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PMID: 9811545 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Crystal structure of methionine aminopeptidase from hyperthermophile, Pyrococcus furiosus.

Journal of molecular biology ·Vol. 284 ·No. 1 ·1998-11-20 ·Pages 101-24

Tahirov TH, Oki H, Tsukihara T, Ogasahara K, Yutani K, Ogata K, Izu Y, Tsunasawa S, Kato I

Abstract

The structure of methionine aminopeptidase from hyperthermophile Pyrococcus furiosus (PfMAP) with an optimal growth temperature of 100 degreesC was determined by the multiple isomorphous replacement method and refined in three different crystal forms, one monoclinic and two hexagonal, at resolutions of 2.8, 2.9, and 3.5 A. The resolution of the monoclinic crystal form was extended to 1.75 A by water-mediated transformation to a low-humidity form, and the obtained diffraction data used for high-resolution structure refinement. This is the first description of a eukaryotic type methionine aminopeptidase structure. The PfMAP molecule is composed of two domains, a catalytic domain and an insertion domain, connected via two antiparallel beta-strands. The catalytic domain, which possesses an internal 2-fold symmetry and contains two cobalt ions in the active site, resembles the structure of a prokaryotic type MAP from Escherichia coli (EcMAP), while the structure of the insertion domain containing three helices has a novel fold and accounts for a major difference between the eukaryotic and prokaryotic types of methionine aminopeptidase. Analysis of the PfMAP structure in comparison with EcMAP and other mesophile proteins reveals several factors which may contribute to the hyperthermostability of PfMAP: (1) a significantly high number of hydrogen bonds and ion-pairs between side-chains of oppositely charged residues involved in the stabilization of helices; (2) an increased number of hydrogen bonds between the positively charged side-chain and neutral oxygen; (3) a larger number of buried water molecules involved in crosslinking the backbone atoms of sequentially separate segments; (4) stabilization of two antiparallel beta-strands connecting the two domains of the molecule by proline residues; (5) shortening of N and C-terminal tails and stabilization of the loop c3E by deletion of three residues.

MeSH Terms
Amino Acid Sequence Aminopeptidases/chemistry,metabolism Binding Sites Crystallization Crystallography, X-Ray Enzyme Stability Escherichia coli/enzymology Hydrogen Bonding Methionyl Aminopeptidases Models, Molecular Molecular Sequence Data Proline Protein Conformation Protein Folding Pyrococcus furiosus/enzymology Sequence Alignment Ureohydrolases/chemistry Water
Chemicals
Water Proline Aminopeptidases Methionyl Aminopeptidases Ureohydrolases creatinase
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Tahirov T H
Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka, 565, Japan.
Oki H
Tsukihara T
Ogasahara K
Yutani K
Ogata K
Izu Y
Tsunasawa S
Kato I
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1998-11-20
Pages
101-24
Language
English
Region
England
NLM ID
2985088R
Subset
IM
Databases
PDB
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