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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:HSF1-CPSF3L

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HSF1-CPSF3L
FusionPDB ID: 37706
FusionGDB2.0 ID: 37706
HgeneTgene
Gene symbol

HSF1

CPSF3L

Gene ID

3297

54973

Gene nameheat shock transcription factor 1integrator complex subunit 11
SynonymsHSTF1CPSF3L|CPSF73L|INT11|RC-68|RC68
Cytomap

8q24.3

1p36.33

Type of geneprotein-codingprotein-coding
Descriptionheat shock factor protein 1integrator complex subunit 11CPSF3-like proteincleavage and polyadenylation specific factor 3-likecleavage and polyadenylation-specific factor 3-like proteinprotein related to CPSF subunits of 68 kDarelated to CPSF subunits 68 kDa
Modification date2020032220200313
UniProtAcc

Q00613

Main function of 5'-partner protein: FUNCTION: Functions as a stress-inducible and DNA-binding transcription factor that plays a central role in the transcriptional activation of the heat shock response (HSR), leading to the expression of a large class of molecular chaperones heat shock proteins (HSPs) that protect cells from cellular insults' damage (PubMed:1871105, PubMed:11447121, PubMed:1986252, PubMed:7760831, PubMed:7623826, PubMed:8946918, PubMed:8940068, PubMed:9341107, PubMed:9121459, PubMed:9727490, PubMed:9499401, PubMed:9535852, PubMed:12659875, PubMed:12917326, PubMed:15016915, PubMed:25963659, PubMed:26754925). In unstressed cells, is present in a HSP90-containing multichaperone complex that maintains it in a non-DNA-binding inactivated monomeric form (PubMed:9727490, PubMed:11583998, PubMed:16278218). Upon exposure to heat and other stress stimuli, undergoes homotrimerization and activates HSP gene transcription through binding to site-specific heat shock elements (HSEs) present in the promoter regions of HSP genes (PubMed:1871105, PubMed:1986252, PubMed:8455624, PubMed:7935471, PubMed:7623826, PubMed:8940068, PubMed:9727490, PubMed:9499401, PubMed:10359787, PubMed:11583998, PubMed:12659875, PubMed:16278218, PubMed:25963659, PubMed:26754925). Activation is reversible, and during the attenuation and recovery phase period of the HSR, returns to its unactivated form (PubMed:11583998, PubMed:16278218). Binds to inverted 5'-NGAAN-3' pentamer DNA sequences (PubMed:1986252, PubMed:26727489). Binds to chromatin at heat shock gene promoters (PubMed:25963659). Plays also several other functions independently of its transcriptional activity. Involved in the repression of Ras-induced transcriptional activation of the c-fos gene in heat-stressed cells (PubMed:9341107). Positively regulates pre-mRNA 3'-end processing and polyadenylation of HSP70 mRNA upon heat-stressed cells in a symplekin (SYMPK)-dependent manner (PubMed:14707147). Plays a role in nuclear export of stress-induced HSP70 mRNA (PubMed:17897941). Plays a role in the regulation of mitotic progression (PubMed:18794143). Plays also a role as a negative regulator of non-homologous end joining (NHEJ) repair activity in a DNA damage-dependent manner (PubMed:26359349). Involved in stress-induced cancer cell proliferation in a IER5-dependent manner (PubMed:26754925). {ECO:0000269|PubMed:10359787, ECO:0000269|PubMed:11447121, ECO:0000269|PubMed:11583998, ECO:0000269|PubMed:12659875, ECO:0000269|PubMed:12917326, ECO:0000269|PubMed:14707147, ECO:0000269|PubMed:15016915, ECO:0000269|PubMed:16278218, ECO:0000269|PubMed:17897941, ECO:0000269|PubMed:1871105, ECO:0000269|PubMed:18794143, ECO:0000269|PubMed:1986252, ECO:0000269|PubMed:25963659, ECO:0000269|PubMed:26359349, ECO:0000269|PubMed:26727489, ECO:0000269|PubMed:26754925, ECO:0000269|PubMed:7623826, ECO:0000269|PubMed:7760831, ECO:0000269|PubMed:7935471, ECO:0000269|PubMed:8455624, ECO:0000269|PubMed:8940068, ECO:0000269|PubMed:8946918, ECO:0000269|PubMed:9121459, ECO:0000269|PubMed:9341107, ECO:0000269|PubMed:9499401, ECO:0000269|PubMed:9535852, ECO:0000269|PubMed:9727490}.; FUNCTION: (Microbial infection) Plays a role in latent human immunodeficiency virus (HIV-1) transcriptional reactivation. Binds to the HIV-1 long terminal repeat promoter (LTR) to reactivate viral transcription by recruiting cellular transcriptional elongation factors, such as CDK9, CCNT1 and EP300. {ECO:0000269|PubMed:27189267}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000528842, ENST00000400780, 
ENST00000528838, 
ENST00000411962, 
ENST00000435064, ENST00000419704, 
ENST00000421495, ENST00000462432, 
ENST00000540437, ENST00000450926, 
ENST00000545578, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 6 X 8=4808 X 8 X 6=384
# samples 1210
** MAII scorelog2(12/480*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/384*10)=-1.94110631094643
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: HSF1 [Title/Abstract] AND CPSF3L [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HSF1 [Title/Abstract] AND CPSF3L [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HSF1(145537302)-CPSF3L(1250998), # samples:1
Anticipated loss of major functional domain due to fusion event.HSF1-CPSF3L 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.
HSF1-CPSF3L 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.
HSF1-CPSF3L 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.
HSF1-CPSF3L 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.
* 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
HgeneHSF1

GO:0000122

negative regulation of transcription by RNA polymerase II

8926278|9341107

HgeneHSF1

GO:0000165

MAPK cascade

12917326

HgeneHSF1

GO:0009299

mRNA transcription

21597468

HgeneHSF1

GO:0034605

cellular response to heat

7935471|9222587|9341107|10359787|10413683|10747973|11514557|11583998|12917326|14707147|16554823|17897941|21085490|26159920

HgeneHSF1

GO:0034620

cellular response to unfolded protein

15016915

HgeneHSF1

GO:0034622

cellular protein-containing complex assembly

11583998

HgeneHSF1

GO:0045944

positive regulation of transcription by RNA polymerase II

9341107|10561509|11514557|12917326|16278218|21085490

HgeneHSF1

GO:0061408

positive regulation of transcription from RNA polymerase II promoter in response to heat stress

7760831|9499401|10747973|12659875|12665592|15016915|25963659|26754925

HgeneHSF1

GO:0071276

cellular response to cadmium ion

10359787|11514557|15016915|25963659

HgeneHSF1

GO:0071280

cellular response to copper ion

15016915

HgeneHSF1

GO:0071480

cellular response to gamma radiation

26359349

HgeneHSF1

GO:0072738

cellular response to diamide

15016915

HgeneHSF1

GO:1900034

regulation of cellular response to heat

11583998

HgeneHSF1

GO:1903936

cellular response to sodium arsenite

15016915

TgeneCPSF3L

GO:0016180

snRNA processing

16239144



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/chr8:145537302/chr1:1250998)
- 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 HSF1 (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 CPSF3L (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)
ENST00000528838HSF1chr8145537302+ENST00000435064CPSF3Lchr11250998-30441408432781912
ENST00000528838HSF1chr8145537302+ENST00000411962CPSF3Lchr11250998-30401408432781912
ENST00000400780HSF1chr8145537302+ENST00000435064CPSF3Lchr11250998-28521216522589845
ENST00000400780HSF1chr8145537302+ENST00000411962CPSF3Lchr11250998-28481216522589845

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
ENST00000528838ENST00000435064HSF1chr8145537302+CPSF3Lchr11250998-0.0174498730.9825501
ENST00000528838ENST00000411962HSF1chr8145537302+CPSF3Lchr11250998-0.0175411010.98245883
ENST00000400780ENST00000435064HSF1chr8145537302+CPSF3Lchr11250998-0.0185938270.9814062
ENST00000400780ENST00000411962HSF1chr8145537302+CPSF3Lchr11250998-0.0187357420.98126423

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 HSF1-CPSF3L

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HSF1chr8145537302CPSF3Lchr112509981216185FSLEHVHGSGPYSAPSPAYSSSSLYA
HSF1chr8145537302CPSF3Lchr112509981408280FSLEHVHGSGPYSAPSPAYSSSSLYA

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Potential FusionNeoAntigen Information of HSF1-CPSF3L 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.
HSF1-CPSF3L_145537302_1250998.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)
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:25YSAPSPAY0.99950.93141119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:02YSAPSPAY0.99890.93921119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:08YSAPSPAY0.99310.88031119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:01YSAPSPAY0.99030.86521119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:05YSAPSPAY0.98350.54271119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:05GPYSAPSPA0.99890.6149918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:02GPYSAPSPA0.99890.6034918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:01VHGSGPYSA0.99360.9328514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:06VHGSGPYSA0.99170.9652514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:10VHGSGPYSA0.72240.5599514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:01GPYSAPSPAY0.98410.9229919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:08GPYSAPSPAY0.9790.9059919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:02GPYSAPSPAY0.96090.9651919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:05GPYSAPSPAY0.95970.7117919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:06HVHGSGPYSA0.63270.9558414
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:06EHVHGSGPYSA0.99920.9725314
HSF1-CPSF3Lchr8145537302chr112509981216HLA-A24:17SGPYSAPSPAY0.49490.6214819
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:21YSAPSPAY0.99890.92611119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C15:04YSAPSPAY0.99770.89831119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:31YSAPSPAY0.99110.86551119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C03:14YSAPSPAY0.97470.97491119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C12:12YSAPSPAY0.96090.9031119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C12:04YSAPSPAY0.95840.9951119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C06:03YSAPSPAY0.9570.99371119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B54:01GPYSAPSPA0.99430.5569918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:09VHGSGPYSA0.99290.8983514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:12GPYSAPSPA0.99120.7018918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:05VHGSGPYSA0.98790.9246514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:04GPYSAPSPA0.92380.6245918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B56:04GPYSAPSPA0.91060.5437918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:21PYSAPSPAY0.82910.91991019
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B78:01GPYSAPSPA0.70030.6878918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B54:01SGPYSAPSPA0.98640.5999818
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:31GPYSAPSPAY0.98270.9277919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:21GPYSAPSPAY0.95730.9504919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:21SGPYSAPSPAY0.98450.9204819
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:39YSAPSPAY0.99940.85951119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:11YSAPSPAY0.99890.90161119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:08YSAPSPAY0.99890.89471119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:11YSAPSPAY0.99870.90791119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:43YSAPSPAY0.99850.89891119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C03:02YSAPSPAY0.99820.9731119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C15:09YSAPSPAY0.99770.89831119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:17YSAPSPAY0.99510.72061119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:30YSAPSPAY0.99510.72061119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:28YSAPSPAY0.99310.90161119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C12:02YSAPSPAY0.99210.96391119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:23YSAPSPAY0.99090.81971119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:20YSAPSPAY0.99030.90961119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:77YSAPSPAY0.99030.86521119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C16:04YSAPSPAY0.97630.97721119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:24YSAPSPAY0.96340.92231119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C12:03YSAPSPAY0.95050.9791119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C16:01YSAPSPAY0.91720.97681119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C16:02YSAPSPAY0.91440.99351119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C02:02YSAPSPAY0.76770.9791119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C02:10YSAPSPAY0.76770.9791119
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:22GPYSAPSPA0.99890.6034918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:09GPYSAPSPA0.99860.6176918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B55:04GPYSAPSPA0.95530.5341918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B56:05GPYSAPSPA0.94030.5398918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B56:02GPYSAPSPA0.91060.5437918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B67:01GPYSAPSPA0.84330.9426918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:09VHGSGPYSA0.79380.8628514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:26GPYSAPSPA0.67580.6157918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B39:11VHGSGPYSA0.56310.903514
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B78:02GPYSAPSPA0.54780.838918
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C14:03PYSAPSPAY0.0110.96951019
HSF1-CPSF3Lchr8145537302chr112509981216HLA-C14:02PYSAPSPAY0.0110.96951019
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B07:09GPYSAPSPAY0.98410.5661919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:77GPYSAPSPAY0.98410.9229919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:23GPYSAPSPAY0.98330.9203919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:20GPYSAPSPAY0.97880.954919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:30GPYSAPSPAY0.97210.8538919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:17GPYSAPSPAY0.97210.8538919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:11GPYSAPSPAY0.96450.9419919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:08GPYSAPSPAY0.93510.9147919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B15:11GPYSAPSPAY0.93310.9189919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:24GPYSAPSPAY0.9230.908919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B35:43GPYSAPSPAY0.91530.9149919
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B78:02SGPYSAPSPA0.7820.8337818
HSF1-CPSF3Lchr8145537302chr112509981216HLA-B18:07GPYSAPSPAY0.2660.9165919

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Potential FusionNeoAntigen Information of HSF1-CPSF3L 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.

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)

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Fusion breakpoint peptide structures of HSF1-CPSF3L

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
3339HGSGPYSAPSPAYSHSF1CPSF3Lchr8145537302chr112509981216

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HSF1-CPSF3L

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-B52:013W393339HGSGPYSAPSPAYS-5.36671-5.36671
HLA-B44:053DX83339HGSGPYSAPSPAYS-6.86648-6.86648

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Vaccine Design for the FusionNeoAntigens of HSF1-CPSF3L

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
HSF1-CPSF3Lchr8145537302chr112509981019PYSAPSPAYCTGCTGGACGTAGATGATGAGCTGGAG
HSF1-CPSF3Lchr8145537302chr112509981119YSAPSPAYCTGGACGTAGATGATGAGCTGGAG
HSF1-CPSF3Lchr8145537302chr11250998314EHVHGSGPYSATTCAGCGTGGACACCAGTGCCCTGCTGGACGTA
HSF1-CPSF3Lchr8145537302chr11250998414HVHGSGPYSAAGCGTGGACACCAGTGCCCTGCTGGACGTA
HSF1-CPSF3Lchr8145537302chr11250998514VHGSGPYSAGTGGACACCAGTGCCCTGCTGGACGTA
HSF1-CPSF3Lchr8145537302chr11250998818SGPYSAPSPAAGTGCCCTGCTGGACGTAGATGATGAGCTG
HSF1-CPSF3Lchr8145537302chr11250998819SGPYSAPSPAYAGTGCCCTGCTGGACGTAGATGATGAGCTGGAG
HSF1-CPSF3Lchr8145537302chr11250998918GPYSAPSPAGCCCTGCTGGACGTAGATGATGAGCTG
HSF1-CPSF3Lchr8145537302chr11250998919GPYSAPSPAYGCCCTGCTGGACGTAGATGATGAGCTGGAG

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

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Information of the samples that have these potential fusion neoantigens of HSF1-CPSF3L

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
Non-CancerHSF1-CPSF3Lchr8145537302ENST00000400780chr11250998ENST0000041196267N

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Potential target of CAR-T therapy development for HSF1-CPSF3L

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 HSF1-CPSF3L

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 HSF1-CPSF3L

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