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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:PFDN5-CAPN2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PFDN5-CAPN2
FusionPDB ID: 64410
FusionGDB2.0 ID: 64410
HgeneTgene
Gene symbol

PFDN5

CAPN2

Gene ID

5204

824

Gene nameprefoldin subunit 5calpain 2
SynonymsMM-1|MM1|PFD5CANP2|CANPL2|CANPml|mCANP
Cytomap

12q13.13

1q41

Type of geneprotein-codingprotein-coding
Descriptionprefoldin subunit 5c-myc binding proteinmyc modulator-1calpain-2 catalytic subunitCANP 2M-calpaincalcium-activated neutral proteinase 2calpain 2, (m/II) large subunitcalpain 2, large [catalytic] subunitcalpain 2, large subunitcalpain M-typecalpain, large polypeptide L2millimolar-calpain
Modification date2020031320200313
UniProtAcc.

P17655

Main function of 5'-partner protein: FUNCTION: Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves MYOC at 'Arg-226' (PubMed:17650508). Proteolytically cleaves CPEB3 following neuronal stimulation which abolishes CPEB3 translational repressor activity, leading to translation of CPEB3 target mRNAs (By similarity). {ECO:0000250|UniProtKB:O08529, ECO:0000269|PubMed:17650508}.
Ensembl transtripts involved in fusion geneENST idsENST00000334478, ENST00000351500, 
ENST00000550846, ENST00000551018, 
ENST00000474026, ENST00000295006, 
ENST00000433674, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 4 X 2=5611 X 7 X 7=539
# samples 711
** MAII scorelog2(7/56*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/539*10)=-2.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PFDN5 [Title/Abstract] AND CAPN2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PFDN5 [Title/Abstract] AND CAPN2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PFDN5(53689423)-CAPN2(223949887), # samples:1
Anticipated loss of major functional domain due to fusion event.PFDN5-CAPN2 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.
PFDN5-CAPN2 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.
PFDN5-CAPN2 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.
PFDN5-CAPN2 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
TgeneCAPN2

GO:0051603

proteolysis involved in cellular protein catabolic process

12150984



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/chr12:53689423/chr1:223949887)
- 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 PFDN5 (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 CAPN2 (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)
ENST00000551018PFDN5chr1253689423+ENST00000433674CAPN2chr1223949887+2045349277885202
ENST00000551018PFDN5chr1253689423+ENST00000295006CAPN2chr1223949887+2047349277885202
ENST00000351500PFDN5chr1253689423+ENST00000433674CAPN2chr1223949887+181111543651202
ENST00000351500PFDN5chr1253689423+ENST00000295006CAPN2chr1223949887+181311543651202
ENST00000550846PFDN5chr1253689423+ENST00000433674CAPN2chr1223949887+180010432640202
ENST00000550846PFDN5chr1253689423+ENST00000295006CAPN2chr1223949887+180210432640202
ENST00000334478PFDN5chr1253689423+ENST00000433674CAPN2chr1223949887+17848816624202
ENST00000334478PFDN5chr1253689423+ENST00000295006CAPN2chr1223949887+17868816624202

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
ENST00000551018ENST00000433674PFDN5chr1253689423+CAPN2chr1223949887+0.0006238290.99937624
ENST00000551018ENST00000295006PFDN5chr1253689423+CAPN2chr1223949887+0.0006214720.99937844
ENST00000351500ENST00000433674PFDN5chr1253689423+CAPN2chr1223949887+0.0004436410.99955636
ENST00000351500ENST00000295006PFDN5chr1253689423+CAPN2chr1223949887+0.0004430750.99955696
ENST00000550846ENST00000433674PFDN5chr1253689423+CAPN2chr1223949887+0.0004910030.999509
ENST00000550846ENST00000295006PFDN5chr1253689423+CAPN2chr1223949887+0.0004905330.99950945
ENST00000334478ENST00000433674PFDN5chr1253689423+CAPN2chr1223949887+0.0005385970.99946135
ENST00000334478ENST00000295006PFDN5chr1253689423+CAPN2chr1223949887+0.0005370550.9994629

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 PFDN5-CAPN2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PFDN5chr1253689423CAPN2chr122394988710423NLPQLEMLKNQLDQFDISEDDIDDGF
PFDN5chr1253689423CAPN2chr122394988711523NLPQLEMLKNQLDQFDISEDDIDDGF
PFDN5chr1253689423CAPN2chr122394988734923NLPQLEMLKNQLDQFDISEDDIDDGF
PFDN5chr1253689423CAPN2chr12239498878823NLPQLEMLKNQLDQFDISEDDIDDGF

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Potential FusionNeoAntigen Information of PFDN5-CAPN2 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.
PFDN5-CAPN2_53689423_223949887.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)
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:01MLKNQLDQF0.99890.7506615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:25MLKNQLDQF0.99270.8437615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:02MLKNQLDQF0.98910.8725615
PFDN5-CAPN2chr1253689423chr122394988788HLA-A32:13MLKNQLDQF0.88120.9225615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:07MLKNQLDQF0.99840.6082615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:04MLKNQLDQF0.97930.7691615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:05MLKNQLDQF0.87140.8431615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:31MLKNQLDQF0.83620.8487615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:125MLKNQLDQF0.99890.7506615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:27MLKNQLDQF0.99890.7733615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:34MLKNQLDQF0.99890.7506615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:33MLKNQLDQF0.99890.7506615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:135MLKNQLDQF0.99880.7657615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:35MLKNQLDQF0.99840.7171615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:50MLKNQLDQF0.99830.8445615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:24MLKNQLDQF0.99780.7983615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:12MLKNQLDQF0.99420.7287615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:39MLKNQLDQF0.99230.7189615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:13MLKNQLDQF0.97380.6593615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B15:20MLKNQLDQF0.87720.9267615
PFDN5-CAPN2chr1253689423chr122394988788HLA-B35:28MLKNQLDQF0.82930.9311615

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Potential FusionNeoAntigen Information of PFDN5-CAPN2 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.
PFDN5-CAPN2_53689423_223949887.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)
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0403LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0403NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0403PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0405LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0405NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0405PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0409LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0409NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0411LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0411NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0411PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0415LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0417LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0417NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0424LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0424NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0424PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0427LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0427NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0429LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0429NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0429PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0430LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0430NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0430PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0436LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0439LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0439NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0439PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0440LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0441LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0441NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0441PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0442LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0445LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0445NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0445PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0446LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0446NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0446PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0448LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0448NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0448PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0449LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0449NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0449PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0450LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0450NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0450PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0451LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0451NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0452LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0452NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0452PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0453LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0456LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0457LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0457NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0457PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0458LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0459LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0459NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0459PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0460LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0460NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0460PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0462LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0465LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0467LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0467NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0467PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0468LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0471LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0471NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0471PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0477LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0477NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0477PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0478LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0479LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0480LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0480NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0480PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0482LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0483LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0483NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0483PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0484LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0484NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0484PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0485LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0485NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0485PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0486LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0486NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0486PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0487LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0487NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0487PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0488LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0488NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0488PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0489LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0489NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0489PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0491LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0491NLPQLEMLKNQLDQF015
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0491PQLEMLKNQLDQFDI217
PFDN5-CAPN2chr1253689423chr122394988788DRB1-0832LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-1002LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-1410LPQLEMLKNQLDQFD116
PFDN5-CAPN2chr1253689423chr122394988788DRB1-1457LPQLEMLKNQLDQFD116

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Fusion breakpoint peptide structures of PFDN5-CAPN2

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
5954MLKNQLDQFDISEDPFDN5CAPN2chr1253689423chr122394988788

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PFDN5-CAPN2

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-B14:023BVN5954MLKNQLDQFDISED-7.9962-8.1096
HLA-B14:023BVN5954MLKNQLDQFDISED-5.70842-6.74372
HLA-B52:013W395954MLKNQLDQFDISED-6.83737-6.95077
HLA-B52:013W395954MLKNQLDQFDISED-4.4836-5.5189
HLA-A11:014UQ25954MLKNQLDQFDISED-10.0067-10.1201
HLA-A11:014UQ25954MLKNQLDQFDISED-9.03915-10.0745
HLA-A24:025HGA5954MLKNQLDQFDISED-6.56204-6.67544
HLA-A24:025HGA5954MLKNQLDQFDISED-5.42271-6.45801
HLA-B44:053DX85954MLKNQLDQFDISED-7.85648-8.89178
HLA-B44:053DX85954MLKNQLDQFDISED-5.3978-5.5112
HLA-A02:016TDR5954MLKNQLDQFDISED-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PFDN5-CAPN2

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
PFDN5-CAPN2chr1253689423chr1223949887615MLKNQLDQFCTCAAGAACCAGCTGGACCAGTTCGAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PFDN5-CAPN2chr1253689423chr1223949887015NLPQLEMLKNQLDQFCTGCCGCAGCTAGAAATGCTCAAGAACCAGCTGGACCAGTTCGAC
PFDN5-CAPN2chr1253689423chr1223949887116LPQLEMLKNQLDQFDCCGCAGCTAGAAATGCTCAAGAACCAGCTGGACCAGTTCGACATC
PFDN5-CAPN2chr1253689423chr1223949887217PQLEMLKNQLDQFDICAGCTAGAAATGCTCAAGAACCAGCTGGACCAGTTCGACATCAGC

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Information of the samples that have these potential fusion neoantigens of PFDN5-CAPN2

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-CancerPFDN5-CAPN2chr1253689423ENST00000334478chr1223949887ENST00000295006131Nd

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Potential target of CAR-T therapy development for PFDN5-CAPN2

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 PFDN5-CAPN2

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 PFDN5-CAPN2

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