Published July 30, 2009 | Version v1
Journal article

Expression, purification and preliminary X-ray crystallographic analysis of UDP-galactopyranose mutase from Deinococcus radiodurans

  • 1. Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon, Saskatchewan S7N 5C9 (Canada)

Description

UDP-galactopyranose mutase was crystallized using the microbatch method. The crystals diffracted to 2.36 Å resolution using synchrotron radiation. UDP-galactopyranose mutase (UGM) catalyzes the interconversion of UDP-galactopyranose and UDP-galactofuranose. A UGM–substrate complex from Deinococccus radiodurans has been expressed, purified and crystallized. Crystals were obtained by the microbatch-under-oil method at room temperature. The crystals diffracted to 2.36 Å resolution at the Canadian Light Source The space group was found to be P212121, with unit-cell parameters a = 134.0, b = 176.6, c = 221.6 Å. The initial structure solution was determined by molecular replacement using UGM from Mycobacterium tuberculosis as a template model

Availability note (English)

Available from http://dx.doi.org/10.1107/S1744309109027754; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720349

Additional details

Publishing Information

Journal Title
Acta Crystallographica. Section F
Journal Volume
65
Journal Issue
Pt 8
Journal Page Range
p. 843-845
ISSN
1744-3091
CODEN
ACSFCL

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46067467
Subject category
S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
Descriptors DEI
CRYSTALS; LIGHT SOURCES; MATHEMATICAL SOLUTIONS; RESOLUTION; SOLUTIONS; SPACE GROUPS; SUBSTRATES; SYNCHROTRON RADIATION
Descriptors DEC
BREMSSTRAHLUNG; DISPERSIONS; ELECTROMAGNETIC RADIATION; HOMOGENEOUS MIXTURES; MIXTURES; RADIATION SOURCES; RADIATIONS; SYMMETRY GROUPS

Optional Information

Copyright
Copyright (c) International Union of Crystallography 2009
Notes
PMCID: PMC2720349; PMID: 19652355; PUBLISHER-ID: hc5085; OAI: oai:pubmedcentral.nih.gov:2720349