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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:TAOK1_EFCAB5

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: TAOK1_EFCAB5
KinaseFusionDB ID: KFG6370
FusionGDB2.0 ID: KFG6370
HgeneTgene
Gene symbol

TAOK1

EFCAB5

Gene ID

57551

374786

Gene nameTAO kinase 1EF-hand calcium binding domain 5
SynonymsDDIB|KFC-B|MAP3K16|MARKK|PSK-2|PSK2|TAO1|hKFC-B|hTAOK1-
Cytomap

17q11.2

17q11.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase TAO1MARK KinaseSTE20-like kinase PSK2kinase from chicken homolog Bmicrotubule affinity regulating kinase kinaseprostate-derived STE20-like kinase 2prostate-derived sterile 20-like kinase 2serine/threonine protein kinEF-hand calcium-binding domain-containing protein 5
Modification date2024040720240403
UniProtAcc

Q7L7X3

A4FU69

Ensembl transtripts involved in fusion geneENST idsENST00000261716, ENST00000536202, 
ENST00000320856, ENST00000378738, 
ENST00000394832, ENST00000394835, 
ENST00000534836, ENST00000536908, 
ENST00000541045, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: TAOK1 [Title/Abstract] AND EFCAB5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TAOK1(27844674)-EFCAB5(28418889), # samples:2
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneTAOK1

GO:0006974

DNA damage response

17396146

HgeneTAOK1

GO:0016310

phosphorylation

12639963

HgeneTAOK1

GO:0046330

positive regulation of JNK cascade

16407310

HgeneTAOK1

GO:0097194

execution phase of apoptosis

16407310


check buttonKinase Fusion gene breakpoints across TAOK1 (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 EFCAB5 (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
ChimerDB4TCGA-AR-A0TY-01ATAOK1chr17

27844674

EFCAB5chr17

28418889

ChimerDB4TCGA-AR-A0TY-01ATAOK1chr17

27844674

EFCAB5chr17

28434852

ChimerDB4TCGA-AR-A0TYTAOK1chr17

27844674

EFCAB5chr17

28434851



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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/:27844674/:28418889)
- 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
TAOK1

Q7L7X3

EFCAB5

A4FU69

FUNCTION: Serine/threonine-protein kinase involved in various processes such as p38/MAPK14 stress-activated MAPK cascade, DNA damage response and regulation of cytoskeleton stability. Phosphorylates MAP2K3, MAP2K6 and MARK2. Acts as an activator of the p38/MAPK14 stress-activated MAPK cascade by mediating phosphorylation and subsequent activation of the upstream MAP2K3 and MAP2K6 kinases. Involved in G-protein coupled receptor signaling to p38/MAPK14. In response to DNA damage, involved in the G2/M transition DNA damage checkpoint by activating the p38/MAPK14 stress-activated MAPK cascade, probably by mediating phosphorylation of MAP2K3 and MAP2K6. Acts as a regulator of cytoskeleton stability by phosphorylating 'Thr-208' of MARK2, leading to activate MARK2 kinase activity and subsequent phosphorylation and detachment of MAPT/TAU from microtubules. Also acts as a regulator of apoptosis: regulates apoptotic morphological changes, including cell contraction, membrane blebbing and apoptotic bodies formation via activation of the MAPK8/JNK cascade. Plays an essential role in the regulation of neuronal development in the central nervous system (PubMed:33565190). Also plays a role in the regulation of neuronal migration to the cortical plate (By similarity). {ECO:0000250|UniProtKB:Q5F2E8, ECO:0000269|PubMed:12665513, ECO:0000269|PubMed:13679851, ECO:0000269|PubMed:16407310, ECO:0000269|PubMed:17396146, ECO:0000269|PubMed:17900936, ECO:0000269|PubMed:33565190}.

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 TAOK1_EFCAB5


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
TAOK1Q7L7X3humanRND3P61587S210KNVKRNKsQRATKRI
TAOK1Q7L7X3humanRND3P61587S218QRATKRIsHMPsRPE
TAOK1Q7L7X3humanTAOK1Q7L7X3T440RNREHFAtIRtAsLV
TAOK1Q7L7X3humanLATS1O95835T1079EHAFyEFtFRRFFDD
TAOK1Q7L7X3humanTAOK1Q7L7X3T443EHFAtIRtAsLVTRQ
TAOK1Q7L7X3humanRND3P61587S240LRKDKAKsCTVM___
TAOK1Q7L7X3humanSEPTIN7Q16181T426EQQNssrtLEKNKKK
TAOK1Q7L7X3humanTAOK1Q7L7X3S181SMAsPANsFVGtPyWPkinase


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
TAOK1IDDescription0.00e+00
TAOK1GO:0000086G2/M transition of mitotic cell cycle3.28e-02
TAOK1GO:0044839cell cycle G2/M phase transition3.28e-02
TAOK1GO:0032956regulation of actin cytoskeleton organization5.94e-02
TAOK1GO:1902855regulation of non-motile cilium assembly5.94e-02
TAOK1GO:0032970regulation of actin filament-based process5.94e-02
TAOK1GO:1902903regulation of supramolecular fiber organization5.94e-02
TAOK1GO:0045786negative regulation of cell cycle5.94e-02
TAOK1GO:0007015actin filament organization5.94e-02
TAOK1GO:0044772mitotic cell cycle phase transition5.94e-02
TAOK1GO:0060644mammary gland epithelial cell differentiation5.94e-02
TAOK1GO:0051220cytoplasmic sequestering of protein6.05e-02
TAOK1GO:0045736negative regulation of cyclin-dependent protein serine/threonine kinase activity6.05e-02
TAOK1GO:1904030negative regulation of cyclin-dependent protein kinase activity6.05e-02
TAOK1GO:1901985positive regulation of protein acetylation6.05e-02
TAOK1GO:0007026negative regulation of microtubule depolymerization6.05e-02
TAOK1GO:0045724positive regulation of cilium assembly6.11e-02
TAOK1GO:0031114regulation of microtubule depolymerization6.16e-02
TAOK1GO:0033146regulation of intracellular estrogen receptor signaling pathway6.27e-02
TAOK1GO:0007095mitotic G2 DNA damage checkpoint signaling6.27e-02
TAOK1GO:0031111negative regulation of microtubule polymerization or depolymerization6.27e-02
TAOK1GO:1900181negative regulation of protein localization to nucleus6.27e-02
TAOK1GO:1901983regulation of protein acetylation6.27e-02
TAOK1GO:0035329hippo signaling6.27e-02
TAOK1GO:0001825blastocyst formation6.27e-02
TAOK1GO:0007019microtubule depolymerization6.27e-02
TAOK1GO:0044818mitotic G2/M transition checkpoint6.68e-02
TAOK1GO:0030520intracellular estrogen receptor signaling pathway6.68e-02
TAOK1GO:0070050neuron cellular homeostasis6.68e-02
TAOK1GO:1905515non-motile cilium assembly6.68e-02
TAOK1GO:0061180mammary gland epithelium development6.68e-02
TAOK1GO:0010972negative regulation of G2/M transition of mitotic cell cycle6.68e-02
TAOK1GO:1901880negative regulation of protein depolymerization6.68e-02
TAOK1GO:1902750negative regulation of cell cycle G2/M phase transition6.68e-02
TAOK1GO:1902017regulation of cilium assembly6.68e-02
TAOK1GO:0033143regulation of intracellular steroid hormone receptor signaling pathway6.68e-02
TAOK1GO:0043242negative regulation of protein-containing complex disassembly6.68e-02
TAOK1GO:0000079regulation of cyclin-dependent protein serine/threonine kinase activity6.68e-02
TAOK1GO:0044773mitotic DNA damage checkpoint signaling6.68e-02
TAOK1GO:1902117positive regulation of organelle assembly6.68e-02
TAOK1GO:1904029regulation of cyclin-dependent protein kinase activity6.68e-02
TAOK1GO:1901879regulation of protein depolymerization6.68e-02
TAOK1GO:0044774mitotic DNA integrity checkpoint signaling6.68e-02
TAOK1GO:0046330positive regulation of JNK cascade6.68e-02
TAOK1GO:0021954central nervous system neuron development6.68e-02
TAOK1GO:0097194execution phase of apoptosis6.68e-02
TAOK1GO:0045185maintenance of protein location6.68e-02
TAOK1GO:0045995regulation of embryonic development6.68e-02
TAOK1GO:0031110regulation of microtubule polymerization or depolymerization6.68e-02
TAOK1GO:0046620regulation of organ growth6.68e-02

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Related Drugs to TAOK1_EFCAB5


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 TAOK1-EFCAB5 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 TAOK1_EFCAB5


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