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:LPCAT3_MAP3K13

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: LPCAT3_MAP3K13
KinaseFusionDB ID: KFG3198
FusionGDB2.0 ID: KFG3198
HgeneTgene
Gene symbol

LPCAT3

MAP3K13

Gene ID

10162

9175

Gene namelysophosphatidylcholine acyltransferase 3mitogen-activated protein kinase kinase kinase 13
SynonymsC3F|LPCAT|LPLAT 5|LPLAT12|LPSAT|MBOAT5|OACT5|nessyLZK|MEKK13|MLK
Cytomap

12p13.31

3q27.2

Type of geneprotein-codingprotein-coding
Descriptionlysophospholipid acyltransferase 51-acylglycerophosphocholine O-acyltransferase1-acylglycerophosphoethanolamine O-acyltransferase1-acylglycerophosphoserine O-acyltransferaseO-acyltransferase (membrane bound) domain containing 5O-acyltransferase domaimitogen-activated protein kinase kinase kinase 13leucine zipper-bearing kinasemixed lineage kinase
Modification date2024033120240305
UniProtAcc

Q6P1A2

O43283

Ensembl transtripts involved in fusion geneENST idsENST00000261407, ENST00000535021, 
ENST00000438798, ENST00000446828, 
ENST00000448876, ENST00000454237, 
ENST00000265026, ENST00000424227, 
ENST00000443863, ENST00000535426, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: LPCAT3 [Title/Abstract] AND MAP3K13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)LPCAT3(7125578)-MAP3K13(185003305), # samples:2
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneLPCAT3

GO:0036150

phosphatidylserine acyl-chain remodeling

18195019|18772128

HgeneLPCAT3

GO:0036151

phosphatidylcholine acyl-chain remodeling

18195019|18772128

HgeneLPCAT3

GO:0036152

phosphatidylethanolamine acyl-chain remodeling

18772128

TgeneMAP3K13

GO:0006468

protein phosphorylation

9353328|11726277

TgeneMAP3K13

GO:0007254

JNK cascade

9353328|11726277

TgeneMAP3K13

GO:0046777

protein autophosphorylation

9353328

TgeneMAP3K13

GO:0051092

positive regulation of NF-kappaB transcription factor activity

12492477

TgeneMAP3K13

GO:0051403

stress-activated MAPK cascade

11726277


check buttonKinase Fusion gene breakpoints across LPCAT3 (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 MAP3K13 (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
ChimerDB4TCGA-BC-A10Y-01ALPCAT3chr12

7125578

MAP3K13chr3

185003305



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/:7125578/:185003305)
- 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
LPCAT3

Q6P1A2

MAP3K13

O43283

FUNCTION: Lysophospholipid O-acyltransferase (LPLAT) that catalyzes the reacylation step of the phospholipid remodeling process also known as the Lands cycle (PubMed:18782225, PubMed:18195019, PubMed:18772128). Catalyzes transfer of the fatty acyl chain from fatty acyl-CoA to 1-acyl lysophospholipid to form various classes of phospholipids. Converts 1-acyl lysophosphatidylcholine (LPC) into phosphatidylcholine (PC) (LPCAT activity), 1-acyl lysophosphatidylserine (LPS) into phosphatidylserine (PS) (LPSAT activity) and 1-acyl lysophosphatidylethanolamine (LPE) into phosphatidylethanolamine (PE) (LPEAT activity) (PubMed:18782225, PubMed:18195019, PubMed:18772128). Favors polyunsaturated fatty acyl-CoAs as acyl donors compared to saturated fatty acyl-CoAs (PubMed:18195019, PubMed:18772128). Has higher activity for LPC acyl acceptors compared to LPEs and LPSs. Can also transfer the fatty acyl chain from fatty acyl-CoA to 1-O-alkyl lysophospholipid or 1-O-alkenyl lysophospholipid with lower efficiency (By similarity). Acts as a major LPC O-acyltransferase in liver and intestine. As a component of the liver X receptor/NR1H3 or NR1H2 signaling pathway, mainly catalyzes the incorporation of arachidonate into PCs of endoplasmic reticulum (ER) membranes, increasing membrane dynamics and enabling triacylglycerols transfer to nascent very low-density lipoprotein (VLDL) particles. Promotes processing of sterol regulatory protein SREBF1 in hepatocytes, likely by facilitating the translocation of SREBF1-SCAP complex from ER to the Golgi apparatus (By similarity). Participates in mechanisms by which the liver X receptor/NR1H3 or NR1H2 signaling pathway counteracts lipid-induced ER stress response and inflammation. Down-regulates hepatic inflammation by limiting arachidonic acid availability for synthesis of inflammatory eicosanoids, such as prostaglandins (By similarity). In enterocytes, acts as a component of a gut-brain feedback loop that coordinates dietary lipid absorption and food intake. Regulates the abundance of PCs containing linoleate and arachidonate in enterocyte membranes, enabling passive diffusion of fatty acids and cholesterol across the membrane for efficient chylomicron assembly (By similarity). In the intestinal crypt, acts as a component of dietary-responsive phospholipid-cholesterol axis, regulating the biosynthesis of cholesterol and its mitogenic effects on intestinal stem cells (By similarity). {ECO:0000250|UniProtKB:Q91V01, ECO:0000269|PubMed:18195019, ECO:0000269|PubMed:18772128, ECO:0000269|PubMed:18782225}.FUNCTION: Activates the JUN N-terminal pathway through activation of the MAP kinase kinase MAP2K7. Acts synergistically with PRDX3 to regulate the activation of NF-kappa-B in the cytosol. This activation is kinase-dependent and involves activating the IKK complex, the IKBKB-containing complex that phosphorylates inhibitors of NF-kappa-B. {ECO:0000269|PubMed:11726277, ECO:0000269|PubMed:12492477, ECO:0000269|PubMed:9353328}.

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 LPCAT3_MAP3K13


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
MAP3K13O43283humanTRIM25Q14258S12CPLAEELsCSICLEP


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
MAP3K13IDDescription0.00e+00
MAP3K13GO:0044790suppression of viral release by host1.50e-02
MAP3K13GO:0046597negative regulation of viral entry into host cell1.50e-02
MAP3K13GO:1903901negative regulation of viral life cycle1.50e-02
MAP3K13GO:0019076viral release from host cell1.50e-02
MAP3K13GO:0035891exit from host cell1.50e-02
MAP3K13GO:0033280response to vitamin D1.50e-02
MAP3K13GO:0006513protein monoubiquitination1.50e-02
MAP3K13GO:0140374antiviral innate immune response1.50e-02
MAP3K13GO:0046596regulation of viral entry into host cell1.50e-02
MAP3K13GO:0052372modulation by symbiont of entry into host1.54e-02
MAP3K13GO:0043903regulation of biological process involved in symbiotic interaction1.58e-02
MAP3K13GO:0043627response to estrogen1.58e-02
MAP3K13GO:0030433ubiquitin-dependent ERAD pathway1.69e-02
MAP3K13GO:0033273response to vitamin1.69e-02
MAP3K13GO:0048525negative regulation of viral process1.70e-02
MAP3K13GO:1990830cellular response to leukemia inhibitory factor1.70e-02
MAP3K13GO:1990823response to leukemia inhibitory factor1.70e-02
MAP3K13GO:0036503ERAD pathway1.70e-02
MAP3K13GO:1903900regulation of viral life cycle1.85e-02
MAP3K13GO:0002753cytosolic pattern recognition receptor signaling pathway1.85e-02
MAP3K13GO:0051092positive regulation of NF-kappaB transcription factor activity1.85e-02
MAP3K13GO:0007584response to nutrient1.85e-02
MAP3K13GO:0046718viral entry into host cell1.85e-02
MAP3K13GO:0044409entry into host1.85e-02
MAP3K13GO:0050792regulation of viral process1.85e-02
MAP3K13GO:0044000movement in host1.99e-02
MAP3K13GO:0043123positive regulation of canonical NF-kappaB signal transduction2.00e-02
MAP3K13GO:0051701biological process involved in interaction with host2.08e-02
MAP3K13GO:0002221pattern recognition receptor signaling pathway2.22e-02
MAP3K13GO:0051091positive regulation of DNA-binding transcription factor activity2.22e-02
MAP3K13GO:0002758innate immune response-activating signaling pathway2.22e-02
MAP3K13GO:0043122regulation of canonical NF-kappaB signal transduction2.22e-02
MAP3K13GO:0034976response to endoplasmic reticulum stress2.22e-02
MAP3K13GO:0002218activation of innate immune response2.24e-02
MAP3K13GO:0007249canonical NF-kappaB signal transduction2.36e-02
MAP3K13GO:0019058viral life cycle2.36e-02
MAP3K13GO:0044403biological process involved in symbiotic interaction2.36e-02
MAP3K13GO:0051607defense response to virus2.36e-02
MAP3K13GO:0140546defense response to symbiont2.36e-02
MAP3K13GO:0045089positive regulation of innate immune response2.36e-02
MAP3K13GO:0030522intracellular receptor signaling pathway2.37e-02
MAP3K13GO:0002833positive regulation of response to biotic stimulus2.42e-02
MAP3K13GO:0006979response to oxidative stress2.54e-02
MAP3K13GO:0051090regulation of DNA-binding transcription factor activity2.54e-02
MAP3K13GO:0045088regulation of innate immune response2.56e-02
MAP3K13GO:0016032viral process2.56e-02
MAP3K13GO:0009615response to virus2.56e-02
MAP3K13GO:0043161proteasome-mediated ubiquitin-dependent protein catabolic process2.63e-02
MAP3K13GO:0002757immune response-activating signaling pathway2.65e-02

Top

Related Drugs to LPCAT3_MAP3K13


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 LPCAT3-MAP3K13 and kinase inhibitors the PubMed Abstract (04-01-2024)

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

Top

Related Diseases to LPCAT3_MAP3K13


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