<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>96(11)</volume><submitter>Yamamura A</submitter><funding>Ministry of Education, Culture, Sports, Science and Technology</funding><pubmed_abstract>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_abstract><journal>Biophysical journal</journal><pagination>4692-700</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2711501</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular mechanism of distinct salt-dependent enzyme activity of two halophilic nucleoside diphosphate kinases.</pubmed_title><pmcid>PMC2711501</pmcid><pubmed_authors>Ichimura T</pubmed_authors><pubmed_authors>Kamekura M</pubmed_authors><pubmed_authors>Okai M</pubmed_authors><pubmed_authors>Mizuki T</pubmed_authors><pubmed_authors>Ohtsuka J</pubmed_authors><pubmed_authors>Miyazono K</pubmed_authors><pubmed_authors>Usami R</pubmed_authors><pubmed_authors>Tanokura M</pubmed_authors><pubmed_authors>Yamamura A</pubmed_authors><pubmed_authors>Nagata K</pubmed_authors><pubmed_authors>Makino T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular mechanism of distinct salt-dependent enzyme activity of two halophilic nucleoside diphosphate kinases.</name><description>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.</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Jun</publication><modification>2024-11-20T10:54:01.823Z</modification><creation>2019-03-27T00:14:01Z</creation></dates><accession>S-EPMC2711501</accession><cross_references><pubmed>19486691</pubmed><doi>10.1016/j.bpj.2009.03.012</doi></cross_references></HashMap>