Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2009-6-2
pubmed:abstractText
Nucleoside diphosphate kinases from haloarchaea Haloarcula quadrata (NDK-q) and H. sinaiiensis (NDK-s) are identical except for one out of 154 residues, i.e., Arg(31) in NDK-q and Cys(31) in NDK-s. However, the salt-dependent activity profiles of NDK-q and NDK-s are quite different: the optimal NaCl concentrations of NDK-q and NDK-s are 1 M and 2 M, respectively. We analyzed the relationships of the secondary, tertiary, and quaternary structures and NDK activity of these NDKs at various salt concentrations, and revealed that 1), NDK-q is present as a hexamer under a wide range of salt concentrations (0.2-4 M NaCl), whereas NDK-s is present as a hexamer at an NaCl concentration above 2 M and as a dimer at NaCl concentrations below 1 M; 2), dimeric NDK-s has lower activity than hexameric NDK-s; and 3), dimeric NDK-s has higher helicity than hexameric NDK-s. We also determined the crystal structure of hexameric NDK-q, and revealed that Arg(31) plays an important role in stabilizing the hexamer. Thus the substitution of Arg (as in NDK-q) to Cys (as in NDK-s) at position 31 destabilizes the hexameric assembly, and causes dissociation to less active dimers at low salt concentrations.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-10222271, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-10320398, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-10805563, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-10980157, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11026680, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11092928, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11517324, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11604538, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11768305, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11768306, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11768309, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-11835509, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-12435508, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-15299374, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-15299926, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-15466238, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-15572765, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-16293253, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-17674972, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-4343790, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-5700707, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-7669763, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-8263923, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-8578593, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-8702707, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-9757107, http://linkedlifedata.com/resource/pubmed/commentcorrection/19486691-9783181
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1542-0086
pubmed:author
pubmed:issnType
Electronic
pubmed:day
3
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4692-700
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed-meshheading:19486691-Amino Acid Sequence, pubmed-meshheading:19486691-Archaeal Proteins, pubmed-meshheading:19486691-Circular Dichroism, pubmed-meshheading:19486691-Crystallization, pubmed-meshheading:19486691-Escherichia coli, pubmed-meshheading:19486691-Haloarcula, pubmed-meshheading:19486691-Models, Molecular, pubmed-meshheading:19486691-Molecular Sequence Data, pubmed-meshheading:19486691-Nucleoside-Diphosphate Kinase, pubmed-meshheading:19486691-Protein Stability, pubmed-meshheading:19486691-Protein Structure, Quaternary, pubmed-meshheading:19486691-Protein Structure, Secondary, pubmed-meshheading:19486691-Protein Structure, Tertiary, pubmed-meshheading:19486691-Sodium Chloride, pubmed-meshheading:19486691-Structural Homology, Protein, pubmed-meshheading:19486691-X-Ray Diffraction
pubmed:year
2009
pubmed:articleTitle
Molecular mechanism of distinct salt-dependent enzyme activity of two halophilic nucleoside diphosphate kinases.
pubmed:affiliation
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't