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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:CYP4A11-CYP4F3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CYP4A11-CYP4F3
FusionPDB ID: 21080
FusionGDB2.0 ID: 21080
HgeneTgene
Gene symbol

CYP4A11

CYP4F3

Gene ID

1579

4051

Gene namecytochrome P450 family 4 subfamily A member 11cytochrome P450 family 4 subfamily F member 3
SynonymsCP4Y|CYP4A2|CYP4AII|CYPIVA11CPF3|CYP4F|CYPIVF3|LTB4H
Cytomap

1p33

19p13.12

Type of geneprotein-codingprotein-coding
Descriptioncytochrome P450 4A1120-HETE synthase20-hydroxyeicosatetraenoic acid synthaseP450HL-omegaalkane-1 monooxygenasecytochrome P-450HK-omegacytochrome P450, family 4, subfamily A, polypeptide 11cytochrome P450, subfamily IVA, polypeptide 11cytochrome P4cytochrome P450 4F320-HETE synthase20-hydroxyeicosatetraenoic acid synthasecytochrome P-450cytochrome P450, family 4, subfamily F, polypeptide 3cytochrome P450, subfamily IVF, polypeptide 3 (leukotriene B4 omega hydroxylase)cytochrome P450-LTB-omega
Modification date2020031320200313
UniProtAcc

Q02928

Main function of 5'-partner protein: FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of fatty acids and their oxygenated derivatives (oxylipins) (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:10553002, PubMed:10660572, PubMed:15611369). 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 (CPR; NADPH-ferrihemoprotein reductase) (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:10553002, PubMed:10660572, PubMed:15611369). Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of saturated and unsaturated fatty acids, the catalytic efficiency decreasing in the following order: dodecanoic > tetradecanoic > (9Z)-octadecenoic > (9Z,12Z)-octadecadienoic > hexadecanoic acid (PubMed:10553002, PubMed:10660572). Acts as a major omega-hydroxylase for dodecanoic (lauric) acid in liver (PubMed:7679927, PubMed:1739747, PubMed:8914854, PubMed:15611369). Participates in omega-hydroxylation of (5Z,8Z,11Z,14Z)-eicosatetraenoic acid (arachidonate) to 20-hydroxyeicosatetraenoic acid (20-HETE), a signaling molecule acting both as vasoconstrictive and natriuretic with overall effect on arterial blood pressure (PubMed:10620324, PubMed:10660572, PubMed:15611369). Can also catalyze the oxidation of the penultimate carbon (omega-1 oxidation) of fatty acids with lower efficiency (PubMed:7679927). May contribute to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acid, thereby initiating chain shortening (PubMed:18182499). Omega-hydroxylates (9R,10S)-epoxy-octadecanoate stereoisomer (PubMed:15145985). Plays a minor role in omega-oxidation of long-chain 3-hydroxy fatty acids (PubMed:18065749). Has little activity toward prostaglandins A1 and E1 (PubMed:7679927). {ECO:0000269|PubMed:10553002, ECO:0000269|PubMed:10620324, ECO:0000269|PubMed:10660572, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15611369, ECO:0000269|PubMed:1739747, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:7679927, ECO:0000269|PubMed:8914854}.

Q08477

Main function of 5'-partner protein: FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids and their oxygenated derivatives (oxylipins) (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15145985, PubMed:16547005, PubMed:16820285, PubMed:18182499, PubMed:18065749, PubMed:18577768). 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 (CPR; NADPH-ferrihemoprotein reductase) (PubMed:9675028). May play a role in inactivation of proinflammatory and anti-inflammatory oxylipins during the resolution of inflammation (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15145985, PubMed:15364545, PubMed:16547005, PubMed:16820285, PubMed:18182499, PubMed:18065749, PubMed:18577768). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15364545, ECO:0000269|PubMed:16547005, ECO:0000269|PubMed:16820285, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768, ECO:0000269|PubMed:8486631, ECO:0000269|PubMed:9675028}.; FUNCTION: [Isoform CYP4F3A]: Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of oxylipins in myeloid cells, displaying higher affinity for arachidonate metabolite leukotriene B4 (LTB4) (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15364545). Inactivates LTB4 via three successive oxidative transformations to 20-hydroxy-LTB4, then to 20-oxo-LTB4 and to 20-carboxy-LTB4 (PubMed:9675028). Has omega-hydroxylase activity toward long-chain fatty acid epoxides with preference for 8,9-epoxy-(5Z,11Z,14Z)-eicosatrienoate (EET) and 9,10-epoxyoctadecanoate (PubMed:15145985). Omega-hydroxylates monohydroxy polyunsaturated fatty acids (PUFAs), including hydroxyeicosatetraenoates (HETEs) and hydroxyeicosapentaenoates (HEPEs), to dihydroxy compounds (PubMed:15364545, PubMed:9675028). Contributes to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acid, thereby initiating chain shortening (PubMed:18182499). Has low hydroxylase activity toward PUFAs (PubMed:18577768, PubMed:11461919). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15364545, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768, ECO:0000269|PubMed:8486631, ECO:0000269|PubMed:9675028}.; FUNCTION: [Isoform CYP4F3B]: Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of polyunsaturated fatty acids (PUFAs) (PubMed:11461919, PubMed:16820285, PubMed:18577768). Participates in the conversion of arachidonic acid to 20-hydroxyeicosatetraenoic acid (20-HETE), a signaling molecule acting both as vasoconstrictive and natriuretic with overall effect on arterial blood pressure (PubMed:11461919, PubMed:16820285, PubMed:18577768). Has high omega-hydroxylase activity toward other PUFAs, including eicosatrienoic acid (ETA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) (PubMed:16820285, PubMed:18577768). Can also catalyze the oxidation of the penultimate carbon (omega-1 oxidation) of PUFAs with lower efficiency (PubMed:18577768). Contributes to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid and hexacosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acids, thereby initiating chain shortening (PubMed:16547005, PubMed:18182499). Omega-hydroxylates long-chain 3-hydroxy fatty acids, likely initiating the oxidative conversion to the corresponding 3-hydroxydicarboxylic fatty acids (PubMed:18065749). Has omega-hydroxylase activity toward long-chain fatty acid epoxides with preference for 8,9-epoxy-(5Z,11Z,14Z)-eicosatrienoate (EET) and 9,10-epoxyoctadecanoate (PubMed:15145985). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:16547005, ECO:0000269|PubMed:16820285, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768}.
Ensembl transtripts involved in fusion geneENST idsENST00000310638, ENST00000371904, 
ENST00000371905, ENST00000457840, 
ENST00000462347, ENST00000496519, 
ENST00000588886, ENST00000221307, 
ENST00000585846, ENST00000586182, 
ENST00000591058, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 2=184 X 4 X 4=64
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CYP4A11 [Title/Abstract] AND CYP4F3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CYP4A11 [Title/Abstract] AND CYP4F3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CYP4A11(47400124)-CYP4F3(15763632), # samples:1
Anticipated loss of major functional domain due to fusion event.CYP4A11-CYP4F3 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.
CYP4A11-CYP4F3 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.
CYP4A11-CYP4F3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CYP4A11-CYP4F3 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneCYP4A11

GO:0001676

long-chain fatty acid metabolic process

18433732

HgeneCYP4A11

GO:0006691

leukotriene metabolic process

9799565

HgeneCYP4A11

GO:0019369

arachidonic acid metabolic process

10660572

HgeneCYP4A11

GO:0019373

epoxygenase P450 pathway

9618440

HgeneCYP4A11

GO:0055114

oxidation-reduction process

9618440|9799565|18433732



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/chr1:47400124/chr19:15763632)
- 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 CYP4A11 (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 CYP4F3 (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)
ENST00000462347CYP4A11chr147400124-ENST00000586182CYP4F3chr1915763632+2092773311350439
ENST00000462347CYP4A11chr147400124-ENST00000591058CYP4F3chr1915763632+2724773311350439
ENST00000462347CYP4A11chr147400124-ENST00000221307CYP4F3chr1915763632+4791773311350439
ENST00000462347CYP4A11chr147400124-ENST00000585846CYP4F3chr1915763632+1737773311350439

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
ENST00000462347ENST00000586182CYP4A11chr147400124-CYP4F3chr1915763632+0.069318380.93068165
ENST00000462347ENST00000591058CYP4A11chr147400124-CYP4F3chr1915763632+0.0317609460.968239
ENST00000462347ENST00000221307CYP4A11chr147400124-CYP4F3chr1915763632+0.0071391170.99286085
ENST00000462347ENST00000585846CYP4A11chr147400124-CYP4F3chr1915763632+0.094325690.9056743

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 CYP4A11-CYP4F3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CYP4A11chr147400124CYP4F3chr1915763632773122GRSDPKSHGSYRFLAPWIGYGLLLLN
CYP4A11chr147400124CYP4F3chr1915763632773127KSHGSYRFLAPWIGYGLLLLNGQTWF

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Potential FusionNeoAntigen Information of CYP4A11-CYP4F3 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.
CYP4A11-CYP4F3_47400124_15763632.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)
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B81:01APWIGYGLL0.1260.5996918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B82:01APWIGYGLL0.10560.6512918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:05YRFLAPWIGY10.8647515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:02YRFLAPWIGY10.5382515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:04YRFLAPWIGY0.99990.6119515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:13FLAPWIGYGL0.99370.5489717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:04FLAPWIGYGL0.99260.7553717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:17FLAPWIGYGL0.99090.6436717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:19FLAPWIGYGL0.9790.503717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:38FLAPWIGYGL0.97790.5479717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B15:18YRFLAPWIGY0.86410.5655515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B81:01APWIGYGLLL0.75850.6656919
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B82:01APWIGYGLLL0.64210.7237919
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B73:01YRFLAPWIG0.9530.8856514
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C01:30LAPWIGYGL0.70010.9563817
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C01:17LAPWIGYGL0.59540.9612817
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B42:02APWIGYGLL0.29860.9309918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B42:01APWIGYGLL0.24720.9265918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:14YRFLAPWIGY0.99990.7737515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:03YRFLAPWIGY0.99950.8769515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:95YRFLAPWIGY0.99890.5801515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:05YRFLAPWIGY0.99880.9564515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:27YRFLAPWIGY0.99870.9364515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:05FLAPWIGYGL0.99740.5214717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:19YRFLAPWIGY0.99220.5609515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:67YRFLAPWIGY0.98860.8959515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:80YRFLAPWIGY0.98860.8959515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:46YRFLAPWIGY0.98660.7517515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:10YRFLAPWIGY0.98620.9499515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C12:16YRFLAPWIGY0.81420.9635515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B42:01APWIGYGLLL0.62770.9449919
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B67:01APWIGYGLL0.73450.8921918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C01:02LAPWIGYGL0.58160.9617817
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C01:03LAPWIGYGL0.46320.8339817
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B82:02APWIGYGLL0.10560.6512918
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:10YRFLAPWIGY0.99990.8028515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:08YRFLAPWIGY0.99990.7288515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:01YRFLAPWIGY0.99920.5141515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B27:09YRFLAPWIGY0.99910.7841515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-A02:03FLAPWIGYGL0.99740.5488717
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:02YRFLAPWIGY0.98860.8959515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-C07:22YRFLAPWIGY0.96860.6633515
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B67:01APWIGYGLLL0.78330.928919
CYP4A11-CYP4F3chr147400124chr1915763632773HLA-B82:02APWIGYGLLL0.64210.7237919

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Potential FusionNeoAntigen Information of CYP4A11-CYP4F3 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.
CYP4A11-CYP4F3_47400124_15763632.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)
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0101SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0101HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0103SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0105SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0105HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0107SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0107HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0109SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0109HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0111SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0111HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0113SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0113HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0115SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0115HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0117SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0117HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0119SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0119HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0121SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0121HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0125SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0125HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0127SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0127HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0129SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0129HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0131SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-0131HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-1001SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-1001HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-1003SHGSYRFLAPWIGYG116
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-1003HGSYRFLAPWIGYGL217
CYP4A11-CYP4F3chr147400124chr1915763632773DRB1-1609SHGSYRFLAPWIGYG116

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Fusion breakpoint peptide structures of CYP4A11-CYP4F3

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
7832RFLAPWIGYGLLLLCYP4A11CYP4F3chr147400124chr1915763632773

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CYP4A11-CYP4F3

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-B14:023BVN7832RFLAPWIGYGLLLL-7.9962-8.1096
HLA-B14:023BVN7832RFLAPWIGYGLLLL-5.70842-6.74372
HLA-B52:013W397832RFLAPWIGYGLLLL-6.83737-6.95077
HLA-B52:013W397832RFLAPWIGYGLLLL-4.4836-5.5189
HLA-A11:014UQ27832RFLAPWIGYGLLLL-10.0067-10.1201
HLA-A11:014UQ27832RFLAPWIGYGLLLL-9.03915-10.0745
HLA-A24:025HGA7832RFLAPWIGYGLLLL-6.56204-6.67544
HLA-A24:025HGA7832RFLAPWIGYGLLLL-5.42271-6.45801
HLA-B44:053DX87832RFLAPWIGYGLLLL-7.85648-8.89178
HLA-B44:053DX87832RFLAPWIGYGLLLL-5.3978-5.5112
HLA-A02:016TDR7832RFLAPWIGYGLLLL-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CYP4A11-CYP4F3

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
CYP4A11-CYP4F3chr147400124chr1915763632514YRFLAPWIGCTGGATATCCTCCTCTTGGCCAAAGCC
CYP4A11-CYP4F3chr147400124chr1915763632515YRFLAPWIGYCTGGATATCCTCCTCTTGGCCAAAGCCATG
CYP4A11-CYP4F3chr147400124chr1915763632717FLAPWIGYGLATCCTCCTCTTGGCCAAAGCCATGACACCA
CYP4A11-CYP4F3chr147400124chr1915763632817LAPWIGYGLCTCCTCTTGGCCAAAGCCATGACACCA
CYP4A11-CYP4F3chr147400124chr1915763632918APWIGYGLLCTCTTGGCCAAAGCCATGACACCACAG
CYP4A11-CYP4F3chr147400124chr1915763632919APWIGYGLLLCTCTTGGCCAAAGCCATGACACCACAGCCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CYP4A11-CYP4F3chr147400124chr1915763632116SHGSYRFLAPWIGYGCATTTGGATTTTCTGGATATCCTCCTCTTGGCCAAAGCCATGACA
CYP4A11-CYP4F3chr147400124chr1915763632217HGSYRFLAPWIGYGLTTGGATTTTCTGGATATCCTCCTCTTGGCCAAAGCCATGACACCA

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Information of the samples that have these potential fusion neoantigens of CYP4A11-CYP4F3

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-CancerCYP4A11-CYP4F3chr147400124ENST00000462347chr1915763632ENST00000221307TCGA-BQ-5879-11A

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Potential target of CAR-T therapy development for CYP4A11-CYP4F3

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 CYP4A11-CYP4F3

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 CYP4A11-CYP4F3

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