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:CUL4A-F7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CUL4A-F7
FusionPDB ID: 20679
FusionGDB2.0 ID: 20679
HgeneTgene
Gene symbol

CUL4A

F7

Gene ID

8451

2155

Gene namecullin 4Acoagulation factor VII
Synonyms-SPCA
Cytomap

13q34

13q34

Type of geneprotein-codingprotein-coding
Descriptioncullin-4ACUL-4Acoagulation factor VIIFVII coagulation proteincoagulation factor VII (serum prothrombin conversion accelerator)eptacog alfaproconvertin
Modification date2020032720200313
UniProtAcc

Q13619

Main function of 5'-partner protein: FUNCTION: Core component of multiple cullin-RING-based E3 ubiquitin-protein ligase complexes which mediate the ubiquitination of target proteins. As a scaffold protein may contribute to catalysis through positioning of the substrate and the ubiquitin-conjugating enzyme. The E3 ubiquitin-protein ligase activity of the complex is dependent on the neddylation of the cullin subunit and is inhibited by the association of the deneddylated cullin subunit with TIP120A/CAND1. The functional specificity of the E3 ubiquitin-protein ligase complex depends on the variable substrate recognition component. DCX(DET1-COP1) directs ubiquitination of JUN. DCX(DDB2) directs ubiquitination of XPC. DCX(DDB2) ubiquitinates histones H3-H4 and is required for efficient histone deposition during replication-coupled (H3.1) and replication-independent (H3.3) nucleosome assembly, probably by facilitating the transfer of H3 from ASF1A/ASF1B to other chaperones involved in histone deposition. DCX(DTL) plays a role in PCNA-dependent polyubiquitination of CDT1 and MDM2-dependent ubiquitination of TP53 in response to radiation-induced DNA damage and during DNA replication. In association with DDB1 and SKP2 probably is involved in ubiquitination of CDKN1B/p27kip. Is involved in ubiquitination of HOXA9. DCX(DTL) directs autoubiquitination of DTL. The DDB1-CUL4A-DTL E3 ligase complex regulates the circadian clock function by mediating the ubiquitination and degradation of CRY1 (PubMed:26431207). With CUL4B, contributes to ribosome biogenesis (PubMed:26711351). {ECO:0000269|PubMed:14578910, ECO:0000269|PubMed:14609952, ECO:0000269|PubMed:15448697, ECO:0000269|PubMed:15548678, ECO:0000269|PubMed:16537899, ECO:0000269|PubMed:16678110, ECO:0000269|PubMed:23478445, ECO:0000269|PubMed:24209620, ECO:0000269|PubMed:26431207, ECO:0000269|PubMed:26711351}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000326335, ENST00000375440, 
ENST00000375441, ENST00000451881, 
ENST00000463426, 
ENST00000473085, 
ENST00000346342, ENST00000375581, 
ENST00000541084, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score12 X 16 X 11=21124 X 4 X 4=64
# samples 195
** MAII scorelog2(19/2112*10)=-3.47453851102751
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CUL4A [Title/Abstract] AND F7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CUL4A [Title/Abstract] AND F7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CUL4A(113893865)-F7(113771787), # samples:2
Anticipated loss of major functional domain due to fusion event.CUL4A-F7 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.
CUL4A-F7 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.
CUL4A-F7 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.
CUL4A-F7 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
HgeneCUL4A

GO:0016567

protein ubiquitination

26431207

TgeneF7

GO:0002690

positive regulation of leukocyte chemotaxis

17991872

TgeneF7

GO:0007596

blood coagulation

8632006|24998411

TgeneF7

GO:0010641

positive regulation of platelet-derived growth factor receptor signaling pathway

17991872

TgeneF7

GO:0016485

protein processing

24998411

TgeneF7

GO:0050927

positive regulation of positive chemotaxis

17991872

TgeneF7

GO:0051897

positive regulation of protein kinase B signaling

18612547



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/chr13:113893865/chr13:113771787)
- 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 CUL4A (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 F7 (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)
ENST00000375441CUL4Achr13113893865+ENST00000541084F7chr13113771787+208512573811976531
ENST00000375441CUL4Achr13113893865+ENST00000346342F7chr13113771787+300012573811976531
ENST00000375441CUL4Achr13113893865+ENST00000375581F7chr13113771787+365012573811976531
ENST00000451881CUL4Achr13113893865+ENST00000541084F7chr13113771787+1812984301703557
ENST00000451881CUL4Achr13113893865+ENST00000346342F7chr13113771787+2727984301703557
ENST00000451881CUL4Achr13113893865+ENST00000375581F7chr13113771787+3377984301703557
ENST00000326335CUL4Achr13113893865+ENST00000541084F7chr13113771787+17238951601614484
ENST00000326335CUL4Achr13113893865+ENST00000346342F7chr13113771787+26388951601614484
ENST00000326335CUL4Achr13113893865+ENST00000375581F7chr13113771787+32888951601614484
ENST00000375440CUL4Achr13113893865+ENST00000541084F7chr13113771787+19471119841838584
ENST00000375440CUL4Achr13113893865+ENST00000346342F7chr13113771787+28621119841838584
ENST00000375440CUL4Achr13113893865+ENST00000375581F7chr13113771787+35121119841838584

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
ENST00000375441ENST00000541084CUL4Achr13113893865+F7chr13113771787+0.0138016590.98619837
ENST00000375441ENST00000346342CUL4Achr13113893865+F7chr13113771787+0.0071719430.9928281
ENST00000375441ENST00000375581CUL4Achr13113893865+F7chr13113771787+0.0094756920.99052435
ENST00000451881ENST00000541084CUL4Achr13113893865+F7chr13113771787+0.0113506060.98864937
ENST00000451881ENST00000346342CUL4Achr13113893865+F7chr13113771787+0.0063197130.99368024
ENST00000451881ENST00000375581CUL4Achr13113893865+F7chr13113771787+0.0089953820.9910046
ENST00000326335ENST00000541084CUL4Achr13113893865+F7chr13113771787+0.0104505090.9895495
ENST00000326335ENST00000346342CUL4Achr13113893865+F7chr13113771787+0.0063254020.99367464
ENST00000326335ENST00000375581CUL4Achr13113893865+F7chr13113771787+0.0091418720.99085814
ENST00000375440ENST00000541084CUL4Achr13113893865+F7chr13113771787+0.0105581380.9894419
ENST00000375440ENST00000346342CUL4Achr13113893865+F7chr13113771787+0.0056485390.9943514
ENST00000375440ENST00000375581CUL4Achr13113893865+F7chr13113771787+0.0080749710.99192506

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 CUL4A-F7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CUL4Achr13113893865F7chr131137717871119345QQALLQHWSEYIKVLLLVNGAQLCGG
CUL4Achr13113893865F7chr131137717871257292QQALLQHWSEYIKVLLLVNGAQLCGG
CUL4Achr13113893865F7chr13113771787895245QQALLQHWSEYIKVLLLVNGAQLCGG
CUL4Achr13113893865F7chr13113771787984318QQALLQHWSEYIKVLLLVNGAQLCGG

Top

Potential FusionNeoAntigen Information of CUL4A-F7 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.
CUL4A-F7_113893865_113771787.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)
CUL4A-F7chr13113893865chr13113771787895HLA-B18:01SEYIKVLL0.99720.914816
CUL4A-F7chr13113893865chr13113771787895HLA-B47:01SEYIKVLL0.9970.5214816
CUL4A-F7chr13113893865chr13113771787895HLA-B41:01SEYIKVLL0.98790.6409816
CUL4A-F7chr13113893865chr13113771787895HLA-B52:01SEYIKVLL0.94960.5535816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:13SEYIKVLL0.93050.7924816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:06QHWSEYIKV0.99910.7725514
CUL4A-F7chr13113893865chr13113771787895HLA-B39:24QHWSEYIKV0.99880.5706514
CUL4A-F7chr13113893865chr13113771787895HLA-B39:01QHWSEYIKV0.99750.8564514
CUL4A-F7chr13113893865chr13113771787895HLA-B38:01QHWSEYIKV0.99690.9481514
CUL4A-F7chr13113893865chr13113771787895HLA-B38:02QHWSEYIKV0.99680.951514
CUL4A-F7chr13113893865chr13113771787895HLA-B13:01SEYIKVLLL0.99030.7986817
CUL4A-F7chr13113893865chr13113771787895HLA-B44:03SEYIKVLLL0.9860.9307817
CUL4A-F7chr13113893865chr13113771787895HLA-B14:01SEYIKVLLL0.97250.6638817
CUL4A-F7chr13113893865chr13113771787895HLA-B14:02SEYIKVLLL0.97250.6638817
CUL4A-F7chr13113893865chr13113771787895HLA-B45:01SEYIKVLLL0.95880.6063817
CUL4A-F7chr13113893865chr13113771787895HLA-B15:10QHWSEYIKV0.95060.5708514
CUL4A-F7chr13113893865chr13113771787895HLA-B18:01SEYIKVLLL0.94280.9134817
CUL4A-F7chr13113893865chr13113771787895HLA-B47:01SEYIKVLLL0.90.5199817
CUL4A-F7chr13113893865chr13113771787895HLA-B41:01SEYIKVLLL0.59030.6691817
CUL4A-F7chr13113893865chr13113771787895HLA-B15:37QHWSEYIKV0.56760.5214514
CUL4A-F7chr13113893865chr13113771787895HLA-B39:13SEYIKVLLL0.48510.8064817
CUL4A-F7chr13113893865chr13113771787895HLA-B38:02SEYIKVLLL0.43620.9577817
CUL4A-F7chr13113893865chr13113771787895HLA-B50:01SEYIKVLLL0.34720.5234817
CUL4A-F7chr13113893865chr13113771787895HLA-B15:37SEYIKVLLL0.29660.6916817
CUL4A-F7chr13113893865chr13113771787895HLA-B52:01SEYIKVLLL0.14370.623817
CUL4A-F7chr13113893865chr13113771787895HLA-B39:01QHWSEYIKVL0.99540.8468515
CUL4A-F7chr13113893865chr13113771787895HLA-B38:01QHWSEYIKVL0.99220.9434515
CUL4A-F7chr13113893865chr13113771787895HLA-B38:02QHWSEYIKVL0.99190.9481515
CUL4A-F7chr13113893865chr13113771787895HLA-B15:10QHWSEYIKVL0.96090.5009515
CUL4A-F7chr13113893865chr13113771787895HLA-B39:01QHWSEYIKVLL0.99960.7942516
CUL4A-F7chr13113893865chr13113771787895HLA-B38:01QHWSEYIKVLL0.99890.9271516
CUL4A-F7chr13113893865chr13113771787895HLA-B38:02QHWSEYIKVLL0.99880.9328516
CUL4A-F7chr13113893865chr13113771787895HLA-B40:06SEYIKVLL0.99990.5286816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:08SEYIKVLL0.97850.6328816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:09QHWSEYIKV0.99840.6482514
CUL4A-F7chr13113893865chr13113771787895HLA-B40:06SEYIKVLLL0.99820.5931817
CUL4A-F7chr13113893865chr13113771787895HLA-B39:12QHWSEYIKV0.99740.8616514
CUL4A-F7chr13113893865chr13113771787895HLA-B39:05QHWSEYIKV0.99620.8515514
CUL4A-F7chr13113893865chr13113771787895HLA-B39:09SEYIKVLLL0.60110.6053817
CUL4A-F7chr13113893865chr13113771787895HLA-C07:05HWSEYIKVL0.5840.9644615
CUL4A-F7chr13113893865chr13113771787895HLA-B39:08SEYIKVLLL0.57610.6695817
CUL4A-F7chr13113893865chr13113771787895HLA-C07:13HWSEYIKVL0.57260.9416615
CUL4A-F7chr13113893865chr13113771787895HLA-B14:03SEYIKVLLL0.57010.7545817
CUL4A-F7chr13113893865chr13113771787895HLA-C07:29HWSEYIKVL0.5190.966615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:10HWSEYIKVL0.4940.9495615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:80HWSEYIKVL0.4750.9316615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:67HWSEYIKVL0.4750.9316615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:19HWSEYIKVL0.4640.6939615
CUL4A-F7chr13113893865chr13113771787895HLA-B39:12SEYIKVLLL0.46240.9156817
CUL4A-F7chr13113893865chr13113771787895HLA-C07:27HWSEYIKVL0.43840.9614615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:46HWSEYIKVL0.4340.8501615
CUL4A-F7chr13113893865chr13113771787895HLA-C12:16HWSEYIKVL0.34570.9672615
CUL4A-F7chr13113893865chr13113771787895HLA-C04:14HWSEYIKVL0.18950.7645615
CUL4A-F7chr13113893865chr13113771787895HLA-B39:09QHWSEYIKVL0.9960.6467515
CUL4A-F7chr13113893865chr13113771787895HLA-B39:05QHWSEYIKVL0.99060.8438515
CUL4A-F7chr13113893865chr13113771787895HLA-B39:05QHWSEYIKVLL0.99890.7906516
CUL4A-F7chr13113893865chr13113771787895HLA-B40:04SEYIKVLL0.99980.6192816
CUL4A-F7chr13113893865chr13113771787895HLA-B18:06SEYIKVLL0.99730.9159816
CUL4A-F7chr13113893865chr13113771787895HLA-B18:05SEYIKVLL0.99720.914816
CUL4A-F7chr13113893865chr13113771787895HLA-B18:08SEYIKVLL0.9970.8986816
CUL4A-F7chr13113893865chr13113771787895HLA-B18:03SEYIKVLL0.99660.9071816
CUL4A-F7chr13113893865chr13113771787895HLA-B18:11SEYIKVLL0.99490.9026816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:02SEYIKVLL0.94310.8031816
CUL4A-F7chr13113893865chr13113771787895HLA-B39:31QHWSEYIKV0.99740.8543514
CUL4A-F7chr13113893865chr13113771787895HLA-B40:04SEYIKVLLL0.99720.6403817
CUL4A-F7chr13113893865chr13113771787895HLA-B38:05QHWSEYIKV0.99690.9481514
CUL4A-F7chr13113893865chr13113771787895HLA-B44:26SEYIKVLLL0.9860.9307817
CUL4A-F7chr13113893865chr13113771787895HLA-B44:07SEYIKVLLL0.9860.9307817
CUL4A-F7chr13113893865chr13113771787895HLA-B44:13SEYIKVLLL0.9860.9307817
CUL4A-F7chr13113893865chr13113771787895HLA-B15:09QHWSEYIKV0.98390.7914514
CUL4A-F7chr13113893865chr13113771787895HLA-B18:07SEYIKVLLL0.95650.8844817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:04SEYIKVLLL0.95130.9215817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:08SEYIKVLLL0.94350.9156817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:05SEYIKVLLL0.94280.9134817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:06SEYIKVLLL0.93780.9157817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:03SEYIKVLLL0.90870.9081817
CUL4A-F7chr13113893865chr13113771787895HLA-B18:11SEYIKVLLL0.77310.8998817
CUL4A-F7chr13113893865chr13113771787895HLA-C14:02HWSEYIKVL0.7180.9719615
CUL4A-F7chr13113893865chr13113771787895HLA-C14:03HWSEYIKVL0.7180.9719615
CUL4A-F7chr13113893865chr13113771787895HLA-C03:67HWSEYIKVL0.69110.9817615
CUL4A-F7chr13113893865chr13113771787895HLA-B39:11QHWSEYIKV0.63850.7594514
CUL4A-F7chr13113893865chr13113771787895HLA-C06:06HWSEYIKVL0.55020.9924615
CUL4A-F7chr13113893865chr13113771787895HLA-B39:31SEYIKVLLL0.54220.911817
CUL4A-F7chr13113893865chr13113771787895HLA-B39:02SEYIKVLLL0.53080.8194817
CUL4A-F7chr13113893865chr13113771787895HLA-C07:02HWSEYIKVL0.4750.9316615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:04HWSEYIKVL0.47120.9432615
CUL4A-F7chr13113893865chr13113771787895HLA-C07:17HWSEYIKVL0.42610.9712615
CUL4A-F7chr13113893865chr13113771787895HLA-C04:04HWSEYIKVL0.41150.9338615
CUL4A-F7chr13113893865chr13113771787895HLA-B15:68SEYIKVLLL0.38270.6295817
CUL4A-F7chr13113893865chr13113771787895HLA-C06:02HWSEYIKVL0.37610.9947615
CUL4A-F7chr13113893865chr13113771787895HLA-C06:17HWSEYIKVL0.37610.9947615
CUL4A-F7chr13113893865chr13113771787895HLA-B50:04SEYIKVLLL0.34720.5234817
CUL4A-F7chr13113893865chr13113771787895HLA-B50:05SEYIKVLLL0.34720.5234817
CUL4A-F7chr13113893865chr13113771787895HLA-C06:08HWSEYIKVL0.34080.9917615
CUL4A-F7chr13113893865chr13113771787895HLA-B48:02SEYIKVLLL0.29750.8876817
CUL4A-F7chr13113893865chr13113771787895HLA-B15:53SEYIKVLLL0.13870.8812817
CUL4A-F7chr13113893865chr13113771787895HLA-B39:31QHWSEYIKVL0.99510.8458515
CUL4A-F7chr13113893865chr13113771787895HLA-B38:05QHWSEYIKVL0.99220.9434515
CUL4A-F7chr13113893865chr13113771787895HLA-B15:09QHWSEYIKVL0.96330.6757515
CUL4A-F7chr13113893865chr13113771787895HLA-B39:11QHWSEYIKVL0.78790.7723515
CUL4A-F7chr13113893865chr13113771787895HLA-B38:05QHWSEYIKVLL0.99890.9271516

Top

Potential FusionNeoAntigen Information of CUL4A-F7 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 CUL4A-F7

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
3550HWSEYIKVLLLVNGCUL4AF7chr13113893865chr13113771787895

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CUL4A-F7

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-B14:023BVN3550HWSEYIKVLLLVNG-7.37157-7.48337
HLA-B14:023BVN3550HWSEYIKVLLLVNG-5.75216-6.79526
HLA-B52:013W393550HWSEYIKVLLLVNG-7.36854-7.48034
HLA-B52:013W393550HWSEYIKVLLLVNG-4.42371-5.46681
HLA-A11:014UQ23550HWSEYIKVLLLVNG-8.60667-9.64977
HLA-A11:014UQ23550HWSEYIKVLLLVNG-5.54504-5.65684
HLA-A24:025HGA3550HWSEYIKVLLLVNG-7.65859-7.77039
HLA-A24:025HGA3550HWSEYIKVLLLVNG-6.03094-7.07404
HLA-B44:053DX83550HWSEYIKVLLLVNG-5.82315-5.93495
HLA-B44:053DX83550HWSEYIKVLLLVNG-2.98805-4.03115

Top

Vaccine Design for the FusionNeoAntigens of CUL4A-F7

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
CUL4A-F7chr13113893865chr13113771787514QHWSEYIKVCAGCACTGGAGCGAGTACATCAAGGTC
CUL4A-F7chr13113893865chr13113771787515QHWSEYIKVLCAGCACTGGAGCGAGTACATCAAGGTCCTG
CUL4A-F7chr13113893865chr13113771787516QHWSEYIKVLLCAGCACTGGAGCGAGTACATCAAGGTCCTGTTG
CUL4A-F7chr13113893865chr13113771787615HWSEYIKVLCACTGGAGCGAGTACATCAAGGTCCTG
CUL4A-F7chr13113893865chr13113771787816SEYIKVLLAGCGAGTACATCAAGGTCCTGTTG
CUL4A-F7chr13113893865chr13113771787817SEYIKVLLLAGCGAGTACATCAAGGTCCTGTTGTTG

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 CUL4A-F7

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
SARCCUL4A-F7chr13113893865ENST00000326335chr13113771787ENST00000346342TCGA-KF-A41W-01A

Top

Potential target of CAR-T therapy development for CUL4A-F7

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

Top

Related Drugs to CUL4A-F7

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

Top

Related Diseases to CUL4A-F7

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