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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:CUL3-DARS

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CUL3-DARS
FusionPDB ID: 20665
FusionGDB2.0 ID: 20665
HgeneTgene
Gene symbol

CUL3

DARS

Gene ID

8452

1615

Gene namecullin 3aspartyl-tRNA synthetase 1
SynonymsCUL-3|PHA2EDARS|HBSL|aspRS
Cytomap

2q36.2

2q21.3

Type of geneprotein-codingprotein-coding
Descriptioncullin-3aspartate--tRNA ligase, cytoplasmicaspartate tRNA ligase 1, cytoplasmicaspartyl-tRNA synthetase, cytoplasmiccell proliferation-inducing gene 40 proteintesticular tissue protein Li 192
Modification date2020032720200313
UniProtAcc

Q13618

Main function of 5'-partner protein: FUNCTION: Core component of multiple cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complexes which mediate the ubiquitination and subsequent proteasomal degradation of target proteins. BCR complexes and ARIH1 collaborate in tandem to mediate ubiquitination of target proteins (PubMed:27565346). 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 BCR complex depends on the BTB domain-containing protein as the substrate recognition component. BCR(KLHL42) is involved in ubiquitination of KATNA1. BCR(SPOP) is involved in ubiquitination of BMI1/PCGF4, BRMS1, MACROH2A1 and DAXX, GLI2 and GLI3. Can also form a cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex containing homodimeric SPOPL or the heterodimer formed by SPOP and SPOPL; these complexes have lower ubiquitin ligase activity. BCR(KLHL9-KLHL13) controls the dynamic behavior of AURKB on mitotic chromosomes and thereby coordinates faithful mitotic progression and completion of cytokinesis. BCR(KLHL12) is involved in ER-Golgi transport by regulating the size of COPII coats, thereby playing a key role in collagen export, which is required for embryonic stem (ES) cells division: BCR(KLHL12) acts by mediating monoubiquitination of SEC31 (SEC31A or SEC31B) (PubMed:22358839, PubMed:27716508). BCR(KLHL3) acts as a regulator of ion transport in the distal nephron; by mediating ubiquitination of WNK4 (PubMed:23387299, PubMed:23453970, PubMed:23576762). The BCR(KLHL20) E3 ubiquitin ligase complex is involved in interferon response and anterograde Golgi to endosome transport: it mediates both ubiquitination leading to degradation and 'Lys-33'-linked ubiquitination (PubMed:20389280, PubMed:21840486, PubMed:21670212, PubMed:24768539). The BCR(KLHL21) E3 ubiquitin ligase complex regulates localization of the chromosomal passenger complex (CPC) from chromosomes to the spindle midzone in anaphase and mediates the ubiquitination of AURKB (PubMed:19995937). The BCR(KLHL22) ubiquitin ligase complex mediates monoubiquitination of PLK1, leading to PLK1 dissociation from phosphoreceptor proteins and subsequent removal from kinetochores, allowing silencing of the spindle assembly checkpoint (SAC) and chromosome segregation (PubMed:23455478). The BCR(KLHL22) ubiquitin ligase complex is also responsible for the amino acid-stimulated 'Lys-48' polyubiquitination and proteasomal degradation of DEPDC5. Through the degradation of DEPDC5, releases the GATOR1 complex-mediated inhibition of the TORC1 pathway (PubMed:29769719). The BCR(KLHL25) ubiquitin ligase complex is involved in translational homeostasis by mediating ubiquitination and subsequent degradation of hypophosphorylated EIF4EBP1 (4E-BP1) (PubMed:22578813). The BCR(KBTBD8) complex acts by mediating monoubiquitination of NOLC1 and TCOF1, leading to remodel the translational program of differentiating cells in favor of neural crest specification (PubMed:26399832). Involved in ubiquitination of cyclin E and of cyclin D1 (in vitro) thus involved in regulation of G1/S transition. Involved in the ubiquitination of KEAP1, ENC1 and KLHL41 (PubMed:15983046). In concert with ATF2 and RBX1, promotes degradation of KAT5 thereby attenuating its ability to acetylate and activate ATM. The BCR(KCTD17) E3 ubiquitin ligase complex mediates ubiquitination and degradation of TCHP, a down-regulator of cilium assembly, thereby inducing ciliogenesis (PubMed:25270598). The BCR(KLHL24) E3 ubiquitin ligase complex mediates ubiquitination of KRT14, controls KRT14 levels during keratinocytes differentiation, and is essential for skin integrity (PubMed:27798626). The BCR(KLHL18) E3 ubiquitin ligase complex mediates the ubiquitination of AURKA leading to its activation at the centrosome which is required for initiating mitotic entry (PubMed:23213400). The BCR(KEAP1) E3 ubiquitin ligase complex acts as a key sensor of oxidative and electrophilic stress by mediating ubiquitination and degradation of NFE2L2/NRF2, a transcription factor regulating expression of many cytoprotective genes (PubMed:15601839, PubMed:16006525). {ECO:0000269|PubMed:10500095, ECO:0000269|PubMed:11311237, ECO:0000269|PubMed:15601839, ECO:0000269|PubMed:15897469, ECO:0000269|PubMed:15983046, ECO:0000269|PubMed:16006525, ECO:0000269|PubMed:16524876, ECO:0000269|PubMed:17543862, ECO:0000269|PubMed:18397884, ECO:0000269|PubMed:19261606, ECO:0000269|PubMed:19995937, ECO:0000269|PubMed:20389280, ECO:0000269|PubMed:21670212, ECO:0000269|PubMed:21840486, ECO:0000269|PubMed:22085717, ECO:0000269|PubMed:22358839, ECO:0000269|PubMed:22578813, ECO:0000269|PubMed:22632832, ECO:0000269|PubMed:23213400, ECO:0000269|PubMed:23387299, ECO:0000269|PubMed:23453970, ECO:0000269|PubMed:23455478, ECO:0000269|PubMed:23576762, ECO:0000269|PubMed:24768539, ECO:0000269|PubMed:25270598, ECO:0000269|PubMed:26399832, ECO:0000269|PubMed:27565346, ECO:0000269|PubMed:27716508, ECO:0000269|PubMed:27798626, ECO:0000269|PubMed:29769719}.

Q6PI48

Main function of 5'-partner protein:
Ensembl transtripts involved in fusion geneENST idsENST00000264414, ENST00000344951, 
ENST00000409096, ENST00000409777, 
ENST00000432260, 
ENST00000463008, 
ENST00000264161, ENST00000537273, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score12 X 12 X 7=10088 X 9 X 5=360
# samples 148
** MAII scorelog2(14/1008*10)=-2.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/360*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CUL3 [Title/Abstract] AND DARS [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CUL3 [Title/Abstract] AND DARS [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CUL3(225378241)-DARS(136670136), # samples:1
Anticipated loss of major functional domain due to fusion event.CUL3-DARS 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.
CUL3-DARS 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.
CUL3-DARS 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.
CUL3-DARS 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.
CUL3-DARS seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
CUL3-DARS seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
CUL3-DARS seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneCUL3

GO:0000209

protein polyubiquitination

19261606

HgeneCUL3

GO:0006511

ubiquitin-dependent protein catabolic process

25401743|27561354

HgeneCUL3

GO:0006513

protein monoubiquitination

22358839

HgeneCUL3

GO:0006888

ER to Golgi vesicle-mediated transport

22358839

HgeneCUL3

GO:0016567

protein ubiquitination

17543862|19782033|19995937|20389280|23213400

HgeneCUL3

GO:0031145

anaphase-promoting complex-dependent catabolic process

10500095

HgeneCUL3

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

19261606|19782033|20389280

HgeneCUL3

GO:0071630

nuclear protein quality control by the ubiquitin-proteasome system

27561354



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/chr2:225378241/chr2:136670136)
- 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 CUL3 (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 DARS (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)
ENST00000264414CUL3chr2225378241-ENST00000264161DARSchr2136670136-19899933391349336
ENST00000264414CUL3chr2225378241-ENST00000537273DARSchr2136670136-14049933391349336
ENST00000344951CUL3chr2225378241-ENST00000264161DARSchr2136670136-18368403841196270
ENST00000344951CUL3chr2225378241-ENST00000537273DARSchr2136670136-12518403841196270
ENST00000409096CUL3chr2225378241-ENST00000264161DARSchr2136670136-1721725531081342
ENST00000409096CUL3chr2225378241-ENST00000537273DARSchr2136670136-1136725531081342

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
ENST00000264414ENST00000264161CUL3chr2225378241-DARSchr2136670136-0.0006730670.99932694
ENST00000264414ENST00000537273CUL3chr2225378241-DARSchr2136670136-0.0018091870.9981908
ENST00000344951ENST00000264161CUL3chr2225378241-DARSchr2136670136-0.0009568770.99904305
ENST00000344951ENST00000537273CUL3chr2225378241-DARSchr2136670136-0.0026911740.99730885
ENST00000409096ENST00000264161CUL3chr2225378241-DARSchr2136670136-0.0002124790.9997875
ENST00000409096ENST00000537273CUL3chr2225378241-DARSchr2136670136-0.0004174960.99958247

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 CUL3-DARS

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CUL3chr2225378241DARSchr2136670136725224EAPFLEMSAEFFQYDTDFYILDKYPL
CUL3chr2225378241DARSchr2136670136840152EAPFLEMSAEFFQYDTDFYILDKYPL
CUL3chr2225378241DARSchr2136670136993218EAPFLEMSAEFFQYDTDFYILDKYPL

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Potential FusionNeoAntigen Information of CUL3-DARS 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.
CUL3-DARS_225378241_136670136.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)
CUL3-DARSchr2225378241chr2136670136993HLA-B15:03FQYDTDFY0.9260.89841119
CUL3-DARSchr2225378241chr2136670136993HLA-A02:04FQYDTDFYI0.98480.5841120
CUL3-DARSchr2225378241chr2136670136993HLA-B15:02EMSAEFFQY0.95720.9304514
CUL3-DARSchr2225378241chr2136670136993HLA-B35:01EMSAEFFQY0.91060.8579514
CUL3-DARSchr2225378241chr2136670136993HLA-B13:02FQYDTDFYI0.88910.77711120
CUL3-DARSchr2225378241chr2136670136993HLA-B13:01FQYDTDFYI0.84090.92981120
CUL3-DARSchr2225378241chr2136670136993HLA-B39:01FQYDTDFYI0.52660.85051120
CUL3-DARSchr2225378241chr2136670136993HLA-B39:13FQYDTDFYI0.48490.87391120
CUL3-DARSchr2225378241chr2136670136993HLA-B38:01FQYDTDFYI0.45120.90881120
CUL3-DARSchr2225378241chr2136670136993HLA-B38:02FQYDTDFYI0.42570.92031120
CUL3-DARSchr2225378241chr2136670136993HLA-B52:01FQYDTDFYI0.090.90291120
CUL3-DARSchr2225378241chr2136670136993HLA-B44:03AEFFQYDTDF0.99660.9557818
CUL3-DARSchr2225378241chr2136670136993HLA-B44:03LEMSAEFFQY0.99450.9664414
CUL3-DARSchr2225378241chr2136670136993HLA-B18:01LEMSAEFFQY0.97980.8759414
CUL3-DARSchr2225378241chr2136670136993HLA-B13:01FQYDTDFYIL0.9130.9411121
CUL3-DARSchr2225378241chr2136670136993HLA-B13:02FFQYDTDFYI0.46960.70121020
CUL3-DARSchr2225378241chr2136670136993HLA-B44:03AEFFQYDTDFY0.99920.9702819
CUL3-DARSchr2225378241chr2136670136993HLA-C04:10QYDTDFYI0.99970.8211220
CUL3-DARSchr2225378241chr2136670136993HLA-C04:07QYDTDFYI0.99960.86591220
CUL3-DARSchr2225378241chr2136670136993HLA-B15:05FQYDTDFY0.9830.91271119
CUL3-DARSchr2225378241chr2136670136993HLA-C04:14QYDTDFYI0.96540.78711220
CUL3-DARSchr2225378241chr2136670136993HLA-C04:10QYDTDFYIL0.99490.8561221
CUL3-DARSchr2225378241chr2136670136993HLA-C04:07QYDTDFYIL0.99410.89851221
CUL3-DARSchr2225378241chr2136670136993HLA-C04:06FQYDTDFYI0.97630.82991120
CUL3-DARSchr2225378241chr2136670136993HLA-B15:21EMSAEFFQY0.96370.9055514
CUL3-DARSchr2225378241chr2136670136993HLA-B15:05EMSAEFFQY0.95150.8178514
CUL3-DARSchr2225378241chr2136670136993HLA-C12:04FQYDTDFYI0.94710.99431120
CUL3-DARSchr2225378241chr2136670136993HLA-C06:03FQYDTDFYI0.94410.99431120
CUL3-DARSchr2225378241chr2136670136993HLA-B15:31EMSAEFFQY0.9220.8293514
CUL3-DARSchr2225378241chr2136670136993HLA-C04:14FQYDTDFYI0.91260.71181120
CUL3-DARSchr2225378241chr2136670136993HLA-C08:03FQYDTDFYI0.84950.9791120
CUL3-DARSchr2225378241chr2136670136993HLA-C07:29QYDTDFYIL0.76270.93121221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:13QYDTDFYIL0.74790.94711221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:10QYDTDFYIL0.70480.96961221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:29FQYDTDFYI0.70240.90721120
CUL3-DARSchr2225378241chr2136670136993HLA-C07:13FQYDTDFYI0.68050.92381120
CUL3-DARSchr2225378241chr2136670136993HLA-C07:80QYDTDFYIL0.67750.95781221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:67QYDTDFYIL0.67750.95781221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:27FQYDTDFYI0.59910.96041120
CUL3-DARSchr2225378241chr2136670136993HLA-C02:06FQYDTDFYI0.58130.95021120
CUL3-DARSchr2225378241chr2136670136993HLA-B39:09FQYDTDFYI0.57990.57851120
CUL3-DARSchr2225378241chr2136670136993HLA-B39:12QYDTDFYIL0.54350.92321221
CUL3-DARSchr2225378241chr2136670136993HLA-C04:14QYDTDFYIL0.51060.81321221
CUL3-DARSchr2225378241chr2136670136993HLA-B39:05FQYDTDFYI0.39190.84161120
CUL3-DARSchr2225378241chr2136670136993HLA-B51:07FQYDTDFYI0.08020.7961120
CUL3-DARSchr2225378241chr2136670136993HLA-C04:10FQYDTDFYIL0.99820.89731121
CUL3-DARSchr2225378241chr2136670136993HLA-C04:07FQYDTDFYIL0.99790.91141121
CUL3-DARSchr2225378241chr2136670136993HLA-C04:14FQYDTDFYIL0.98660.73321121
CUL3-DARSchr2225378241chr2136670136993HLA-C04:01QYDTDFYI0.99960.86591220
CUL3-DARSchr2225378241chr2136670136993HLA-C18:01QYDTDFYI0.99930.88511220
CUL3-DARSchr2225378241chr2136670136993HLA-B15:53FQYDTDFY0.99530.95231119
CUL3-DARSchr2225378241chr2136670136993HLA-B15:54FQYDTDFY0.99110.94071119
CUL3-DARSchr2225378241chr2136670136993HLA-B15:20FQYDTDFY0.98350.93751119
CUL3-DARSchr2225378241chr2136670136993HLA-B35:28FQYDTDFY0.97760.94311119
CUL3-DARSchr2225378241chr2136670136993HLA-B35:20FQYDTDFY0.96350.94941119
CUL3-DARSchr2225378241chr2136670136993HLA-B18:04FQYDTDFY0.94080.9191119
CUL3-DARSchr2225378241chr2136670136993HLA-B48:02FQYDTDFY0.78690.92811119
CUL3-DARSchr2225378241chr2136670136993HLA-C04:01QYDTDFYIL0.99410.89851221
CUL3-DARSchr2225378241chr2136670136993HLA-C18:01QYDTDFYIL0.99220.89351221
CUL3-DARSchr2225378241chr2136670136993HLA-A02:03FQYDTDFYI0.98380.57531120
CUL3-DARSchr2225378241chr2136670136993HLA-B15:12EMSAEFFQY0.98290.8571514
CUL3-DARSchr2225378241chr2136670136993HLA-B15:08EMSAEFFQY0.97260.8038514
CUL3-DARSchr2225378241chr2136670136993HLA-A25:01EMSAEFFQY0.95880.8959514
CUL3-DARSchr2225378241chr2136670136993HLA-C04:04FQYDTDFYI0.95480.7361120
CUL3-DARSchr2225378241chr2136670136993HLA-B15:20EMSAEFFQY0.95180.8816514
CUL3-DARSchr2225378241chr2136670136993HLA-C17:01FQYDTDFYI0.92080.71731120
CUL3-DARSchr2225378241chr2136670136993HLA-B35:28EMSAEFFQY0.91930.8816514
CUL3-DARSchr2225378241chr2136670136993HLA-B35:77EMSAEFFQY0.91060.8579514
CUL3-DARSchr2225378241chr2136670136993HLA-B35:23EMSAEFFQY0.90790.8593514
CUL3-DARSchr2225378241chr2136670136993HLA-B35:20EMSAEFFQY0.90110.9017514
CUL3-DARSchr2225378241chr2136670136993HLA-B15:73FQYDTDFYI0.88370.95061120
CUL3-DARSchr2225378241chr2136670136993HLA-C08:01FQYDTDFYI0.84950.9791120
CUL3-DARSchr2225378241chr2136670136993HLA-C06:02FQYDTDFYI0.8410.99381120
CUL3-DARSchr2225378241chr2136670136993HLA-C06:17FQYDTDFYI0.8410.99381120
CUL3-DARSchr2225378241chr2136670136993HLA-B35:24EMSAEFFQY0.76430.8715514
CUL3-DARSchr2225378241chr2136670136993HLA-B15:13EMSAEFFQY0.76010.6372514
CUL3-DARSchr2225378241chr2136670136993HLA-C06:06FQYDTDFYI0.74930.98191120
CUL3-DARSchr2225378241chr2136670136993HLA-C03:06FQYDTDFYI0.73840.99161120
CUL3-DARSchr2225378241chr2136670136993HLA-C04:04QYDTDFYIL0.68380.82531221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:17QYDTDFYIL0.68130.96961221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:02QYDTDFYIL0.67750.95781221
CUL3-DARSchr2225378241chr2136670136993HLA-C07:04FQYDTDFYI0.61730.91241120
CUL3-DARSchr2225378241chr2136670136993HLA-B39:02FQYDTDFYI0.58560.87061120
CUL3-DARSchr2225378241chr2136670136993HLA-C07:04QYDTDFYIL0.53980.93431221
CUL3-DARSchr2225378241chr2136670136993HLA-C06:08FQYDTDFYI0.52420.99221120
CUL3-DARSchr2225378241chr2136670136993HLA-C02:02FQYDTDFYI0.51380.96931120
CUL3-DARSchr2225378241chr2136670136993HLA-C02:10FQYDTDFYI0.51380.96931120
CUL3-DARSchr2225378241chr2136670136993HLA-B38:05FQYDTDFYI0.45120.90881120
CUL3-DARSchr2225378241chr2136670136993HLA-B18:04EMSAEFFQY0.42370.8406514
CUL3-DARSchr2225378241chr2136670136993HLA-B18:07EMSAEFFQY0.240.783514
CUL3-DARSchr2225378241chr2136670136993HLA-B15:09FQYDTDFYI0.08640.70691120
CUL3-DARSchr2225378241chr2136670136993HLA-C14:03FFQYDTDFY0.06910.96511019
CUL3-DARSchr2225378241chr2136670136993HLA-C14:02FFQYDTDFY0.06910.96511019
CUL3-DARSchr2225378241chr2136670136993HLA-C04:01FQYDTDFYIL0.99790.91141121
CUL3-DARSchr2225378241chr2136670136993HLA-C18:01FQYDTDFYIL0.9970.91121121
CUL3-DARSchr2225378241chr2136670136993HLA-B44:13AEFFQYDTDF0.99660.9557818
CUL3-DARSchr2225378241chr2136670136993HLA-B44:26AEFFQYDTDF0.99660.9557818
CUL3-DARSchr2225378241chr2136670136993HLA-B44:07AEFFQYDTDF0.99660.9557818
CUL3-DARSchr2225378241chr2136670136993HLA-B44:13LEMSAEFFQY0.99450.9664414
CUL3-DARSchr2225378241chr2136670136993HLA-B44:07LEMSAEFFQY0.99450.9664414
CUL3-DARSchr2225378241chr2136670136993HLA-B44:26LEMSAEFFQY0.99450.9664414
CUL3-DARSchr2225378241chr2136670136993HLA-B18:08LEMSAEFFQY0.98690.8531414
CUL3-DARSchr2225378241chr2136670136993HLA-B15:73FQYDTDFYIL0.98320.92831121
CUL3-DARSchr2225378241chr2136670136993HLA-B18:05LEMSAEFFQY0.97980.8759414
CUL3-DARSchr2225378241chr2136670136993HLA-B18:11LEMSAEFFQY0.95340.8674414
CUL3-DARSchr2225378241chr2136670136993HLA-B44:26AEFFQYDTDFY0.99920.9702819
CUL3-DARSchr2225378241chr2136670136993HLA-B44:07AEFFQYDTDFY0.99920.9702819
CUL3-DARSchr2225378241chr2136670136993HLA-B44:13AEFFQYDTDFY0.99920.9702819

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Potential FusionNeoAntigen Information of CUL3-DARS 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.
CUL3-DARS_225378241_136670136.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)
CUL3-DARSchr2225378241chr2136670136993DRB1-1222EAPFLEMSAEFFQYD015
CUL3-DARSchr2225378241chr2136670136993DRB3-0101AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0101SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0104AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0104SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0105AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0105SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0108AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0108SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0109AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0111AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0111SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0112AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0112SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0113AEFFQYDTDFYILDK823
CUL3-DARSchr2225378241chr2136670136993DRB3-0113SAEFFQYDTDFYILD722
CUL3-DARSchr2225378241chr2136670136993DRB3-0114AEFFQYDTDFYILDK823

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Fusion breakpoint peptide structures of CUL3-DARS

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
6009MSAEFFQYDTDFYICUL3DARSchr2225378241chr2136670136993

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CUL3-DARS

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-B14:023BVN6009MSAEFFQYDTDFYI-8.85616-8.96956
HLA-B14:023BVN6009MSAEFFQYDTDFYI-5.66423-6.69953
HLA-B52:013W396009MSAEFFQYDTDFYI-6.49489-6.60829
HLA-B52:013W396009MSAEFFQYDTDFYI-3.99785-5.03315
HLA-A11:014UQ26009MSAEFFQYDTDFYI-4.90759-5.94289
HLA-A24:025HGA6009MSAEFFQYDTDFYI-7.27887-7.39227
HLA-A24:025HGA6009MSAEFFQYDTDFYI-7.11524-8.15054
HLA-B27:056PYJ6009MSAEFFQYDTDFYI-6.11615-6.22955
HLA-B27:056PYJ6009MSAEFFQYDTDFYI-4.78818-5.82348
HLA-B44:053DX86009MSAEFFQYDTDFYI-7.22602-7.33942
HLA-B44:053DX86009MSAEFFQYDTDFYI-4.86671-5.90201

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Vaccine Design for the FusionNeoAntigens of CUL3-DARS

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
CUL3-DARSchr2225378241chr21366701361019FFQYDTDFYTTTTTTCAGTATGATACAGATTTTTAT
CUL3-DARSchr2225378241chr21366701361020FFQYDTDFYITTTTTTCAGTATGATACAGATTTTTATATT
CUL3-DARSchr2225378241chr21366701361119FQYDTDFYTTTCAGTATGATACAGATTTTTAT
CUL3-DARSchr2225378241chr21366701361120FQYDTDFYITTTCAGTATGATACAGATTTTTATATT
CUL3-DARSchr2225378241chr21366701361121FQYDTDFYILTTTCAGTATGATACAGATTTTTATATTCTT
CUL3-DARSchr2225378241chr21366701361220QYDTDFYICAGTATGATACAGATTTTTATATT
CUL3-DARSchr2225378241chr21366701361221QYDTDFYILCAGTATGATACAGATTTTTATATTCTT
CUL3-DARSchr2225378241chr2136670136414LEMSAEFFQYTTGGAAATGTCTGCAGAATTTTTTCAGTAT
CUL3-DARSchr2225378241chr2136670136514EMSAEFFQYGAAATGTCTGCAGAATTTTTTCAGTAT
CUL3-DARSchr2225378241chr2136670136818AEFFQYDTDFGCAGAATTTTTTCAGTATGATACAGATTTT
CUL3-DARSchr2225378241chr2136670136819AEFFQYDTDFYGCAGAATTTTTTCAGTATGATACAGATTTTTAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CUL3-DARSchr2225378241chr2136670136015EAPFLEMSAEFFQYDGAGGCTCCTTTTTTGGAAATGTCTGCAGAATTTTTTCAGTATGAT
CUL3-DARSchr2225378241chr2136670136722SAEFFQYDTDFYILDTCTGCAGAATTTTTTCAGTATGATACAGATTTTTATATTCTTGAT
CUL3-DARSchr2225378241chr2136670136823AEFFQYDTDFYILDKGCAGAATTTTTTCAGTATGATACAGATTTTTATATTCTTGATAAA

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Information of the samples that have these potential fusion neoantigens of CUL3-DARS

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
KIRCCUL3-DARSchr2225378241ENST00000264414chr2136670136ENST00000264161TCGA-CJ-4636-01A

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Potential target of CAR-T therapy development for CUL3-DARS

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 CUL3-DARS

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 CUL3-DARS

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