Guided entry of tail-anchored proteins factor 1 (WRB)

The protein contains 174 amino acids for an estimated molecular weight of 19780 Da.

 

Required for the post-translational delivery of tail-anchored (TA) proteins to the endoplasmic reticulum (ER) (PubMed:21444755, PubMed:23041287, PubMed:24392163, PubMed:27226539). Together with CAMLG/GET2, acts as a membrane receptor for soluble GET3/TRC40, which recognizes and selectively binds the transmembrane domain of TA proteins in the cytosol (PubMed:21444755, PubMed:23041287, PubMed:24392163, PubMed:27226539). Required to ensure correct topology and ER insertion of CAMLG (PubMed:31417168, PubMed:32187542). (updated: June 2, 2021)

Protein identification was indicated in the following studies:

  1. 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.

This protein is predicted to be membranous by TOPCONS.


Interpro domains
Total structural coverage: 0%
Model score: 45

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VariantDescription
dbSNP:rs35946782

No binding partner found

The reference OMIM entry for this protein is 602915

Tryptophan-rich basic protein; wrb
Congenital heart disease 5 gene, formerly; chd5, formerly

CLONING

Egeo et al. (1998) used direct cDNA selection to identify over 300 fetal heart and cultured cardiac fibroblast cDNAs from chromosome 21q22.2-q22.3 in order to screen for genes that may contribute to congenital heart defects in Down syndrome (190685) patients. One clone, designated WRB, encoded a predicted 174-amino acid protein with a pI of 10.5. The WRB protein has a tryptophan-rich C-terminal region and a potential nuclear localization signal. By immunofluorescence, Egeo et al. (1998) localized WRB to the cell nucleus. Northern blot analysis of human adult and fetal tissues showed wide expression of WRB as 1.4- and 1.6-kb mRNAs.

MAPPING

By analysis of genomic clones and somatic cell hybrids, Egeo et al. (1998) mapped the WRB gene to chromosome 21q22.3, near HMG14 (163920). ... More on the omim web site

Subscribe to this protein entry history

July 1, 2021: Protein entry updated
Automatic update: Entry updated from uniprot information.

April 25, 2020: Protein entry updated
Automatic update: Entry updated from uniprot information.

Feb. 23, 2019: Protein entry updated
Automatic update: model status changed

Oct. 20, 2018: Protein entry updated
Automatic update: OMIM entry 602915 was added.

Oct. 19, 2018: Additional information
Initial protein addition to the database. This entry was referenced in Bryk and co-workers. (2017).