LGALS7

Lectin, galactoside-binding, soluble, 7

PDB rendering based on 1bkz.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols LGALS7 ; GAL7; LGALS7A
External IDs OMIM: 600615 MGI: 1316742 HomoloGene: 100509 ChEMBL: 5008 GeneCards: LGALS7 Gene
Orthologs
Species Human Mouse
Entrez 3963 16858
Ensembl ENSG00000205076 ENSMUSG00000053522
UniProt P47929 D3Z141
RefSeq (mRNA) NM_002307 NM_008496
RefSeq (protein) NP_002298 NP_032522
Location (UCSC) Chr 19:
38.77 – 38.77 Mb
Chr 7:
28.86 – 28.87 Mb
PubMed search

Galectin-7 is a protein that in humans is encoded by the LGALS7 gene.[1][2][3]

The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell–cell and cell–matrix interactions. Differential and in situ hybridizations indicate that this lectin is specifically expressed in keratinocytes. It is expressed at all stages of epidermal differentiation (i.e., in basal and suprabasal layers). It is moderately repressed by retinoic acid. The protein was found mainly in stratified squamous epithelium. The antigen localized to basal keratinocytes, although it was also found, albeit at lower levels, in the suprabasal layers where it concentrated to areas of cell-to-cell contact. The cellular localization and its striking down-regulation in cultured keratinocytes imply a role in cell–cell and/or cell–matrix interactions necessary for normal growth control.[3]

References

  1. Madsen P, Rasmussen HH, Flint T, Gromov P, Kruse TA, Honore B, Vorum H, Celis JE (Apr 1995). "Cloning, expression, and chromosome mapping of human galectin-7". J Biol Chem 270 (11): 5823–29. doi:10.1074/jbc.270.11.5823. PMID 7534301.
  2. Magnaldo T, Bernerd F, Darmon M (May 1995). "Galectin-7, a human 14-kDa S-lectin, specifically expressed in keratinocytes and sensitive to retinoic acid". Dev Biol 168 (2): 259–71. doi:10.1006/dbio.1995.1078. PMID 7729568.
  3. 1 2 "Entrez Gene: LGALS7 lectin, galactoside-binding, soluble, 7 (galectin 7)".

Further reading

This article is issued from Wikipedia - version of the Tuesday, September 01, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.