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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:PRKAR1B-MAD1L1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRKAR1B-MAD1L1
FusionPDB ID: 68671
FusionGDB2.0 ID: 68671
HgeneTgene
Gene symbol

PRKAR1B

MAD1L1

Gene ID

5575

8379

Gene nameprotein kinase cAMP-dependent type I regulatory subunit betamitotic arrest deficient 1 like 1
SynonymsPRKAR1MAD1|PIG9|TP53I9|TXBP181
Cytomap

7p22.3

7p22.3

Type of geneprotein-codingprotein-coding
DescriptioncAMP-dependent protein kinase type I-beta regulatory subunitprotein kinase, cAMP-dependent, regulatory subunit type I betaprotein kinase, cAMP-dependent, regulatory, type I, betamitotic spindle assembly checkpoint protein MAD1MAD1 mitotic arrest deficient like 1MAD1-like protein 1mitotic arrest deficient 1-like protein 1mitotic checkpoint MAD1 protein homologmitotic-arrest deficient 1, yeast, homolog-like 1tax-binding prote
Modification date2020032720200313
UniProtAcc.

Q9Y6D9

Main function of 5'-partner protein: FUNCTION: Component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate (PubMed:10049595, PubMed:20133940, PubMed:29162720). Forms a heterotetrameric complex with the closed conformation form of MAD2L1 (C-MAD2) at unattached kinetochores during prometaphase, recruits an open conformation of MAD2L1 (O-MAD2) and promotes the conversion of O-MAD2 to C-MAD2, which ensures mitotic checkpoint signaling (PubMed:29162720). {ECO:0000269|PubMed:10049595, ECO:0000269|PubMed:20133940, ECO:0000269|PubMed:29162720}.
Ensembl transtripts involved in fusion geneENST idsENST00000360274, ENST00000403562, 
ENST00000406797, ENST00000537384, 
ENST00000544935, ENST00000488474, 
ENST00000486340, ENST00000265854, 
ENST00000399654, ENST00000402746, 
ENST00000406869, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 5=18023 X 16 X 12=4416
# samples 737
** MAII scorelog2(7/180*10)=-1.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(37/4416*10)=-3.57714299626186
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PRKAR1B [Title/Abstract] AND MAD1L1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PRKAR1B [Title/Abstract] AND MAD1L1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAD1L1(2108828)-PRKAR1B(591107), # samples:1
PRKAR1B(645830)-MAD1L1(2020176), # samples:1
Anticipated loss of major functional domain due to fusion event.PRKAR1B-MAD1L1 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.
PRKAR1B-MAD1L1 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.
PRKAR1B-MAD1L1 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.
PRKAR1B-MAD1L1 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.
MAD1L1-PRKAR1B seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MAD1L1-PRKAR1B seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
MAD1L1-PRKAR1B seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
MAD1L1-PRKAR1B seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PRKAR1B-MAD1L1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PRKAR1B-MAD1L1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PRKAR1B-MAD1L1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PRKAR1B-MAD1L1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgenePRKAR1B

GO:2000480

negative regulation of cAMP-dependent protein kinase activity

21812984

TgeneMAD1L1

GO:0007094

mitotic spindle assembly checkpoint

18981471

TgeneMAD1L1

GO:0090235

regulation of metaphase plate congression

20133940



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/chr7:2108828/chr7:591107)
- 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 PRKAR1B (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 MAD1L1 (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)
ENST00000544935PRKAR1Bchr7645830-ENST00000402746MAD1L1chr72020176-16816641151404429
ENST00000544935PRKAR1Bchr7645830-ENST00000399654MAD1L1chr72020176-16816641151404429
ENST00000544935PRKAR1Bchr7645830-ENST00000406869MAD1L1chr72020176-16816641151404429
ENST00000544935PRKAR1Bchr7645830-ENST00000265854MAD1L1chr72020176-16646641151404429
ENST00000406797PRKAR1Bchr7645830-ENST00000402746MAD1L1chr72020176-17417241361464442
ENST00000406797PRKAR1Bchr7645830-ENST00000399654MAD1L1chr72020176-17417241361464442
ENST00000406797PRKAR1Bchr7645830-ENST00000406869MAD1L1chr72020176-17417241361464442
ENST00000406797PRKAR1Bchr7645830-ENST00000265854MAD1L1chr72020176-17247241361464442
ENST00000403562PRKAR1Bchr7645830-ENST00000402746MAD1L1chr72020176-1649632831372429
ENST00000403562PRKAR1Bchr7645830-ENST00000399654MAD1L1chr72020176-1649632831372429
ENST00000403562PRKAR1Bchr7645830-ENST00000406869MAD1L1chr72020176-1649632831372429
ENST00000403562PRKAR1Bchr7645830-ENST00000265854MAD1L1chr72020176-1632632831372429

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
ENST00000544935ENST00000402746PRKAR1Bchr7645830-MAD1L1chr72020176-0.0130608370.9869392
ENST00000544935ENST00000399654PRKAR1Bchr7645830-MAD1L1chr72020176-0.0130608370.9869392
ENST00000544935ENST00000406869PRKAR1Bchr7645830-MAD1L1chr72020176-0.0130608370.9869392
ENST00000544935ENST00000265854PRKAR1Bchr7645830-MAD1L1chr72020176-0.0125701610.9874298
ENST00000406797ENST00000402746PRKAR1Bchr7645830-MAD1L1chr72020176-0.0110247170.9889753
ENST00000406797ENST00000399654PRKAR1Bchr7645830-MAD1L1chr72020176-0.0110247170.9889753
ENST00000406797ENST00000406869PRKAR1Bchr7645830-MAD1L1chr72020176-0.0110247170.9889753
ENST00000406797ENST00000265854PRKAR1Bchr7645830-MAD1L1chr72020176-0.0105274470.98947257
ENST00000403562ENST00000402746PRKAR1Bchr7645830-MAD1L1chr72020176-0.0119679520.988032
ENST00000403562ENST00000399654PRKAR1Bchr7645830-MAD1L1chr72020176-0.0119679520.988032
ENST00000403562ENST00000406869PRKAR1Bchr7645830-MAD1L1chr72020176-0.0119679520.988032
ENST00000403562ENST00000265854PRKAR1Bchr7645830-MAD1L1chr72020176-0.011394090.9886059

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 PRKAR1B-MAD1L1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PRKAR1Bchr7645830MAD1L1chr72020176632183GDNFYVVDQGEVDLEMELKMLKSQSS
PRKAR1Bchr7645830MAD1L1chr72020176664183GDNFYVVDQGEVDLEMELKMLKSQSS
PRKAR1Bchr7645830MAD1L1chr72020176724196GDNFYVVDQGEVDLEMELKMLKSQSS

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Potential FusionNeoAntigen Information of PRKAR1B-MAD1L1 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.
PRKAR1B-MAD1L1_645830_2020176.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)
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B13:01GEVDLEMEL0.99550.897918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B44:03GEVDLEMEL0.98840.9736918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B50:02GEVDLEMEL0.98630.6598918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B47:01GEVDLEMEL0.97430.629918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B45:01GEVDLEMEL0.92160.9182918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B15:37DQGEVDLEM0.71140.7932716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:01GEVDLEMEL0.69360.9479918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:13GEVDLEMEL0.59180.9717918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B50:01GEVDLEMEL0.43140.7053918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B41:01GEVDLEMEL0.41130.9258918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:15EVDLEMEL10.91731018
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:10VVDQGEVDL0.99970.7896514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:09VVDQGEVDL0.99970.98514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:07VVDQGEVDL0.99960.819514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B40:06GEVDLEMEL0.99960.616918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:15VVDQGEVDL0.99950.9832514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:06VVDQGEVDL0.92240.8303514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B15:31DQGEVDLEM0.78160.9716716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:04VVDQGEVDL0.74530.9722514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:13VVDQGEVDL0.74530.9722514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:08GEVDLEMEL0.70490.864918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:14VVDQGEVDL0.66470.7978514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:05DQGEVDLEM0.56030.9659716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:05GEVDLEMEL0.47730.9559918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:03VVDQGEVDL0.44990.9883514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:09YVVDQGEVDL0.99830.9674414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:15YVVDQGEVDL0.99670.9523414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:09VVDQGEVDLEM10.984516
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:15VVDQGEVDLEM10.9835516
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:07FYVVDQGEVDL0.99930.6375314
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:10FYVVDQGEVDL0.99930.6426314
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:02EVDLEMEL10.91731018
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:03EVDLEMEL10.8421018
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:03VVDQGEVDL0.99970.8389514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:01VVDQGEVDL0.99970.98514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:01VVDQGEVDL0.99960.819514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C18:01VVDQGEVDL0.99950.8982514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B40:04GEVDLEMEL0.99950.6938918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:02VVDQGEVDL0.99950.9832514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C01:03VVDQGEVDL0.99930.9079514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B44:07GEVDLEMEL0.98840.9736918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B44:26GEVDLEMEL0.98840.9736918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B44:13GEVDLEMEL0.98840.9736918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:04DQGEVDLEM0.88670.9632716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B35:20DQGEVDLEM0.76550.9905716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C03:06VVDQGEVDL0.74140.9859514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:06DQGEVDLEM0.7210.9612716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:05GEVDLEMEL0.69360.9479918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:11GEVDLEMEL0.68130.8198918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:06GEVDLEMEL0.65930.9551918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:11GEVDLEMEL0.65520.9346918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B18:03GEVDLEMEL0.65280.9418918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:11DQGEVDLEM0.59270.9456716
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:02GEVDLEMEL0.56580.9717918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B39:31GEVDLEMEL0.55980.9647918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B41:03GEVDLEMEL0.55610.6613918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C17:01VVDQGEVDL0.47610.8637514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:01VVDQGEVDL0.44990.9883514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B48:02GEVDLEMEL0.44120.9474918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B50:05GEVDLEMEL0.43140.7053918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B50:04GEVDLEMEL0.43140.7053918
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B07:13VVDQGEVDL0.08080.8052514
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:01YVVDQGEVDL0.99830.9674414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:03YVVDQGEVDL0.99810.9013414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:02YVVDQGEVDL0.99670.9523414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C03:06YVVDQGEVDL0.98520.9779414
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B40:04QGEVDLEMEL0.54660.8117818
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B41:03QGEVDLEMEL0.45940.8343818
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C05:01VVDQGEVDLEM10.984516
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:03VVDQGEVDLEM10.9652516
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C08:02VVDQGEVDLEM10.9835516
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-B40:04GEVDLEMELKM0.99950.6826920
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C04:01FYVVDQGEVDL0.99930.6375314
PRKAR1B-MAD1L1chr7645830chr72020176632HLA-C18:01FYVVDQGEVDL0.99870.6564314

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Potential FusionNeoAntigen Information of PRKAR1B-MAD1L1 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.
PRKAR1B-MAD1L1_645830_2020176.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)
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0409GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0409DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0462GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0462DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0807GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0819GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0825GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0834GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-0905GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-1333GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-1333DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB1-1468GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0101GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0101DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0104GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0104DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0105GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0105DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0108GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0108DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0109GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0109DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0111GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0111DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0112GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0112DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0113GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0113DNFYVVDQGEVDLEM116
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0114GDNFYVVDQGEVDLE015
PRKAR1B-MAD1L1chr7645830chr72020176632DRB3-0114DNFYVVDQGEVDLEM116

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Fusion breakpoint peptide structures of PRKAR1B-MAD1L1

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
9864VDQGEVDLEMELKMPRKAR1BMAD1L1chr7645830chr72020176632

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PRKAR1B-MAD1L1

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-B14:023BVN9864VDQGEVDLEMELKM-7.9962-8.1096
HLA-B14:023BVN9864VDQGEVDLEMELKM-5.70842-6.74372
HLA-B52:013W399864VDQGEVDLEMELKM-6.83737-6.95077
HLA-B52:013W399864VDQGEVDLEMELKM-4.4836-5.5189
HLA-A11:014UQ29864VDQGEVDLEMELKM-10.0067-10.1201
HLA-A11:014UQ29864VDQGEVDLEMELKM-9.03915-10.0745
HLA-A24:025HGA9864VDQGEVDLEMELKM-6.56204-6.67544
HLA-A24:025HGA9864VDQGEVDLEMELKM-5.42271-6.45801
HLA-B44:053DX89864VDQGEVDLEMELKM-7.85648-8.89178
HLA-B44:053DX89864VDQGEVDLEMELKM-5.3978-5.5112
HLA-A02:016TDR9864VDQGEVDLEMELKM-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PRKAR1B-MAD1L1

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
PRKAR1B-MAD1L1chr7645830chr720201761018EVDLEMELGAAGTGGATCTGGAGATGGAGCTG
PRKAR1B-MAD1L1chr7645830chr72020176314FYVVDQGEVDLTTCTATGTCGTTGATCAAGGGGAAGTGGATCTG
PRKAR1B-MAD1L1chr7645830chr72020176414YVVDQGEVDLTATGTCGTTGATCAAGGGGAAGTGGATCTG
PRKAR1B-MAD1L1chr7645830chr72020176514VVDQGEVDLGTCGTTGATCAAGGGGAAGTGGATCTG
PRKAR1B-MAD1L1chr7645830chr72020176516VVDQGEVDLEMGTCGTTGATCAAGGGGAAGTGGATCTGGAGATG
PRKAR1B-MAD1L1chr7645830chr72020176716DQGEVDLEMGATCAAGGGGAAGTGGATCTGGAGATG
PRKAR1B-MAD1L1chr7645830chr72020176818QGEVDLEMELCAAGGGGAAGTGGATCTGGAGATGGAGCTG
PRKAR1B-MAD1L1chr7645830chr72020176918GEVDLEMELGGGGAAGTGGATCTGGAGATGGAGCTG
PRKAR1B-MAD1L1chr7645830chr72020176920GEVDLEMELKMGGGGAAGTGGATCTGGAGATGGAGCTGAAGATG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PRKAR1B-MAD1L1chr7645830chr72020176015GDNFYVVDQGEVDLEGGAGACAACTTCTATGTCGTTGATCAAGGGGAAGTGGATCTGGAG
PRKAR1B-MAD1L1chr7645830chr72020176116DNFYVVDQGEVDLEMGACAACTTCTATGTCGTTGATCAAGGGGAAGTGGATCTGGAGATG

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Information of the samples that have these potential fusion neoantigens of PRKAR1B-MAD1L1

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
STADPRKAR1B-MAD1L1chr7645830ENST00000403562chr72020176ENST00000265854TCGA-BR-8078-01A

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Potential target of CAR-T therapy development for PRKAR1B-MAD1L1

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 PRKAR1B-MAD1L1

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 PRKAR1B-MAD1L1

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