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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:NOL4_PLK2

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: NOL4_PLK2
KinaseFusionDB ID: KFG4224
FusionGDB2.0 ID: KFG4224
HgeneTgene
Gene symbol

NOL4

PLK2

Gene ID

8715

10769

Gene namenucleolar protein 4polo like kinase 2
SynonymsCT125|HRIHFB2255|NOLPSNK|hPlk2|hSNK
Cytomap

18q12.1

5q11.2

Type of geneprotein-codingprotein-coding
Descriptionnucleolar protein 4cancer/testis antigen 125nucleolar localized proteinserine/threonine-protein kinase PLK2PLK-2serine/threonine-protein kinase SNKserum-inducible kinase
Modification date2024040320240305
UniProtAcc

O94818

Q9NYY3

Ensembl transtripts involved in fusion geneENST idsENST00000261592, ENST00000269185, 
ENST00000535384, ENST00000535475, 
ENST00000538587, ENST00000589544, 
ENST00000590846, 
ENST00000274289, 
ENST00000502671, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: NOL4 [Title/Abstract] AND PLK2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NOL4(31712694)-PLK2(57749813), # 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
TgenePLK2

GO:0006468

protein phosphorylation

20352051

TgenePLK2

GO:0007052

mitotic spindle organization

19001868

TgenePLK2

GO:0010508

positive regulation of autophagy

23983262

TgenePLK2

GO:0018105

peptidyl-serine phosphorylation

23983262

TgenePLK2

GO:0045732

positive regulation of protein catabolic process

23983262

TgenePLK2

GO:0046599

regulation of centriole replication

19001868|20352051|20531387


check buttonKinase Fusion gene breakpoints across NOL4 (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 PLK2 (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
ChiTaRS5.0BI494851NOL4chr18

31712694

PLK2chr5

57749813



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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/:31712694/:57749813)
- 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
NOL4

O94818

PLK2

Q9NYY3

FUNCTION: Tumor suppressor serine/threonine-protein kinase involved in synaptic plasticity, centriole duplication and G1/S phase transition. Polo-like kinases act by binding and phosphorylating proteins that are already phosphorylated on a specific motif recognized by the POLO box domains. Phosphorylates CENPJ, NPM1, RAPGEF2, RASGRF1, SNCA, SIPA1L1 and SYNGAP1. Plays a key role in synaptic plasticity and memory by regulating the Ras and Rap protein signaling: required for overactivity-dependent spine remodeling by phosphorylating the Ras activator RASGRF1 and the Rap inhibitor SIPA1L1 leading to their degradation by the proteasome. Conversely, phosphorylates the Rap activator RAPGEF2 and the Ras inhibitor SYNGAP1, promoting their activity. Also regulates synaptic plasticity independently of kinase activity, via its interaction with NSF that disrupts the interaction between NSF and the GRIA2 subunit of AMPARs, leading to a rapid rundown of AMPAR-mediated current that occludes long term depression. Required for procentriole formation and centriole duplication by phosphorylating CENPJ and NPM1, respectively. Its induction by p53/TP53 suggests that it may participate in the mitotic checkpoint following stress. {ECO:0000269|PubMed:15242618, ECO:0000269|PubMed:19001868, ECO:0000269|PubMed:20352051, ECO:0000269|PubMed:20531387}.

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 NOL4_PLK2


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
PLK2Q9NYY3humanCRYABP02511S19RPFFPFHsPsrLFDQCrystallin
PLK2Q9NYY3humanYWHAEP62258T208DAIAELDtLsEEsyk14-3-3
PLK2Q9NYY3humanCALUO43852S44kVHNDAQsFDyDHDA
PLK2Q9NYY3humanCENPJQ9HC77S595IsFSSNSsFVLKILE
PLK2Q9NYY3humanFBXW7Q969H0S349IKPGFIHsPWKSAYI
PLK2Q9NYY3humanCALUO43852T60LGAEEAktFDQLtPE
PLK2Q9NYY3humanSNCBQ16143S118LMEPEGEsYEDPPQESynuclein
PLK2Q9NYY3humanPLK1P53350S137LELCRRRsLLELHkRPkinase
PLK2Q9NYY3humanSNCAP37840S129NEAyEMPsEEGyQDySynuclein
PLK2Q9NYY3humanCENPJQ9HC77S589EQAADEIsFSSNSsF
PLK2Q9NYY3humanTP73O15350S48VVGGTDssMDVFHLE
PLK2Q9NYY3humanCALUO43852T196KDIVVQEtMEDIDKNEF-hand_5
PLK2Q9NYY3humanNPM1P06748S4____MEDsMDMDMsP
PLK2Q9NYY3humanFBXW7Q969H0S176KRKLDHGsEVRSFSL
PLK2Q9NYY3humanFBXW7Q969H0S25sLRGNPSssQVDEEQ


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
PLK2IDDescription0.00e+00
PLK2GO:1903829positive regulation of protein localization4.10e-05
PLK2GO:0031647regulation of protein stability1.47e-04
PLK2GO:0031648protein destabilization5.54e-04
PLK2GO:0032886regulation of microtubule-based process1.43e-03
PLK2GO:0031398positive regulation of protein ubiquitination3.51e-03
PLK2GO:0045936negative regulation of phosphate metabolic process3.51e-03
PLK2GO:0010563negative regulation of phosphorus metabolic process3.51e-03
PLK2GO:1903322positive regulation of protein modification by small protein conjugation or removal3.51e-03
PLK2GO:0031109microtubule polymerization or depolymerization3.51e-03
PLK2GO:0007098centrosome cycle3.51e-03
PLK2GO:0031400negative regulation of protein modification process3.51e-03
PLK2GO:0051443positive regulation of ubiquitin-protein transferase activity3.51e-03
PLK2GO:0031023microtubule organizing center organization3.51e-03
PLK2GO:1901987regulation of cell cycle phase transition3.51e-03
PLK2GO:0046599regulation of centriole replication3.51e-03
PLK2GO:1901875positive regulation of post-translational protein modification3.51e-03
PLK2GO:0070507regulation of microtubule cytoskeleton organization3.51e-03
PLK2GO:0006469negative regulation of protein kinase activity4.55e-03
PLK2GO:0033673negative regulation of kinase activity5.30e-03
PLK2GO:0090169regulation of spindle assembly5.30e-03
PLK2GO:0031396regulation of protein ubiquitination5.41e-03
PLK2GO:0050821protein stabilization6.33e-03
PLK2GO:1902115regulation of organelle assembly6.33e-03
PLK2GO:0051438regulation of ubiquitin-protein transferase activity6.33e-03
PLK2GO:0051348negative regulation of transferase activity6.33e-03
PLK2GO:0042417dopamine metabolic process6.33e-03
PLK2GO:0043523regulation of neuron apoptotic process6.33e-03
PLK2GO:0060236regulation of mitotic spindle organization6.33e-03
PLK2GO:1990000amyloid fibril formation6.33e-03
PLK2GO:0007099centriole replication6.42e-03
PLK2GO:1903320regulation of protein modification by small protein conjugation or removal6.51e-03
PLK2GO:0090224regulation of spindle organization6.89e-03
PLK2GO:0010824regulation of centrosome duplication6.97e-03
PLK2GO:0098534centriole assembly7.06e-03
PLK2GO:0051402neuron apoptotic process8.45e-03
PLK2GO:0046605regulation of centrosome cycle8.45e-03
PLK2GO:1901873regulation of post-translational protein modification8.63e-03
PLK2GO:0006584catecholamine metabolic process8.69e-03
PLK2GO:0009712catechol-containing compound metabolic process8.69e-03
PLK2GO:0007062sister chromatid cohesion9.08e-03
PLK2GO:0001933negative regulation of protein phosphorylation9.50e-03
PLK2GO:0034504protein localization to nucleus9.82e-03
PLK2GO:1904951positive regulation of establishment of protein localization1.09e-02
PLK2GO:0042326negative regulation of phosphorylation1.10e-02
PLK2GO:0032386regulation of intracellular transport1.14e-02
PLK2GO:0048488synaptic vesicle endocytosis1.14e-02
PLK2GO:0140238presynaptic endocytosis1.15e-02
PLK2GO:0051298centrosome duplication1.20e-02
PLK2GO:0045862positive regulation of proteolysis1.20e-02

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Related Drugs to NOL4_PLK2


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 NOL4-PLK2 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 NOL4_PLK2


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