Please use this identifier to cite or link to this item: https://doi.org/10.1007/s10969-012-9143-5
DC FieldValue
dc.titleCrystal structure of mouse RhoA:GTPcS complex in a centered lattice
dc.contributor.authorJobichen, C.
dc.contributor.authorPal, K.
dc.contributor.authorSwaminathan, K.
dc.date.accessioned2014-10-27T08:25:01Z
dc.date.available2014-10-27T08:25:01Z
dc.date.issued2012-12
dc.identifier.citationJobichen, C.,Pal, K.,Swaminathan, K. (2012-12). Crystal structure of mouse RhoA:GTPcS complex in a centered lattice. Journal of Structural and Functional Genomics 13 (4) : 241-245. ScholarBank@NUS Repository. <a href="https://doi.org/10.1007/s10969-012-9143-5" target="_blank">https://doi.org/10.1007/s10969-012-9143-5</a>
dc.identifier.issn1345711X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/100366
dc.description.abstractRhoA, a member of the Rho sub-family of small GTPases, plays a significant signaling role in cell morphogenesis, migration, neuronal development, cell division and adhesion. So far, 4 structures of RhoA:GDP/GTP analogs and 14 structures of RhoA in complex with other proteins have been reported. All RhoA:GDP/GTP analog complexes have been crystallized in primitive lattices and RhoA is monomeric. This is the first time a RhoA:GTP analog complex has been crystallized as a dimer in a centered lattice. The present structure reveals structural differences in the switch-I (residues 28-42) and switch-II (residues 61-66) regions, which play important roles in interactions with downstream targets to transduce signals, when compared to the previously reported structures. © Springer Science+Business Media B.V. 2012.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s10969-012-9143-5
dc.sourceScopus
dc.subjectCrystal structure
dc.subjectDimer
dc.subjectGTPγS
dc.subjectRhoA
dc.subjectSmall GTPases
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1007/s10969-012-9143-5
dc.description.sourcetitleJournal of Structural and Functional Genomics
dc.description.volume13
dc.description.issue4
dc.description.page241-245
dc.description.codenJSFGA
dc.identifier.isiutNOT_IN_WOS
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