UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Kinase Fusion Gene Summary

leaf

Kinase Fusion Gene Sample Information

leaf

Kinase Fusion ORF Analysis

leaf

Kinase Fusion Amino Acid Sequences

leaf

Multiple Sequence Alignment of All Fusion Protein Isoforms

leaf

Kinase Fusion Protein Functional Features

leaf

Kinase Fusion Protein Structures

leaf

Comparison of Fusion Protein Isoforms

leaf

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

leaf

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

leaf

Ramachandran Plot of Kinase Fusion Protein Structure

leaf

Potential Active Site Information

leaf

Virtual Screening Results

leaf

Kinase-Substrate Information

leaf

Related Drugs with This Kinase Fusion Protein

leaf

Related Disease with This Kinase Fusion Protein

leaf

Clinical Trials of the Found Drugs/Small Molecules

Kinase Fusion Gene:HSP90AA1_CSNK2A2

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: HSP90AA1_CSNK2A2
KinaseFusionDB ID: KFG2757
FusionGDB2.0 ID: KFG2757
HgeneTgene
Gene symbol

HSP90AA1

CSNK2A2

Gene ID

3320

1459

Gene nameheat shock protein 90 alpha family class A member 1casein kinase 2 alpha 2
SynonymsEL52|HEL-S-65p|HSP86|HSP89A|HSP90A|HSP90N|HSPC1|HSPCA|HSPCAL1|HSPCAL4|HSPN|Hsp103|Hsp89|Hsp90|LAP-2|LAP2CK2A2|CK2alpha'|CSNK2A1
Cytomap

14q32.31

16q21

Type of geneprotein-codingprotein-coding
Descriptionheat shock protein HSP 90-alphaHSP 86LPS-associated protein 2epididymis luminal secretory protein 52epididymis secretory sperm binding protein Li 65pheat shock 86 kDaheat shock 90kD protein 1, alphaheat shock 90kD protein 1, alpha-like 4heat shockcasein kinase II subunit alpha'CK II alpha'casein kinase 2 alpha'casein kinase 2, alpha prime polypeptide
Modification date2024040720240407
UniProtAcc

P07900

P19784

Ensembl transtripts involved in fusion geneENST idsENST00000216281, ENST00000334701, 
ENST00000441629, ENST00000558600, 
ENST00000566813, ENST00000262506, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: HSP90AA1 [Title/Abstract] AND CSNK2A2 [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
HgeneHSP90AA1

GO:0001934

positive regulation of protein phosphorylation

19363271

HgeneHSP90AA1

GO:0002218

activation of innate immune response

20628368

HgeneHSP90AA1

GO:0002230

positive regulation of defense response to virus by host

20628368

HgeneHSP90AA1

GO:0007004

telomere maintenance via telomerase

10197982

HgeneHSP90AA1

GO:0031396

regulation of protein ubiquitination

16809764

HgeneHSP90AA1

GO:0032273

positive regulation of protein polymerization

19363271

HgeneHSP90AA1

GO:0032728

positive regulation of interferon-beta production

20628368

HgeneHSP90AA1

GO:0042981

regulation of apoptotic process

25609812

HgeneHSP90AA1

GO:0045040

protein insertion into mitochondrial outer membrane

15644312

HgeneHSP90AA1

GO:0051131

chaperone-mediated protein complex assembly

15644312

HgeneHSP90AA1

GO:0051973

positive regulation of telomerase activity

10197982

HgeneHSP90AA1

GO:0098586

cellular response to virus

25609812

HgeneHSP90AA1

GO:1902949

positive regulation of tau-protein kinase activity

19363271

HgeneHSP90AA1

GO:1905323

telomerase holoenzyme complex assembly

10197982

TgeneCSNK2A2

GO:0006302

double-strand break repair

22325354

TgeneCSNK2A2

GO:0018105

peptidyl-serine phosphorylation

28031292


check buttonKinase Fusion gene breakpoints across HSP90AA1 (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 CSNK2A2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.


Top

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
CCLEU266B1HSP90AA1chr14

102551172

CSNK2A2chr16

58220749



Top

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)

Top

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



Top

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
HSP90AA1

P07900

CSNK2A2

P19784

FUNCTION: Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle that is linked to its ATPase activity which is essential for its chaperone activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:11274138, PubMed:15577939, PubMed:15937123, PubMed:27353360, PubMed:29127155, PubMed:12526792). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself (PubMed:29127155). Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:27295069, PubMed:26991466). Plays a critical role in mitochondrial import, delivers preproteins to the mitochondrial import receptor TOMM70 (PubMed:12526792). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels (PubMed:25973397). In the first place, they alter the steady-state levels of certain transcription factors in response to various physiological cues(PubMed:25973397). Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment (PubMed:25973397). Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Binds bacterial lipopolysaccharide (LPS) and mediates LPS-induced inflammatory response, including TNF secretion by monocytes (PubMed:11276205). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Mediates the association of TOMM70 with IRF3 or TBK1 in mitochondrial outer membrane which promotes host antiviral response (PubMed:20628368, PubMed:25609812). {ECO:0000269|PubMed:11274138, ECO:0000269|PubMed:11276205, ECO:0000269|PubMed:12526792, ECO:0000269|PubMed:15577939, ECO:0000269|PubMed:15937123, ECO:0000269|PubMed:20628368, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:25609812, ECO:0000269|PubMed:27353360, ECO:0000269|PubMed:29127155, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.; FUNCTION: (Microbial infection) Seems to interfere with N.meningitidis NadA-mediated invasion of human cells. Decreasing HSP90 levels increases adhesion and entry of E.coli expressing NadA into human Chang cells; increasing its levels leads to decreased adhesion and invasion. {ECO:0000305|PubMed:22066472}.FUNCTION: Catalytic subunit of a constitutively active serine/threonine-protein kinase complex that phosphorylates a large number of substrates containing acidic residues C-terminal to the phosphorylated serine or threonine (PubMed:11239457, PubMed:11704824, PubMed:16193064, PubMed:30898438). Regulates numerous cellular processes, such as cell cycle progression, apoptosis and transcription, as well as viral infection (PubMed:11704824, PubMed:16193064, PubMed:30898438). May act as a regulatory node which integrates and coordinates numerous signals leading to an appropriate cellular response (PubMed:12631575, PubMed:19387552, PubMed:19387551). During mitosis, functions as a component of the p53/TP53-dependent spindle assembly checkpoint (SAC) that maintains cyclin-B-CDK1 activity and G2 arrest in response to spindle damage (PubMed:12631575, PubMed:19387552, PubMed:19387551). Also required for p53/TP53-mediated apoptosis, phosphorylating 'Ser-392' of p53/TP53 following UV irradiation (PubMed:11239457). Phosphorylates a number of DNA repair proteins in response to DNA damage, such as MDC1, RAD9A, RAD51 and HTATSF1, promoting their recruitment to DNA damage sites (PubMed:20545769, PubMed:21482717, PubMed:22325354, PubMed:26811421, PubMed:30898438, PubMed:35597237). Can also negatively regulate apoptosis (PubMed:19387552, PubMed:19387551). Phosphorylates the caspases CASP9 and CASP2 and the apoptotic regulator NOL3 (PubMed:12631575, PubMed:19387552, PubMed:19387551). Phosphorylation protects CASP9 from cleavage and activation by CASP8, and inhibits the dimerization of CASP2 and activation of CASP8 (PubMed:12631575, PubMed:19387552, PubMed:19387551). Regulates transcription by direct phosphorylation of RNA polymerases I, II, III and IV (PubMed:12631575, PubMed:19387552, PubMed:19387551). Also phosphorylates and regulates numerous transcription factors including NF-kappa-B, STAT1, CREB1, IRF1, IRF2, ATF1, SRF, MAX, JUN, FOS, MYC and MYB (PubMed:12631575, PubMed:19387552, PubMed:19387551). Phosphorylates Hsp90 and its co-chaperones FKBP4 and CDC37, which is essential for chaperone function (PubMed:19387550). Regulates Wnt signaling by phosphorylating CTNNB1 and the transcription factor LEF1 (PubMed:19387549). Acts as an ectokinase that phosphorylates several extracellular proteins (PubMed:12631575, PubMed:19387552, PubMed:19387551). During viral infection, phosphorylates various proteins involved in the viral life cycles of EBV, HSV, HBV, HCV, HIV, CMV and HPV (PubMed:12631575, PubMed:19387552, PubMed:19387551). {ECO:0000269|PubMed:11239457, ECO:0000269|PubMed:11704824, ECO:0000269|PubMed:16193064, ECO:0000269|PubMed:20545769, ECO:0000269|PubMed:21482717, ECO:0000269|PubMed:22325354, ECO:0000269|PubMed:26811421, ECO:0000269|PubMed:30898438, ECO:0000269|PubMed:35597237, ECO:0000303|PubMed:12631575, ECO:0000303|PubMed:19387549, ECO:0000303|PubMed:19387550, ECO:0000303|PubMed:19387551, ECO:0000303|PubMed:19387552}.

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


Top

Kinase-Substrate Information of HSP90AA1_CSNK2A2


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
CSNK2A2P19784humanCTNNB1P35222T112EGMQIPstQFdAAHP
CSNK2A2P19784humanSMC3Q9UQE7S1067GDVEGsQsQDEGEGsSMC_N
CSNK2A2P19784humanCSNK2BP67870S3_____MsssEEVsWI
CSNK2A2P19784humanCCNHP51946T315KHEEEEWtDDDLVEs
CSNK2A2P19784humanXRCC1P18887T523AGstDENtDsEEHQE
CSNK2A2P19784humanCDC37Q16543S13VWDHIEVsDDEDETHCDC37_N
CSNK2A2P19784humanCTNNB1P35222T102RAAMFPEtLDEGMQI
CSNK2A2P19784humanTP73O15350T27SSLEPDStyFDLPQS
CSNK2A2P19784humanTYMSP04818S124FLDsLGFsTREEGDLThymidylat_synt
CSNK2A2P19784humanNKX3-1Q99801T93EAEtLAEtEPERHLG
CSNK2A2P19784humanXRCC1P18887T488GAEDsGDtEDELRRV
CSNK2A2P19784humanSUZ12Q15022S583PQEMEVDsEDEKDPEVEFS-Box
CSNK2A2P19784humanSRPK1Q96SB4S555DYLFEPHsGEEYTRDPkinase
CSNK2A2P19784humanXRCC1P18887S485QDNGAEDsGDtEDEL
CSNK2A2P19784humanSRPK1Q96SB4S51QEEEILGsDDDEQED
CSNK2A2P19784humanCTNNB1P35222S29VsHWQQQsyLDsGIH
CSNK2A2P19784humanXRCC1P18887S518GEDPyAGstDENtDs
CSNK2A2P19784humanXRCC1P18887T519EDPyAGstDENtDsE
CSNK2A2P19784humanNKX3-1Q99801T89AAPEEAEtLAEtEPE
CSNK2A2P19784humanHSF1Q00613T142DsVTKLLtDVQLMKG
CSNK2A2P19784humanCSNK2BP67870S2______MsssEEVsW


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
CSNK2A2IDDescription0.00e+00
CSNK2A2GO:0009410response to xenobiotic stimulus1.05e-04
CSNK2A2GO:0060768regulation of epithelial cell proliferation involved in prostate gland development6.06e-03
CSNK2A2GO:0060767epithelial cell proliferation involved in prostate gland development6.06e-03
CSNK2A2GO:0048709oligodendrocyte differentiation7.47e-03
CSNK2A2GO:0003159morphogenesis of an endothelium7.47e-03
CSNK2A2GO:0061154endothelial tube morphogenesis7.47e-03
CSNK2A2GO:0060479lung cell differentiation1.55e-02
CSNK2A2GO:0060487lung epithelial cell differentiation1.55e-02
CSNK2A2GO:1901654response to ketone2.68e-02
CSNK2A2GO:0060428lung epithelium development2.69e-02
CSNK2A2GO:0033574response to testosterone2.69e-02
CSNK2A2GO:0048713regulation of oligodendrocyte differentiation2.69e-02
CSNK2A2GO:0030850prostate gland development3.02e-02
CSNK2A2GO:0010001glial cell differentiation3.02e-02
CSNK2A2GO:0007062sister chromatid cohesion3.65e-02
CSNK2A2GO:0006303double-strand break repair via nonhomologous end joining3.65e-02
CSNK2A2GO:0001666response to hypoxia3.65e-02
CSNK2A2GO:0051054positive regulation of DNA metabolic process3.65e-02
CSNK2A2GO:0001655urogenital system development3.65e-02
CSNK2A2GO:0001822kidney development3.65e-02
CSNK2A2GO:0036293response to decreased oxygen levels3.65e-02
CSNK2A2GO:0030858positive regulation of epithelial cell differentiation3.65e-02
CSNK2A2GO:0097193intrinsic apoptotic signaling pathway3.65e-02
CSNK2A2GO:0072001renal system development3.66e-02
CSNK2A2GO:0060562epithelial tube morphogenesis3.68e-02
CSNK2A2GO:0042063gliogenesis3.68e-02
CSNK2A2GO:0045685regulation of glial cell differentiation3.68e-02
CSNK2A2GO:0070482response to oxygen levels3.69e-02
CSNK2A2GO:0000079regulation of cyclin-dependent protein serine/threonine kinase activity3.69e-02
CSNK2A2GO:1904029regulation of cyclin-dependent protein kinase activity3.83e-02
CSNK2A2GO:0048525negative regulation of viral process4.38e-02
CSNK2A2GO:0001656metanephros development4.38e-02
CSNK2A2GO:0032204regulation of telomere maintenance5.19e-02
CSNK2A2GO:0014013regulation of gliogenesis5.63e-02
CSNK2A2GO:0032355response to estradiol5.76e-02
CSNK2A2GO:0048732gland development5.87e-02
CSNK2A2GO:0010720positive regulation of cell development5.87e-02
CSNK2A2GO:0002065columnar/cuboidal epithelial cell differentiation6.05e-02
CSNK2A2GO:0021761limbic system development6.05e-02
CSNK2A2GO:0002761regulation of myeloid leukocyte differentiation6.05e-02
CSNK2A2GO:0045931positive regulation of mitotic cell cycle6.17e-02
CSNK2A2GO:0048565digestive tract development6.17e-02
CSNK2A2GO:0003158endothelium development6.17e-02
CSNK2A2GO:1903900regulation of viral life cycle6.17e-02
CSNK2A2GO:0051053negative regulation of DNA metabolic process6.17e-02
CSNK2A2GO:0055123digestive system development6.17e-02
CSNK2A2GO:0007584response to nutrient6.17e-02
CSNK2A2GO:0000723telomere maintenance6.17e-02
CSNK2A2GO:0048754branching morphogenesis of an epithelial tube6.17e-02

Top

Related Drugs to HSP90AA1_CSNK2A2


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 HSP90AA1-CSNK2A2 and kinase inhibitors the PubMed Abstract (04-01-2024)

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

Top

Related Diseases to HSP90AA1_CSNK2A2


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


Top

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