FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ACPP-NEDD4L

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ACPP-NEDD4L
FusionPDB ID: 1455
FusionGDB2.0 ID: 1455
HgeneTgene
Gene symbol

ACPP

NEDD4L

Gene ID

55

23327

Gene nameacid phosphatase 3NEDD4 like E3 ubiquitin protein ligase
Synonyms5'-NT|ACP-3|ACPP|TM-PAPNEDD4-2|NEDD4.2|PVNH7|RSP5|hNEDD4-2
Cytomap

3q22.1

18q21.31

Type of geneprotein-codingprotein-coding
Descriptionprostatic acid phosphataseTMPaseacid phosphatase, prostateecto-5'-nucleotidaseprostatic acid phosphotasethiamine monophosphataseE3 ubiquitin-protein ligase NEDD4-likeHECT-type E3 ubiquitin transferase NED4Lneural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligaseubiquitin-protein ligase Rsp5
Modification date2020031320200329
UniProtAcc.

Q96PU5

Main function of 5'-partner protein: FUNCTION: E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Inhibits TGF-beta signaling by triggering SMAD2 and TGFBR1 ubiquitination and proteasome-dependent degradation. Promotes ubiquitination and internalization of various plasma membrane channels such as ENaC, SCN2A/Nav1.2, SCN3A/Nav1.3, SCN5A/Nav1.5, SCN9A/Nav1.7, SCN10A/Nav1.8, KCNA3/Kv1.3, KCNH2, EAAT1, KCNQ2/Kv7.2, KCNQ3/Kv7.3 or CLC5 (PubMed:26363003, PubMed:27445338). Promotes ubiquitination and degradation of SGK1 and TNK2. Ubiquitinates BRAT1 and this ubiquitination is enhanced in the presence of NDFIP1 (PubMed:25631046). Plays a role in dendrite formation by melanocytes (PubMed:23999003). Involved in the regulation of TOR signaling (PubMed:27694961). Ubiquitinates and regulates protein levels of NTRK1 once this one is activated by NGF (PubMed:27445338). {ECO:0000250|UniProtKB:Q8CFI0, ECO:0000269|PubMed:12911626, ECO:0000269|PubMed:15040001, ECO:0000269|PubMed:15217910, ECO:0000269|PubMed:15489223, ECO:0000269|PubMed:15496141, ECO:0000269|PubMed:15576372, ECO:0000269|PubMed:19144635, ECO:0000269|PubMed:23999003, ECO:0000269|PubMed:25631046, ECO:0000269|PubMed:26363003, ECO:0000269|PubMed:27445338, ECO:0000269|PubMed:27694961}.
Ensembl transtripts involved in fusion geneENST idsENST00000336375, ENST00000351273, 
ENST00000475741, ENST00000489084, 
ENST00000588516, ENST00000256830, 
ENST00000256832, ENST00000357895, 
ENST00000382850, ENST00000435432, 
ENST00000456986, ENST00000586263, 
ENST00000431212, ENST00000456173, 
ENST00000589054, ENST00000356462, 
ENST00000400345, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score28 X 17 X 4=190427 X 28 X 6=4536
# samples 3132
** MAII scorelog2(31/1904*10)=-2.61869335803371
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/4536*10)=-3.82527683005487
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ACPP [Title/Abstract] AND NEDD4L [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ACPP [Title/Abstract] AND NEDD4L [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ACPP(132056398)-NEDD4L(55833020), # samples:1
Anticipated loss of major functional domain due to fusion event.ACPP-NEDD4L 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.
ACPP-NEDD4L 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.
ACPP-NEDD4L 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.
ACPP-NEDD4L 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
HgeneACPP

GO:0046085

adenosine metabolic process

18940592

TgeneNEDD4L

GO:0003254

regulation of membrane depolarization

15217910

TgeneNEDD4L

GO:0006511

ubiquitin-dependent protein catabolic process

21463633

TgeneNEDD4L

GO:0010038

response to metal ion

11244092

TgeneNEDD4L

GO:0016567

protein ubiquitination

15217910|25631046

TgeneNEDD4L

GO:0034765

regulation of ion transmembrane transport

17289006

TgeneNEDD4L

GO:0042391

regulation of membrane potential

17289006

TgeneNEDD4L

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

21463633

TgeneNEDD4L

GO:0060306

regulation of membrane repolarization

21463633

TgeneNEDD4L

GO:0070936

protein K48-linked ubiquitination

21463633

TgeneNEDD4L

GO:1901016

regulation of potassium ion transmembrane transporter activity

17289006

TgeneNEDD4L

GO:1901017

negative regulation of potassium ion transmembrane transporter activity

21463633

TgeneNEDD4L

GO:1901380

negative regulation of potassium ion transmembrane transport

21463633

TgeneNEDD4L

GO:1902306

negative regulation of sodium ion transmembrane transport

15217910

TgeneNEDD4L

GO:1903861

positive regulation of dendrite extension

23999003

TgeneNEDD4L

GO:2000009

negative regulation of protein localization to cell surface

21463633

TgeneNEDD4L

GO:2000650

negative regulation of sodium ion transmembrane transporter activity

15217910



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/chr3:132056398/chr18:55833020)
- 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 ACPP (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 NEDD4L (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000336375ACPPchr3132056398+ENST00000356462NEDD4Lchr1855833020+36386456633321088
ENST00000336375ACPPchr3132056398+ENST00000400345NEDD4Lchr1855833020+39616456635241152
ENST00000351273ACPPchr3132056398+ENST00000356462NEDD4Lchr1855833020+35986052632921088
ENST00000351273ACPPchr3132056398+ENST00000400345NEDD4Lchr1855833020+39216052634841152

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
ENST00000336375ENST00000356462ACPPchr3132056398+NEDD4Lchr1855833020+0.0005891110.99941087
ENST00000336375ENST00000400345ACPPchr3132056398+NEDD4Lchr1855833020+0.0003095330.99969053
ENST00000351273ENST00000356462ACPPchr3132056398+NEDD4Lchr1855833020+0.0006257220.99937433
ENST00000351273ENST00000400345ACPPchr3132056398+NEDD4Lchr1855833020+0.0003237030.99967635

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

Top

Fusion Protein Breakpoint Sequences for ACPP-NEDD4L

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ACPPchr3132056398NEDD4Lchr1855833020605193KSEEFQKRLHPYKGESRILRVKVVSG
ACPPchr3132056398NEDD4Lchr1855833020645193KSEEFQKRLHPYKGESRILRVKVVSG

Top

Potential FusionNeoAntigen Information of ACPP-NEDD4L 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.
ACPP-NEDD4L_132056398_55833020.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)
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:03HPYKGESRI0.91780.8824918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:02HPYKGESRI0.91390.9319918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:04HPYKGESRI0.91390.9319918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A74:09RLHPYKGESR0.98450.7498717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A74:03RLHPYKGESR0.98450.7498717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A74:11RLHPYKGESR0.98450.7498717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A31:02RLHPYKGESR0.96110.7428717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A31:06RLHPYKGESR0.90870.6698717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:03HPYKGESRIL0.84940.7601919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:04HPYKGESRIL0.72020.8434919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:02HPYKGESRIL0.72020.8434919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B27:05KRLHPYKGESR0.99990.6122617
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:12HPYKGESRI0.91390.9319918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B39:10HPYKGESRI0.41130.8489918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A31:01RLHPYKGESR0.98620.7123717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B39:10HPYKGESRIL0.77470.7376919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:12HPYKGESRIL0.72020.8434919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:13HPYKGESRI0.91430.8895918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:09HPYKGESRI0.91390.9319918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B67:01HPYKGESRI0.59930.6672918
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-A74:01RLHPYKGESR0.98450.7498717
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:13HPYKGESRIL0.86180.7726919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B67:01HPYKGESRIL0.75980.5706919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B35:09HPYKGESRIL0.72020.8434919
ACPP-NEDD4Lchr3132056398chr1855833020645HLA-B27:10KRLHPYKGESR0.99990.8017617

Top

Potential FusionNeoAntigen Information of ACPP-NEDD4L 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.
ACPP-NEDD4L_132056398_55833020.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)
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0305LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0305RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0340LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0340RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0340HPYKGESRILRVKVV924
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-0340KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1114LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1114RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1120LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1120RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1168LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1168RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1168HPYKGESRILRVKVV924
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1173RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1173LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1179LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1179RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1302LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1302RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1323LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1323RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1329LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1329RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1329HPYKGESRILRVKVV924
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1334LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1334RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1336LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1336RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1339LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1339RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1341LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1341RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1341HPYKGESRILRVKVV924
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1341KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1373LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1373RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1374LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1374RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1385LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1385RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1386LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1386RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1396LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1396RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1396HPYKGESRILRVKVV924
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1397LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1397RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1399LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1399RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1419LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1419RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1430LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1430RLHPYKGESRILRVK722
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1498LHPYKGESRILRVKV823
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1501QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1504QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1505QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1506QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1509QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1510QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1510FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1510EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1510KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1513QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1516QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1518QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1520QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1522QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1524QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1528QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1532QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1533QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1535QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1535FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1537QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1537FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1537EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1540QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1541QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1542QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1543QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1545QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1546QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB1-1549QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0103QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0106QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0106FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0106EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0106KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0106EEFQKRLHPYKGESR217
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0111QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0111FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0111EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0111KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0202QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0202FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0202EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0202KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0202EEFQKRLHPYKGESR217
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0203QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0203FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0203EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0203KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0204QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0204FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0204EFQKRLHPYKGESRI318
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0204KRLHPYKGESRILRV621
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0205QKRLHPYKGESRILR520
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0205FQKRLHPYKGESRIL419
ACPP-NEDD4Lchr3132056398chr1855833020645DRB5-0205EFQKRLHPYKGESRI318

Top

Fusion breakpoint peptide structures of ACPP-NEDD4L

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
4564KRLHPYKGESRILRACPPNEDD4Lchr3132056398chr1855833020645

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ACPP-NEDD4L

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-B14:023BVN4564KRLHPYKGESRILR-7.9962-8.1096
HLA-B14:023BVN4564KRLHPYKGESRILR-5.70842-6.74372
HLA-B52:013W394564KRLHPYKGESRILR-6.83737-6.95077
HLA-B52:013W394564KRLHPYKGESRILR-4.4836-5.5189
HLA-A11:014UQ24564KRLHPYKGESRILR-10.0067-10.1201
HLA-A11:014UQ24564KRLHPYKGESRILR-9.03915-10.0745
HLA-A24:025HGA4564KRLHPYKGESRILR-6.56204-6.67544
HLA-A24:025HGA4564KRLHPYKGESRILR-5.42271-6.45801
HLA-B44:053DX84564KRLHPYKGESRILR-7.85648-8.89178
HLA-B44:053DX84564KRLHPYKGESRILR-5.3978-5.5112
HLA-A02:016TDR4564KRLHPYKGESRILR-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of ACPP-NEDD4L

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
ACPP-NEDD4Lchr3132056398chr1855833020617KRLHPYKGESRAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGT
ACPP-NEDD4Lchr3132056398chr1855833020717RLHPYKGESRAGGCTGCACCCTTATAAGGGAGAGTCCCGT
ACPP-NEDD4Lchr3132056398chr1855833020918HPYKGESRICACCCTTATAAGGGAGAGTCCCGTATT
ACPP-NEDD4Lchr3132056398chr1855833020919HPYKGESRILCACCCTTATAAGGGAGAGTCCCGTATTCTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ACPP-NEDD4Lchr3132056398chr1855833020217EEFQKRLHPYKGESRGAGGAATTCCAGAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGT
ACPP-NEDD4Lchr3132056398chr1855833020318EFQKRLHPYKGESRIGAATTCCAGAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGTATT
ACPP-NEDD4Lchr3132056398chr1855833020419FQKRLHPYKGESRILTTCCAGAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGTATTCTC
ACPP-NEDD4Lchr3132056398chr1855833020520QKRLHPYKGESRILRCAGAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGTATTCTCAGA
ACPP-NEDD4Lchr3132056398chr1855833020621KRLHPYKGESRILRVAAGAGGCTGCACCCTTATAAGGGAGAGTCCCGTATTCTCAGAGTA
ACPP-NEDD4Lchr3132056398chr1855833020722RLHPYKGESRILRVKAGGCTGCACCCTTATAAGGGAGAGTCCCGTATTCTCAGAGTAAAA
ACPP-NEDD4Lchr3132056398chr1855833020823LHPYKGESRILRVKVCTGCACCCTTATAAGGGAGAGTCCCGTATTCTCAGAGTAAAAGTT
ACPP-NEDD4Lchr3132056398chr1855833020924HPYKGESRILRVKVVCACCCTTATAAGGGAGAGTCCCGTATTCTCAGAGTAAAAGTTGTT

Top

Information of the samples that have these potential fusion neoantigens of ACPP-NEDD4L

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
PRADACPP-NEDD4Lchr3132056398ENST00000336375chr1855833020ENST00000356462TCGA-HC-7210-01A

Top

Potential target of CAR-T therapy development for ACPP-NEDD4L

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

Top

Related Drugs to ACPP-NEDD4L

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to ACPP-NEDD4L

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