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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:MAP2K2-PSMD9

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MAP2K2-PSMD9
FusionPDB ID: 51191
FusionGDB2.0 ID: 51191
HgeneTgene
Gene symbol

MAP2K2

PSMD9

Gene ID

5605

5715

Gene namemitogen-activated protein kinase kinase 2proteasome 26S subunit, non-ATPase 9
SynonymsCFC4|MAPKK2|MEK2|MKK2|PRKMK2Rpn4|p27
Cytomap

19p13.3

12q24.31

Type of geneprotein-codingprotein-coding
Descriptiondual specificity mitogen-activated protein kinase kinase 2ERK activator kinase 2MAP kinase kinase 2MAPK/ERK kinase 2mitogen-activated protein kinase kinase 2, p4526S proteasome non-ATPase regulatory subunit 926S proteasome regulatory subunit p27homolog of rat Bridge 1proteasome (prosome, macropain) 26S subunit, non-ATPase, 9proteasome 26S non-ATPase regulatory subunit 9
Modification date2020032720200314
UniProtAcc

P36507

Main function of 5'-partner protein: FUNCTION: Catalyzes the concomitant phosphorylation of a threonine and a tyrosine residue in a Thr-Glu-Tyr sequence located in MAP kinases. Activates the ERK1 and ERK2 MAP kinases (By similarity). Activates BRAF in a KSR1 or KSR2-dependent manner; by binding to KSR1 or KSR2 releases the inhibitory intramolecular interaction between KSR1 or KSR2 protein kinase and N-terminal domains which promotes KSR1 or KSR2-BRAF dimerization and BRAF activation (PubMed:29433126). {ECO:0000250|UniProtKB:Q63932, ECO:0000269|PubMed:29433126}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000262948, ENST00000394867, 
ENST00000599345, 
ENST00000261817, 
ENST00000340175, ENST00000542602, 
ENST00000541212, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 6 X 6=3603 X 4 X 3=36
# samples 105
** MAII scorelog2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/36*10)=0.473931188332412
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: MAP2K2 [Title/Abstract] AND PSMD9 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MAP2K2 [Title/Abstract] AND PSMD9 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAP2K2(4110507)-PSMD9(122353762), # samples:2
Anticipated loss of major functional domain due to fusion event.MAP2K2-PSMD9 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.
MAP2K2-PSMD9 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.
MAP2K2-PSMD9 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
MAP2K2-PSMD9 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
MAP2K2-PSMD9 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
MAP2K2-PSMD9 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene 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
HgeneMAP2K2

GO:0036289

peptidyl-serine autophosphorylation

8388392

HgeneMAP2K2

GO:0071902

positive regulation of protein serine/threonine kinase activity

8388392



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/chr19:4110507/chr12:122353762)
- 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 MAP2K2 (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 PSMD9 (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)
ENST00000262948MAP2K2chr194110507-ENST00000541212PSMD9chr12122353762+2807704254820188

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
ENST00000262948ENST00000541212MAP2K2chr194110507-PSMD9chr12122353762+0.0051750540.994825

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 MAP2K2-PSMD9

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MAP2K2chr194110507PSMD9chr12122353762704150YSDGEISICMEHMKPLNVTVIRRGEK

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Potential FusionNeoAntigen Information of MAP2K2-PSMD9 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.
MAP2K2-PSMD9_4110507_122353762.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)
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:06EHMKPLNV0.99970.69251018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B14:01EHMKPLNV0.99960.53971018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B14:02EHMKPLNV0.99960.53971018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:01EHMKPLNV0.99930.84091018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:02EHMKPLNV0.99930.90821018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:10EHMKPLNV0.99660.52821018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:37EHMKPLNV0.98640.50591018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B45:01MEHMKPLNV0.99860.7619918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:22HMKPLNVTV0.99690.5911120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:13HMKPLNVTV0.99620.72331120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:06EHMKPLNVT0.99270.77481019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:27HMKPLNVTV0.99090.56231120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A30:08HMKPLNVTV0.99070.80711120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:01EHMKPLNVT0.98810.91861019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:38HMKPLNVTV0.98470.72991120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:11HMKPLNVTV0.97390.56011120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:30HMKPLNVTV0.97320.52911120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:67HMKPLNVTV0.97320.52911120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:24HMKPLNVTV0.97320.52911120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:60HMKPLNVTV0.97230.54281120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:04HMKPLNVTV0.97160.69351120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:17HMKPLNVTV0.96820.60061120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:16HMKPLNVTV0.96680.54651120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B08:09HMKPLNVTV0.96530.72371120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B08:01HMKPLNVTV0.96520.73431120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:21HMKPLNVTV0.9630.6661120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B08:09MEHMKPLNV0.95750.732918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:35HMKPLNVTV0.95730.53361120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:10EHMKPLNVT0.93330.56231019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B41:01MEHMKPLNV0.92230.8977918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:29HMKPLNVTV0.88720.52731120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:20HMKPLNVTV0.8620.53591120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:37EHMKPLNVT0.67730.55661019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B50:01MEHMKPLNV0.60580.7019918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:13MEHMKPLNV0.34230.8367918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B48:01HMKPLNVTV0.31730.54661120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B13:02HMKPLNVTV0.27230.57431120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B13:01HMKPLNVTV0.18360.96171120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B52:01HMKPLNVTV0.16680.96871120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B52:01MEHMKPLNV0.16370.7934918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:06EHMKPLNVTV0.99850.79941020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:01EHMKPLNVTV0.99780.94731020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:01EHMKPLNVTV0.99710.96391020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:02EHMKPLNVTV0.99640.9771020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:10EHMKPLNVTV0.97920.60731020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:37EHMKPLNVTV0.9170.6341020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:01EHMKPLNVTVI0.99740.94451021
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:02EHMKPLNVTVI0.99730.95641021
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A31:02HMKPLNVTVIR0.9790.51581122
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:05EHMKPLNV0.99910.81531018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:12EHMKPLNV0.9990.84381018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B14:03EHMKPLNV0.84780.85311018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B40:06MEHMKPLNV0.99970.518918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-C12:04HMKPLNVTV0.99970.98631120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-C06:03HMKPLNVTV0.99970.9891120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:05HMKPLNVTV0.9970.57331120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:09EHMKPLNVT0.98640.75051019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:12EHMKPLNVT0.98450.92041019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:05EHMKPLNVT0.98150.9021019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:04HMKPLNVTV0.97330.90361120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:01HMKPLNVTV0.97320.52911120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B73:01EHMKPLNVT0.26280.69321019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B51:07HMKPLNVTV0.15940.95531120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B51:07MEHMKPLNV0.10060.6995918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:09EHMKPLNVTV0.99750.81531020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:12EHMKPLNVTV0.99750.94911020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:05EHMKPLNVTV0.99610.93961020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:31EHMKPLNV0.99940.83761018
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:03HMKPLNVTV0.9990.67231120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B40:04MEHMKPLNV0.99690.6718918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A30:01HMKPLNVTV0.99040.91761120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:31EHMKPLNVT0.98740.91661019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:73HMKPLNVTV0.97020.94021120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B08:18HMKPLNVTV0.96520.73431120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:14HMKPLNVTV0.96460.61471120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A02:06HMKPLNVTV0.9630.6661120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:30HMKPLNVTV0.9070.84091120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B41:03MEHMKPLNV0.90010.6744918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B08:12HMKPLNVTV0.85880.86571120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B18:03MEHMKPLNV0.83610.658918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-A32:01HMKPLNVTV0.78610.93221120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:11EHMKPLNVT0.71360.92261019
MAP2K2-PSMD9chr194110507chr12122353762704HLA-C07:04HMKPLNVTV0.62290.9331120
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B50:05MEHMKPLNV0.60580.7019918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B50:04MEHMKPLNV0.60580.7019918
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:31EHMKPLNVTV0.9980.94661020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:05EHMKPLNVTV0.99710.96391020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B15:09EHMKPLNVTV0.98730.58551020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B39:11EHMKPLNVTV0.87570.93281020
MAP2K2-PSMD9chr194110507chr12122353762704HLA-B38:05EHMKPLNVTVI0.99740.94451021

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Potential FusionNeoAntigen Information of MAP2K2-PSMD9 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 MAP2K2-PSMD9

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
8636SICMEHMKPLNVTVMAP2K2PSMD9chr194110507chr12122353762704

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MAP2K2-PSMD9

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-B14:023BVN8636SICMEHMKPLNVTV-6.15779-7.19309
HLA-B14:023BVN8636SICMEHMKPLNVTV-5.42154-5.53494
HLA-B52:013W398636SICMEHMKPLNVTV-6.31003-7.34533
HLA-B52:013W398636SICMEHMKPLNVTV-5.72549-5.83889
HLA-A11:014UQ28636SICMEHMKPLNVTV-10.3617-10.4751
HLA-A11:014UQ28636SICMEHMKPLNVTV-6.62574-7.66104
HLA-A24:025HGA8636SICMEHMKPLNVTV-7.32817-7.44157
HLA-A24:025HGA8636SICMEHMKPLNVTV-5.51285-6.54815
HLA-B44:053DX88636SICMEHMKPLNVTV-6.27581-7.31111
HLA-B44:053DX88636SICMEHMKPLNVTV-5.0724-5.1858
HLA-A02:016TDR8636SICMEHMKPLNVTV-2.75053-2.86393

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Vaccine Design for the FusionNeoAntigens of MAP2K2-PSMD9

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
MAP2K2-PSMD9chr194110507chr121223537621018EHMKPLNVGAACACATGAAGCCCCTGAATGTG
MAP2K2-PSMD9chr194110507chr121223537621019EHMKPLNVTGAACACATGAAGCCCCTGAATGTGACA
MAP2K2-PSMD9chr194110507chr121223537621020EHMKPLNVTVGAACACATGAAGCCCCTGAATGTGACAGTG
MAP2K2-PSMD9chr194110507chr121223537621021EHMKPLNVTVIGAACACATGAAGCCCCTGAATGTGACAGTGATC
MAP2K2-PSMD9chr194110507chr121223537621120HMKPLNVTVCACATGAAGCCCCTGAATGTGACAGTG
MAP2K2-PSMD9chr194110507chr121223537621122HMKPLNVTVIRCACATGAAGCCCCTGAATGTGACAGTGATCCGC
MAP2K2-PSMD9chr194110507chr12122353762918MEHMKPLNVATGGAACACATGAAGCCCCTGAATGTG

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 MAP2K2-PSMD9

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
HNSCMAP2K2-PSMD9chr194110507ENST00000262948chr12122353762ENST00000541212TCGA-BA-A4IG-01A

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Potential target of CAR-T therapy development for MAP2K2-PSMD9

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 MAP2K2-PSMD9

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 MAP2K2-PSMD9

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