SNX5

In today's world, SNX5 has become increasingly important. Whether in the field of health, technology, education or any other field, SNX5 has captured the attention of experts and the general public. Over the years, we have witnessed how SNX5 has evolved and become a key issue in our society. In this article, we will thoroughly explore all facets of SNX5, from its history to its current applications, with the goal of providing a complete and detailed overview of its importance in today's world.

SNX5
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSNX5, sorting nexin 5
External IDsOMIM: 605937; MGI: 1916428; HomoloGene: 40944; GeneCards: SNX5; OMA:SNX5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_152227
NM_001282454
NM_014426

NM_001199188
NM_024225

RefSeq (protein)

NP_001269383
NP_055241
NP_689413

NP_001186117
NP_077187

Location (UCSC)Chr 20: 17.94 – 17.97 MbChr 2: 144.09 – 144.11 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Sorting nexin-5 is a protein that in humans is encoded by the SNX5 gene.[5][6][7]

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein is a component of the mammalian retromer complex,[6] which facilitates cargo retrieval from endosomes to the trans-Golgi network. It has also been shown to bind to the Fanconi anemia, complementation group A protein. This gene results in two transcript variants encoding the same protein.[7]

Interactions

SNX5 has been shown to interact with FANCA.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000089006Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027423Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Otsuki T; Kajigaya S; Ozawa K; Liu JM (Jan 2000). "SNX5, a new member of the sorting nexin family, binds to the Fanconi anemia complementation group A protein". Biochem Biophys Res Commun. 265 (3): 630–5. doi:10.1006/bbrc.1999.1731. PMID 10600472.
  6. ^ a b Wassmer T; Attar N; Bujny MV; Oakley J; Traer CJ; Cullen PJ (Dec 2006). "A loss-of-function screen reveals SNX5 and SNX6 as potential components of the mammalian retromer". J Cell Sci. 120 (Pt 1): 45–54. doi:10.1242/jcs.03302. PMID 17148574.
  7. ^ a b "Entrez Gene: SNX5 sorting nexin 5".

Further reading