LANCL1: Difference between revisions

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==Function==
==Function==


This gene encodes a loosely associated peripheral membrane protein related to the LanC family of bacterial membrane-associated proteins involved in the biosynthesis of antimicrobial peptides. This protein may play a role as a peptide-modifying enzyme component in eukaryotic cells. Previously considered a member of the G-protein-coupled receptor superfamily, this protein is now in the LanC family. Multiple alternatively spliced variants, encoding the same protein, have been identified.
This gene encodes a loosely associated peripheral [[membrane protein]] related to the LanC family of bacterial membrane-associated proteins involved in the biosynthesis of antimicrobial peptides. This protein may play a role as a [[peptide]]-modifying [[enzyme]] component in eukaryotic cells. Previously considered a member of the [[G protein–coupled receptor|G-protein-coupled receptor]] superfamily, this protein is now in the LanC family. Multiple [[alternatively spliced]] variants, encoding the same protein, have been identified.


== References ==
== References ==

Latest revision as of 16:05, 16 February 2018

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

n/a

n/a

RefSeq (protein)

n/a

n/a

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

LanC like 1 is a protein that in humans is encoded by the LANCL1 gene. [1]

Function

This gene encodes a loosely associated peripheral membrane protein related to the LanC family of bacterial membrane-associated proteins involved in the biosynthesis of antimicrobial peptides. This protein may play a role as a peptide-modifying enzyme component in eukaryotic cells. Previously considered a member of the G-protein-coupled receptor superfamily, this protein is now in the LanC family. Multiple alternatively spliced variants, encoding the same protein, have been identified.

References

  1. "Entrez Gene: LanC like 1". Retrieved 2016-04-20.

Further reading

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