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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:MYCBP2-CPB2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MYCBP2-CPB2
FusionPDB ID: 56200
FusionGDB2.0 ID: 56200
HgeneTgene
Gene symbol

MYCBP2

CPB2

Gene ID

23077

1361

Gene nameMYC binding protein 2carboxypeptidase B2
SynonymsMyc-bp2|PAM|PHR1|PhrCPU|PCPB|TAFI
Cytomap

13q22.3

13q14.13

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase MYCBP2HighwireMYC binding protein 2, E3 ubiquitin protein ligasePAM/Highwire/RPM-1 protein 1RING-type E3 ubiquitin transferase MYCBP2myc-binding protein 2pam/highwire/rpm-1 proteinprotein associated with Myccarboxypeptidase B2carboxypeptidase B-like proteincarboxypeptidase B2 (plasma)carboxypeptidase B2 (plasma, carboxypeptidase U)carboxypeptidase Rthrombin-activable fibrinolysis inhibitorthrombin-activatable fibrinolysis inhibitor
Modification date2020031320200313
UniProtAcc

O75592

Main function of 5'-partner protein: FUNCTION: Atypical E3 ubiquitin-protein ligase which specifically mediates ubiquitination of threonine and serine residues on target proteins, instead of ubiquitinating lysine residues (PubMed:29643511). Shows esterification activity towards both threonine and serine, with a preference for threonine, and acts via two essential catalytic cysteine residues that relay ubiquitin to its substrate via thioester intermediates (PubMed:29643511). Interacts with the E2 enzymes UBE2D1, UBE2D3, UBE2E1 and UBE2L3 (PubMed:18308511, PubMed:29643511). Plays a key role in neural development, probably by mediating ubiquitination of threonine residues on target proteins (Probable). Involved in different processes such as regulation of neurite outgrowth, synaptic growth, synaptogenesis and axon degeneration (By similarity). Required for the formation of major central nervous system axon tracts (By similarity). Required for proper axon growth by regulating axon navigation and axon branching: acts by regulating the subcellular location and stability of MAP3K12/DLK (By similarity). Required for proper localization of retinogeniculate projections but not for eye-specific segregation (By similarity). Regulates axon guidance in the olfactory system (By similarity). Involved in Wallerian axon degeneration, an evolutionarily conserved process that drives the loss of damaged axons: acts by promoting destabilization of NMNAT2, probably via ubiquitination of NMNAT2 (By similarity). Catalyzes ubiquitination of threonine and/or serine residues on NMNAT2, consequences of threonine and/or serine ubiquitination are however unknown (PubMed:29643511). Regulates the internalization of TRPV1 in peripheral sensory neurons (By similarity). Mediates ubiquitination and subsequent proteasomal degradation of TSC2/tuberin (PubMed:18308511, PubMed:27278822). Independently of the E3 ubiquitin-protein ligase activity, also acts as a guanosine exchange factor (GEF) for RAN in neurons of dorsal root ganglia (PubMed:26304119). May function as a facilitator or regulator of transcriptional activation by MYC (PubMed:9689053). Acts in concert with HUWE1 to regulate the circadian clock gene expression by promoting the lithium-induced ubiquination and degradation of NR1D1 (PubMed:20534529). {ECO:0000250|UniProtKB:Q7TPH6, ECO:0000269|PubMed:18308511, ECO:0000269|PubMed:20534529, ECO:0000269|PubMed:26304119, ECO:0000269|PubMed:27278822, ECO:0000269|PubMed:29643511, ECO:0000269|PubMed:9689053}.

Q96IY4

Main function of 5'-partner protein: FUNCTION: Cleaves C-terminal arginine or lysine residues from biologically active peptides such as kinins or anaphylatoxins in the circulation thereby regulating their activities. Down-regulates fibrinolysis by removing C-terminal lysine residues from fibrin that has already been partially degraded by plasmin. {ECO:0000269|PubMed:10574983}.
Ensembl transtripts involved in fusion geneENST idsENST00000360084, ENST00000357337, 
ENST00000407578, ENST00000544440, 
ENST00000482517, 
ENST00000181383, 
ENST00000439329, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 16 X 8=17922 X 2 X 2=8
# samples 152
** MAII scorelog2(15/1792*10)=-3.57853623156172
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Fusion gene context

PubMed: MYCBP2 [Title/Abstract] AND CPB2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MYCBP2 [Title/Abstract] AND CPB2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MYCBP2(77862296)-CPB2(46638876), # samples:3
Anticipated loss of major functional domain due to fusion event.MYCBP2-CPB2 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.
MYCBP2-CPB2 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.
MYCBP2-CPB2 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.
MYCBP2-CPB2 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.
MYCBP2-CPB2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MYCBP2-CPB2 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
HgeneMYCBP2

GO:0016567

protein ubiquitination

29643511

HgeneMYCBP2

GO:0031398

positive regulation of protein ubiquitination

20534529



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/chr13:77862296/chr13:46638876)
- 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 MYCBP2 (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 CPB2 (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)
ENST00000544440MYCBP2chr1377862296-ENST00000181383CPB2chr1346638876-1496498121067351
ENST00000544440MYCBP2chr1377862296-ENST00000439329CPB2chr1346638876-144349812989325
ENST00000407578MYCBP2chr1377862296-ENST00000181383CPB2chr1346638876-18598611831430415
ENST00000407578MYCBP2chr1377862296-ENST00000439329CPB2chr1346638876-18068611831352389

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
ENST00000544440ENST00000181383MYCBP2chr1377862296-CPB2chr1346638876-0.0010259550.9989741
ENST00000544440ENST00000439329MYCBP2chr1377862296-CPB2chr1346638876-0.0012113240.99878865
ENST00000407578ENST00000181383MYCBP2chr1377862296-CPB2chr1346638876-0.0016039960.998396
ENST00000407578ENST00000439329MYCBP2chr1377862296-CPB2chr1346638876-0.0015445650.9984554

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 MYCBP2-CPB2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MYCBP2chr1377862296CPB2chr1346638876498162EEESKEPPIKLPKNRMWRKNRSFYAN
MYCBP2chr1377862296CPB2chr1346638876861226EEESKEPPIKLPKNRMWRKNRSFYAN

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Potential FusionNeoAntigen Information of MYCBP2-CPB2 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.
MYCBP2-CPB2_77862296_46638876.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)
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A74:09KLPKNRMWR0.96870.7987918
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A74:03KLPKNRMWR0.96870.7987918
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A74:11KLPKNRMWR0.96870.7987918
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A31:06KLPKNRMWR0.84150.5321918
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A31:02KLPKNRMWR0.8160.8153918
MYCBP2-CPB2chr1377862296chr1346638876861HLA-B58:02IKLPKNRMW0.43860.9227817
MYCBP2-CPB2chr1377862296chr1346638876861HLA-A74:01KLPKNRMWR0.96870.7987918

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Potential FusionNeoAntigen Information of MYCBP2-CPB2 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.
MYCBP2-CPB2_77862296_46638876.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)
MYCBP2-CPB2chr1377862296chr1346638876861DRB3-0205PKNRMWRKNRSFYAN1126
MYCBP2-CPB2chr1377862296chr1346638876861DRB3-0211PKNRMWRKNRSFYAN1126

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Fusion breakpoint peptide structures of MYCBP2-CPB2

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
6865PPIKLPKNRMWRKNMYCBP2CPB2chr1377862296chr1346638876861

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MYCBP2-CPB2

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-B14:023BVN6865PPIKLPKNRMWRKN-7.9962-8.1096
HLA-B14:023BVN6865PPIKLPKNRMWRKN-5.70842-6.74372
HLA-B52:013W396865PPIKLPKNRMWRKN-6.83737-6.95077
HLA-B52:013W396865PPIKLPKNRMWRKN-4.4836-5.5189
HLA-A11:014UQ26865PPIKLPKNRMWRKN-10.0067-10.1201
HLA-A11:014UQ26865PPIKLPKNRMWRKN-9.03915-10.0745
HLA-A24:025HGA6865PPIKLPKNRMWRKN-6.56204-6.67544
HLA-A24:025HGA6865PPIKLPKNRMWRKN-5.42271-6.45801
HLA-B44:053DX86865PPIKLPKNRMWRKN-7.85648-8.89178
HLA-B44:053DX86865PPIKLPKNRMWRKN-5.3978-5.5112
HLA-A02:016TDR6865PPIKLPKNRMWRKN-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of MYCBP2-CPB2

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
MYCBP2-CPB2chr1377862296chr1346638876817IKLPKNRMWATCAAGCTTCCAAAGAATCGAATGTGG
MYCBP2-CPB2chr1377862296chr1346638876918KLPKNRMWRAAGCTTCCAAAGAATCGAATGTGGAGA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MYCBP2-CPB2chr1377862296chr13466388761126PKNRMWRKNRSFYANCCAAAGAATCGAATGTGGAGAAAGAACCGTTCTTTCTATGCGAAC

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Information of the samples that have these potential fusion neoantigens of MYCBP2-CPB2

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
BLCAMYCBP2-CPB2chr1377862296ENST00000407578chr1346638876ENST00000181383TCGA-UY-A78N-01A

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Potential target of CAR-T therapy development for MYCBP2-CPB2

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 MYCBP2-CPB2

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 MYCBP2-CPB2

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