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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:PARP14-CYP2C8

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PARP14-CYP2C8
FusionPDB ID: 62814
FusionGDB2.0 ID: 62814
HgeneTgene
Gene symbol

PARP14

CYP2C8

Gene ID

54625

1558

Gene namepoly(ADP-ribose) polymerase family member 14cytochrome P450 family 2 subfamily C member 8
SynonymsARTD8|BAL2|PARP-14|pART8CPC8|CYP2C8DM|CYPIIC8|MP-12/MP-20
Cytomap

3q21.1

10q23.33

Type of geneprotein-codingprotein-coding
Descriptionprotein mono-ADP-ribosyltransferase PARP14ADP-ribosyltransferase diphtheria toxin-like 8B-aggressive lymphoma 2b aggressive lymphoma protein 2collaborator of STAT6poly [ADP-ribose] polymerase 14cytochrome P450 2C8P450 form 1cytochrome P450 IIC2cytochrome P450 MP-12cytochrome P450 MP-20cytochrome P450 form 1cytochrome P450, family 2, subfamily C, polypeptide 8cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 8flavopr
Modification date2020031320200320
UniProtAcc.

P10632

Main function of 5'-partner protein: FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids, steroid hormones and vitamins (PubMed:7574697, PubMed:11093772, PubMed:14559847, PubMed:15766564, PubMed:19965576). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase) (PubMed:7574697, PubMed:11093772, PubMed:14559847, PubMed:15766564, PubMed:19965576). Primarily catalyzes the epoxidation of double bonds of polyunsaturated fatty acids (PUFA) with a preference for the last double bond (PubMed:7574697, PubMed:15766564, PubMed:19965576). Catalyzes the hydroxylation of carbon-hydrogen bonds. Metabolizes all trans-retinoic acid toward its 4-hydroxylated form (PubMed:11093772). Displays 16-alpha hydroxylase activity toward estrogen steroid hormones, 17beta-estradiol (E2) and estrone (E1) (PubMed:14559847). Plays a role in the oxidative metabolism of xenobiotics. It is the principal enzyme responsible for the metabolism of the anti-cancer drug paclitaxel (taxol) (PubMed:26427316). {ECO:0000269|PubMed:11093772, ECO:0000269|PubMed:14559847, ECO:0000269|PubMed:15766564, ECO:0000269|PubMed:19965576, ECO:0000269|PubMed:26427316, ECO:0000269|PubMed:7574697}.
Ensembl transtripts involved in fusion geneENST idsENST00000475640, ENST00000474629, 
ENST00000371270, ENST00000539050, 
ENST00000535898, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 7 X 5=2806 X 2 X 5=60
# samples 96
** MAII scorelog2(9/280*10)=-1.63742992061529
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/60*10)=0
Fusion gene context

PubMed: PARP14 [Title/Abstract] AND CYP2C8 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PARP14 [Title/Abstract] AND CYP2C8 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PARP14(122439235)-CYP2C8(96827448), # samples:1
Anticipated loss of major functional domain due to fusion event.PARP14-CYP2C8 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.
PARP14-CYP2C8 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.
PARP14-CYP2C8 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.
PARP14-CYP2C8 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
HgenePARP14

GO:0006471

protein ADP-ribosylation

27796300

TgeneCYP2C8

GO:0002933

lipid hydroxylation

14559847

TgeneCYP2C8

GO:0006082

organic acid metabolic process

19651758

TgeneCYP2C8

GO:0008202

steroid metabolic process

14559847

TgeneCYP2C8

GO:0008210

estrogen metabolic process

12865317|14559847

TgeneCYP2C8

GO:0017144

drug metabolic process

19651758

TgeneCYP2C8

GO:0019373

epoxygenase P450 pathway

7574697

TgeneCYP2C8

GO:0042573

retinoic acid metabolic process

11093772

TgeneCYP2C8

GO:0042738

exogenous drug catabolic process

18619574

TgeneCYP2C8

GO:0046456

icosanoid biosynthetic process

15766564

TgeneCYP2C8

GO:0055114

oxidation-reduction process

19651758

TgeneCYP2C8

GO:0070989

oxidative demethylation

18619574



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/chr3:122439235/chr10:96827448)
- 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 PARP14 (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 CYP2C8 (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)
ENST00000474629PARP14chr3122439235+ENST00000371270CYP2C8chr1096827448-6867520726065112083

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
ENST00000474629ENST00000371270PARP14chr3122439235+CYP2C8chr1096827448-0.0002236750.9997763

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 PARP14-CYP2C8

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PARP14chr3122439235CYP2C8chr109682744852071649KFNQTCSHFRIEKFSKVYGPVFTVYF

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Potential FusionNeoAntigen Information of PARP14-CYP2C8 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.
PARP14-CYP2C8_122439235_96827448.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)
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:01IEKFSKVY0.99850.75181018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:02SHFRIEKF0.99670.5462614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:01SHFRIEKF0.99670.5462614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:10SHFRIEKF0.99190.6031614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B38:01SHFRIEKF0.98540.9539614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:18SHFRIEKF0.98320.7459614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B38:02SHFRIEKF0.98270.9595614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:37SHFRIEKF0.97560.7144614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:02FRIEKFSKV0.99990.5736817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:05FRIEKFSKV0.99990.891817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:04FRIEKFSKV0.99980.6982817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:06FRIEKFSKV0.99870.7165817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:01FRIEKFSKV0.99680.5067817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:02FRIEKFSKV0.99680.5067817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:01FRIEKFSKV0.99390.9206817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:01RIEKFSKVY0.97660.8773918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:25RIEKFSKVY0.95480.7937918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:37FRIEKFSKV0.47330.6533817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:05FRIEKFSKVY0.99990.7207818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:12SHFRIEKF0.99450.8964614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:05SHFRIEKF0.97560.875614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:03SHFRIEKF0.85280.6798614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:14FRIEKFSKV0.99990.8007817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B73:01FRIEKFSKV0.99880.6027817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:05FRIEKFSKV0.99670.9643817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:12FRIEKFSKV0.99530.9261817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:27FRIEKFSKV0.99120.9541817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:95FRIEKFSKV0.98970.6545817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:03FRIEKFSKV0.98680.9097817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:29FRIEKFSKV0.96080.9492817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:46FRIEKFSKV0.92630.8446817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:19FRIEKFSKV0.89040.5811817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:07RIEKFSKVY0.88930.6076918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:10FRIEKFSKV0.86350.9505817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:13FRIEKFSKV0.86210.942817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:80FRIEKFSKV0.85720.9334817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:67FRIEKFSKV0.85720.9334817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:05RIEKFSKVY0.71720.8049918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B14:03FRIEKFSKV0.43650.6001817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:03FRIEKFSKV0.37610.9932817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C12:16FRIEKFSKV0.03040.9614817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:03FRIEKFSKVY0.99930.7762818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:27FRIEKFSKVY0.99820.897818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:05FRIEKFSKVY0.99810.8802818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:80FRIEKFSKVY0.99750.8437818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:67FRIEKFSKVY0.99750.8437818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:10FRIEKFSKVY0.99640.8826818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:46FRIEKFSKVY0.99640.6447818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C12:16FRIEKFSKVY0.97260.9524818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:08IEKFSKVY0.99870.59451018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:04IEKFSKVY0.99870.78211018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:05IEKFSKVY0.99850.75181018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:06IEKFSKVY0.99850.74291018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:03IEKFSKVY0.99830.74141018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:53IEKFSKVY0.99560.74511018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B18:11IEKFSKVY0.99470.66151018
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:31SHFRIEKF0.99310.893614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B38:05SHFRIEKF0.98540.9539614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:09SHFRIEKF0.95460.5304614
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:08FRIEKFSKV0.99990.778817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:09FRIEKFSKV0.99980.8806817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:06FRIEKFSKV0.99980.7271817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:10FRIEKFSKV0.99980.808817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B39:31FRIEKFSKV0.99650.9214817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:01FRIEKFSKV0.99140.6314817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-A30:01HFRIEKFSK0.98380.7337716
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:12RIEKFSKVY0.98190.8284918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:27RIEKFSKVY0.97780.8626918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:125RIEKFSKVY0.97660.8773918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:33RIEKFSKVY0.97660.8773918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:34RIEKFSKVY0.97660.8773918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:135RIEKFSKVY0.97580.8681918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:08FRIEKFSKV0.97350.978817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:50RIEKFSKVY0.96980.8169918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:04FRIEKFSKV0.96410.9304817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:39RIEKFSKVY0.95890.6743918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:17FRIEKFSKV0.95160.9561817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:35RIEKFSKVY0.92490.8447918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:02FRIEKFSKV0.85720.9334817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:22FRIEKFSKV0.77920.7911817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:20RIEKFSKVY0.72030.8623918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B35:28RIEKFSKVY0.63420.859918
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C18:01FRIEKFSKV0.54260.7377817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C04:04FRIEKFSKV0.52310.8537817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:06FRIEKFSKV0.39880.9742817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:17FRIEKFSKV0.31330.992817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:02FRIEKFSKV0.31330.992817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C03:67FRIEKFSKV0.25840.9771817
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:10FRIEKFSKVY0.99990.6363818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B27:08FRIEKFSKVY0.99990.5222818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:02FRIEKFSKVY0.99750.8437818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:17FRIEKFSKVY0.99650.9355818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-B15:54FRIEKFSKVY0.98210.8421818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C07:22FRIEKFSKVY0.97970.6247818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:17FRIEKFSKVY0.96280.9874818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:02FRIEKFSKVY0.96280.9874818
PARP14-CYP2C8chr3122439235chr10968274485207HLA-C06:08FRIEKFSKVY0.90240.9745818

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Potential FusionNeoAntigen Information of PARP14-CYP2C8 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.
PARP14-CYP2C8_122439235_96827448.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)
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-0828SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-0828HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1125SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1125HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1148SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1167SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1167HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1308SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1309SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1309HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1317SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1317HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1318SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1318HFRIEKFSKVYGPVF722
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1370SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1372SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1384SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1437SHFRIEKFSKVYGPV621
PARP14-CYP2C8chr3122439235chr10968274485207DRB1-1437HFRIEKFSKVYGPVF722

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Fusion breakpoint peptide structures of PARP14-CYP2C8

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
8618SHFRIEKFSKVYGPPARP14CYP2C8chr3122439235chr10968274485207

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PARP14-CYP2C8

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-B14:023BVN8618SHFRIEKFSKVYGP-7.9962-8.1096
HLA-B14:023BVN8618SHFRIEKFSKVYGP-5.70842-6.74372
HLA-B52:013W398618SHFRIEKFSKVYGP-6.83737-6.95077
HLA-B52:013W398618SHFRIEKFSKVYGP-4.4836-5.5189
HLA-A11:014UQ28618SHFRIEKFSKVYGP-10.0067-10.1201
HLA-A11:014UQ28618SHFRIEKFSKVYGP-9.03915-10.0745
HLA-A24:025HGA8618SHFRIEKFSKVYGP-6.56204-6.67544
HLA-A24:025HGA8618SHFRIEKFSKVYGP-5.42271-6.45801
HLA-B44:053DX88618SHFRIEKFSKVYGP-7.85648-8.89178
HLA-B44:053DX88618SHFRIEKFSKVYGP-5.3978-5.5112
HLA-A02:016TDR8618SHFRIEKFSKVYGP-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PARP14-CYP2C8

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
PARP14-CYP2C8chr3122439235chr10968274481018IEKFSKVYATAGAGAAGTTCTCAAAAGTCTAT
PARP14-CYP2C8chr3122439235chr1096827448614SHFRIEKFTCACACTTCAGAATAGAGAAGTTC
PARP14-CYP2C8chr3122439235chr1096827448716HFRIEKFSKCACTTCAGAATAGAGAAGTTCTCAAAA
PARP14-CYP2C8chr3122439235chr1096827448817FRIEKFSKVTTCAGAATAGAGAAGTTCTCAAAAGTC
PARP14-CYP2C8chr3122439235chr1096827448818FRIEKFSKVYTTCAGAATAGAGAAGTTCTCAAAAGTCTAT
PARP14-CYP2C8chr3122439235chr1096827448918RIEKFSKVYAGAATAGAGAAGTTCTCAAAAGTCTAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PARP14-CYP2C8chr3122439235chr1096827448621SHFRIEKFSKVYGPVTCACACTTCAGAATAGAGAAGTTCTCAAAAGTCTATGGTCCTGTG
PARP14-CYP2C8chr3122439235chr1096827448722HFRIEKFSKVYGPVFCACTTCAGAATAGAGAAGTTCTCAAAAGTCTATGGTCCTGTGTTC

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Information of the samples that have these potential fusion neoantigens of PARP14-CYP2C8

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
Non-CancerPARP14-CYP2C8chr3122439235ENST00000474629chr1096827448ENST00000371270TCGA-DD-A1EH-11A

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Potential target of CAR-T therapy development for PARP14-CYP2C8

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 PARP14-CYP2C8

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 PARP14-CYP2C8

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