CACYBP

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Template:Short description An Error has occurred retrieving Wikidata item for infobox Calcyclin-binding protein is a protein that in humans is encoded by the CACYBP gene.[1][2][3]

The protein encoded by this gene is a calcyclin binding protein. It may be involved in calcium-dependent ubiquitination and subsequent proteosomal degradation of target proteins. It probably serves as a molecular bridge in ubiquitin E3 complexes and participates in the ubiquitin-mediated degradation of beta-catenin. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene.[3]

Protein Interactions

CACYBP has been shown to interact with SKP1A[4] and SIAH1.[1]

The CacyBP/SIP complex instead, is known to be a part of stress respons, since it interacts with chaperone HSP90.[5]

References

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  1. ^ a b Page Module:Citation/CS1/styles.css has no content.Matsuzawa SI, Reed JC (May 2001). "Siah-1, SIP, and Ebi collaborate in a novel pathway for beta-catenin degradation linked to p53 responses". Molecular Cell. 7 (5): 915–26. doi:10.1016/S1097-2765(01)00242-8. PMID 11389839.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Matsuzawa S, Li C, Ni CZ, Takayama S, Reed JC, Ely KR (January 2003). "Structural analysis of Siah1 and its interactions with Siah-interacting protein (SIP)". The Journal of Biological Chemistry. 278 (3): 1837–40. doi:10.1074/jbc.M210263200. PMID 12421809.
  3. ^ a b Page Module:Citation/CS1/styles.css has no content."Entrez Gene: CACYBP calcyclin binding protein".
  4. ^ Page Module:Citation/CS1/styles.css has no content.Matsuzawa SI, Reed JC (May 2001). "Siah-1, SIP, and Ebi collaborate in a novel pathway for beta-catenin degradation linked to p53 responses". Molecular Cell. 7 (5): 915–26. doi:10.1016/S1097-2765(01)00242-8. PMID 11389839.
  5. ^ Page Module:Citation/CS1/styles.css has no content.Filipek, Anna; Leśniak, Wiesława (2018-12-29). "Aktualny pogląd na komórkową funkcję S100A6 i jego ligandów, CacyBP/SIP i Sgt1". Postępy Biochemii (in polski). 64 (3): 242–252. doi:10.18388/pb.2018_136. ISSN 0032-5422. PMID 30656909.

Further reading

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