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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:DAPK1-GRIN2D

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DAPK1-GRIN2D
FusionPDB ID: 21349
FusionGDB2.0 ID: 21349
HgeneTgene
Gene symbol

DAPK1

GRIN2D

Gene ID

1612

2906

Gene namedeath associated protein kinase 1glutamate ionotropic receptor NMDA type subunit 2D
SynonymsDAPK|ROCO3EB11|EIEE46|GluN2D|NMDAR2D|NR2D
Cytomap

9q21.33

19q13.33

Type of geneprotein-codingprotein-coding
Descriptiondeath-associated protein kinase 1DAP kinase 1glutamate receptor ionotropic, NMDA 2DN-methyl D-aspartate receptor subtype 2DN-methyl-d-aspartate receptor subunit 2Destrogen receptor binding CpG islandglutamate [NMDA] receptor subunit epsilon-4glutamate receptor, ionotropic, N-methyl D-aspartate
Modification date2020031320200313
UniProtAcc

P53355

Main function of 5'-partner protein: FUNCTION: Calcium/calmodulin-dependent serine/threonine kinase involved in multiple cellular signaling pathways that trigger cell survival, apoptosis, and autophagy. Regulates both type I apoptotic and type II autophagic cell deaths signal, depending on the cellular setting. The former is caspase-dependent, while the latter is caspase-independent and is characterized by the accumulation of autophagic vesicles. Phosphorylates PIN1 resulting in inhibition of its catalytic activity, nuclear localization, and cellular function. Phosphorylates TPM1, enhancing stress fiber formation in endothelial cells. Phosphorylates STX1A and significantly decreases its binding to STXBP1. Phosphorylates PRKD1 and regulates JNK signaling by binding and activating PRKD1 under oxidative stress. Phosphorylates BECN1, reducing its interaction with BCL2 and BCL2L1 and promoting the induction of autophagy. Phosphorylates TSC2, disrupting the TSC1-TSC2 complex and stimulating mTORC1 activity in a growth factor-dependent pathway. Phosphorylates RPS6, MYL9 and DAPK3. Acts as a signaling amplifier of NMDA receptors at extrasynaptic sites for mediating brain damage in stroke. Cerebral ischemia recruits DAPK1 into the NMDA receptor complex and it phosphorylates GRINB at Ser-1303 inducing injurious Ca(2+) influx through NMDA receptor channels, resulting in an irreversible neuronal death. Required together with DAPK3 for phosphorylation of RPL13A upon interferon-gamma activation which is causing RPL13A involvement in transcript-selective translation inhibition.; FUNCTION: Isoform 2 cannot induce apoptosis but can induce membrane blebbing.

O15399

Main function of 5'-partner protein: FUNCTION: Component of NMDA receptor complexes that function as heterotetrameric, ligand-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Channel activation requires binding of the neurotransmitter glutamate to the epsilon subunit, glycine binding to the zeta subunit, plus membrane depolarization to eliminate channel inhibition by Mg(2+) (PubMed:9489750, PubMed:27616483, PubMed:26875626, PubMed:28126851). Sensitivity to glutamate and channel kinetics depend on the subunit composition (PubMed:9489750). {ECO:0000269|PubMed:26875626, ECO:0000269|PubMed:27616483, ECO:0000269|PubMed:28095420, ECO:0000269|PubMed:28126851, ECO:0000269|PubMed:9489750}.
Ensembl transtripts involved in fusion geneENST idsENST00000358077, ENST00000408954, 
ENST00000469640, ENST00000472284, 
ENST00000491893, ENST00000466188, 
ENST00000263269, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 13 X 5=9105 X 9 X 5=225
# samples 148
** MAII scorelog2(14/910*10)=-2.70043971814109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/225*10)=-1.49185309632967
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: DAPK1 [Title/Abstract] AND GRIN2D [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: DAPK1 [Title/Abstract] AND GRIN2D [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DAPK1(90296541)-GRIN2D(48922842), # samples:2
Anticipated loss of major functional domain due to fusion event.DAPK1-GRIN2D 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.
DAPK1-GRIN2D 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.
DAPK1-GRIN2D 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.
DAPK1-GRIN2D 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
HgeneDAPK1

GO:0006468

protein phosphorylation

10629061

HgeneDAPK1

GO:0017148

negative regulation of translation

18995835

HgeneDAPK1

GO:0035556

intracellular signal transduction

10629061

HgeneDAPK1

GO:0043280

positive regulation of cysteine-type endopeptidase activity involved in apoptotic process

16132846

HgeneDAPK1

GO:0046777

protein autophosphorylation

10629061|12730201

HgeneDAPK1

GO:0071346

cellular response to interferon-gamma

18995835

TgeneGRIN2D

GO:0097553

calcium ion transmembrane import into cytosol

26875626



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/chr9:90296541/chr19:48922842)
- 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 DAPK1 (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 GRIN2D (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)
ENST00000358077DAPK1chr990296541+ENST00000263269GRIN2Dchr1948922842+5551240718345561457
ENST00000472284DAPK1chr990296541+ENST00000263269GRIN2Dchr1948922842+5568242420045731457
ENST00000469640DAPK1chr990296541+ENST00000263269GRIN2Dchr1948922842+5743259937547481457
ENST00000408954DAPK1chr990296541+ENST00000263269GRIN2Dchr1948922842+5703255933547081457
ENST00000491893DAPK1chr990296541+ENST00000263269GRIN2Dchr1948922842+544122977344461457

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
ENST00000358077ENST00000263269DAPK1chr990296541+GRIN2Dchr1948922842+0.0037831090.99621683
ENST00000472284ENST00000263269DAPK1chr990296541+GRIN2Dchr1948922842+0.0039205270.9960795
ENST00000469640ENST00000263269DAPK1chr990296541+GRIN2Dchr1948922842+0.004290220.9957098
ENST00000408954ENST00000263269DAPK1chr990296541+GRIN2Dchr1948922842+0.0040965230.99590355
ENST00000491893ENST00000263269DAPK1chr990296541+GRIN2Dchr1948922842+0.0032441650.9967558

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 DAPK1-GRIN2D

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
DAPK1chr990296541GRIN2Dchr194892284222971032AEAAPPPAKPPPPPQPLPSPAYPAPR
DAPK1chr990296541GRIN2Dchr19489228422297739NSSRFPPSPLASKPTGPGGSTFTIGK
DAPK1chr990296541GRIN2Dchr194892284224071032AEAAPPPAKPPPPPQPLPSPAYPAPR
DAPK1chr990296541GRIN2Dchr19489228422407739NSSRFPPSPLASKPTGPGGSTFTIGK
DAPK1chr990296541GRIN2Dchr194892284224241032AEAAPPPAKPPPPPQPLPSPAYPAPR
DAPK1chr990296541GRIN2Dchr19489228422424739NSSRFPPSPLASKPTGPGGSTFTIGK
DAPK1chr990296541GRIN2Dchr194892284225591032AEAAPPPAKPPPPPQPLPSPAYPAPR
DAPK1chr990296541GRIN2Dchr19489228422559739NSSRFPPSPLASKPTGPGGSTFTIGK
DAPK1chr990296541GRIN2Dchr194892284225991032AEAAPPPAKPPPPPQPLPSPAYPAPR
DAPK1chr990296541GRIN2Dchr19489228422599739NSSRFPPSPLASKPTGPGGSTFTIGK

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Potential FusionNeoAntigen Information of DAPK1-GRIN2D 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.
DAPK1-GRIN2D_90296541_48922842.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)
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:10KPPPPPQPL0.99960.542817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B14:01KPPPPPQPL0.96080.9167817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B14:02KPPPPPQPL0.96080.9167817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:24KPPPPPQPL0.93480.5691817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:03KPPPPPQPL0.92840.8818817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:08KPPPPPQPL0.8910.7913817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:04KPPPPPQPL0.80660.9604817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:02KPPPPPQPL0.80660.9604817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:05KPPPPPQPL0.80490.7068817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:01KPPPPPQPL0.79530.9221817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B15:10KPPPPPQPL0.76160.6713817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B08:01KPPPPPQPL0.56290.506817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B08:09KPPPPPQPL0.48460.7295817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B81:01AKPPPPPQPL0.9510.5376717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B48:01AKPPPPPQPL0.93960.6581717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:10AKPPPPPQPL0.91070.6747717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:02AKPPPPPQPL0.8980.6292717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:03AKPPPPPQPL0.85340.8972717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:08PPQPLPSPAY0.79350.62131222
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:12KPPPPPQPL0.99710.5914817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B14:03KPPPPPQPL0.98290.9146817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:08KPPPPPQPL0.89740.9098817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:09KPPPPPQPL0.85890.7692817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:10KPPPPPQPL0.84890.9315817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:08KPPPPPQPL0.83560.8138817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:12KPPPPPQPL0.80660.9604817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:06KPPPPPQPL0.79750.9459817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B51:07KPPPPPQPL0.77190.8947817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B42:02KPPPPPQPL0.72680.5251817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B78:01KPPPPPQPL0.72630.5156817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:13KPPPPPQPL0.69790.9799817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:04KPPPPPQPL0.69790.9799817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:03KPPPPPQPL0.69190.985817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:30KPPPPPQPL0.68990.9568817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:13KPPPPPQPL0.67620.8951817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B42:01KPPPPPQPL0.65250.5167817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:17KPPPPPQPL0.59840.9436817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:14KPPPPPQPL0.58810.908817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:29KPPPPPQPL0.55170.9094817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:19KPPPPPQPL0.54810.8322817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:07KPPPPPQPL0.36370.8652817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:10KPPPPPQPL0.35160.8626817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:15KPPPPPQPL0.26430.9762817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:09AKPPPPPQPL0.99340.8661717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:17AKPPPPPQPL0.99180.9534717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:10AKPPPPPQPL0.99110.9613717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:30AKPPPPPQPL0.98370.969717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:13AKPPPPPQPL0.98360.9334717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:29AKPPPPPQPL0.97950.9321717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B56:04AKPPPPPQPL0.94840.5136717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:12AKPPPPPQPL0.93490.6903717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:04AKPPPPPQPL0.87520.6241717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B42:02AKPPPPPQPL0.87160.587717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B42:01AKPPPPPQPL0.84590.5788717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:13KPPPPPQPL0.99950.8637817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:05KPPPPPQPL0.97880.9374817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:17KPPPPPQPL0.97460.9569817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:67KPPPPPQPL0.96120.9824817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:04KPPPPPQPL0.95210.9885817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:03KPPPPPQPL0.95210.9885817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:13KPPPPPQPL0.92030.881817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:23KPPPPPQPL0.87220.8944817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:02KPPPPPQPL0.83630.9519817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B67:01KPPPPPQPL0.83510.8574817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:09KPPPPPQPL0.80660.9604817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:30KPPPPPQPL0.80610.8353817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:17KPPPPPQPL0.80610.8353817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:11KPPPPPQPL0.79980.9288817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C07:04KPPPPPQPL0.79560.926817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:04KPPPPPQPL0.77920.9334817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B78:02KPPPPPQPL0.77820.6349817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B39:11KPPPPPQPL0.76860.761817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C03:06KPPPPPQPL0.71550.9864817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:01KPPPPPQPL0.69190.985817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B08:12KPPPPPQPL0.62930.7122817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B08:18KPPPPPQPL0.56290.506817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:02KPPPPPQPL0.55250.9414817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B15:09KPPPPPQPL0.52680.7055817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:03KPPPPPQPL0.41850.9225817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C18:01KPPPPPQPL0.39890.8652817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:03KPPPPPQPL0.39030.8781817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C04:01KPPPPPQPL0.36370.8652817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:43KPPPPPQPL0.28220.908817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B15:08KPPPPPQPL0.27370.9011817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B15:11KPPPPPQPL0.26760.9223817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C08:02KPPPPPQPL0.26430.9762817
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:03AKPPPPPQPL0.98990.9525717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-C01:02AKPPPPPQPL0.98990.9518717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B67:01AKPPPPPQPL0.98720.9136717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:26AKPPPPPQPL0.98550.5441717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B56:02AKPPPPPQPL0.94840.5136717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:09AKPPPPPQPL0.91850.5942717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B07:22AKPPPPPQPL0.8980.6292717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B35:22AKPPPPPQPL0.87390.504717
DAPK1-GRIN2Dchr990296541chr19489228422407HLA-B15:11PPQPLPSPAY0.79370.65731222

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Potential FusionNeoAntigen Information of DAPK1-GRIN2D 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.

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)

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Fusion breakpoint peptide structures of DAPK1-GRIN2D

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
6488PAKPPPPPQPLPSPDAPK1GRIN2Dchr990296541chr19489228422407

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of DAPK1-GRIN2D

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-B14:023BVN6488PAKPPPPPQPLPSP-7.9962-8.1096
HLA-B14:023BVN6488PAKPPPPPQPLPSP-5.70842-6.74372
HLA-B52:013W396488PAKPPPPPQPLPSP-6.83737-6.95077
HLA-B52:013W396488PAKPPPPPQPLPSP-4.4836-5.5189
HLA-A11:014UQ26488PAKPPPPPQPLPSP-10.0067-10.1201
HLA-A11:014UQ26488PAKPPPPPQPLPSP-9.03915-10.0745
HLA-A24:025HGA6488PAKPPPPPQPLPSP-6.56204-6.67544
HLA-A24:025HGA6488PAKPPPPPQPLPSP-5.42271-6.45801
HLA-B44:053DX86488PAKPPPPPQPLPSP-7.85648-8.89178
HLA-B44:053DX86488PAKPPPPPQPLPSP-5.3978-5.5112
HLA-A02:016TDR6488PAKPPPPPQPLPSP-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of DAPK1-GRIN2D

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
DAPK1-GRIN2Dchr990296541chr19489228421222PPQPLPSPAYCAGGCCCTGGCGGTTCAACCTTCACCATTG
DAPK1-GRIN2Dchr990296541chr1948922842717AKPPPPPQPLTGGCTTCTAAGCCCACAGGCCCTGGCGGTT
DAPK1-GRIN2Dchr990296541chr1948922842817KPPPPPQPLCTTCTAAGCCCACAGGCCCTGGCGGTT

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

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Information of the samples that have these potential fusion neoantigens of DAPK1-GRIN2D

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
BRCADAPK1-GRIN2Dchr990296541ENST00000358077chr1948922842ENST00000263269TCGA-B6-A0I8-01A

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Potential target of CAR-T therapy development for DAPK1-GRIN2D

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
TgeneGRIN2Dchr9:90296541chr19:48922842ENST00000263269713658_67301337.0TransmembraneHelical
TgeneGRIN2Dchr9:90296541chr19:48922842ENST00000263269713845_86401337.0TransmembraneHelical

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 DAPK1-GRIN2D

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 DAPK1-GRIN2D

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