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Center for Computational Systems Medicine
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Kinase Fusion Gene Summary

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Kinase Fusion Gene Sample Information

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Kinase Fusion ORF Analysis

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Kinase Fusion Amino Acid Sequences

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Multiple Sequence Alignment of All Fusion Protein Isoforms

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Kinase Fusion Protein Functional Features

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Kinase Fusion Protein Structures

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Comparison of Fusion Protein Isoforms

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Comparison of Fusion Protein Sequences/Structures with Known Sequences/Structures from PDB

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pLDDT Scores and Difference Analysis of pLDDT Scores Between the Active Sites (Best) and Non-Active Sites.

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Ramachandran Plot of Kinase Fusion Protein Structure

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Potential Active Site Information

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Virtual Screening Results

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Kinase-Substrate Information

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Related Drugs with This Kinase Fusion Protein

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Related Disease with This Kinase Fusion Protein

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Clinical Trials of the Found Drugs/Small Molecules

Kinase Fusion Gene:MAP2K7_MAP2K7

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: MAP2K7_MAP2K7
KinaseFusionDB ID: KFG3337
FusionGDB2.0 ID: KFG3337
HgeneTgene
Gene symbol

MAP2K7

MAP2K7

Gene ID

5609

5609

Gene namemitogen-activated protein kinase kinase 7mitogen-activated protein kinase kinase 7
SynonymsJNKK2|MAPKK7|MEK|MEK 7|MKK7|PRKMK7|SAPKK-4|SAPKK4JNKK2|MAPKK7|MEK|MEK 7|MKK7|PRKMK7|SAPKK-4|SAPKK4
Cytomap

19p13.2

19p13.2

Type of geneprotein-codingprotein-coding
Descriptiondual specificity mitogen-activated protein kinase kinase 7JNK-activating kinase 2MAP kinase kinase 7MAPK/ERK kinase 7SAPK kinase 4c-Jun N-terminal kinase kinase 2stress-activated protein kinase kinase 4dual specificity mitogen-activated protein kinase kinase 7JNK-activating kinase 2MAP kinase kinase 7MAPK/ERK kinase 7SAPK kinase 4c-Jun N-terminal kinase kinase 2stress-activated protein kinase kinase 4
Modification date2024041620240416
UniProtAcc

O14733

O14733

Ensembl transtripts involved in fusion geneENST idsENST00000397979, ENST00000397981, 
ENST00000397983, ENST00000545011, 
ENST00000397979, ENST00000397981, 
ENST00000397983, ENST00000545011, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: MAP2K7 [Title/Abstract] AND MAP2K7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAP2K7(7978422)-MAP2K7(7979080), # samples:1
MAP2K7(7974313)-MAP2K7(7969905), # samples:1
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneMAP2K7

GO:0006970

response to osmotic stress

9535930

HgeneMAP2K7

GO:0009408

response to heat

9535930

HgeneMAP2K7

GO:0009411

response to UV

9535930

HgeneMAP2K7

GO:0034612

response to tumor necrosis factor

9535930

HgeneMAP2K7

GO:0051403

stress-activated MAPK cascade

9535930

TgeneMAP2K7

GO:0006970

response to osmotic stress

9535930

TgeneMAP2K7

GO:0009408

response to heat

9535930

TgeneMAP2K7

GO:0009411

response to UV

9535930

TgeneMAP2K7

GO:0034612

response to tumor necrosis factor

9535930

TgeneMAP2K7

GO:0051403

stress-activated MAPK cascade

9535930


check buttonKinase Fusion gene breakpoints across MAP2K7 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonKinase Fusion gene breakpoints across MAP2K7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.


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Kinase Fusion Gene Sample Information

check buttonKinase Fusion gene information.
check button Kinase Fusion gene information from four resources (ChiTars 5.0, ChimerDB 4.0, COSMIC, and CCLE)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceSampleHgeneHchrHbpTgeneTchrTbp
ChiTaRS5.0AW072158MAP2K7chr19

7978422

MAP2K7chr19

7979080

ChiTaRS5.0DA497564MAP2K7chr19

7974313

MAP2K7chr19

7969905



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Kinase Fusion ORF Analysis


check buttonKinase Fusion information from ORFfinder translation from full-length transcript sequence from KinaseFusionDB.
HenstTenstHgeneHchrHbpTgeneTchrTbpSeq length
(transcript)
Seq length
(amino acids)

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Kinase Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from KinaseFusionDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>Henst_Tenst_Hgene_Hchr_Hbp_Tgene_Tchr_Tbp_length(fusion AA)_AAseq

Multiple Sequence Alignment of All Fusion Protein Isoforms



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Kinase Fusion Protein Functional Features


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/:7978422/:7979080)
- 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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MAP2K7

O14733

MAP2K7

O14733

FUNCTION: Dual specificity protein kinase which acts as an essential component of the MAP kinase signal transduction pathway. Essential component of the stress-activated protein kinase/c-Jun N-terminal kinase (SAP/JNK) signaling pathway. With MAP2K4/MKK4, is the one of the only known kinase to directly activate the stress-activated protein kinase/c-Jun N-terminal kinases MAPK8/JNK1, MAPK9/JNK2 and MAPK10/JNK3. MAP2K4/MKK4 and MAP2K7/MKK7 both activate the JNKs by phosphorylation, but they differ in their preference for the phosphorylation site in the Thr-Pro-Tyr motif. MAP2K4/MKK4 shows preference for phosphorylation of the Tyr residue and MAP2K7/MKK7 for the Thr residue. The monophosphorylation of JNKs on the Thr residue is sufficient to increase JNK activity indicating that MAP2K7/MKK7 is important to trigger JNK activity, while the additional phosphorylation of the Tyr residue by MAP2K4/MKK4 ensures optimal JNK activation. Has a specific role in JNK signal transduction pathway activated by pro-inflammatory cytokines. The MKK/JNK signaling pathway is also involved in mitochondrial death signaling pathway, including the release cytochrome c, leading to apoptosis. Part of a non-canonical MAPK signaling pathway, composed of the upstream MAP3K12 kinase and downstream MAP kinases MAPK1/ERK2 and MAPK3/ERK1, that enhances the AP-1-mediated transcription of APP in response to APOE (PubMed:28111074). {ECO:0000269|PubMed:28111074, ECO:0000269|PubMed:9312068, ECO:0000269|PubMed:9372971, ECO:0000269|PubMed:9535930, ECO:0000269|Ref.5}.FUNCTION: Dual specificity protein kinase which acts as an essential component of the MAP kinase signal transduction pathway. Essential component of the stress-activated protein kinase/c-Jun N-terminal kinase (SAP/JNK) signaling pathway. With MAP2K4/MKK4, is the one of the only known kinase to directly activate the stress-activated protein kinase/c-Jun N-terminal kinases MAPK8/JNK1, MAPK9/JNK2 and MAPK10/JNK3. MAP2K4/MKK4 and MAP2K7/MKK7 both activate the JNKs by phosphorylation, but they differ in their preference for the phosphorylation site in the Thr-Pro-Tyr motif. MAP2K4/MKK4 shows preference for phosphorylation of the Tyr residue and MAP2K7/MKK7 for the Thr residue. The monophosphorylation of JNKs on the Thr residue is sufficient to increase JNK activity indicating that MAP2K7/MKK7 is important to trigger JNK activity, while the additional phosphorylation of the Tyr residue by MAP2K4/MKK4 ensures optimal JNK activation. Has a specific role in JNK signal transduction pathway activated by pro-inflammatory cytokines. The MKK/JNK signaling pathway is also involved in mitochondrial death signaling pathway, including the release cytochrome c, leading to apoptosis. Part of a non-canonical MAPK signaling pathway, composed of the upstream MAP3K12 kinase and downstream MAP kinases MAPK1/ERK2 and MAPK3/ERK1, that enhances the AP-1-mediated transcription of APP in response to APOE (PubMed:28111074). {ECO:0000269|PubMed:28111074, ECO:0000269|PubMed:9312068, ECO:0000269|PubMed:9372971, ECO:0000269|PubMed:9535930, ECO:0000269|Ref.5}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.

check button - Retained domain in the 5'-partner of fusion protein (protein functional feature from UniProt).
PartnerHgeneeneHbpTgeneeneTbpENSTBPexonTotalExonProtein feature lociBPlociTotalLenFeatureNote


check button - Retained domain in the 3'-partner of fusion protein (protein functional feature from UniProt).
PartnerHgeneeneHbpTgeneeneTbpENSTBPexonTotalExonProtein feature lociBPlociTotalLenFeatureNote


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Kinase-Substrate Information of MAP2K7_MAP2K7


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
MAP2K7O14733humanMAPK10P53779-2T221AGTSFMMtPyVVTRYPkinase
MAP2K7O14733humanMAPK9P45984T183ACtNFMMtPyVVtRYPkinase
MAP2K7O14733humanMAPK8P45983Y185tsFMMtPyVVtRYYRPkinase
MAP2K7O14733humanMAPK9P45984S407STEQtLAsDTDSSLD
MAP2K7O14733humanMAPK8P45983T183AGtsFMMtPyVVtRYPkinase
MAP2K7O14733humanFADDQ13158S194QNRsGAMsPMsWNsD
MAP2K7O14733humanMAPK9P45984T404SSMSTEQtLAsDTDS
MAP2K7O14733humanMAPK8P45983-2T183AGTSFMMtPyVVTRYPkinase
MAP2K7O14733humanMAPK10P53779T221AGtsFMMtPyVVtRYPkinase


check button Biological Network Integration of This Kinase and Substrates
(GeneMANIA website)

check button Enriched GO biological processes of the phosphorylation target genes of the kinase
KinaseGOIDGO termP.adjust
MAP2K7IDDescription0.00e+00
MAP2K7GO:0038095Fc-epsilon receptor signaling pathway2.57e-06
MAP2K7GO:0038093Fc receptor signaling pathway1.55e-05
MAP2K7GO:0090398cellular senescence6.69e-05
MAP2K7GO:0042752regulation of circadian rhythm6.69e-05
MAP2K7GO:0007254JNK cascade1.57e-04
MAP2K7GO:0007623circadian rhythm2.58e-04
MAP2K7GO:0051403stress-activated MAPK cascade3.07e-04
MAP2K7GO:0031098stress-activated protein kinase signaling cascade3.07e-04
MAP2K7GO:0048511rhythmic process5.25e-04
MAP2K7GO:0071276cellular response to cadmium ion6.86e-04
MAP2K7GO:0002768immune response-regulating cell surface receptor signaling pathway6.86e-04
MAP2K7GO:0046686response to cadmium ion1.50e-03
MAP2K7GO:0002764immune response-regulating signaling pathway1.75e-03
MAP2K7GO:0071260cellular response to mechanical stimulus1.92e-03
MAP2K7GO:0031343positive regulation of cell killing1.99e-03
MAP2K7GO:0031341regulation of cell killing3.99e-03
MAP2K7GO:2001235positive regulation of apoptotic signaling pathway6.41e-03
MAP2K7GO:0034614cellular response to reactive oxygen species6.83e-03
MAP2K7GO:0031334positive regulation of protein-containing complex assembly1.03e-02
MAP2K7GO:0071248cellular response to metal ion1.03e-02
MAP2K7GO:0000302response to reactive oxygen species1.04e-02
MAP2K7GO:0009612response to mechanical stimulus1.07e-02
MAP2K7GO:0001906cell killing1.12e-02
MAP2K7GO:0071241cellular response to inorganic substance1.13e-02
MAP2K7GO:0034599cellular response to oxidative stress1.34e-02
MAP2K7GO:0018105peptidyl-serine phosphorylation1.72e-02
MAP2K7GO:0018209peptidyl-serine modification1.79e-02
MAP2K7GO:0062197cellular response to chemical stress1.79e-02
MAP2K7GO:0009416response to light stimulus1.79e-02
MAP2K7GO:0071214cellular response to abiotic stimulus1.84e-02
MAP2K7GO:0104004cellular response to environmental stimulus1.84e-02
MAP2K7GO:0045089positive regulation of innate immune response1.84e-02
MAP2K7GO:0071496cellular response to external stimulus1.84e-02
MAP2K7GO:0045862positive regulation of proteolysis1.84e-02
MAP2K7GO:0010038response to metal ion1.84e-02
MAP2K7GO:0071803positive regulation of podosome assembly1.84e-02
MAP2K7GO:0002833positive regulation of response to biotic stimulus1.89e-02
MAP2K7GO:1901030positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway1.95e-02
MAP2K7GO:2001233regulation of apoptotic signaling pathway1.95e-02
MAP2K7GO:0006979response to oxidative stress1.95e-02
MAP2K7GO:0036462TRAIL-activated apoptotic signaling pathway1.95e-02
MAP2K7GO:0071801regulation of podosome assembly1.95e-02
MAP2K7GO:0072683T cell extravasation1.95e-02
MAP2K7GO:0043254regulation of protein-containing complex assembly1.95e-02
MAP2K7GO:0045088regulation of innate immune response1.95e-02
MAP2K7GO:0048148behavioral response to cocaine1.95e-02
MAP2K7GO:0097202activation of cysteine-type endopeptidase activity1.95e-02
MAP2K7GO:0009314response to radiation1.95e-02
MAP2K7GO:0045651positive regulation of macrophage differentiation2.16e-02

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Related Drugs to MAP2K7_MAP2K7


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

check button Distribution of the number of studies mentioning MAP2K7-MAP2K7 and kinase inhibitors the PubMed Abstract (04-01-2024)

Fusion gene - drug pair 1Fusion gene - drug pair 2PMIDPublication dateDOIStudy title

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Related Diseases to MAP2K7_MAP2K7


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Related diseases from the literature mentioned this fusion gene and drug.
(PubMed, 04-01-2024)
MeSH IDMeSH term

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource


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Clinical Trials of the Found Drugs/Small Molecules


check button Statistics of the Clinical Trials of the Found Kinase Inibitors from clinicaltrials.gov (06-17-2024)

check button Clinical Trials from clinicaltrials.gov (06-17-2024)

Fusion GeneKinase InhibitorNCT IDStudy StatusPhasesDisease# EnrolmentDate