SMIM15(small integral membrane protein 15) is a protein in humans that is encoded by the SMIM15 gene.[1] It is a transmembrane protein that interacts with PBX4.[2] Deletions where SMIM15 is located have produced mental defects and physical deformities.[3] [4] The gene has been found to have ubiquitous but variable expression in many tissues throughout the body.[1]
Small integral membrane protein 15 (SMIM15) is a protein in humans that is encoded by the SMIM15 gene.[1] It has also been known under the aliases C5orf43[1] and GC05M060454.[1] It is made up of 74 amino acids. It is located at 5q12.1.[1] SMIM15 has 4741 base pairs with three exons[1] [5]
SMIM15 has zero isoforms[1] The 5' UTR region spans 420 bases and the 3' UTR spans 2243 bases.[5]
| Number of Base Pairs | Start and End Locations | ||
| 1 | 252 | 61162217 – 61162468 | |
| 2 | 140 | 61161088 – 61161227 | |
| 3 | 2496 | 61157704 – 61160199 |
Primary sequence of SMIM15 is:[6] MFDIKAWAEY VVEWAAKDPY GFLTTVILAL TPLFLASAVL SWKLAKMIEA REKEQKKKQK. RQENIAKAKR LKKD
Molecular weight of SMIM15 has been found to be 8.6 kdal and it has a pI of 9.82.[7] There are no significant compositional features compositional features like charge clusters, hydrophobic segments, charge runs, patterns, multiplets or periodicities.[8]
There is one transmembrane domain located from amino acids 20 – 42.[9] [10]
The other domains include a luminal domain from amino acids 1 - 19 and cytosolic domain from amino acids 43 - 74.
The secondary structure for SMIM15 is largely alpha-helical with alpha helices making up 62.16% (46 amino acids) of the protein.[11] Random coil makes up 25.68% (19 amino acids) and extended strands make up 12.16% (9 amino acids) of the SMIM15 protein.
There are a number of post-translational modifications of the SMIM15 protein, which are shown in the Conceptual Translation of Human SMIM15 as shown in figure 1.
The predicted sites for sumoylation are at positions: 5, 67, 69, 72, 73.[12] It is known to affect protein stability, protect from degradation, cellular localization, protein-protein interactions and DNA binding.
The predicted sites for glycation are at positions: 5, 43, 58, 72, 73.[13] Glycation can lead to the creation of AGE (advanced glycation end products.[14] Glycation is a process in which proteins react with reducing sugar molecules, which will lead to impairment of the function and changes the characteristics of the protein.[15]
Finally, there are four predicted sites for phosphorylation of tyrosine on position 20, threonine on positions 25 and 31, and serine on position 41.[16] Phosphorylation will affect different cellular processes and thus regulating protein function.[17]
SMIM15 has a transmembrane domain found within amino acids 20–42. There are cleavage sites at the C-terminous and nuclear localization signals.[18]
SMIM15 has been found to have ubiquitous but variable expression in many different tissues throughout the body. it has the highest level of expression within the prostate.[19] There are lower levels of expression within skeletal muscles compared to other tissues within the body.[20]
SMIM15 has one CpG island within the promoter. SMIM15 has lower levels of H3K4Me1 but higher levels of H3K4Me3 and H3K27Ac across all of their cell lines[21]
The Promoter region for SMIM15 is 1049 base pairs long. and it is known as GXP_922465. There are 431 different transcription binding factor sites, some of these binding factors include GATA1, TGIF, LMX1A, and NKX61
There are no known micro-RNA targets in the 3' UTR. mRNA secondary structures exhibited a high number of predicted stem-loop structures. This could indicate high stability of the mRNA transcript, and some binding sites for regulatory mechanisms.
The function of SMIM15 is currently not well understood.
There is only one interacting protein currently identified.[22] [23] This protein is PBX4 which is known for playing critical roles in embryonic development and cellular differentiation both as Hox cofactors and through Hox - independent pathways. PBX4 is also a member of the pre-B cell leukemia transcription factor family.[24]
Deletion of 5q12.1 can lead to the development of mental retardation and ocular defects. Another deletion in the 5q12.1 - 5q12.3 region lead to mental-motor retardation and dysmorphia. In terms of diseases, Caries is a multifactorial disease and little is still known about the host genetic factors influencing susceptibility. The interval 5q12.1-5q13.3 as linked to low caries susceptibility in Filipino families.[25]
SMIM15 is conserved in both vertebrates and invertebrates. It is not found in insects or fungi. SMIM15 does not have any paralogs[1] and the farthest known relative of the Homo sapiens SMIM15 is found within Trichoplax sp.H2 with a date of divergence 747 MYA[26]