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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:AP1M1-CYP4F11

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: AP1M1-CYP4F11
FusionPDB ID: 5189
FusionGDB2.0 ID: 5189
HgeneTgene
Gene symbol

AP1M1

CYP4F11

Gene ID

8907

57834

Gene nameadaptor related protein complex 1 subunit mu 1cytochrome P450 family 4 subfamily F member 11
SynonymsAP47|CLAPM2|CLTNM|MU-1ACYPIVF11
Cytomap

19p13.11

19p13.12

Type of geneprotein-codingprotein-coding
DescriptionAP-1 complex subunit mu-1AP-mu chain family member mu1AHA1 47 kDa subunitadapter-related protein complex 1 subunit mu-1adaptor protein complex AP-1 mu-1 subunitadaptor protein complex AP-1 subunit mu-1adaptor related protein complex 1 mu 1 subunitccytochrome P450 4F113-hydroxy fatty acids omega-hydroxylase CYP4F11cytochrome P450, family 4, subfamily F, polypeptide 11cytochrome P450, subfamily IVF, polypeptide 11docosahexaenoic acid omega-hydroxylaselong-chain fatty acid omega-monooxygenasephy
Modification date2020031320200313
UniProtAcc

Q9BXS5

Main function of 5'-partner protein: FUNCTION: Subunit of clathrin-associated adaptor protein complex 1 that plays a role in protein sorting in the trans-Golgi network (TGN) and endosomes. The AP complexes mediate the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules.

Q9HBI6

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:24138531, PubMed:15364545, PubMed:18065749). 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:15364545, PubMed:18065749, PubMed:24138531). Catalyzes with high efficiency the oxidation of the terminal carbon (omega-oxidation) of 3-hydroxy fatty acids, such as 3-hydroxyhexadecanoic and 3-hydroxyoctadecanoic acids, likely participating in the biosynthesis of long-chain 3-hydroxydicarboxylic acids (PubMed:18065749, PubMed:19932081). Omega-hydroxylates and inactivates phylloquinone (vitamin K1), and menaquinone-4 (MK-4, a form of vitamin K2), both acting as cofactors in blood coagulation (PubMed:24138531). Metabolizes with low efficiciency fatty acids, including (5Z,8Z,11Z,14Z)-eicosatetraenoic acid (arachidonate) and its oxygenated metabolite 8-hydroxyeicosatetraenoic acid (8-HETE) (PubMed:15364545, PubMed:19932081). Catalyzes N- and O-demethylation of drugs such as erythromycin, benzphetamine, ethylmorphine, chlorpromazine, imipramine and verapamil (PubMed:15364545). {ECO:0000269|PubMed:15364545, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:19932081, ECO:0000269|PubMed:24138531}.
Ensembl transtripts involved in fusion geneENST idsENST00000291439, ENST00000429941, 
ENST00000444449, ENST00000541844, 
ENST00000590756, 
ENST00000248041, 
ENST00000326742, ENST00000402119, 
ENST00000591841, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 5=2102 X 3 X 2=12
# samples 82
** MAII scorelog2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/12*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: AP1M1 [Title/Abstract] AND CYP4F11 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: AP1M1 [Title/Abstract] AND CYP4F11 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)AP1M1(16319988)-CYP4F11(16040411), # samples:1
AP1M1(16319988)-CYP4F11(16045219), # samples:1
Anticipated loss of major functional domain due to fusion event.AP1M1-CYP4F11 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.
AP1M1-CYP4F11 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
TgeneCYP4F11

GO:0006631

fatty acid metabolic process

18065749

TgeneCYP4F11

GO:0042361

menaquinone catabolic process

24138531

TgeneCYP4F11

GO:0042376

phylloquinone catabolic process

24138531

TgeneCYP4F11

GO:0042377

vitamin K catabolic process

24138531



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/chr19:16319988/chr19:16040411)
- 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 AP1M1 (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 CYP4F11 (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)
ENST00000291439AP1M1chr1916319988+ENST00000248041CYP4F11chr1916040411-37379954252371648
ENST00000291439AP1M1chr1916319988+ENST00000326742CYP4F11chr1916040411-36689954252161578
ENST00000291439AP1M1chr1916319988+ENST00000402119CYP4F11chr1916040411-35319954252371648
ENST00000541844AP1M1chr1916319988+ENST00000248041CYP4F11chr1916040411-32455031491879576
ENST00000541844AP1M1chr1916319988+ENST00000326742CYP4F11chr1916040411-31765031491669506
ENST00000541844AP1M1chr1916319988+ENST00000402119CYP4F11chr1916040411-30395031491879576
ENST00000590756AP1M1chr1916319988+ENST00000248041CYP4F11chr1916040411-32455031491879576
ENST00000590756AP1M1chr1916319988+ENST00000326742CYP4F11chr1916040411-31765031491669506
ENST00000590756AP1M1chr1916319988+ENST00000402119CYP4F11chr1916040411-30395031491879576
ENST00000429941AP1M1chr1916319988+ENST00000248041CYP4F11chr1916040411-3404662922038648
ENST00000429941AP1M1chr1916319988+ENST00000326742CYP4F11chr1916040411-3335662921828578
ENST00000429941AP1M1chr1916319988+ENST00000402119CYP4F11chr1916040411-3198662922038648
ENST00000444449AP1M1chr1916319988+ENST00000248041CYP4F11chr1916040411-3381639692015648
ENST00000444449AP1M1chr1916319988+ENST00000326742CYP4F11chr1916040411-3312639691805578
ENST00000444449AP1M1chr1916319988+ENST00000402119CYP4F11chr1916040411-3175639692015648

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
ENST00000291439ENST00000248041AP1M1chr1916319988+CYP4F11chr1916040411-0.0044488610.9955511
ENST00000291439ENST00000326742AP1M1chr1916319988+CYP4F11chr1916040411-0.0049902920.99500966
ENST00000291439ENST00000402119AP1M1chr1916319988+CYP4F11chr1916040411-0.0048688710.99513113
ENST00000541844ENST00000248041AP1M1chr1916319988+CYP4F11chr1916040411-0.0045232630.9954768
ENST00000541844ENST00000326742AP1M1chr1916319988+CYP4F11chr1916040411-0.0038382350.9961617
ENST00000541844ENST00000402119AP1M1chr1916319988+CYP4F11chr1916040411-0.005058630.99494135
ENST00000590756ENST00000248041AP1M1chr1916319988+CYP4F11chr1916040411-0.0042776140.9957224
ENST00000590756ENST00000326742AP1M1chr1916319988+CYP4F11chr1916040411-0.0037036690.99629635
ENST00000590756ENST00000402119AP1M1chr1916319988+CYP4F11chr1916040411-0.0048642240.9951357
ENST00000429941ENST00000248041AP1M1chr1916319988+CYP4F11chr1916040411-0.0043798350.9956202
ENST00000429941ENST00000326742AP1M1chr1916319988+CYP4F11chr1916040411-0.0049611090.9950389
ENST00000429941ENST00000402119AP1M1chr1916319988+CYP4F11chr1916040411-0.0047509550.99524903
ENST00000444449ENST00000248041AP1M1chr1916319988+CYP4F11chr1916040411-0.004507160.9954928
ENST00000444449ENST00000326742AP1M1chr1916319988+CYP4F11chr1916040411-0.0051045920.9948954
ENST00000444449ENST00000402119AP1M1chr1916319988+CYP4F11chr1916040411-0.0049035530.9950964

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 AP1M1-CYP4F11

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
AP1M1chr1916319988CYP4F11chr1916040411503118EVFLDVIESVNLLVTPTEEGMKTLTQ
AP1M1chr1916319988CYP4F11chr1916040411503123VIESVNLLVTPTEEGMKTLTQLVTTY
AP1M1chr1916319988CYP4F11chr1916040411639190EVFLDVIESVNLLVTPTEEGMKTLTQ
AP1M1chr1916319988CYP4F11chr1916040411639195VIESVNLLVTPTEEGMKTLTQLVTTY
AP1M1chr1916319988CYP4F11chr1916040411662190EVFLDVIESVNLLVTPTEEGMKTLTQ
AP1M1chr1916319988CYP4F11chr1916040411662195VIESVNLLVTPTEEGMKTLTQLVTTY
AP1M1chr1916319988CYP4F11chr1916040411995190EVFLDVIESVNLLVTPTEEGMKTLTQ
AP1M1chr1916319988CYP4F11chr1916040411995195VIESVNLLVTPTEEGMKTLTQLVTTY

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Potential FusionNeoAntigen Information of AP1M1-CYP4F11 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.
AP1M1-CYP4F11_16319988_16040411.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)
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B44:03EEGMKTLTQL0.93630.91631222
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:03TPTEEGMKTL0.83410.9375919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:04TPTEEGMKTL0.57720.9879919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:02TPTEEGMKTL0.57720.9879919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B81:01TPTEEGMKTL0.50080.54919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B39:08TEEGMKTL0.98750.83631119
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B07:12TPTEEGMKTL0.94840.5007919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B39:10TPTEEGMKTL0.57940.9527919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:12TPTEEGMKTL0.57720.9879919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B42:01TPTEEGMKTL0.52830.6957919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-C01:17VTPTEEGMKTL0.99930.9609819
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B40:04TEEGMKTL0.99980.74641119
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B41:03TEEGMKTL0.96320.6171119
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B44:07EEGMKTLTQL0.93630.91631222
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B44:13EEGMKTLTQL0.93630.91631222
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B44:26EEGMKTLTQL0.93630.91631222
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B40:04EEGMKTLTQL0.86550.73541222
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:13TPTEEGMKTL0.8060.9384919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:22TPTEEGMKTL0.64880.5305919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B67:01TPTEEGMKTL0.62820.9145919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B35:09TPTEEGMKTL0.57720.9879919
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-C01:02VTPTEEGMKTL0.99950.9572819
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B40:04TEEGMKTLTQL0.99950.76631122
AP1M1-CYP4F11chr1916319988chr1916040411995HLA-B41:03TEEGMKTLTQL0.98020.63461122

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Potential FusionNeoAntigen Information of AP1M1-CYP4F11 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.
AP1M1-CYP4F11_16319988_16040411.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)
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0403SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0403ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0403IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0413SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0413ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0415SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0422SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0427SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0427ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0436SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0439SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0439ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0439IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0440SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0440ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0441SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0441ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0441IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0444SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0444ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0446SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0446ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0446IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0449SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0449ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0449IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0450SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0450ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0450IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0451SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0451ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0451IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0452SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0452ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0452IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0455SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0456SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0456ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0459SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0459ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0460SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0460ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0460IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0468SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0468ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0470SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0470ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0471SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0471ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0471IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0478SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0478ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0479SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0479ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0485SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0485ESVNLLVTPTEEGMK217
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0485IESVNLLVTPTEEGM116
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0488SVNLLVTPTEEGMKT318
AP1M1-CYP4F11chr1916319988chr1916040411995DRB1-0488ESVNLLVTPTEEGMK217

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Fusion breakpoint peptide structures of AP1M1-CYP4F11

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
5289LLVTPTEEGMKTLTAP1M1CYP4F11chr1916319988chr1916040411995

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of AP1M1-CYP4F11

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-B14:023BVN5289LLVTPTEEGMKTLT-8.55667-8.74867
HLA-B14:023BVN5289LLVTPTEEGMKTLT-3.49457-4.25557
HLA-B52:013W395289LLVTPTEEGMKTLT-7.26725-7.45925
HLA-B52:013W395289LLVTPTEEGMKTLT-4.01461-4.77561
HLA-A24:025HGA5289LLVTPTEEGMKTLT-7.65911-8.42011
HLA-A24:025HGA5289LLVTPTEEGMKTLT-7.10204-7.29404
HLA-B44:053DX85289LLVTPTEEGMKTLT-7.5556-8.3166
HLA-B44:053DX85289LLVTPTEEGMKTLT-2.76159-2.95359

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Vaccine Design for the FusionNeoAntigens of AP1M1-CYP4F11

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
AP1M1-CYP4F11chr1916319988chr19160404111119TEEGMKTLCTCTTGGTCACTCCCACGGAAGAG
AP1M1-CYP4F11chr1916319988chr19160404111122TEEGMKTLTQLCTCTTGGTCACTCCCACGGAAGAGGGCATGAAG
AP1M1-CYP4F11chr1916319988chr19160404111222EEGMKTLTQLTTGGTCACTCCCACGGAAGAGGGCATGAAG
AP1M1-CYP4F11chr1916319988chr1916040411819VTPTEEGMKTLTCTGTCAACCTCTTGGTCACTCCCACGGAAGAG
AP1M1-CYP4F11chr1916319988chr1916040411919TPTEEGMKTLGTCAACCTCTTGGTCACTCCCACGGAAGAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
AP1M1-CYP4F11chr1916319988chr1916040411116IESVNLLVTPTEEGMGTGTTCTTGGACGTCATCGAGTCTGTCAACCTCTTGGTCACTCCC
AP1M1-CYP4F11chr1916319988chr1916040411217ESVNLLVTPTEEGMKTTCTTGGACGTCATCGAGTCTGTCAACCTCTTGGTCACTCCCACG
AP1M1-CYP4F11chr1916319988chr1916040411318SVNLLVTPTEEGMKTTTGGACGTCATCGAGTCTGTCAACCTCTTGGTCACTCCCACGGAA

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Information of the samples that have these potential fusion neoantigens of AP1M1-CYP4F11

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
LUADAP1M1-CYP4F11chr1916319988ENST00000291439chr1916040411ENST00000248041TCGA-05-4426-01A

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Potential target of CAR-T therapy development for AP1M1-CYP4F11

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 AP1M1-CYP4F11

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 AP1M1-CYP4F11

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