FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

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

leaf

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

leaf

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

leaf

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

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

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

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:PRKAB2-FBP2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRKAB2-FBP2
FusionPDB ID: 68614
FusionGDB2.0 ID: 68614
HgeneTgene
Gene symbol

PRKAB2

FBP2

Gene ID

5565

64430

Gene nameprotein kinase AMP-activated non-catalytic subunit beta 2pecanex 4
Synonyms-C14orf135|FBP2|PCNXL4
Cytomap

1q21.1

14q23.1

Type of geneprotein-codingprotein-coding
Description5'-AMP-activated protein kinase subunit beta-25'-AMP-activated protein kinase, beta-2 subunitAMP-activated protein kinase beta 2 non-catalytic subunitAMPK beta 2AMPK beta-2 chainAMPK subunit beta-2protein kinase, AMP-activated, beta 2 non-catalytic pecanex-like protein 4HCV F protein-binding protein 2HCV F-interacting proteinhepatitis C virus F protein-binding protein 2pecanex homolog 4pecanex homolog protein 4pecanex-like 4pecanex-like protein C14orf135
Modification date2020032720200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000254101, ENST00000425272, 
ENST00000496858, 
ENST00000375337, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 2=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Fusion gene context

PubMed: PRKAB2 [Title/Abstract] AND FBP2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PRKAB2 [Title/Abstract] AND FBP2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PRKAB2(146643568)-FBP2(97349751), # samples:3
Anticipated loss of major functional domain due to fusion event.PRKAB2-FBP2 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.
PRKAB2-FBP2 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.
PRKAB2-FBP2 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.
PRKAB2-FBP2 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.
PRKAB2-FBP2 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PRKAB2-FBP2 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
PRKAB2-FBP2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PRKAB2-FBP2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PRKAB2-FBP2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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)

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/chr1:146643568/chr9:97349751)
- 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 PRKAB2 (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 FBP2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000425272PRKAB2chr1146643568-ENST00000375337FBP2chr997349751-1286218541067337

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
ENST00000425272ENST00000375337PRKAB2chr1146643568-FBP2chr997349751-0.0030564970.99694353

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

Top

Fusion Protein Breakpoint Sequences for PRKAB2-FBP2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PRKAB2chr1146643568FBP2chr99734975121854VRTTPACSASLTPRYGIAGSVNVTGD

Top

Potential FusionNeoAntigen Information of PRKAB2-FBP2 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.
PRKAB2-FBP2_146643568_97349751.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)
PRKAB2-FBP2chr1146643568chr997349751218HLA-B15:17CSASLTPRY0.99120.763615
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:02TPRYGIAGSV0.99880.67351121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:05TPRYGIAGSV0.99880.56581121
PRKAB2-FBP2chr1146643568chr997349751218HLA-C15:04CSASLTPRY0.73720.7443615
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:12TPRYGIAGSV0.97150.73671121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B54:01TPRYGIAGSV0.96080.66711121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:04TPRYGIAGSV0.9550.6741121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B42:01TPRYGIAGSV0.94290.73881121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B78:01TPRYGIAGSV0.80150.63261121
PRKAB2-FBP2chr1146643568chr997349751218HLA-C16:02SASLTPRY0.95790.9778715
PRKAB2-FBP2chr1146643568chr997349751218HLA-C16:01SASLTPRY0.84230.9446715
PRKAB2-FBP2chr1146643568chr997349751218HLA-C15:09CSASLTPRY0.73720.7443615
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:22TPRYGIAGSV0.99880.67351121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:09TPRYGIAGSV0.99860.66781121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B55:04TPRYGIAGSV0.7870.59531121
PRKAB2-FBP2chr1146643568chr997349751218HLA-B07:26TPRYGIAGSV0.74120.53591121

Top

Potential FusionNeoAntigen Information of PRKAB2-FBP2 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.
PRKAB2-FBP2_146643568_97349751.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)
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0101TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0103TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0105TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0107TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0109TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0111TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0113TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0113LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0115TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0117TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0117LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0119TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0121TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0121LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0125TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0127TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0129TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0131TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0469TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0701TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0701LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0701SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0703TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0703LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0703SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0704TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0704LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0705TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0705LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0705SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0706TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0706LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0707TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0707LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0707SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0708TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0708LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0708SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0709TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0709LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0709SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0711TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0711LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0711SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0712TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0712LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0712SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0713TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0713LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0713SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0714TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0714LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0714SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0715TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0715LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0715SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0716TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0716LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0716SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0717TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0717LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0717SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0719TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0719LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0719SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0901TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0901LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0901SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0902TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0903TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0904TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0904LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0905TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0905LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0907TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0907LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0907SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0908TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0909TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0909LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-0909SLTPRYGIAGSVNVT924
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1511TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1527TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1534TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1534LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1601TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1601LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1602TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1602LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1603TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1603LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1604TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1605TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1607TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1608TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1608LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1611TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1611LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1612TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1612LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1614TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1614LTPRYGIAGSVNVTG1025
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1616TPRYGIAGSVNVTGD1126
PRKAB2-FBP2chr1146643568chr997349751218DRB1-1616LTPRYGIAGSVNVTG1025

Top

Fusion breakpoint peptide structures of PRKAB2-FBP2

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
929CSASLTPRYGIAGSPRKAB2FBP2chr1146643568chr997349751218

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PRKAB2-FBP2

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-B14:023BVN929CSASLTPRYGIAGS-4.62424-5.65954
HLA-B14:023BVN929CSASLTPRYGIAGS-4.1114-4.2248
HLA-B52:013W39929CSASLTPRYGIAGS-6.8001-6.9135
HLA-B52:013W39929CSASLTPRYGIAGS-6.46104-7.49634
HLA-A24:025HGA929CSASLTPRYGIAGS-9.1447-9.2581
HLA-A24:025HGA929CSASLTPRYGIAGS-6.01279-7.04809
HLA-B44:053DX8929CSASLTPRYGIAGS-5.02862-5.14202
HLA-B44:053DX8929CSASLTPRYGIAGS-4.60714-5.64244

Top

Vaccine Design for the FusionNeoAntigens of PRKAB2-FBP2

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
PRKAB2-FBP2chr1146643568chr9973497511121TPRYGIAGSVTCCAAGGTATGGAATCGCAGGAAGCGTTAA
PRKAB2-FBP2chr1146643568chr997349751615CSASLTPRYTTCAGCCTCCCTGACTCCAAGGTATGG
PRKAB2-FBP2chr1146643568chr997349751715SASLTPRYAGCCTCCCTGACTCCAAGGTATGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PRKAB2-FBP2chr1146643568chr9973497511025LTPRYGIAGSVNVTGGACTCCAAGGTATGGAATCGCAGGAAGCGTTAACGTGACGGGAGA
PRKAB2-FBP2chr1146643568chr9973497511126TPRYGIAGSVNVTGDTCCAAGGTATGGAATCGCAGGAAGCGTTAACGTGACGGGAGATGA
PRKAB2-FBP2chr1146643568chr997349751924SLTPRYGIAGSVNVTCCTGACTCCAAGGTATGGAATCGCAGGAAGCGTTAACGTGACGGG

Top

Information of the samples that have these potential fusion neoantigens of PRKAB2-FBP2

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
KIRCPRKAB2-FBP2chr1146643568ENST00000425272chr997349751ENST00000375337TCGA-CZ-5452-01A

Top

Potential target of CAR-T therapy development for PRKAB2-FBP2

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

Top

Related Drugs to PRKAB2-FBP2

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

Top

Related Diseases to PRKAB2-FBP2

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