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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:TRIM8_PRKX

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: TRIM8_PRKX
KinaseFusionDB ID: KFG6787
FusionGDB2.0 ID: KFG6787
HgeneTgene
Gene symbol

TRIM8

PRKX

Gene ID

81603

5613

Gene nametripartite motif containing 8protein kinase cAMP-dependent X-linked catalytic subunit
SynonymsFSGSNEDS|GERP|RNF27PKX1
Cytomap

10q24.32

Xp22.33

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase TRIM8RING-type E3 ubiquitin transferase TRIM8glioblastoma-expressed RING finger proteinprobable E3 ubiquitin-protein ligase TRIM8ring finger protein 27tripartite motif protein TRIM8cAMP-dependent protein kinase catalytic subunit PRKXprotein kinase PKX1protein kinase Xprotein kinase X-linkedserine/threonine-protein kinase PRKX
Modification date2024030520240411
UniProtAcc

Q9BZR9

P51817

Ensembl transtripts involved in fusion geneENST idsENST00000302424, ENST00000487927, 
ENST00000262848, ENST00000425240, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: TRIM8 [Title/Abstract] AND PRKX [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneTRIM8

GO:0007249

canonical NF-kappaB signal transduction

27995356

HgeneTRIM8

GO:0043123

positive regulation of canonical NF-kappaB signal transduction

23077300

HgeneTRIM8

GO:0044790

suppression of viral release by host

18248090

HgeneTRIM8

GO:0045087

innate immune response

18248090

HgeneTRIM8

GO:0051091

positive regulation of DNA-binding transcription factor activity

23077300

HgeneTRIM8

GO:0051092

positive regulation of NF-kappaB transcription factor activity

23077300

HgeneTRIM8

GO:0070534

protein K63-linked ubiquitination

27995356

TgenePRKX

GO:0018105

peptidyl-serine phosphorylation

16491121

TgenePRKX

GO:0030099

myeloid cell differentiation

9860982

TgenePRKX

GO:0030155

regulation of cell adhesion

17980165

TgenePRKX

GO:0030334

regulation of cell migration

17980165

TgenePRKX

GO:0046777

protein autophosphorylation

10026146|16491121

TgenePRKX

GO:0060562

epithelial tube morphogenesis

17980165

TgenePRKX

GO:0060993

kidney morphogenesis

17980165

TgenePRKX

GO:2000696

regulation of epithelial cell differentiation involved in kidney development

17980165


check buttonKinase Fusion gene breakpoints across TRIM8 (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 PRKX (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
CCLESW1463TRIM8chr10

104404364

PRKXchrX

3525338



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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/:/:)
- 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
TRIM8

Q9BZR9

PRKX

P51817

FUNCTION: E3 ubiquitin-protein ligase that participates in multiple biological processes including cell survival, differentiation, apoptosis, and in particular, the innate immune response (PubMed:27981609, PubMed:28747347). Participates in the activation of interferon-gamma signaling by promoting proteasomal degradation of the repressor SOCS1 (PubMed:12163497). Plays a positive role in the TNFalpha and IL-1beta signaling pathways. Mechanistically, induces the 'Lys-63'-linked polyubiquitination of MAP3K7/TAK1 component leading to the activation of NF-kappa-B (PubMed:22084099, PubMed:23152791, PubMed:27981609, PubMed:34871740). Modulates also STAT3 activity through negative regulation of PIAS3, either by degradation of PIAS3 through the ubiquitin-proteasome pathway or exclusion of PIAS3 from the nucleus (PubMed:20516148). Negatively regulates TLR3/4-mediated innate immune response by catalyzing 'Lys-6'- and 'Lys-33'-linked polyubiquitination of TICAM1 and thereby disrupting the TICAM1-TBK1 interaction (PubMed:28747347). {ECO:0000269|PubMed:12163497, ECO:0000269|PubMed:20516148, ECO:0000269|PubMed:22084099, ECO:0000269|PubMed:23152791, ECO:0000269|PubMed:28747347, ECO:0000269|PubMed:34871740}.FUNCTION: Serine/threonine protein kinase regulated by and mediating cAMP signaling in cells. Acts through phosphorylation of downstream targets that may include CREB, SMAD6 and PKD1 and has multiple functions in cellular differentiation and epithelial morphogenesis. Regulates myeloid cell differentiation through SMAD6 phosphorylation. Involved in nephrogenesis by stimulating renal epithelial cell migration and tubulogenesis. Also involved in angiogenesis through stimulation of endothelial cell proliferation, migration and vascular-like structure formation. {ECO:0000269|PubMed:12082174, ECO:0000269|PubMed:16236808, ECO:0000269|PubMed:16491121, ECO:0000269|PubMed:17980165, ECO:0000269|PubMed:19367327, ECO:0000269|PubMed:21684272, ECO:0000269|PubMed:9860982}.

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 TRIM8_PRKX


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
PRKXP51817humanSMAD6O43541S435RKVPPGYsIKVFDFEMH2
PRKXP51817humanPKD1P98161S4166EPLPSRSsRGsKVSP


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
PRKXIDDescription0.00e+00
PRKXGO:0034405response to fluid shear stress6.30e-04
PRKXGO:0072163mesonephric epithelium development1.48e-03
PRKXGO:0072164mesonephric tubule development1.48e-03
PRKXGO:0001823mesonephros development1.48e-03
PRKXGO:0072073kidney epithelium development2.51e-03
PRKXGO:0001822kidney development8.40e-03
PRKXGO:0072001renal system development8.40e-03
PRKXGO:0031589cell-substrate adhesion8.87e-03
PRKXGO:0072014proximal tubule development1.44e-02
PRKXGO:0072205metanephric collecting duct development1.44e-02
PRKXGO:0072173metanephric tubule morphogenesis1.44e-02
PRKXGO:0003183mitral valve morphogenesis1.44e-02
PRKXGO:0009950dorsal/ventral axis specification1.44e-02
PRKXGO:0072017distal tubule development1.44e-02
PRKXGO:0072070loop of Henle development1.44e-02
PRKXGO:0003174mitral valve development1.44e-02
PRKXGO:0034616response to laminar fluid shear stress1.44e-02
PRKXGO:0042994cytoplasmic sequestering of transcription factor1.44e-02
PRKXGO:0045737positive regulation of cyclin-dependent protein serine/threonine kinase activity1.44e-02
PRKXGO:0051290protein heterotetramerization1.44e-02
PRKXGO:0072044collecting duct development1.44e-02
PRKXGO:0072176nephric duct development1.44e-02
PRKXGO:0032926negative regulation of activin receptor signaling pathway1.47e-02
PRKXGO:1904031positive regulation of cyclin-dependent protein kinase activity1.47e-02
PRKXGO:0001502cartilage condensation1.47e-02
PRKXGO:0003184pulmonary valve morphogenesis1.47e-02
PRKXGO:0051220cytoplasmic sequestering of protein1.47e-02
PRKXGO:0072234metanephric nephron tubule development1.47e-02
PRKXGO:0003177pulmonary valve development1.47e-02
PRKXGO:0036303lymph vessel morphogenesis1.47e-02
PRKXGO:0060392negative regulation of SMAD protein signal transduction1.47e-02
PRKXGO:0098743cell aggregation1.47e-02
PRKXGO:0003148outflow tract septum morphogenesis1.47e-02
PRKXGO:0072273metanephric nephron morphogenesis1.47e-02
PRKXGO:0072170metanephric tubule development1.47e-02
PRKXGO:0072243metanephric nephron epithelium development1.47e-02
PRKXGO:0003181atrioventricular valve morphogenesis1.49e-02
PRKXGO:0032925regulation of activin receptor signaling pathway1.49e-02
PRKXGO:0051291protein heterooligomerization1.49e-02
PRKXGO:0003171atrioventricular valve development1.49e-02
PRKXGO:0072207metanephric epithelium development1.49e-02
PRKXGO:0001945lymph vessel development1.49e-02
PRKXGO:0003338metanephros morphogenesis1.49e-02
PRKXGO:0060674placenta blood vessel development1.49e-02
PRKXGO:0090162establishment of epithelial cell polarity1.60e-02
PRKXGO:0003180aortic valve morphogenesis1.75e-02
PRKXGO:0030279negative regulation of ossification1.78e-02
PRKXGO:0072210metanephric nephron development1.78e-02
PRKXGO:0000578embryonic axis specification1.78e-02

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Related Drugs to TRIM8_PRKX


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 TRIM8-PRKX 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 TRIM8_PRKX


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