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Fusion Protein:SAT1-MPHOSPH8 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: SAT1-MPHOSPH8 | FusionPDB ID: 79249 | FusionGDB2.0 ID: 79249 | Hgene | Tgene | Gene symbol | SAT1 | MPHOSPH8 | Gene ID | 81539 | 54737 |
| Gene name | solute carrier family 38 member 1 | M-phase phosphoprotein 8 | |
| Synonyms | ATA1|NAT2|SAT1|SNAT1 | HSMPP8|TWA3|mpp8 | |
| Cytomap | 12q13.11 | 13q12.11 | |
| Type of gene | protein-coding | protein-coding | |
| Description | sodium-coupled neutral amino acid transporter 1N-system amino acid transporter 2amino acid transporter A1amino acid transporter system A1system A amino acid transporter 1system N amino acid transporter 1 | M-phase phosphoprotein 8M-phase phosphoprotein, mppM-phase phosphoprotein, mpp8two hybrid-associated protein 3 with RanBPM | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | . | Q99549 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000489394, ENST00000379254, ENST00000379270, ENST00000379251, ENST00000379253, | ENST00000361479, ENST00000414242, ENST00000496525, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 10 X 13 X 4=520 | 25 X 17 X 10=4250 |
| # samples | 15 | 30 | |
| ** MAII score | log2(15/520*10)=-1.79354912253257 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(30/4250*10)=-3.82442843541655 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: SAT1 [Title/Abstract] AND MPHOSPH8 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | MPHOSPH8(20224305)-SAT1(23803938), # samples:1 SAT1(23803938)-MPHOSPH8(20224305), # samples:2 | ||
| Anticipated loss of major functional domain due to fusion event. | SAT1-MPHOSPH8 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF. SAT1-MPHOSPH8 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. | ||
| * DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Tgene | MPHOSPH8 | GO:0045814 | negative regulation of gene expression, epigenetic | 26022416|28581500|29211708 |
| Tgene | MPHOSPH8 | GO:0090309 | positive regulation of methylation-dependent chromatin silencing | 28581500|29211708 |
| Fusion gene breakpoints across SAT1 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across MPHOSPH8 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChiTaRS5.0 | N/A | BM263362 | SAT1 | chrX | 23803938 | - | MPHOSPH8 | chr13 | 20224305 | - |
| ChiTaRS5.0 | N/A | CA848235 | SAT1 | chrX | 23803938 | - | MPHOSPH8 | chr13 | 20224305 | - |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
| ENST00000379270 | SAT1 | chrX | 23803938 | - | ENST00000414242 | MPHOSPH8 | chr13 | 20224305 | - | 2052 | 929 | 1041 | 2051 | 336 |
| ENST00000379270 | SAT1 | chrX | 23803938 | - | ENST00000361479 | MPHOSPH8 | chr13 | 20224305 | - | 3615 | 929 | 1041 | 2030 | 329 |
| DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
| ENST00000379270 | ENST00000414242 | SAT1 | chrX | 23803938 | - | MPHOSPH8 | chr13 | 20224305 | - | 0.001030163 | 0.9989698 |
| ENST00000379270 | ENST00000361479 | SAT1 | chrX | 23803938 | - | MPHOSPH8 | chr13 | 20224305 | - | 0.000519914 | 0.99948007 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >79249_79249_1_SAT1-MPHOSPH8_SAT1_chrX_23803938_ENST00000379270_MPHOSPH8_chr13_20224305_ENST00000361479_length(amino acids)=329AA_BP= MSLGMDLQLEWMKLEDFQKHLDGKDENFAATDAIPSNVLRDAVKNGDYITVKVALNSNEEYNLDQEDSSGMTLVMLAAAGGQDDLLRLLI TKGAKVNGRQKNGTTALIHAAEKNFLTTVAILLEAGAFVNVQQSNGETALMKACKRGNSDIVRLVIECGADCNILSKHQNSALHFAKQSN NVLVYDLLKNHLETLSRVAEETIKDYFEARLALLEPVFPIACHRLCEGPDFSTDFNYKPPQNIPEGSGILLFIFHANFLGKEVIARLCGP -------------------------------------------------------------- >79249_79249_2_SAT1-MPHOSPH8_SAT1_chrX_23803938_ENST00000379270_MPHOSPH8_chr13_20224305_ENST00000414242_length(amino acids)=336AA_BP=293 MSLGMDLQLEWMKLEDFQKHLDGKDENFAATDAIPSNVLRDAVKNGDYITVKVALNSNEEYNLDQEDSSGMTLVMLAAAGGQDDLLRLLI TKGAKVNGRQKNGTTALIHAAEKNFLTTVAILLEAGAFVNVQQSNGETALMKACKRGNSDIVRLVIECGADCNILSKHQNSALHFAKQSN NVLVYDLLKNHLETLSRVAEETIKDYFEARLALLEPVFPIACHRLCEGPDFSTDFNYKPPQNIPEGSGILLFIFHANFLGKEVIARLCGP -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chrX:20224305/chr13:23803938) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| . | MPHOSPH8 |
| FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. | FUNCTION: Heterochromatin component that specifically recognizes and binds methylated 'Lys-9' of histone H3 (H3K9me) and promotes recruitment of proteins that mediate epigenetic repression (PubMed:20871592, PubMed:26022416). Mediates recruitment of the HUSH complex to H3K9me3 sites: the HUSH complex is recruited to genomic loci rich in H3K9me3 and is required to maintain transcriptional silencing by promoting recruitment of SETDB1, a histone methyltransferase that mediates further deposition of H3K9me3, as well as MORC2 (PubMed:26022416, PubMed:28581500). Binds H3K9me and promotes DNA methylation by recruiting DNMT3A to target CpG sites; these can be situated within the coding region of the gene (PubMed:20871592). Mediates down-regulation of CDH1 expression (PubMed:20871592). Also represses L1 retrotransposons in collaboration with MORC2 and, probably, SETDB1, the silencing is dependent of repressive epigenetic modifications, such as H3K9me3 mark. Silencing events often occur within introns of transcriptionally active genes, and lead to the down-regulation of host gene expression (PubMed:29211708). The HUSH complex is also involved in the silencing of unintegrated retroviral DNA by being recruited by ZNF638: some part of the retroviral DNA formed immediately after infection remains unintegrated in the host genome and is transcriptionally repressed (PubMed:30487602). {ECO:0000269|PubMed:20871592, ECO:0000269|PubMed:26022416, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:30487602}. |
| Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
| - Retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 151_256 | 0 | 861.0 | Compositional bias | Note=Lys-rich | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 151_256 | 0 | 868.0 | Compositional bias | Note=Lys-rich | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 59_118 | 0 | 861.0 | Domain | Chromo | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 59_118 | 0 | 868.0 | Domain | Chromo | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 80_87 | 0 | 861.0 | Region | Histone H3K9me3 binding | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 80_87 | 0 | 868.0 | Region | Histone H3K9me3 binding | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 600_629 | 0 | 861.0 | Repeat | Note=ANK 1 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 633_662 | 0 | 861.0 | Repeat | Note=ANK 2 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 666_695 | 0 | 861.0 | Repeat | Note=ANK 3 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000361479 | 0 | 14 | 699_728 | 0 | 861.0 | Repeat | Note=ANK 4 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 600_629 | 0 | 868.0 | Repeat | Note=ANK 1 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 633_662 | 0 | 868.0 | Repeat | Note=ANK 2 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 666_695 | 0 | 868.0 | Repeat | Note=ANK 3 | |
| Tgene | MPHOSPH8 | chrX:23803938 | chr13:20224305 | ENST00000414242 | 0 | 13 | 699_728 | 0 | 868.0 | Repeat | Note=ANK 4 |
| - Not-retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 4_171 | 0 | 172.0 | Domain | N-acetyltransferase |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 102_107 | 0 | 172.0 | Region | Acetyl-CoA binding |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 126_128 | 0 | 172.0 | Region | Substrate binding |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 133_136 | 0 | 172.0 | Region | Acetyl-CoA binding |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 140_143 | 0 | 172.0 | Region | Acetyl-CoA binding |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 27_28 | 0 | 172.0 | Region | Substrate binding |
| Hgene | SAT1 | chrX:23803938 | chr13:20224305 | ENST00000379270 | - | 1 | 6 | 94_96 | 0 | 172.0 | Region | Acetyl-CoA binding |
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Fusion Protein Structures |
| PDB and CIF files of the predicted fusion proteins * Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format. |
| Fusion protein PDB link (fusion AA seq ID in FusionPDB) | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | AA seq | Len(AA seq) |
| PDB file >>>634_SAT1_23803938_MPHOSPH8_20224305_ranked_0.pdb | SAT1 | 23803938 | 23803938 | ENST00000361479 | MPHOSPH8 | chr13 | 20224305 | - | MSLGMDLQLEWMKLEDFQKHLDGKDENFAATDAIPSNVLRDAVKNGDYITVKVALNSNEEYNLDQEDSSGMTLVMLAAAGGQDDLLRLLI TKGAKVNGRQKNGTTALIHAAEKNFLTTVAILLEAGAFVNVQQSNGETALMKACKRGNSDIVRLVIECGADCNILSKHQNSALHFAKQSN NVLVYDLLKNHLETLSRVAEETIKDYFEARLALLEPVFPIACHRLCEGPDFSTDFNYKPPQNIPEGSGILLFIFHANFLGKEVIARLCGP | 336 |
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pLDDT score distribution |
| pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2 * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
SAT1_pLDDT.png  |
MPHOSPH8_pLDDT.png  |
| pLDDT score distribution of the predicted fusion protein structures from AlphaFold2 * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
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Ramachandran Plot of Fusion Protein Structure |
| Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide. |
| Fusion AA seq ID in FusionPDB and their Ramachandran plots |
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Fusion Protein-Protein Interaction |
| Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
| Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| SAT1 | |
| MPHOSPH8 |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to SAT1-MPHOSPH8 |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to SAT1-MPHOSPH8 |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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