Transmembrane protein 53


Transmembrane protein 53, or TMEM53, is a protein that is encoded on chromosome 1 in humans. It has no paralogs but is predicted to have many orthologs across eukaryotes.

Properties and Structure

General Properties

Source:

Secondary Structure

The secondary structure of TMEM53 is predicted to consist of alternating pairs of alpha helices and beta sheets.

Alternative Splicing

TMEM53 has 3 exons. Twelve alternative splice forms have been identified using 26 alternative exons. The following table includes the predicted post-translational modifications for each isoform.
AceView Splice Form# Amino Acids% ID with RefSeq# of Clones FoundDUF829CK2 sitesPKC sitesTyr sitesPumilio siteN-Myristoylation sitesExtras
a277RefSeq64X23112
b24788.8%6X22112
c20464.4%1X21112Microbody C-terminal targeting signal
d20473.6%10X22111
e22357.5%2X143
f14321.4%1X133Amidation site, Asn glycosylation site, cAMP-dependent phosphorylation site
g142n/a1131
h13745.1%2X132Protein prenyltransferase repeat
i12932.1%1X42
j13927.2%21X23
k110n/a1143Amidation site, Asn glycosylation site, cAMP-dependent phosphorylation site
l106n/a53

Function

The function of TMEM53 is not fully understood. It contains a domain of unknown function, DUF829, which is approximately 240 amino acids long. This domain has not been found in proteins other than TMEM53 and its orthologs.

Expression

Based on human and mouse EST profiles and a human tissue GEO profile, TMEM53 appears to be expressed ubiquitously at low levels in both normal and cancerous tissues.
More specific expression patterns have also been observed:

Homology

Transmembrane protein 53 has no paralogs. It does, however, have orthologs extending throughout eukaryotes, from primates to amoeba. The following table presents a selection of orthologs found using searches in BLAST and BLAT. It is not a comprehensive list, but rather a small selection meant to display the diversity of species in which orthologs are found.
Scientific nameCommon nameAccession numberSequence lengthPercent identityPercent Similarity
Homo sapiensHumanNP_078863277 aa--
Macaca mulattaRhesus monkeyXP_001093396.1204 aa97%98%
Canis lupus familiarisDogXP_539639.2278 aa88%92%
Mus musculusMouseNP_081113.1276 aa86%91%
Monodelphis domesticaOpossumXP_001376124.1405 aa69%82%
Gallus gallusChickenXP_422420.1276 aa56%70%
Xenopus laevisFrogNP_001086490.1285 aa54%69%
Danio rerioZebrafishNP_001002637.1281 aa47%66%
Ciona intestinalisSea squirtXP_002127410.1290 aa37%51%
Drosophila melanogasterFruit flyNP_610178.2368 aa35%56%
Apis melliferaHoney beeXP_392954.1326 aa32%52%
Strongylocentrotus purpuratusPurple sea urchinXP_788598.1287 aa32%52%
Oryza sativaRiceEEC81354.1412 aa31%45%
Nematostella vectensisSea anemoneXP_001628968.1242 aa29%52%
Populus trichocarpaBlack cottonwoodXP_002306371.1443 aa29%45%
Aspergillus nidulansFungusXP_657927.1285 aa27%44%
Dictyostelium discoideumAmoebaXP_644630.1354 aa27%44%

Based on ClustalW multiple sequence alignments of 38 orthologs, including the ones above, 11 amino acids are completely conserved throughout all species with this protein.

Predicted Post-Translational Modification

Using bioinformatic analysis tools like MyHits Motif Scan and various tools at ExPASy and comparing to multiple sequence alignments, highly conserved potential sites of post-translational modification were identified. The following is not a comprehensive list of predicted modification sites; it includes only the ones that use highly conserved amino acids.
  • CK2 phosphorylation sites 140-143, 217-220
  • Tyrosine phosphorylation sites 209-216, 263
  • PKC phosphorylation site 19-21 conserved in mammals
  • N-myristoylation site 27-32 conserved in mammals
  • N-myristoylation site 153-158 conserved in vertebrates
T216, the tyrosine for a tyrosine phosphorylation site, and S217, the serine for a predicted CK2 phosphorylation site, are completely conserved throughout the protein's evolutionary history. This suggests high likelihood that these sites are real and important for the protein's function.