84:1321-1327.Entities:
Keywords: C-terminal cleavage; Ni binding; hyperthermophilic archaea; protease; substrate recognition
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Year: 2016 PMID: 27192667 DOI: 10.1002/prot.25070
Source DB: PubMed Journal: Proteins ISSN: 0887-3585