ZFYVE27

ZFYVE27
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesZFYVE27, PROTRUDIN, SPG33, zinc finger FYVE-type containing 27
External IDsMGI: 1919602 HomoloGene: 16939 GeneCards: ZFYVE27
Gene location (Human)
Chr.Chromosome 10 (human)[1]
Band10q24.2Start97,737,121 bp[1]
End97,760,907 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

118813

319740

Ensembl

ENSG00000155256

ENSMUSG00000018820

UniProt

Q5T4F4

Q3TXX3

RefSeq (mRNA)

NM_001164531
NM_177319

RefSeq (protein)

NP_001158003
NP_796293

Location (UCSC)Chr 10: 97.74 – 97.76 MbChr 19: 42.16 – 42.19 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Zinc finger, FYVE domain containing 27 is a protein that in humans is encoded by the ZFYVE27 gene.[5]

Function

This gene encodes a protein with several Transmembrane domains, a Rab11-binding domain and a lipid-binding FYVE finger domain. The encoded protein appears to promote Neuriteformation. A mutation in this gene has been reported to be associated with Hereditary spastic paraplegia, however the Pathogenicity of the mutation, which may simply represent a Polymorphism (biology), is unclear. [provided by RefSeq, Mar 2010].

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000155256 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000018820 - Ensembl, May 2017
  3. "Human PubMed Reference:".
  4. "Mouse PubMed Reference:".
  5. "Entrez Gene: Zinc finger, FYVE domain containing 27".

Further reading

  • Zhang C, Li D, Ma Y, Yan J, Yang B, Li P, Yu A, Lu C, Ma X (July 2012). "Role of spastin and protrudin in neurite outgrowth". Journal of Cellular Biochemistry. 113 (7): 2296–307. doi:10.1002/jcb.24100. PMID 22573551.
  • Saita S, Shirane M, Natume T, Iemura S, Nakayama KI (May 2009). "Promotion of neurite extension by protrudin requires its interaction with vesicle-associated membrane protein-associated protein". The Journal of Biological Chemistry. 284 (20): 13766–77. doi:10.1074/jbc.M807938200. PMC 2679478. PMID 19289470.
  • Mannan AU, Krawen P, Sauter SM, Boehm J, Chronowska A, Paulus W, Neesen J, Engel W (August 2006). "ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia". American Journal of Human Genetics. 79 (2): 351–7. doi:10.1086/504927. PMC 1559503. PMID 16826525.
  • Martignoni M, Riano E, Rugarli EI (July 2008). "The role of ZFYVE27/protrudin in hereditary spastic paraplegia". American Journal of Human Genetics. 83 (1): 127–8, author reply 128–30. doi:10.1016/j.ajhg.2008.05.014. PMC 2443834. PMID 18606302.
  • Matsuzaki F, Shirane M, Matsumoto M, Nakayama KI (December 2011). "Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation". Molecular Biology of the Cell. 22 (23): 4602–20. doi:10.1091/mbc.E11-01-0068. PMC 3226478. PMID 21976701.
  • Shirane M, Nakayama KI (November 2006). "Protrudin induces neurite formation by directional membrane trafficking". Science. 314 (5800): 818–21. doi:10.1126/science.1134027. PMID 17082457.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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