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:AKT3-PTPRR

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: AKT3-PTPRR
FusionPDB ID: 3504
FusionGDB2.0 ID: 3504
HgeneTgene
Gene symbol

AKT3

PTPRR

Gene ID

10000

5801

Gene nameAKT serine/threonine kinase 3protein tyrosine phosphatase receptor type R
SynonymsMPPH|MPPH2|PKB-GAMMA|PKBG|PRKBG|RAC-PK-gamma|RAC-gamma|STK-2EC-PTP|PCPTP1|PTP-SL|PTPBR7|PTPRQ
Cytomap

1q43-q44

12q15

Type of geneprotein-codingprotein-coding
DescriptionRAC-gamma serine/threonine-protein kinasePKB gammaRAC-gamma serine/threonine protein kinasev-akt murine thymoma viral oncogene homolog 3 (protein kinase B, gamma)receptor-type tyrosine-protein phosphatase RCh-1 PTPaseNC-PTPCOM1R-PTP-Rch-1PTPaseprotein tyrosine phosphatase Cr1PTPaseprotein-tyrosine phosphatase NC-PTPCOM1protein-tyrosine phosphatase PCPTP1
Modification date2020031320200313
UniProtAcc

Q9Y243

Main function of 5'-partner protein: FUNCTION: AKT3 is one of 3 closely related serine/threonine-protein kinases (AKT1, AKT2 and AKT3) called the AKT kinase, and which regulate many processes including metabolism, proliferation, cell survival, growth and angiogenesis. This is mediated through serine and/or threonine phosphorylation of a range of downstream substrates. Over 100 substrate candidates have been reported so far, but for most of them, no isoform specificity has been reported. AKT3 is the least studied AKT isoform. It plays an important role in brain development and is crucial for the viability of malignant glioma cells. AKT3 isoform may also be the key molecule in up-regulation and down-regulation of MMP13 via IL13. Required for the coordination of mitochondrial biogenesis with growth factor-induced increases in cellular energy demands. Down-regulation by RNA interference reduces the expression of the phosphorylated form of BAD, resulting in the induction of caspase-dependent apoptosis. {ECO:0000269|PubMed:18524868, ECO:0000269|PubMed:21191416}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000263826, ENST00000336199, 
ENST00000366539, ENST00000366540, 
ENST00000492957, 
ENST00000342084, 
ENST00000378778, ENST00000537619, 
ENST00000549308, ENST00000283228, 
ENST00000440835, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 15 X 7=189038 X 16 X 13=7904
# samples 2142
** MAII scorelog2(21/1890*10)=-3.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(42/7904*10)=-4.23412171391856
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: AKT3 [Title/Abstract] AND PTPRR [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: AKT3 [Title/Abstract] AND PTPRR [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)AKT3(243776973)-PTPRR(71078044), # samples:3
Anticipated loss of major functional domain due to fusion event.AKT3-PTPRR 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.
AKT3-PTPRR 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.
AKT3-PTPRR 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.
AKT3-PTPRR 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.
AKT3-PTPRR seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
AKT3-PTPRR seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
AKT3-PTPRR seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
AKT3-PTPRR seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneAKT3

GO:0043536

positive regulation of blood vessel endothelial cell migration

28254819

HgeneAKT3

GO:1905564

positive regulation of vascular endothelial cell proliferation

28254819



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/chr1:243776973/chr12:71078044)
- 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 AKT3 (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 PTPRR (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)
ENST00000336199AKT3chr1243776973-ENST00000283228PTPRRchr1271078044-2479762421376444
ENST00000336199AKT3chr1243776973-ENST00000440835PTPRRchr1271078044-2488762421376444
ENST00000366540AKT3chr1243776973-ENST00000283228PTPRRchr1271078044-25668491291463444
ENST00000366540AKT3chr1243776973-ENST00000440835PTPRRchr1271078044-25758491291463444
ENST00000263826AKT3chr1243776973-ENST00000283228PTPRRchr1271078044-2494777571391444
ENST00000263826AKT3chr1243776973-ENST00000440835PTPRRchr1271078044-2503777571391444

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
ENST00000336199ENST00000283228AKT3chr1243776973-PTPRRchr1271078044-0.0002778840.99972206
ENST00000336199ENST00000440835AKT3chr1243776973-PTPRRchr1271078044-0.0002747940.99972516
ENST00000366540ENST00000283228AKT3chr1243776973-PTPRRchr1271078044-0.0003450170.999655
ENST00000366540ENST00000440835AKT3chr1243776973-PTPRRchr1271078044-0.0003386730.9996613
ENST00000263826ENST00000283228AKT3chr1243776973-PTPRRchr1271078044-0.0003369750.999663
ENST00000263826ENST00000440835AKT3chr1243776973-PTPRRchr1271078044-0.0003300830.9996699

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 AKT3-PTPRR

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
AKT3chr1243776973PTPRRchr1271078044762240RLCFVMEYVNGGEGYSGKEKAFIATQ
AKT3chr1243776973PTPRRchr1271078044777240RLCFVMEYVNGGEGYSGKEKAFIATQ
AKT3chr1243776973PTPRRchr1271078044849240RLCFVMEYVNGGEGYSGKEKAFIATQ

Top

Potential FusionNeoAntigen Information of AKT3-PTPRR 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.
AKT3-PTPRR_243776973_71078044.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)
AKT3-PTPRRchr1243776973chr1271078044777HLA-B44:03MEYVNGGEGY0.99680.8938515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:01MEYVNGGEGY0.98940.7804515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B45:01GEGYSGKEKA0.97220.95221121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B50:02GEGYSGKEKA0.920.78841121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B41:01GEGYSGKEKA0.8660.97381121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B50:01GEGYSGKEKA0.83350.80351121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B15:21EYVNGGEGY0.56310.7944615
AKT3-PTPRRchr1243776973chr1271078044777HLA-B40:06GEGYSGKEKA0.94660.96211121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B44:07MEYVNGGEGY0.99680.8938515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B44:13MEYVNGGEGY0.99680.8938515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B44:26MEYVNGGEGY0.99680.8938515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:04MEYVNGGEGY0.99430.7982515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:08MEYVNGGEGY0.99030.5837515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:05MEYVNGGEGY0.98940.7804515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B15:53MEYVNGGEGY0.98930.7754515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:06MEYVNGGEGY0.98650.7601515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:03MEYVNGGEGY0.98020.7648515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B18:11MEYVNGGEGY0.98010.7782515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B35:28MEYVNGGEGY0.94050.7959515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B35:20MEYVNGGEGY0.92020.8124515
AKT3-PTPRRchr1243776973chr1271078044777HLA-B50:05GEGYSGKEKA0.83350.80351121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B50:04GEGYSGKEKA0.83350.80351121
AKT3-PTPRRchr1243776973chr1271078044777HLA-B48:02MEYVNGGEGY0.81960.7718515

Top

Potential FusionNeoAntigen Information of AKT3-PTPRR 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)

Top

Fusion breakpoint peptide structures of AKT3-PTPRR

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
2275EYVNGGEGYSGKEKAKT3PTPRRchr1243776973chr1271078044777

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of AKT3-PTPRR

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-B14:023BVN2275EYVNGGEGYSGKEK-7.9962-8.1096
HLA-B14:023BVN2275EYVNGGEGYSGKEK-5.70842-6.74372
HLA-B52:013W392275EYVNGGEGYSGKEK-6.83737-6.95077
HLA-B52:013W392275EYVNGGEGYSGKEK-4.4836-5.5189
HLA-A11:014UQ22275EYVNGGEGYSGKEK-10.0067-10.1201
HLA-A11:014UQ22275EYVNGGEGYSGKEK-9.03915-10.0745
HLA-A24:025HGA2275EYVNGGEGYSGKEK-6.56204-6.67544
HLA-A24:025HGA2275EYVNGGEGYSGKEK-5.42271-6.45801
HLA-B44:053DX82275EYVNGGEGYSGKEK-7.85648-8.89178
HLA-B44:053DX82275EYVNGGEGYSGKEK-5.3978-5.5112
HLA-A02:016TDR2275EYVNGGEGYSGKEK-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of AKT3-PTPRR

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
AKT3-PTPRRchr1243776973chr12710780441121GEGYSGKEKAGGCGAGGGCTACAGTGGCAAGGAGAAAGCC
AKT3-PTPRRchr1243776973chr1271078044515MEYVNGGEGYATGGAATATGTTAATGGGGGCGAGGGCTAC
AKT3-PTPRRchr1243776973chr1271078044615EYVNGGEGYGAATATGTTAATGGGGGCGAGGGCTAC

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

Top

Information of the samples that have these potential fusion neoantigens of AKT3-PTPRR

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
SKCMAKT3-PTPRRchr1243776973ENST00000263826chr1271078044ENST00000283228TCGA-ER-A197-06A

Top

Potential target of CAR-T therapy development for AKT3-PTPRR

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
TgenePTPRRchr1:243776973chr12:71078044ENST00000440835410228_2480413.0TransmembraneHelical
TgenePTPRRchr1:243776973chr12:71078044ENST00000549308511228_2480413.0TransmembraneHelical

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 AKT3-PTPRR

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

Top

Related Diseases to AKT3-PTPRR

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