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PP1C binds to SHOC2 through a hydrophobic N-terminal disordered region that is complimentary to the <scene name='95/952695/Rvxf_motif/2'>RVXF Motif on SHOC2</scene> and adjacent to a catalytic metal ions <ref name="Liau">PMID: 35768504</ref>.  In the RAS/RAF signaling cascade, the region of RAF that is C-terminal to the phosphate group binds to this hydrophobic groove, and the remaining residues bind to the hydrophobic region of SHOC2 <ref name="Hauseman">PMID:35830882</ref>. RAF binding to this region of SHOC2 is what allows PP1C to be specific when in the SMP complex in comparison to PP1C on its own <ref name="Hauseman">PMID:35830882</ref>. Similarly to SHOC2, PP1C does not undergo a <scene name='95/952694/Pp1coverlay/4'>significant conformational change</scene> when SHOC2 and MRAS-GTP bind. The lack of conformational change shows that the structure of PP1C is not dependent on the SMP complex, but in order to act as a phosphatase it must be bound to the complex <ref name="Liau">PMID: 35768504</ref>.  
PP1C binds to SHOC2 through a hydrophobic N-terminal disordered region that is complimentary to the <scene name='95/952695/Rvxf_motif/2'>RVXF Motif on SHOC2</scene> and adjacent to a catalytic metal ions <ref name="Liau">PMID: 35768504</ref>.  In the RAS/RAF signaling cascade, the region of RAF that is C-terminal to the phosphate group binds to this hydrophobic groove, and the remaining residues bind to the hydrophobic region of SHOC2 <ref name="Hauseman">PMID:35830882</ref>. RAF binding to this region of SHOC2 is what allows PP1C to be specific when in the SMP complex in comparison to PP1C on its own <ref name="Hauseman">PMID:35830882</ref>. Similarly to SHOC2, PP1C does not undergo a <scene name='95/952694/Pp1coverlay/4'>significant conformational change</scene> when SHOC2 and MRAS-GTP bind. The lack of conformational change shows that the structure of PP1C is not dependent on the SMP complex, but in order to act as a phosphatase it must be bound to the complex <ref name="Liau">PMID: 35768504</ref>.  


PP1C is involved in many different cellular signaling pathways including [https://www.ncbi.nlm.nih.gov/books/NBK545161/. protein synthesis], [https://www.ncbi.nlm.nih.gov/books/NBK559006/. muscle contraction,] and even [https://pubmed.ncbi.nlm.nih.gov/11237211/] carbohydrate metabolism]<ref name="Kelker">PMID: 18992256</ref>. In all these pathways, including the SMP pathway, PP1C does not exist as a monomer, it is present in holoenzyme form complex with one of two regulatory subunits ensuring there is no sporadic pathway activation <ref name="Liau">PMID: 35768504</ref>.
PP1C is involved in many different cellular signaling pathways including [https://www.ncbi.nlm.nih.gov/books/NBK545161/. protein synthesis], [https://www.ncbi.nlm.nih.gov/books/NBK559006/. muscle contraction,] and even [https://pubmed.ncbi.nlm.nih.gov/11237211. carbohydrate metabolism]<ref name="Kelker">PMID: 18992256</ref>. In all these pathways, including the SMP pathway, PP1C does not exist as a monomer, it is present in holoenzyme form complex with one of two regulatory subunits ensuring there is no sporadic pathway activation <ref name="Liau">PMID: 35768504</ref>.
===RAS/RAF ===
===RAS/RAF ===


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OCA, Jaime Prilusky, Kayla Wilhoite, Sloan August, Rosa Trippel, R. Jeremy Johnson