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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:PDPK1-MAPK8IP3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PDPK1-MAPK8IP3
FusionPDB ID: 64033
FusionGDB2.0 ID: 64038
HgeneTgene
Gene symbol

PDPK1

MAPK8IP3

Gene ID

5170

23162

Gene name3-phosphoinositide dependent protein kinase 1mitogen-activated protein kinase 8 interacting protein 3
SynonymsPDK1|PDPK2|PDPK2P|PRO0461JIP-3|JIP3|JSAP1|NEDBA|SYD2|syd
Cytomap

16p13.3

16p13.3

Type of geneprotein-codingprotein-coding
Description3-phosphoinositide-dependent protein kinase 13-phosphoinositide-dependent protein kinase 2 pseudogenePkB kinase like gene 1C-Jun-amino-terminal kinase-interacting protein 3C-jun-amino-terminal kinase interacting protein 3JNK MAP kinase scaffold protein 3JNK-interacting protein 3JNK/SAPK-associated protein-1JNK/stress-activated protein kinase-associated protein 1homolog
Modification date2020031320200313
UniProtAcc.

Q9UPT6

Main function of 5'-partner protein: FUNCTION: The JNK-interacting protein (JIP) group of scaffold proteins selectively mediates JNK signaling by aggregating specific components of the MAPK cascade to form a functional JNK signaling module (PubMed:12189133). May function as a regulator of vesicle transport, through interactions with the JNK-signaling components and motor proteins (By similarity). Promotes neuronal axon elongation in a kinesin- and JNK-dependent manner. Activates cofilin at axon tips via local activation of JNK, thereby regulating filopodial dynamics and enhancing axon elongation. Its binding to kinesin heavy chains (KHC), promotes kinesin-1 motility along microtubules and is essential for axon elongation and regeneration. Regulates cortical neuronal migration by mediating NTRK2/TRKB anterograde axonal transport during brain development (By similarity). Acts as an adapter that bridges the interaction between NTRK2/TRKB and KLC1 and drives NTRK2/TRKB axonal but not dendritic anterograde transport, which is essential for subsequent BDNF-triggered signaling and filopodia formation (PubMed:21775604). {ECO:0000250|UniProtKB:Q9ESN9, ECO:0000269|PubMed:12189133, ECO:0000269|PubMed:21775604}.
Ensembl transtripts involved in fusion geneENST idsENST00000471311, ENST00000342085, 
ENST00000354836, ENST00000389224, 
ENST00000441549, ENST00000268673, 
ENST00000250894, ENST00000356010, 
ENST00000568271, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 11 X 6=7268 X 8 X 6=384
# samples 129
** MAII scorelog2(12/726*10)=-2.59693514238723
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/384*10)=-2.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PDPK1 [Title/Abstract] AND MAPK8IP3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PDPK1 [Title/Abstract] AND MAPK8IP3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PDPK1(2616454)-MAPK8IP3(1809958), # samples:1
PDPK1(2616454)-MAPK8IP3(1809959), # samples:1
Anticipated loss of major functional domain due to fusion event.PDPK1-MAPK8IP3 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.
PDPK1-MAPK8IP3 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.
PDPK1-MAPK8IP3 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.
PDPK1-MAPK8IP3 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.
PDPK1-MAPK8IP3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PDPK1-MAPK8IP3 seems lost the major protein functional domain in Hgene partner, which is a kinase 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
HgenePDPK1

GO:0006468

protein phosphorylation

14585963

HgenePDPK1

GO:0006469

negative regulation of protein kinase activity

9373175

HgenePDPK1

GO:0018107

peptidyl-threonine phosphorylation

9368760

HgenePDPK1

GO:0030512

negative regulation of transforming growth factor beta receptor signaling pathway

17327236

HgenePDPK1

GO:0032148

activation of protein kinase B activity

9368760

HgenePDPK1

GO:0035556

intracellular signal transduction

14749367

HgenePDPK1

GO:0051281

positive regulation of release of sequestered calcium ion into cytosol

22454520



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/chr16:2616454/chr16:1809958)
- 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 PDPK1 (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 MAPK8IP3 (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)
ENST00000342085PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809958+51198588936251178
ENST00000342085PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809958+39428588936251178
ENST00000441549PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809958+50868255635921178
ENST00000441549PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809958+39098255635921178
ENST00000389224PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809958+5554129366540601131
ENST00000389224PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809958+4377129366540601131
ENST00000342085PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809959+51198588936251178
ENST00000342085PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809959+39428588936251178
ENST00000441549PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809959+50868255635921178
ENST00000441549PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809959+39098255635921178
ENST00000389224PDPK1chr162616454+ENST00000250894MAPK8IP3chr161809959+5554129366540601131
ENST00000389224PDPK1chr162616454+ENST00000356010MAPK8IP3chr161809959+4377129366540601131

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
ENST00000342085ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809958+0.0039237970.99607617
ENST00000342085ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809958+0.0043451910.9956548
ENST00000441549ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809958+0.0038321430.99616784
ENST00000441549ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809958+0.0043232960.9956767
ENST00000389224ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809958+0.004995390.9950046
ENST00000389224ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809958+0.0051585070.9948415
ENST00000342085ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809959+0.0039237970.99607617
ENST00000342085ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809959+0.0043451910.9956548
ENST00000441549ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809959+0.0038321430.99616784
ENST00000441549ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809959+0.0043232960.9956767
ENST00000389224ENST00000250894PDPK1chr162616454+MAPK8IP3chr161809959+0.004995390.9950046
ENST00000389224ENST00000356010PDPK1chr162616454+MAPK8IP3chr161809959+0.0051585070.9948415

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 PDPK1-MAPK8IP3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PDPK1chr162616454MAPK8IP3chr1618099581293209FGTAKVLSPESKQGMGKEVGNLLLEN
PDPK1chr162616454MAPK8IP3chr161809958825256FGTAKVLSPESKQGMGKEVGNLLLEN
PDPK1chr162616454MAPK8IP3chr161809958858256FGTAKVLSPESKQGMGKEVGNLLLEN
PDPK1chr162616454MAPK8IP3chr1618099591293209FGTAKVLSPESKQGMGKEVGNLLLEN
PDPK1chr162616454MAPK8IP3chr161809959825256FGTAKVLSPESKQGMGKEVGNLLLEN
PDPK1chr162616454MAPK8IP3chr161809959858256FGTAKVLSPESKQGMGKEVGNLLLEN

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Potential FusionNeoAntigen Information of PDPK1-MAPK8IP3 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.
PDPK1-MAPK8IP3_2616454_1809958.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)
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:17LSPESKQGM0.93550.904615
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:30LSPESKQGM0.89170.9245615
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:17VLSPESKQGM0.97760.9049515
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:02LSPESKQGM0.94150.9043615
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:03LSPESKQGM0.92340.9045615
PDPK1-MAPK8IP3chr162616454chr161809958858HLA-C01:02VLSPESKQGM0.98190.9068515

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Potential FusionNeoAntigen Information of PDPK1-MAPK8IP3 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 PDPK1-MAPK8IP3

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
5647LSPESKQGMGKEVGPDPK1MAPK8IP3chr162616454chr161809958858

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PDPK1-MAPK8IP3

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-B14:023BVN5647LSPESKQGMGKEVG-7.9962-8.1096
HLA-B14:023BVN5647LSPESKQGMGKEVG-5.70842-6.74372
HLA-B52:013W395647LSPESKQGMGKEVG-6.83737-6.95077
HLA-B52:013W395647LSPESKQGMGKEVG-4.4836-5.5189
HLA-A11:014UQ25647LSPESKQGMGKEVG-10.0067-10.1201
HLA-A11:014UQ25647LSPESKQGMGKEVG-9.03915-10.0745
HLA-A24:025HGA5647LSPESKQGMGKEVG-6.56204-6.67544
HLA-A24:025HGA5647LSPESKQGMGKEVG-5.42271-6.45801
HLA-B44:053DX85647LSPESKQGMGKEVG-7.85648-8.89178
HLA-B44:053DX85647LSPESKQGMGKEVG-5.3978-5.5112
HLA-A02:016TDR5647LSPESKQGMGKEVG-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PDPK1-MAPK8IP3

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
PDPK1-MAPK8IP3chr162616454chr161809958515VLSPESKQGMTCTTATCCCCAGAGAGCAAACAAGGAATGG
PDPK1-MAPK8IP3chr162616454chr161809958615LSPESKQGMTATCCCCAGAGAGCAAACAAGGAATGG

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 PDPK1-MAPK8IP3

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
BRCAPDPK1-MAPK8IP3chr162616454ENST00000342085chr161809958ENST00000250894TCGA-A8-A06Z

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Potential target of CAR-T therapy development for PDPK1-MAPK8IP3

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 PDPK1-MAPK8IP3

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 PDPK1-MAPK8IP3

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