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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:STK10_XIAP

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: STK10_XIAP
KinaseFusionDB ID: KFG6125
FusionGDB2.0 ID: KFG6125
HgeneTgene
Gene symbol

STK10

XIAP

Gene ID

6793

331

Gene nameserine/threonine kinase 10X-linked inhibitor of apoptosis
SynonymsLOK|PRO2729API3|BIRC4|IAP-3|ILP1|MIHA|XLP2|hIAP-3|hIAP3
Cytomap

5q35.1

Xq25

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase 10lymphocyte-oriented kinaseE3 ubiquitin-protein ligase XIAPIAP-like protein 1RING-type E3 ubiquitin transferase XIAPX-linked IAPX-linked inhibitor of apoptosis, E3 ubiquitin protein ligasebaculoviral IAP repeat-containing protein 4inhibitor of apoptosis protein 3
Modification date2024030520240407
UniProtAcc

O94804

P98170

Ensembl transtripts involved in fusion geneENST idsENST00000176763, ENST00000517775, 
ENST00000355640, ENST00000371199, 
ENST00000434753, ENST00000468691, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: STK10 [Title/Abstract] AND XIAP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)STK10(171607186)-XIAP(122999413), # samples:1
STK10(171606716)-XIAP(122999320), # 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
HgeneSTK10

GO:0046777

protein autophosphorylation

12639966|18239682

TgeneXIAP

GO:0010804

negative regulation of tumor necrosis factor-mediated signaling pathway

11865055

TgeneXIAP

GO:0031398

positive regulation of protein ubiquitination

21931591

TgeneXIAP

GO:0032481

positive regulation of type I interferon production

36394357

TgeneXIAP

GO:0042742

defense response to bacterium

29452636

TgeneXIAP

GO:0042981

regulation of apoptotic process

11865055

TgeneXIAP

GO:0043066

negative regulation of apoptotic process

11257230

TgeneXIAP

GO:0043123

positive regulation of canonical NF-kappaB signal transduction

19667203|22607974

TgeneXIAP

GO:0043154

negative regulation of cysteine-type endopeptidase activity involved in apoptotic process

11583623

TgeneXIAP

GO:0046330

positive regulation of JNK cascade

11865055

TgeneXIAP

GO:0070427

nucleotide-binding oligomerization domain containing 1 signaling pathway

29452636

TgeneXIAP

GO:0070431

nucleotide-binding oligomerization domain containing 2 signaling pathway

19667203|22607974|29452636

TgeneXIAP

GO:0070534

protein K63-linked ubiquitination

29452636

TgeneXIAP

GO:0097340

inhibition of cysteine-type endopeptidase activity

11865055

TgeneXIAP

GO:1902530

positive regulation of protein linear polyubiquitination

21931591|22607974


check buttonKinase Fusion gene breakpoints across STK10 (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 XIAP (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
ChiTaRS5.0BM930492STK10chr5

171607186

XIAPchrX

122999413

ChiTaRS5.0BQ187681STK10chr5

171606716

XIAPchrX

122999320



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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/:171607186/:122999413)
- 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
STK10

O94804

XIAP

P98170

FUNCTION: Serine/threonine-protein kinase involved in regulation of lymphocyte migration. Phosphorylates MSN, and possibly PLK1. Involved in regulation of lymphocyte migration by mediating phosphorylation of ERM proteins such as MSN. Acts as a negative regulator of MAP3K1/MEKK1. May also act as a cell cycle regulator by acting as a polo kinase kinase: mediates phosphorylation of PLK1 in vitro; however such data require additional evidences in vivo. {ECO:0000269|PubMed:11903060, ECO:0000269|PubMed:12639966, ECO:0000269|PubMed:19255442}.FUNCTION: Multi-functional protein which regulates not only caspases and apoptosis, but also modulates inflammatory signaling and immunity, copper homeostasis, mitogenic kinase signaling, cell proliferation, as well as cell invasion and metastasis (PubMed:11447297, PubMed:12121969, PubMed:9230442, PubMed:11257230, PubMed:11257231, PubMed:12620238, PubMed:17967870, PubMed:19473982, PubMed:20154138, PubMed:22103349, PubMed:17560374). Acts as a direct caspase inhibitor (PubMed:11257230, PubMed:11257231, PubMed:12620238). Directly bind to the active site pocket of CASP3 and CASP7 and obstructs substrate entry (PubMed:11257230, PubMed:11257231, PubMed:16352606, PubMed:16916640). Inactivates CASP9 by keeping it in a monomeric, inactive state (PubMed:12620238). Acts as an E3 ubiquitin-protein ligase regulating NF-kappa-B signaling and the target proteins for its E3 ubiquitin-protein ligase activity include: RIPK1, RIPK2, MAP3K2/MEKK2, DIABLO/SMAC, AIFM1, CCS, PTEN and BIRC5/survivin (PubMed:17967870, PubMed:19473982, PubMed:20154138, PubMed:22103349, PubMed:22607974, PubMed:30026309, PubMed:29452636, PubMed:17560374). Acts as an important regulator of innate immunity by mediating 'Lys-63'-linked polyubiquitination of RIPK2 downstream of NOD1 and NOD2, thereby transforming RIPK2 into a scaffolding protein for downstream effectors, ultimately leading to activation of the NF-kappa-B and MAP kinases signaling (PubMed:19667203, PubMed:22607974, PubMed:30026309, PubMed:29452636). 'Lys-63'-linked polyubiquitination of RIPK2 also promotes recruitment of the LUBAC complex to RIPK2 (PubMed:22607974, PubMed:29452636). Regulates the BMP signaling pathway and the SMAD and MAP3K7/TAK1 dependent pathways leading to NF-kappa-B and JNK activation (PubMed:17560374). Ubiquitination of CCS leads to enhancement of its chaperone activity toward its physiologic target, SOD1, rather than proteasomal degradation (PubMed:20154138). Ubiquitination of MAP3K2/MEKK2 and AIFM1 does not lead to proteasomal degradation (PubMed:17967870, PubMed:22103349). Plays a role in copper homeostasis by ubiquitinating COMMD1 and promoting its proteasomal degradation (PubMed:14685266). Can also function as E3 ubiquitin-protein ligase of the NEDD8 conjugation pathway, targeting effector caspases for neddylation and inactivation (PubMed:21145488). Ubiquitinates and therefore mediates the proteasomal degradation of BCL2 in response to apoptosis (PubMed:29020630). Protects cells from spontaneous formation of the ripoptosome, a large multi-protein complex that has the capability to kill cancer cells in a caspase-dependent and caspase-independent manner (PubMed:22095281). Suppresses ripoptosome formation by ubiquitinating RIPK1 and CASP8 (PubMed:22095281). Acts as a positive regulator of Wnt signaling and ubiquitinates TLE1, TLE2, TLE3, TLE4 and AES (PubMed:22304967). Ubiquitination of TLE3 results in inhibition of its interaction with TCF7L2/TCF4 thereby allowing efficient recruitment and binding of the transcriptional coactivator beta-catenin to TCF7L2/TCF4 that is required to initiate a Wnt-specific transcriptional program (PubMed:22304967). {ECO:0000269|PubMed:11257230, ECO:0000269|PubMed:11257231, ECO:0000269|PubMed:11447297, ECO:0000269|PubMed:12121969, ECO:0000269|PubMed:12620238, ECO:0000269|PubMed:14685266, ECO:0000269|PubMed:16352606, ECO:0000269|PubMed:16916640, ECO:0000269|PubMed:17560374, ECO:0000269|PubMed:17967870, ECO:0000269|PubMed:19473982, ECO:0000269|PubMed:19667203, ECO:0000269|PubMed:20154138, ECO:0000269|PubMed:21145488, ECO:0000269|PubMed:22103349, ECO:0000269|PubMed:22304967, ECO:0000269|PubMed:22607974, ECO:0000269|PubMed:29020630, ECO:0000269|PubMed:29452636, ECO:0000269|PubMed:30026309, ECO:0000269|PubMed:9230442, ECO:0000303|PubMed:22095281}.

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 STK10_XIAP


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
STK10O94804humanRDXP35241T564AGRDKyKtLRQIRQGERM_C
STK10O94804humanEZRP15311T567QGRDkyKtLRQIRQGERM_C
STK10O94804humanPLK1P53350T210YDGERKktLCGtPNyPkinase
STK10O94804humanMSNP26038T558LGRDKyKtLRQIRQGERM_C


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
STK10IDDescription0.00e+00
STK10GO:1902946protein localization to early endosome1.25e-07
STK10GO:1905668positive regulation of protein localization to endosome1.25e-07
STK10GO:1905666regulation of protein localization to endosome1.25e-07
STK10GO:1903651positive regulation of cytoplasmic transport1.49e-07
STK10GO:2000641regulation of early endosome to late endosome transport2.54e-07
STK10GO:0036010protein localization to endosome6.39e-07
STK10GO:0045732positive regulation of protein catabolic process7.22e-07
STK10GO:1902115regulation of organelle assembly7.22e-07
STK10GO:1903649regulation of cytoplasmic transport7.22e-07
STK10GO:0045022early endosome to late endosome transport1.73e-06
STK10GO:0061028establishment of endothelial barrier2.01e-06
STK10GO:0098927vesicle-mediated transport between endosomal compartments2.01e-06
STK10GO:0042176regulation of protein catabolic process3.85e-06
STK10GO:0001885endothelial cell development3.89e-06
STK10GO:1903829positive regulation of protein localization9.79e-06
STK10GO:0045446endothelial cell differentiation2.53e-05
STK10GO:0008360regulation of cell shape3.43e-05
STK10GO:0003158endothelium development3.46e-05
STK10GO:0072697protein localization to cell cortex3.58e-05
STK10GO:0016482cytosolic transport6.43e-05
STK10GO:0032388positive regulation of intracellular transport8.26e-05
STK10GO:0002064epithelial cell development9.52e-05
STK10GO:0022604regulation of cell morphogenesis1.40e-04
STK10GO:0032386regulation of intracellular transport3.38e-04
STK10GO:0010737protein kinase A signaling3.47e-04
STK10GO:1990778protein localization to cell periphery3.61e-04
STK10GO:0032535regulation of cellular component size4.01e-04
STK10GO:0140694non-membrane-bounded organelle assembly5.18e-04
STK10GO:0022406membrane docking1.77e-03
STK10GO:1904375regulation of protein localization to cell periphery3.80e-03
STK10GO:0030010establishment of cell polarity4.77e-03
STK10GO:0051017actin filament bundle assembly4.92e-03
STK10GO:0061572actin filament bundle organization5.01e-03
STK10GO:0008361regulation of cell size6.24e-03
STK10GO:0007051spindle organization7.07e-03
STK10GO:0007163establishment or maintenance of cell polarity8.75e-03
STK10GO:0072659protein localization to plasma membrane1.37e-02
STK10GO:1901990regulation of mitotic cell cycle phase transition1.84e-02
STK10GO:0030953astral microtubule organization1.84e-02
STK10GO:0051081nuclear membrane disassembly1.84e-02
STK10GO:0051660establishment of centrosome localization1.84e-02
STK10GO:0071803positive regulation of podosome assembly1.84e-02
STK10GO:0010639negative regulation of organelle organization1.84e-02
STK10GO:0030397membrane disassembly1.94e-02
STK10GO:0034111negative regulation of homotypic cell-cell adhesion1.97e-02
STK10GO:0071394cellular response to testosterone stimulus1.97e-02
STK10GO:0032530regulation of microvillus organization1.97e-02
STK10GO:0032536regulation of cell projection size1.97e-02
STK10GO:0070486leukocyte aggregation1.97e-02

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Related Drugs to STK10_XIAP


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 STK10-XIAP 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 STK10_XIAP


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