1zw6
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(New page: 200px<br /> <applet load="1zw6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1zw6, resolution 1.50Å" /> '''Crystal Structure o...)
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Revision as of 18:35, 12 November 2007
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Crystal Structure of the GTP-bound form of RasQ61G
Contents |
Overview
The flexibility of the conserved 57DTAGQ61 motif is essential for Ras, proper cycling in response to growth factors. Here, we increase the, flexibility of the 57DTAGQ61 motif by mutating Gln61 to Gly. The crystal, structure of the RasQ61G mutant reveals a new conformation of switch 2, that bears remarkable structural homology to an intermediate for GTP, hydrolysis revealed by targeted molecular dynamics simulations. The, mutation increased retention of GTP and inhibited Ras binding to the, catalytic site, but not to the distal site of Sos. Most importantly, the, thermodynamics of RafRBD binding to Ras are altered even though the, structure of switch 1 is not affected by the mutation. Our results suggest, that interplay and transmission of structural information between the, switch regions are important factors for Ras function. They propose that, initiation of GTP hydrolysis sets off the separation of the Ras/effector, complex even before the GDP conformation is reached.
Disease
Known diseases associated with this structure: Bladder cancer, somatic OMIM:[190020], Costello syndrome OMIM:[190020], Thyroid carcinoma, follicular, somatic OMIM:[190020]
About this Structure
1ZW6 is a Single protein structure of sequence from Homo sapiens with MG, CA and GNP as ligands. Full crystallographic information is available from OCA.
Reference
Structure of a transient intermediate for GTP hydrolysis by ras., Ford B, Hornak V, Kleinman H, Nassar N, Structure. 2006 Mar;14(3):427-36. PMID:16531227
Page seeded by OCA on Mon Nov 12 20:42:15 2007
Categories: Homo sapiens | Single protein | Ford, B. | Hornak, V. | Kleinman, H. | Nassar, N. | CA | GNP | MG | G-protein | Gtp | Gtpase | Ras
