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From Proteopedia
This page, as it appeared on March 17, 2023, was featured in this article in the journal Biochemistry and Molecular Biology Education.
SHOC2-PP1C-MRAS
IntroductionSHOC2-PP1C-MRAS is a ternary complex formed by the individual proteins: SHOC2, PP1C, and MRAS. Formation of this complex begins with a signal binding to a receptor tyrosine kinase receptor(RTK). This causes membrane bound MRAS to exchange GDP for GTP. From here the complex comes together and is able to dephosphorylate the RAF complex leading to further downstream signaling effects.
Overall StructureSHOC2
PP1C
MRAS
Key Ligand Interactions![]() Figure 3: Electrostatic illustration of the amphipathic binding pocket of the LPA1 receptor. This binding pocket was revealed by cutting away the exterior or the protein. This binding pocket, located in the interior of the protein, has both polar and nonpolar regions. The blue and red coloration highlight the positively and negatively charged regions, respectively, and the white color shows the nonpolar region of the binding pocket. SHOC2 and PP1CSHOC2 and MRASPP1C and MRASSignaling Pathway
Disease RelevanceCancerRASopathiesFuture Studies3D structures of lysophosphatidic acid receptor4z34, 4z35, 4z36 - hLPA1 + antagonist - human References
Proteopedia ResourcesCategory:Lysophosphatidic acid binding Category:Lysophosphatidic acid Butler University Proteopedia Pages See also: |
Student Contributors
Madeline Gilbert Inaya Patel Rushda Hussein