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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:MAP4K5-NIN

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MAP4K5-NIN
FusionPDB ID: 51424
FusionGDB2.0 ID: 51424
HgeneTgene
Gene symbol

MAP4K5

NIN

Gene ID

11183

51199

Gene namemitogen-activated protein kinase kinase kinase kinase 5ninein
SynonymsGCKR|KHS|KHS1|MAPKKKK5SCKL7
Cytomap

14q22.1

14q22.1

Type of geneprotein-codingprotein-coding
Descriptionmitogen-activated protein kinase kinase kinase kinase 5MAPK/ERK kinase kinase kinase 5MEK kinase kinase 5MEKKK 5germinal center kinase-relatedkinase homologous to SPS1/STE20nineinglycogen synthase kinase 3 beta-interacting proteinhNineinninein (GSK3B interacting protein)ninein centrosomal protein
Modification date2020031320200328
UniProtAcc

Q9Y4K4

Main function of 5'-partner protein: FUNCTION: May play a role in the response to environmental stress. Appears to act upstream of the JUN N-terminal pathway. {ECO:0000269|PubMed:9038372}.

Q9Y2I6

Main function of 5'-partner protein: FUNCTION: Involved in the microtubule organization in interphase cells. Overexpression induces the fragmentation of the Golgi, and causes lysosomes to disperse toward the cell periphery; it also interferes with mitotic spindle assembly. May play a role in ovarian carcinogenesis. {ECO:0000269|PubMed:12852856, ECO:0000269|PubMed:16254247, ECO:0000269|PubMed:18538832}.
Ensembl transtripts involved in fusion geneENST idsENST00000013125, ENST00000557578, 
ENST00000486200, ENST00000245441, 
ENST00000324330, ENST00000382041, 
ENST00000382043, ENST00000389868, 
ENST00000453196, ENST00000530997, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score21 X 18 X 10=37807 X 9 X 4=252
# samples 2710
** MAII scorelog2(27/3780*10)=-3.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/252*10)=-1.33342373372519
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: MAP4K5 [Title/Abstract] AND NIN [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MAP4K5 [Title/Abstract] AND NIN [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NIN(51277460)-MAP4K5(50886555), # samples:1
MAP4K5(50971518)-NIN(51205004), # samples:3
Anticipated loss of major functional domain due to fusion event.MAP4K5-NIN 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.
MAP4K5-NIN 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.
MAP4K5-NIN seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MAP4K5-NIN seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
MAP4K5-NIN seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
MAP4K5-NIN seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
MAP4K5-NIN seems lost the major protein functional domain in Tgene partner, which is a essential 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
HgeneMAP4K5

GO:0006468

protein phosphorylation

9038372

HgeneMAP4K5

GO:0035556

intracellular signal transduction

9038372



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/chr14:51277460/chr14:50886555)
- 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 MAP4K5 (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 NIN (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)
ENST00000013125MAP4K5chr1450971518-ENST00000245441NINchr1451205004-49594854821258258
ENST00000013125MAP4K5chr1450971518-ENST00000389868NINchr1451205004-50204857951319174
ENST00000013125MAP4K5chr1450971518-ENST00000530997NINchr1451205004-32254854821258258
ENST00000013125MAP4K5chr1450971518-ENST00000382043NINchr1451205004-11754854821129215
ENST00000013125MAP4K5chr1450971518-ENST00000382041NINchr1451205004-11624854821129215
ENST00000013125MAP4K5chr1450971518-ENST00000324330NINchr1451205004-11914857951190131
ENST00000013125MAP4K5chr1450971518-ENST00000453196NINchr1451205004-1451485482997171
ENST00000013125MAP4K5chr1450971518-ENST00000245441NINchr1451210247-54004854821699405
ENST00000013125MAP4K5chr1450971518-ENST00000389868NINchr1451210247-54614854821267261
ENST00000013125MAP4K5chr1450971518-ENST00000530997NINchr1451210247-36664854821699405
ENST00000013125MAP4K5chr1450971518-ENST00000382043NINchr1451210247-16164854821570362
ENST00000013125MAP4K5chr1450971518-ENST00000382041NINchr1451210247-16034854821570362
ENST00000013125MAP4K5chr1450971518-ENST00000324330NINchr1451210247-16324854821267261
ENST00000013125MAP4K5chr1450971518-ENST00000453196NINchr1451210247-18924854821438318
ENST00000013125MAP4K5chr1450971517-ENST00000245441NINchr1451205004-49594854821258258
ENST00000013125MAP4K5chr1450971517-ENST00000389868NINchr1451205004-50204857951319174
ENST00000013125MAP4K5chr1450971517-ENST00000530997NINchr1451205004-32254854821258258
ENST00000013125MAP4K5chr1450971517-ENST00000382043NINchr1451205004-11754854821129215
ENST00000013125MAP4K5chr1450971517-ENST00000382041NINchr1451205004-11624854821129215
ENST00000013125MAP4K5chr1450971517-ENST00000324330NINchr1451205004-11914857951190131
ENST00000013125MAP4K5chr1450971517-ENST00000453196NINchr1451205004-1451485482997171

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
ENST00000013125ENST00000245441MAP4K5chr1450971518-NINchr1451205004-0.0005188120.99948126
ENST00000013125ENST00000389868MAP4K5chr1450971518-NINchr1451205004-0.0025148220.99748516
ENST00000013125ENST00000530997MAP4K5chr1450971518-NINchr1451205004-0.0006659540.99933404
ENST00000013125ENST00000382043MAP4K5chr1450971518-NINchr1451205004-0.0083297180.99167025
ENST00000013125ENST00000382041MAP4K5chr1450971518-NINchr1451205004-0.0079469090.99205303
ENST00000013125ENST00000324330MAP4K5chr1450971518-NINchr1451205004-0.034986330.9650137
ENST00000013125ENST00000453196MAP4K5chr1450971518-NINchr1451205004-0.0071371540.9928629
ENST00000013125ENST00000245441MAP4K5chr1450971518-NINchr1451210247-0.0002571030.9997429
ENST00000013125ENST00000389868MAP4K5chr1450971518-NINchr1451210247-0.00074640.9992536
ENST00000013125ENST00000530997MAP4K5chr1450971518-NINchr1451210247-0.0007061070.9992939
ENST00000013125ENST00000382043MAP4K5chr1450971518-NINchr1451210247-0.010414810.9895852
ENST00000013125ENST00000382041MAP4K5chr1450971518-NINchr1451210247-0.0108363140.98916376
ENST00000013125ENST00000324330MAP4K5chr1450971518-NINchr1451210247-0.0070501390.99294984
ENST00000013125ENST00000453196MAP4K5chr1450971518-NINchr1451210247-0.0043498190.99565023
ENST00000013125ENST00000245441MAP4K5chr1450971517-NINchr1451205004-0.0005188120.99948126
ENST00000013125ENST00000389868MAP4K5chr1450971517-NINchr1451205004-0.0025148220.99748516
ENST00000013125ENST00000530997MAP4K5chr1450971517-NINchr1451205004-0.0006659540.99933404
ENST00000013125ENST00000382043MAP4K5chr1450971517-NINchr1451205004-0.0083297180.99167025
ENST00000013125ENST00000382041MAP4K5chr1450971517-NINchr1451205004-0.0079469090.99205303
ENST00000013125ENST00000324330MAP4K5chr1450971517-NINchr1451205004-0.034986330.9650137
ENST00000013125ENST00000453196MAP4K5chr1450971517-NINchr1451205004-0.0071371540.9928629

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 MAP4K5-NIN

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

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Potential FusionNeoAntigen Information of MAP4K5-NIN 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.

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)

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Potential FusionNeoAntigen Information of MAP4K5-NIN 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 MAP4K5-NIN

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.

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MAP4K5-NIN

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

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Vaccine Design for the FusionNeoAntigens of MAP4K5-NIN

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

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 MAP4K5-NIN

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

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Potential target of CAR-T therapy development for MAP4K5-NIN

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 MAP4K5-NIN

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 MAP4K5-NIN

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
TgeneNINC3553870SECKEL SYNDROME 72GENOMICS_ENGLAND;ORPHANET;UNIPROT