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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:FBXW11-STK10

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: FBXW11-STK10
FusionPDB ID: 29890
FusionGDB2.0 ID: 29890
HgeneTgene
Gene symbol

FBXW11

STK10

Gene ID

23291

6793

Gene nameF-box and WD repeat domain containing 11serine/threonine kinase 10
SynonymsBTRC2|BTRCP2|FBW1B|FBXW1B|Fbw11|HosLOK|PRO2729
Cytomap

5q35.1

5q35.1

Type of geneprotein-codingprotein-coding
DescriptionF-box/WD repeat-containing protein 11F-box and WD repeats protein beta-TrCP2F-box and WD-40 domain protein 11F-box and WD-40 domain protein 1BF-box protein Fbw1bF-box/WD repeat-containing protein 1Bbeta-transducin repeat-containing protein 2homologserine/threonine-protein kinase 10lymphocyte-oriented kinase
Modification date2020032920200313
UniProtAcc

Q9UKB1

Main function of 5'-partner protein: FUNCTION: Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably recognizes and binds to phosphorylated target proteins. SCF(FBXW11) mediates the ubiquitination of phosphorylated CTNNB1 and participates in Wnt signaling. SCF(FBXW11) mediates the ubiquitination of phosphorylated NFKBIA, which degradation frees the associated NFKB1 to translocate into the nucleus and to activate transcription. SCF(FBXW11) mediates the ubiquitination of IFNAR1. SCF(FBXW11) mediates the ubiquitination of CEP68; this is required for centriole separation during mitosis (PubMed:25503564). Involved in the oxidative stress-induced a ubiquitin-mediated decrease in RCAN1. Mediates the degradation of CDC25A induced by ionizing radiation in cells progressing through S phase and thus may function in the intra-S-phase checkpoint. Has an essential role in the control of the clock-dependent transcription via degradation of phosphorylated PER1 and phosphorylated PER2. SCF(FBXW11) mediates the ubiquitination of CYTH1, and probably CYTH2 (PubMed:29420262). {ECO:0000269|PubMed:10321728, ECO:0000269|PubMed:10437795, ECO:0000269|PubMed:10644755, ECO:0000269|PubMed:10648623, ECO:0000269|PubMed:14532120, ECO:0000269|PubMed:14603323, ECO:0000269|PubMed:15917222, ECO:0000269|PubMed:18575781, ECO:0000269|PubMed:19966869, ECO:0000269|PubMed:20347421, ECO:0000269|PubMed:25503564, ECO:0000269|PubMed:29420262}.; FUNCTION: (Microbial infection) Target of human immunodeficiency virus type 1 (HIV-1) protein VPU to polyubiquitinate and deplete BST2 from cells and antagonize its antiviral action. {ECO:0000269|PubMed:19730691}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000265094, ENST00000296933, 
ENST00000393802, ENST00000425623, 
ENST00000522891, 
ENST00000517775, 
ENST00000176763, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 6 X 9=70216 X 15 X 7=1680
# samples 1317
** MAII scorelog2(13/702*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1680*10)=-3.30485458152842
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: FBXW11 [Title/Abstract] AND STK10 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: FBXW11 [Title/Abstract] AND STK10 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)FBXW11(171433462)-STK10(171554425), # samples:1
FBXW11(171423894)-STK10(171554425), # samples:1
Anticipated loss of major functional domain due to fusion event.FBXW11-STK10 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.
FBXW11-STK10 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.
FBXW11-STK10 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.
FBXW11-STK10 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
HgeneFBXW11

GO:0000209

protein polyubiquitination

20347421

HgeneFBXW11

GO:0016567

protein ubiquitination

16885022

HgeneFBXW11

GO:0031146

SCF-dependent proteasomal ubiquitin-dependent protein catabolic process

20347421

HgeneFBXW11

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

20347421

TgeneSTK10

GO:0046777

protein autophosphorylation

12639966|18239682



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/chr5:171433462/chr5:171554425)
- 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 FBXW11 (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 STK10 (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)
ENST00000296933FBXW11chr5171433462-ENST00000176763STK10chr5171554425-58114162903001903
ENST00000265094FBXW11chr5171433462-ENST00000176763STK10chr5171554425-5578183572768903
ENST00000393802FBXW11chr5171433462-ENST00000176763STK10chr5171554425-5588193672778903

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
ENST00000296933ENST00000176763FBXW11chr5171433462-STK10chr5171554425-0.0078122850.99218774
ENST00000265094ENST00000176763FBXW11chr5171433462-STK10chr5171554425-0.0080227410.9919773
ENST00000393802ENST00000176763FBXW11chr5171433462-STK10chr5171554425-0.0080252120.9919748

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 FBXW11-STK10

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
FBXW11chr5171433462STK10chr517155442518340MEPDSVIEDKTIELMIMIEFCPGGAV
FBXW11chr5171433462STK10chr517155442519340MEPDSVIEDKTIELMIMIEFCPGGAV
FBXW11chr5171433462STK10chr517155442541640MEPDSVIEDKTIELMIMIEFCPGGAV

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Potential FusionNeoAntigen Information of FBXW11-STK10 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.
FBXW11-STK10_171433462_171554425.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)
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:01IELMIMIEF0.9970.83771120
FBXW11-STK10chr5171433462chr5171554425183HLA-B58:01KTIELMIMI0.99630.7262918
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:01KTIELMIMI0.99510.8179918
FBXW11-STK10chr5171433462chr5171554425183HLA-B58:02KTIELMIMI0.99430.7462918
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:03KTIELMIMI0.99430.8341918
FBXW11-STK10chr5171433462chr5171554425183HLA-B15:16KTIELMIMI0.99380.619918
FBXW11-STK10chr5171433462chr5171554425183HLA-B15:17KTIELMIMI0.99370.7388918
FBXW11-STK10chr5171433462chr5171554425183HLA-B44:03IELMIMIEF0.98820.92071120
FBXW11-STK10chr5171433462chr5171554425183HLA-A30:08KTIELMIMI0.98440.6116918
FBXW11-STK10chr5171433462chr5171554425183HLA-A32:13KTIELMIMI0.98090.9179918
FBXW11-STK10chr5171433462chr5171554425183HLA-B13:02KTIELMIMI0.6880.5314918
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:01KTIELMIMIEF0.99990.9288920
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:03KTIELMIMIEF0.99950.9356920
FBXW11-STK10chr5171433462chr5171554425183HLA-C15:04KTIELMIMI0.9990.907918
FBXW11-STK10chr5171433462chr5171554425183HLA-C15:06KTIELMIMI0.99880.896918
FBXW11-STK10chr5171433462chr5171554425183HLA-C15:02KTIELMIMI0.99920.9003918
FBXW11-STK10chr5171433462chr5171554425183HLA-C15:09KTIELMIMI0.9990.907918
FBXW11-STK10chr5171433462chr5171554425183HLA-C15:05KTIELMIMI0.99890.9128918
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:07IELMIMIEF0.99780.79911120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:04IELMIMIEF0.99760.85711120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:08IELMIMIEF0.99710.76381120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:05IELMIMIEF0.9970.83771120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:06IELMIMIEF0.99660.83611120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:03IELMIMIEF0.99570.83091120
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:10KTIELMIMI0.99510.8179918
FBXW11-STK10chr5171433462chr5171554425183HLA-B58:06KTIELMIMI0.99490.6409918
FBXW11-STK10chr5171433462chr5171554425183HLA-A32:01KTIELMIMI0.99270.9319918
FBXW11-STK10chr5171433462chr5171554425183HLA-B44:26IELMIMIEF0.98820.92071120
FBXW11-STK10chr5171433462chr5171554425183HLA-B44:13IELMIMIEF0.98820.92071120
FBXW11-STK10chr5171433462chr5171554425183HLA-B44:07IELMIMIEF0.98820.92071120
FBXW11-STK10chr5171433462chr5171554425183HLA-B18:11IELMIMIEF0.96720.761120
FBXW11-STK10chr5171433462chr5171554425183HLA-A69:01KTIELMIMI0.93640.5531918
FBXW11-STK10chr5171433462chr5171554425183HLA-B48:02IELMIMIEF0.59630.79431120
FBXW11-STK10chr5171433462chr5171554425183HLA-B57:10KTIELMIMIEF0.99990.9288920

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Potential FusionNeoAntigen Information of FBXW11-STK10 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.
FBXW11-STK10_171433462_171554425.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)
FBXW11-STK10chr5171433462chr5171554425183DRB1-0310EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB1-0310PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB1-1476EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB1-1476PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB1-1476MEPDSVIEDKTIELM015
FBXW11-STK10chr5171433462chr5171554425183DRB1-1479EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB1-1479PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB1-1479MEPDSVIEDKTIELM015
FBXW11-STK10chr5171433462chr5171554425183DRB1-1525EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB1-1525PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0101EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0101PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0104EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0104PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0105EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0105PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0108EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0108PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0111EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0111PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0112EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0112PDSVIEDKTIELMIM217
FBXW11-STK10chr5171433462chr5171554425183DRB3-0113EPDSVIEDKTIELMI116
FBXW11-STK10chr5171433462chr5171554425183DRB3-0113PDSVIEDKTIELMIM217

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Fusion breakpoint peptide structures of FBXW11-STK10

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
3638IEDKTIELMIMIEFFBXW11STK10chr5171433462chr5171554425183

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of FBXW11-STK10

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-B14:023BVN3638IEDKTIELMIMIEF-7.9962-8.1096
HLA-B14:023BVN3638IEDKTIELMIMIEF-5.70842-6.74372
HLA-B52:013W393638IEDKTIELMIMIEF-6.83737-6.95077
HLA-B52:013W393638IEDKTIELMIMIEF-4.4836-5.5189
HLA-A11:014UQ23638IEDKTIELMIMIEF-10.0067-10.1201
HLA-A11:014UQ23638IEDKTIELMIMIEF-9.03915-10.0745
HLA-A24:025HGA3638IEDKTIELMIMIEF-6.56204-6.67544
HLA-A24:025HGA3638IEDKTIELMIMIEF-5.42271-6.45801
HLA-B44:053DX83638IEDKTIELMIMIEF-7.85648-8.89178
HLA-B44:053DX83638IEDKTIELMIMIEF-5.3978-5.5112
HLA-A02:016TDR3638IEDKTIELMIMIEF-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of FBXW11-STK10

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
FBXW11-STK10chr5171433462chr51715544251120IELMIMIEFCTCATGATCATGATTGAGTTCTGTCCA
FBXW11-STK10chr5171433462chr5171554425918KTIELMIMIATCGAGCTCATGATCATGATTGAGTTC
FBXW11-STK10chr5171433462chr5171554425920KTIELMIMIEFATCGAGCTCATGATCATGATTGAGTTCTGTCCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
FBXW11-STK10chr5171433462chr5171554425015MEPDSVIEDKTIELMCCCGACTCGGTGATTGAGGACAAGACCATCGAGCTCATGATCATG
FBXW11-STK10chr5171433462chr5171554425116EPDSVIEDKTIELMIGACTCGGTGATTGAGGACAAGACCATCGAGCTCATGATCATGATT
FBXW11-STK10chr5171433462chr5171554425217PDSVIEDKTIELMIMTCGGTGATTGAGGACAAGACCATCGAGCTCATGATCATGATTGAG

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Information of the samples that have these potential fusion neoantigens of FBXW11-STK10

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
OVFBXW11-STK10chr5171433462ENST00000265094chr5171554425ENST00000176763TCGA-61-2000-01A

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Potential target of CAR-T therapy development for FBXW11-STK10

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 FBXW11-STK10

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 FBXW11-STK10

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