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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:PCMT1-CCT2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PCMT1-CCT2
FusionPDB ID: 63351
FusionGDB2.0 ID: 63351
HgeneTgene
Gene symbol

PCMT1

CCT2

Gene ID

5110

10576

Gene nameprotein-L-isoaspartate (D-aspartate) O-methyltransferasechaperonin containing TCP1 subunit 2
SynonymsPIMT99D8.1|CCT-beta|CCTB|HEL-S-100n|PRO1633|TCP-1-beta
Cytomap

6q25.1

12q15

Type of geneprotein-codingprotein-coding
Descriptionprotein-L-isoaspartate(D-aspartate) O-methyltransferaseL-isoaspartyl protein carboxyl methyltransferaseepididymis secretory sperm binding proteinprotein L-isoaspartyl/D-aspartyl methyltransferaseprotein-beta-aspartate methyltransferaseT-complex protein 1 subunit betaT-complex protein 1, beta subunitchaperonin containing TCP1, subunit 2 (beta)chaperonin containing t-complex polypeptide 1, beta subunitchaperonin containing t-complex polypeptide 1, subunit 2epididymis secretory sperm
Modification date2020031320200313
UniProtAcc.

P78371

Main function of 5'-partner protein: FUNCTION: Component of the chaperonin-containing T-complex (TRiC), a molecular chaperone complex that assists the folding of proteins upon ATP hydrolysis (PubMed:25467444). The TRiC complex mediates the folding of WRAP53/TCAB1, thereby regulating telomere maintenance (PubMed:25467444). As part of the TRiC complex may play a role in the assembly of BBSome, a complex involved in ciliogenesis regulating transports vesicles to the cilia (PubMed:20080638). The TRiC complex plays a role in the folding of actin and tubulin (Probable). {ECO:0000269|PubMed:20080638, ECO:0000269|PubMed:25467444, ECO:0000305}.
Ensembl transtripts involved in fusion geneENST idsENST00000367378, ENST00000367380, 
ENST00000367384, ENST00000464889, 
ENST00000544496, ENST00000480010, 
ENST00000299300, ENST00000543146, 
ENST00000544368, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 4 X 4=8014 X 13 X 9=1638
# samples 516
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1638*10)=-3.35579154675365
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PCMT1 [Title/Abstract] AND CCT2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PCMT1 [Title/Abstract] AND CCT2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PCMT1(150094305)-CCT2(69981285), # samples:1
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr6:150094305/chr12:69981285)
- 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.
FGviewer

check buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across PCMT1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across CCT2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Amino Acid Sequences


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000367384PCMT1chr6150094305+ENST00000299300CCT2chr1269981285+23606511562114652
ENST00000367384PCMT1chr6150094305+ENST00000544368CCT2chr1269981285+21736511562099647
ENST00000367384PCMT1chr6150094305+ENST00000543146CCT2chr1269981285+23556511562114652
ENST00000367378PCMT1chr6150094305+ENST00000299300CCT2chr1269981285+23596501552113652
ENST00000367378PCMT1chr6150094305+ENST00000544368CCT2chr1269981285+21726501552098647
ENST00000367378PCMT1chr6150094305+ENST00000543146CCT2chr1269981285+23546501552113652
ENST00000464889PCMT1chr6150094305+ENST00000299300CCT2chr1269981285+23596501552113652
ENST00000464889PCMT1chr6150094305+ENST00000544368CCT2chr1269981285+21726501552098647
ENST00000464889PCMT1chr6150094305+ENST00000543146CCT2chr1269981285+23546501552113652
ENST00000367380PCMT1chr6150094305+ENST00000299300CCT2chr1269981285+2108399331862609
ENST00000367380PCMT1chr6150094305+ENST00000544368CCT2chr1269981285+1921399331847604
ENST00000367380PCMT1chr6150094305+ENST00000543146CCT2chr1269981285+2103399331862609
ENST00000544496PCMT1chr6150094305+ENST00000299300CCT2chr1269981285+1924215591678539
ENST00000544496PCMT1chr6150094305+ENST00000544368CCT2chr1269981285+1737215591663534
ENST00000544496PCMT1chr6150094305+ENST00000543146CCT2chr1269981285+1919215591678539

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000367384ENST00000299300PCMT1chr6150094305+CCT2chr1269981285+0.0057347140.99426526
ENST00000367384ENST00000544368PCMT1chr6150094305+CCT2chr1269981285+0.0058092540.99419075
ENST00000367384ENST00000543146PCMT1chr6150094305+CCT2chr1269981285+0.005814240.9941857
ENST00000367378ENST00000299300PCMT1chr6150094305+CCT2chr1269981285+0.0057707620.9942292
ENST00000367378ENST00000544368PCMT1chr6150094305+CCT2chr1269981285+0.005848940.99415106
ENST00000367378ENST00000543146PCMT1chr6150094305+CCT2chr1269981285+0.0058508650.9941492
ENST00000464889ENST00000299300PCMT1chr6150094305+CCT2chr1269981285+0.0057707620.9942292
ENST00000464889ENST00000544368PCMT1chr6150094305+CCT2chr1269981285+0.005848940.99415106
ENST00000464889ENST00000543146PCMT1chr6150094305+CCT2chr1269981285+0.0058508650.9941492
ENST00000367380ENST00000299300PCMT1chr6150094305+CCT2chr1269981285+0.0054461080.9945539
ENST00000367380ENST00000544368PCMT1chr6150094305+CCT2chr1269981285+0.0055247540.9944753
ENST00000367380ENST00000543146PCMT1chr6150094305+CCT2chr1269981285+0.0055350730.99446493
ENST00000544496ENST00000299300PCMT1chr6150094305+CCT2chr1269981285+0.0018557670.99814427
ENST00000544496ENST00000544368PCMT1chr6150094305+CCT2chr1269981285+0.0018188980.9981811
ENST00000544496ENST00000543146PCMT1chr6150094305+CCT2chr1269981285+0.0019054380.9980946

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for PCMT1-CCT2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PCMT1chr6150094305CCT2chr126998128521552LRSFQATISAPHMDKILLSSGRDASL
PCMT1chr6150094305CCT2chr1269981285399122SIGFQATISAPHMDKILLSSGRDASL
PCMT1chr6150094305CCT2chr1269981285650165SIGFQATISAPHMDKILLSSGRDASL
PCMT1chr6150094305CCT2chr1269981285651165SIGFQATISAPHMDKILLSSGRDASL

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Potential FusionNeoAntigen Information of PCMT1-CCT2 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
PCMT1-CCT2_150094305_69981285.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
PCMT1-CCT2chr6150094305chr1269981285215HLA-B15:16ISAPHMDKI0.96760.5081716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:03APHMDKILL0.90790.694918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B52:01ISAPHMDKI0.79760.7718716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:04APHMDKILL0.72130.6682918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:02APHMDKILL0.72130.6682918
PCMT1-CCT2chr6150094305chr1269981285215HLA-A11:03ATISAPHMDK0.99920.5165515
PCMT1-CCT2chr6150094305chr1269981285215HLA-A30:08ATISAPHMDK0.97350.7646515
PCMT1-CCT2chr6150094305chr1269981285215HLA-B57:03ISAPHMDKILL0.99890.8349718
PCMT1-CCT2chr6150094305chr1269981285215HLA-C03:07ISAPHMDKI0.99780.9248716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C15:06ISAPHMDKI0.99740.7838716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B07:12APHMDKILL0.98880.5598918
PCMT1-CCT2chr6150094305chr1269981285215HLA-C04:06ISAPHMDKI0.97770.7015716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C06:03ISAPHMDKI0.90270.974716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C12:04ISAPHMDKI0.90140.9783716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C12:12ISAPHMDKI0.82530.8137716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:12APHMDKILL0.72130.6682918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B39:10APHMDKILL0.71450.7612918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B42:02APHMDKILL0.69750.6085918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B42:01APHMDKILL0.66080.6002918
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:17SAPHMDKIL0.52680.9531817
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:30SAPHMDKIL0.43340.9705817
PCMT1-CCT2chr6150094305chr1269981285215HLA-C02:06ISAPHMDKI0.23850.8783716
PCMT1-CCT2chr6150094305chr1269981285215HLA-A11:01ATISAPHMDK0.99920.5612515
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:17SAPHMDKILL0.95320.9534818
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:30SAPHMDKILL0.91970.9642818
PCMT1-CCT2chr6150094305chr1269981285215HLA-B07:12SAPHMDKILL0.72470.5254818
PCMT1-CCT2chr6150094305chr1269981285215HLA-C15:05ISAPHMDKI0.99760.8257716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C15:02ISAPHMDKI0.99750.7582716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C03:17SAPHMDKIL0.96510.9559817
PCMT1-CCT2chr6150094305chr1269981285215HLA-B57:02ISAPHMDKI0.95320.7433716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C03:06ISAPHMDKI0.95190.9408716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:13APHMDKILL0.8910.7049918
PCMT1-CCT2chr6150094305chr1269981285215HLA-C12:03ISAPHMDKI0.83850.9366716
PCMT1-CCT2chr6150094305chr1269981285215HLA-C16:02ISAPHMDKI0.83840.9758716
PCMT1-CCT2chr6150094305chr1269981285215HLA-B35:09APHMDKILL0.72130.6682918
PCMT1-CCT2chr6150094305chr1269981285215HLA-B67:01APHMDKILL0.69360.687918
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:02SAPHMDKIL0.53170.9512817
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:03SAPHMDKIL0.36620.8516817
PCMT1-CCT2chr6150094305chr1269981285215HLA-C17:01ISAPHMDKI0.10880.5741716
PCMT1-CCT2chr6150094305chr1269981285215HLA-A11:02ATISAPHMDK0.99920.5612515
PCMT1-CCT2chr6150094305chr1269981285215HLA-A30:01ATISAPHMDK0.96930.801515
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:03SAPHMDKILL0.95260.8565818
PCMT1-CCT2chr6150094305chr1269981285215HLA-C01:02SAPHMDKILL0.9480.9517818
PCMT1-CCT2chr6150094305chr1269981285215HLA-B67:01SAPHMDKILL0.63570.5689818

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Potential FusionNeoAntigen Information of PCMT1-CCT2 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
PCMT1-CCT2_150094305_69981285.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0407SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0407LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0419SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0431SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0431LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0443SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0447SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0447LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0454SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0454LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0461SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0464SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0469SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0469LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0474SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0474LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0482SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0482LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0701SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0701LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0703SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0703LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0705SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0705LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0706SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0706LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0707SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0707LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0708SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0708LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0709SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0712SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0712LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0713SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0713LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0714SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0714LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0715SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0715LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0716SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0716LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0717SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0717LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0719SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0719LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0901SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0902SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0902LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0902RSFQATISAPHMDKI116
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0903SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0903LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0904SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0907SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0907LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0908SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB1-0908LRSFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB1-0909SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285650DRB5-0112SIGFQATISAPHMDK015
PCMT1-CCT2chr6150094305chr1269981285215DRB5-0112LRSFQATISAPHMDK015

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Fusion breakpoint peptide structures of PCMT1-CCT2

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
9415TISAPHMDKILLSSPCMT1CCT2chr6150094305chr1269981285215

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PCMT1-CCT2

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN9415TISAPHMDKILLSS-7.15543-7.26883
HLA-B14:023BVN9415TISAPHMDKILLSS-4.77435-5.80965
HLA-B52:013W399415TISAPHMDKILLSS-6.80875-6.92215
HLA-B52:013W399415TISAPHMDKILLSS-4.20386-5.23916
HLA-A11:014UQ29415TISAPHMDKILLSS-7.5194-8.5547
HLA-A11:014UQ29415TISAPHMDKILLSS-6.9601-7.0735
HLA-A24:025HGA9415TISAPHMDKILLSS-7.52403-7.63743
HLA-A24:025HGA9415TISAPHMDKILLSS-5.82433-6.85963
HLA-B27:056PYJ9415TISAPHMDKILLSS-3.28285-4.31815
HLA-B44:053DX89415TISAPHMDKILLSS-5.91172-6.94702
HLA-B44:053DX89415TISAPHMDKILLSS-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of PCMT1-CCT2

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
PCMT1-CCT2chr6150094305chr1269981285515ATISAPHMDKGCAACAATCAGTGCTCCACACATGGACAAA
PCMT1-CCT2chr6150094305chr1269981285716ISAPHMDKIATCAGTGCTCCACACATGGACAAAATT
PCMT1-CCT2chr6150094305chr1269981285718ISAPHMDKILLATCAGTGCTCCACACATGGACAAAATTCTTCTA
PCMT1-CCT2chr6150094305chr1269981285817SAPHMDKILAGTGCTCCACACATGGACAAAATTCTT
PCMT1-CCT2chr6150094305chr1269981285818SAPHMDKILLAGTGCTCCACACATGGACAAAATTCTTCTA
PCMT1-CCT2chr6150094305chr1269981285918APHMDKILLGCTCCACACATGGACAAAATTCTTCTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PCMT1-CCT2chr6150094305chr1269981285015LRSFQATISAPHMDKCTCCGCAGTTTCCAAGCAACAATCAGTGCTCCACACATGGACAAA
PCMT1-CCT2chr6150094305chr1269981285015SIGFQATISAPHMDKTCAATAGGTTTCCAAGCAACAATCAGTGCTCCACACATGGACAAA
PCMT1-CCT2chr6150094305chr1269981285116RSFQATISAPHMDKICGCAGTTTCCAAGCAACAATCAGTGCTCCACACATGGACAAAATT

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Information of the samples that have these potential fusion neoantigens of PCMT1-CCT2

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
SKCMPCMT1-CCT2chr6150094305ENST00000544496chr1269981285ENST00000299300TCGA-ER-A197-06A

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Potential target of CAR-T therapy development for PCMT1-CCT2

check button Predicted 3D structure. We used RoseTTAFold.

check buttonRetention 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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to PCMT1-CCT2

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to PCMT1-CCT2

check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource