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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:PGK1-TP53BP1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PGK1-TP53BP1
FusionPDB ID: 64613
FusionGDB2.0 ID: 64613
HgeneTgene
Gene symbol

PGK1

TP53BP1

Gene ID

5230

7158

Gene namephosphoglycerate kinase 1tumor protein p53 binding protein 1
SynonymsHEL-S-68p|MIG10|PGKA53BP1|TDRD30|p202|p53BP1
Cytomap

Xq21.1

15q15.3

Type of geneprotein-codingprotein-coding
Descriptionphosphoglycerate kinase 1PRP 2cell migration-inducing gene 10 proteinepididymis secretory sperm binding protein Li 68pprimer recognition protein 2TP53-binding protein 1p53-binding protein 1tumor protein 53-binding protein, 1tumor suppressor p53-binding protein 1
Modification date2020031320200322
UniProtAcc.

Q12888

Main function of 5'-partner protein: FUNCTION: Double-strand break (DSB) repair protein involved in response to DNA damage, telomere dynamics and class-switch recombination (CSR) during antibody genesis (PubMed:12364621, PubMed:22553214, PubMed:23333306, PubMed:17190600, PubMed:21144835, PubMed:27153538, PubMed:28241136). Plays a key role in the repair of double-strand DNA breaks (DSBs) in response to DNA damage by promoting non-homologous end joining (NHEJ)-mediated repair of DSBs and specifically counteracting the function of the homologous recombination (HR) repair protein BRCA1 (PubMed:22553214, PubMed:23727112, PubMed:23333306, PubMed:27153538). In response to DSBs, phosphorylation by ATM promotes interaction with RIF1 and dissociation from NUDT16L1/TIRR, leading to recruitment to DSBs sites (PubMed:28241136). Recruited to DSBs sites by recognizing and binding histone H2A monoubiquitinated at 'Lys-15' (H2AK15Ub) and histone H4 dimethylated at 'Lys-20' (H4K20me2), two histone marks that are present at DSBs sites (PubMed:23760478, PubMed:27153538, PubMed:28241136, PubMed:17190600). Required for immunoglobulin class-switch recombination (CSR) during antibody genesis, a process that involves the generation of DNA DSBs (PubMed:23345425). Participates in the repair and the orientation of the broken DNA ends during CSR (By similarity). In contrast, it is not required for classic NHEJ and V(D)J recombination (By similarity). Promotes NHEJ of dysfunctional telomeres via interaction with PAXIP1 (PubMed:23727112). {ECO:0000250|UniProtKB:P70399, ECO:0000269|PubMed:12364621, ECO:0000269|PubMed:17190600, ECO:0000269|PubMed:21144835, ECO:0000269|PubMed:22553214, ECO:0000269|PubMed:23333306, ECO:0000269|PubMed:23345425, ECO:0000269|PubMed:23727112, ECO:0000269|PubMed:23760478, ECO:0000269|PubMed:27153538, ECO:0000269|PubMed:28241136}.
Ensembl transtripts involved in fusion geneENST idsENST00000476531, ENST00000373316, 
ENST00000442431, ENST00000537456, 
ENST00000263801, ENST00000382039, 
ENST00000382044, ENST00000450115, 
ENST00000605155, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 5 X 3=756 X 6 X 3=108
# samples 66
** MAII scorelog2(6/75*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PGK1 [Title/Abstract] AND TP53BP1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PGK1 [Title/Abstract] AND TP53BP1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PGK1(77380895)-TP53BP1(43705524), # samples:1
Anticipated loss of major functional domain due to fusion event.PGK1-TP53BP1 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.
PGK1-TP53BP1 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.
PGK1-TP53BP1 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.
PGK1-TP53BP1 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
HgenePGK1

GO:0071456

cellular response to hypoxia

11130727

TgeneTP53BP1

GO:0006303

double-strand break repair via nonhomologous end joining

23333306|23760478|28241136

TgeneTP53BP1

GO:0006974

cellular response to DNA damage stimulus

17500065|28241136

TgeneTP53BP1

GO:0045830

positive regulation of isotype switching

23345425

TgeneTP53BP1

GO:0051260

protein homooligomerization

23345425

TgeneTP53BP1

GO:2000042

negative regulation of double-strand break repair via homologous recombination

23333306|23345425



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/chrX:77380895/chr15:43705524)
- 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 PGK1 (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 TP53BP1 (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)
ENST00000373316PGK1chrX77380895+ENST00000263801TP53BP1chr1543705524-231913081251495456
ENST00000373316PGK1chrX77380895+ENST00000382039TP53BP1chr1543705524-231413081251495456
ENST00000373316PGK1chrX77380895+ENST00000382044TP53BP1chr1543705524-231413081251495456
ENST00000373316PGK1chrX77380895+ENST00000450115TP53BP1chr1543705524-231413081252146673
ENST00000442431PGK1chrX77380895+ENST00000263801TP53BP1chr1543705524-1830819441006320
ENST00000442431PGK1chrX77380895+ENST00000382039TP53BP1chr1543705524-18258199661322
ENST00000442431PGK1chrX77380895+ENST00000382044TP53BP1chr1543705524-18258199661322
ENST00000442431PGK1chrX77380895+ENST00000450115TP53BP1chr1543705524-1825819441657537
ENST00000537456PGK1chrX77380895+ENST00000263801TP53BP1chr1543705524-239713862091573454
ENST00000537456PGK1chrX77380895+ENST00000382039TP53BP1chr1543705524-239213862091573454
ENST00000537456PGK1chrX77380895+ENST00000382044TP53BP1chr1543705524-239213862091573454
ENST00000537456PGK1chrX77380895+ENST00000450115TP53BP1chr1543705524-239213862092224671

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
ENST00000373316ENST00000263801PGK1chrX77380895+TP53BP1chr1543705524-0.001087880.9989121
ENST00000373316ENST00000382039PGK1chrX77380895+TP53BP1chr1543705524-0.0011241230.9988759
ENST00000373316ENST00000382044PGK1chrX77380895+TP53BP1chr1543705524-0.0011241230.9988759
ENST00000373316ENST00000450115PGK1chrX77380895+TP53BP1chr1543705524-0.0011682330.9988318
ENST00000442431ENST00000263801PGK1chrX77380895+TP53BP1chr1543705524-0.00183270.9981673
ENST00000442431ENST00000382039PGK1chrX77380895+TP53BP1chr1543705524-0.0018646720.9981353
ENST00000442431ENST00000382044PGK1chrX77380895+TP53BP1chr1543705524-0.0018646720.9981353
ENST00000442431ENST00000450115PGK1chrX77380895+TP53BP1chr1543705524-0.0015706890.99842924
ENST00000537456ENST00000263801PGK1chrX77380895+TP53BP1chr1543705524-0.0022658990.99773407
ENST00000537456ENST00000382039PGK1chrX77380895+TP53BP1chr1543705524-0.0023554670.9976445
ENST00000537456ENST00000382044PGK1chrX77380895+TP53BP1chr1543705524-0.0023554670.9976445
ENST00000537456ENST00000450115PGK1chrX77380895+TP53BP1chr1543705524-0.0027923790.9972076

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 PGK1-TP53BP1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PGK1chrX77380895TP53BP1chr15437055241308394ITIIGGASLELLEVGAGEFVSPCESG
PGK1chrX77380895TP53BP1chr15437055241386392ITIIGGASLELLEVGAGEFVSPCESG
PGK1chrX77380895TP53BP1chr1543705524819258ITIIGGASLELLEVGAGEFVSPCESG

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Potential FusionNeoAntigen Information of PGK1-TP53BP1 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.
PGK1-TP53BP1_77380895_43705524.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)
PGK1-TP53BP1chrX77380895chr15437055241308HLA-B18:01LEVGAGEF0.99330.9261119
PGK1-TP53BP1chrX77380895chr15437055241308HLA-C02:06GASLELLEV0.84110.9897514
PGK1-TP53BP1chrX77380895chr15437055241308HLA-B18:05LEVGAGEF0.99330.9261119
PGK1-TP53BP1chrX77380895chr15437055241308HLA-B18:11LEVGAGEF0.98920.93851119

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Potential FusionNeoAntigen Information of PGK1-TP53BP1 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 PGK1-TP53BP1

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
598ASLELLEVGAGEFVPGK1TP53BP1chrX77380895chr15437055241308

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PGK1-TP53BP1

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-B52:013W39598ASLELLEVGAGEFV-5.34702-5.34702
HLA-B44:053DX8598ASLELLEVGAGEFV-3.7485-3.7485

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Vaccine Design for the FusionNeoAntigens of PGK1-TP53BP1

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
PGK1-TP53BP1chrX77380895chr15437055241119LEVGAGEFTGGAAGTAGGGGCAGGAGAGTTTG
PGK1-TP53BP1chrX77380895chr1543705524514GASLELLEVGTGCCAGTTTGGAGCTCCTGGAAGTAG

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 PGK1-TP53BP1

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
N/APGK1-TP53BP1chrX77380895ENST00000373316chr1543705524ENST00000450115BQ349520

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Potential target of CAR-T therapy development for PGK1-TP53BP1

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 PGK1-TP53BP1

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 PGK1-TP53BP1

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
TgeneTP53BP1C0006142Malignant neoplasm of breast1CTD_human
TgeneTP53BP1C0007102Malignant tumor of colon1CTD_human
TgeneTP53BP1C0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneTP53BP1C0009375Colonic Neoplasms1CTD_human
TgeneTP53BP1C0017636Glioblastoma1CTD_human
TgeneTP53BP1C0024232Lymphatic Metastasis1CTD_human
TgeneTP53BP1C0334588Giant Cell Glioblastoma1CTD_human
TgeneTP53BP1C0678222Breast Carcinoma1CTD_human
TgeneTP53BP1C0919267ovarian neoplasm1CTD_human
TgeneTP53BP1C1140680Malignant neoplasm of ovary1CTD_human
TgeneTP53BP1C1257931Mammary Neoplasms, Human1CTD_human
TgeneTP53BP1C1458155Mammary Neoplasms1CTD_human
TgeneTP53BP1C1621958Glioblastoma Multiforme1CTD_human
TgeneTP53BP1C4704874Mammary Carcinoma, Human1CTD_human