Suprabasin (SBSN)

The protein contains 590 amino acids for an estimated molecular weight of 60541 Da.

 

No function (updated: March 4, 2015)

Protein identification was indicated in the following studies:

  1. Goodman and co-workers. (2013) The proteomics and interactomics of human erythrocytes. Exp Biol Med (Maywood) 238(5), 509-518.
  2. Hegedűs and co-workers. (2015) Inconsistencies in the red blood cell membrane proteome analysis: generation of a database for research and diagnostic applications. Database (Oxford) 1-8.
  3. Bryk and co-workers. (2017) Quantitative Analysis of Human Red Blood Cell Proteome. J Proteome Res. 16(8), 2752-2761.
  4. D'Alessandro and co-workers. (2017) Red blood cell proteomics update: is there more to discover? Blood Transfus. 15(2), 182-187.

Methods

The following articles were analysed to gather the proteome content of erythrocytes.

The gene or protein list provided in the studies were processed using the ID mapping API of Uniprot in September 2018. The number of proteins identified and mapped without ambiguity in these studies is indicated below.
Only Swiss-Prot entries (reviewed) were considered for protein evidence assignation.

PublicationIdentification 1Uniprot mapping 2Not mapped /
Obsolete
TrEMBLSwiss-Prot
Goodman (2013)2289 (gene list)227853205992269
Lange (2014)123412347281224
Hegedus (2015)2638262202352387
Wilson (2016)165815281702911068
d'Alessandro (2017)18261817201815
Bryk (2017)20902060101081942
Chu (2018)18531804553621387

1 as available in the article and/or in supplementary material
2 uniprot mapping returns all protein isoforms as one entry

The compilation of older studies can be retrieved from the Red Blood Cell Collection database.

The data and differentiation stages presented below come from the proteomic study and analysis performed by our partners of the GReX consortium, more details are available in their published work.

No sequence conservation computed yet.

Interpro domains
Total structural coverage: 36%
Model score: 0
No model available.

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VariantDescription
dbSNP:rs10775583

No binding partner found

Biological Process

Molecular Function

The reference OMIM entry for this protein is 609969

Suprabasin
Sbsn

CLONING

By subtractive hybridization to identify genes expressed in differentiated mouse keratinocytes, Park et al. (2002) cloned Sbsn. The deduced 700-amino acid protein has a calculated molecular mass of 72 kD. Sbsn contains an N-terminal transmembrane domain, a central domain with glycine-, alanine-, and histidine-rich short tandem repeats, and several phosphorylation and myristoylation sites. An alternatively spliced transcript encodes a protein lacking the central repetitive region. By RT-PCR of skin RNA, Park et al. (2002) cloned a partial human SBSN cDNA. Northern blot analysis of human tissues detected 2.2- and 1.1-kb SBSN transcripts in skin, esophagus, uterus, thymus, and a keratinocyte cell line. Northern blot analysis detected 2 Sbsn transcripts at embryonic day 15.5 in mice, coinciding with epidermal stratification. In situ hybridization of embryonic and adult mice showed Sbsn expression in the suprabasal layers of the epithelia in tongue, stomach, and epidermis. Northern and RNA dot blot analyses of adult mouse tissues revealed expression in uterus and thyroid, but not in heart, brain, spleen, lung, liver, smooth muscle, and kidney. Fluorescence-tagged Sbsn showed a punctate cytoplasmic distribution in transfected mouse keratinocytes that did not overlap with lysosomal or mitochondrial markers.

GENE FUNCTION

Park et al. (2002) found that expression of Sbsn in primary mouse epidermal keratinocytes was induced by calcium and phorbol esters and inhibited by a PKC (see PRKCA; 176960) inhibitor. Monomeric recombinant Sbsn was cross-linked into a high molecular mass form by the transglutaminases Tgm2 (190196) and Tgm3 (600238). Park et al. (2002) concluded that SBSN may have a role in epidermal differentiation.

GENE STRUCTURE

Park et al. (2002) determined that the mouse Sbsn gene contains 4 exons.

MAPPING

By genomic sequence analysis, Park et al. (2002) mapped the SBSN gene to chromosome 19q13.1. They mapped the mouse Sbsn gene to a region of chromosome 7B2-B3 that shares homology of synteny with human chromosome 19q13.1. ... More on the omim web site

Subscribe to this protein entry history

Feb. 2, 2018: Protein entry updated
Automatic update: Uniprot description updated

Dec. 19, 2017: Protein entry updated
Automatic update: Uniprot description updated

March 25, 2017: Additional information
No protein expression data in P. Mayeux work for SBSN

March 16, 2016: Protein entry updated
Automatic update: OMIM entry 609969 was added.