GOLGA4

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VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Golgin subfamily A member 4 is a protein that in humans is encoded by the GOLGA4 gene.[1][2]

The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The golgins are a family of proteins, of which the protein encoded by this gene is a member, that are localized to the Golgi. This protein has been postulated to play a role in Rab6-regulated membrane-tethering events in the Golgi apparatus. Alternative splice variants have been described but their full-length nature has not been determined.[2]

Interactions

GOLGA4 has been shown to interact with ARL1.[3][4]

References

  1. Erlich R, Gleeson PA, Campbell P, Dietzsch E, Toh BH (June 1996). "Molecular characterization of trans-Golgi p230. A human peripheral membrane protein encoded by a gene on chromosome 6p12-22 contains extensive coiled-coil alpha-helical domains and a granin motif". J Biol Chem. 271 (14): 8328–8337. doi:10.1074/jbc.271.14.8328. PMID 8626529.
  2. 2.0 2.1 "Entrez Gene: GOLGA4 golgi autoantigen, golgin subfamily a, 4".
  3. Lu, Lei; Hong Wanjin (September 2003). "Interaction of Arl1-GTP with GRIP Domains Recruits Autoantigens Golgin-97 and Golgin-245/p230 onto the Golgi". Mol. Biol. Cell. United States. 14 (9): 3767–3781. doi:10.1091/mbc.E03-01-0864. ISSN 1059-1524. PMC 196566. PMID 12972563.
  4. Van Valkenburgh, H; Shern J F; Sharer J D; Zhu X; Kahn R A (June 2001). "ADP-ribosylation factors (ARFs) and ARF-like 1 (ARL1) have both specific and shared effectors: characterizing ARL1-binding proteins". J. Biol. Chem. United States. 276 (25): 22826–22837. doi:10.1074/jbc.M102359200. ISSN 0021-9258. PMID 11303027.

Further reading