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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:TNIK_EIF5A2

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: TNIK_EIF5A2
KinaseFusionDB ID: KFG6647
FusionGDB2.0 ID: KFG6647
HgeneTgene
Gene symbol

TNIK

EIF5A2

Gene ID

23043

56648

Gene nameTRAF2 and NCK interacting kinaseeukaryotic translation initiation factor 5A2
SynonymsMRT54EIF-5A2|eIF5AII
Cytomap

3q26.2-q26.31

3q26.2

Type of geneprotein-codingprotein-coding
DescriptionTRAF2 and NCK-interacting protein kinaseeukaryotic translation initiation factor 5A-2eIF-5A-2eukaryotic initiation factor 5A
Modification date2024040720240416
UniProtAcc

Q9UKE5

Q9GZV4

Ensembl transtripts involved in fusion geneENST idsENST00000284483, ENST00000341852, 
ENST00000357327, ENST00000369326, 
ENST00000436636, ENST00000460047, 
ENST00000464785, ENST00000465393, 
ENST00000470834, ENST00000475336, 
ENST00000488470, ENST00000538048, 
ENST00000295822, ENST00000460117, 
ENST00000474096, ENST00000487522, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: TNIK [Title/Abstract] AND EIF5A2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TNIK(170785460)-EIF5A2(170612662), # 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
HgeneTNIK

GO:0006468

protein phosphorylation

10521462|15342639|22797597

HgeneTNIK

GO:0030036

actin cytoskeleton organization

15342639

HgeneTNIK

GO:0035556

intracellular signal transduction

10521462

HgeneTNIK

GO:0046330

positive regulation of JNK cascade

15342639

HgeneTNIK

GO:0046777

protein autophosphorylation

10521462|15342639

HgeneTNIK

GO:0048814

regulation of dendrite morphogenesis

20159449


check buttonKinase Fusion gene breakpoints across TNIK (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 EIF5A2 (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
ChiTaRS5.0EC495694TNIKchr3

170785460

EIF5A2chr3

170612662

CCLEMKN1TNIKchr3

171177796

EIF5A2chr3

170612212



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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/chr3:170785460/chr3:170612662)
- 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
TNIK

Q9UKE5

EIF5A2

Q9GZV4

FUNCTION: Serine/threonine kinase that acts as an essential activator of the Wnt signaling pathway. Recruited to promoters of Wnt target genes and required to activate their expression. May act by phosphorylating TCF4/TCF7L2. Appears to act upstream of the JUN N-terminal pathway. May play a role in the response to environmental stress. Part of a signaling complex composed of NEDD4, RAP2A and TNIK which regulates neuronal dendrite extension and arborization during development. More generally, it may play a role in cytoskeletal rearrangements and regulate cell spreading. Phosphorylates SMAD1 on Thr-322. {ECO:0000269|PubMed:10521462, ECO:0000269|PubMed:15342639, ECO:0000269|PubMed:19061864, ECO:0000269|PubMed:19816403, ECO:0000269|PubMed:20159449, ECO:0000269|PubMed:21690388}.FUNCTION: Translation factor that promotes translation elongation and termination, particularly upon ribosome stalling at specific amino acid sequence contexts (PubMed:14622290). Binds between the exit (E) and peptidyl (P) site of the ribosome and promotes rescue of stalled ribosome: specifically required for efficient translation of polyproline-containing peptides as well as other motifs that stall the ribosome. Acts as a ribosome quality control (RQC) cofactor by joining the RQC complex to facilitate peptidyl transfer during CAT tailing step (By similarity). Also involved in actin dynamics and cell cycle progression, mRNA decay and probably in a pathway involved in stress response and maintenance of cell wall integrity (By similarity). {ECO:0000250|UniProtKB:P23301, ECO:0000250|UniProtKB:P63241, ECO:0000269|PubMed:14622290}.

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 TNIK_EIF5A2


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
TNIKQ9UKE5humanSMAD1Q15797T322sNVNRNStIENTRRHMH2
TNIKQ9UKE5humanTCF7L2Q9NQB0S177QALkDARsPsPAHIVCTNNB1_binding
TNIKQ9UKE5humanHTTP42858S13kLMkAFEsLksFQQQ
TNIKQ9UKE5humanHTTP42858T3_____MAtLEkLMkA


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
TNIKIDDescription0.00e+00
TNIKGO:2001237negative regulation of extrinsic apoptotic signaling pathway2.23e-02
TNIKGO:2001236regulation of extrinsic apoptotic signaling pathway2.78e-02
TNIKGO:0097191extrinsic apoptotic signaling pathway2.78e-02
TNIKGO:2001234negative regulation of apoptotic signaling pathway2.78e-02
TNIKGO:0033002muscle cell proliferation2.78e-02
TNIKGO:0045165cell fate commitment3.10e-02
TNIKGO:2001233regulation of apoptotic signaling pathway4.35e-02
TNIKGO:0097050type B pancreatic cell apoptotic process4.35e-02
TNIKGO:0098598learned vocalization behavior or vocal learning4.35e-02
TNIKGO:0099004calmodulin dependent kinase signaling pathway4.35e-02
TNIKGO:0031223auditory behavior4.35e-02
TNIKGO:0007638mechanosensory behavior4.35e-02
TNIKGO:0042762regulation of sulfur metabolic process4.35e-02
TNIKGO:1903599positive regulation of autophagy of mitochondrion4.35e-02
TNIKGO:2000479regulation of cAMP-dependent protein kinase activity4.35e-02
TNIKGO:0001710mesodermal cell fate commitment4.35e-02
TNIKGO:1901522positive regulation of transcription from RNA polymerase II promoter involved in cellular response to chemical stimulus4.35e-02
TNIKGO:0045721negative regulation of gluconeogenesis4.38e-02
TNIKGO:0031053primary miRNA processing4.38e-02
TNIKGO:0010560positive regulation of glycoprotein biosynthetic process4.38e-02
TNIKGO:1903020positive regulation of glycoprotein metabolic process4.38e-02
TNIKGO:0045724positive regulation of cilium assembly4.38e-02
TNIKGO:1903672positive regulation of sprouting angiogenesis4.38e-02
TNIKGO:1901021positive regulation of calcium ion transmembrane transporter activity4.38e-02
TNIKGO:0010996response to auditory stimulus4.38e-02
TNIKGO:0060795cell fate commitment involved in formation of primary germ layer4.38e-02
TNIKGO:0061036positive regulation of cartilage development4.38e-02
TNIKGO:0015012heparan sulfate proteoglycan biosynthetic process4.38e-02
TNIKGO:0048333mesodermal cell differentiation4.38e-02
TNIKGO:0000132establishment of mitotic spindle orientation4.38e-02
TNIKGO:0003161cardiac conduction system development4.38e-02
TNIKGO:0032350regulation of hormone metabolic process4.38e-02
TNIKGO:0040001establishment of mitotic spindle localization4.38e-02
TNIKGO:1903146regulation of autophagy of mitochondrion4.38e-02
TNIKGO:0051281positive regulation of release of sequestered calcium ion into cytosol4.38e-02
TNIKGO:0051294establishment of spindle orientation4.38e-02
TNIKGO:0047496vesicle transport along microtubule4.38e-02
TNIKGO:0035196miRNA processing4.38e-02
TNIKGO:0043666regulation of phosphoprotein phosphatase activity4.38e-02
TNIKGO:0031648protein destabilization4.38e-02
TNIKGO:2001259positive regulation of cation channel activity4.38e-02
TNIKGO:0006890retrograde vesicle-mediated transpor8.24e-03
TNIKGO:0006111regulation of gluconeogenesis4.38e-02
TNIKGO:0010559regulation of glycoprotein biosynthetic process4.38e-02
TNIKGO:0045912negative regulation of carbohydrate metabolic process4.38e-02
TNIKGO:0051293establishment of spindle localization4.38e-02
TNIKGO:0010718positive regulation of epithelial to mesenchymal transition4.38e-02
TNIKGO:0060038cardiac muscle cell proliferation4.38e-02
TNIKGO:0010921regulation of phosphatase activity4.38e-02

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Related Drugs to TNIK_EIF5A2


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 TNIK-EIF5A2 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 TNIK_EIF5A2


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