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Fusion Protein:LIMK1-GNAT3 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: LIMK1-GNAT3 | FusionPDB ID: 44711 | FusionGDB2.0 ID: 44711 | Hgene | Tgene | Gene symbol | LIMK1 | GNAT3 | Gene ID | 3984 | 346562 |
Gene name | LIM domain kinase 1 | G protein subunit alpha transducin 3 | |
Synonyms | LIMK|LIMK-1 | GDCA | |
Cytomap | 7q11.23 | 7q21.11 | |
Type of gene | protein-coding | protein-coding | |
Description | LIM domain kinase 1LIM motif-containing protein kinase | guanine nucleotide-binding protein G(t) subunit alpha-3guanine nucleotide binding protein, alpha transducing 3gustatory G proteingustducin alpha-3 chaingustducin, alpha polypeptide | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | P53667 | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000336180, ENST00000418310, ENST00000538333, ENST00000491052, | ENST00000398291, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 7 X 6 X 4=168 | 3 X 3 X 3=27 |
# samples | 6 | 3 | |
** MAII score | log2(6/168*10)=-1.48542682717024 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(3/27*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: LIMK1 [Title/Abstract] AND GNAT3 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | LIMK1(73530288)-GNAT3(80123963), # samples:3 | ||
Anticipated loss of major functional domain due to fusion event. | LIMK1-GNAT3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. LIMK1-GNAT3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. LIMK1-GNAT3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. LIMK1-GNAT3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | LIMK1 | GO:0006468 | protein phosphorylation | 17512523|22328514 |
Hgene | LIMK1 | GO:0032233 | positive regulation of actin filament bundle assembly | 17512523 |
Hgene | LIMK1 | GO:0051444 | negative regulation of ubiquitin-protein transferase activity | 17512523 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | SARC | TCGA-X6-A8C6-01A | LIMK1 | chr7 | 73530288 | - | GNAT3 | chr7 | 80123963 | - |
ChimerDB4 | SARC | TCGA-X6-A8C6-01A | LIMK1 | chr7 | 73530288 | + | GNAT3 | chr7 | 80123963 | - |
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Fusion ORF Analysis |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000418310 | LIMK1 | chr7 | 73530288 | + | ENST00000398291 | GNAT3 | chr7 | 80123963 | - | 2706 | 1759 | 96 | 2705 | 869 |
ENST00000336180 | LIMK1 | chr7 | 73530288 | + | ENST00000398291 | GNAT3 | chr7 | 80123963 | - | 2565 | 1618 | 51 | 2564 | 837 |
ENST00000538333 | LIMK1 | chr7 | 73530288 | + | ENST00000398291 | GNAT3 | chr7 | 80123963 | - | 2583 | 1636 | 171 | 2582 | 803 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000418310 | ENST00000398291 | LIMK1 | chr7 | 73530288 | + | GNAT3 | chr7 | 80123963 | - | 0.00234379 | 0.9976562 |
ENST00000336180 | ENST00000398291 | LIMK1 | chr7 | 73530288 | + | GNAT3 | chr7 | 80123963 | - | 0.002325742 | 0.9976743 |
ENST00000538333 | ENST00000398291 | LIMK1 | chr7 | 73530288 | + | GNAT3 | chr7 | 80123963 | - | 0.002479037 | 0.997521 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >44711_44711_1_LIMK1-GNAT3_LIMK1_chr7_73530288_ENST00000336180_GNAT3_chr7_80123963_ENST00000398291_length(amino acids)=837AA_BP=522 MRLTLLCCTWREERMGEEGSELPVCASCGQRIYDGQYLQALNADWHADCFRCCDCSASLSHQYYEKDGQLFCKKDYWARYGESCHGCSEQ ITKGLVMVAGELKYHPECFICLTCGTFIGDGDTYTLVEHSKLYCGHCYYQTVVTPVIEQILPDSPGSHLPHTVTLVSIPASSHGKRGLSV SIDPPHGPPGCGTEHSHTVRVQGVDPGCMSPDVKNSIHVGDRILEINGTPIRNVPLDEIDLLIQETSRLLQLTLEHDPHDTLGHGLGPET SPLSSPAYTPSGEAGSSARQKPVLRSCSIDRSPGAGSLGSPASQRKDLGRSESLRVVCRPHRIFRPSDLIHGEVLGKGCFGQAIKVTHRE TGEVMVMKELIRFDEETQRTFLKEVKVMRCLEHPNVLKFIGVLYKDKRLNFITEYIKGGTLRGIIKSMDSQYPWSQRVSFAKDIASGMAY LHSMNIIHRDLNSHNCLVRENKNVVVADFGLARLMVDEKTQPEGLRSLKKPDRKKRYTVVGNPYWMAPEMINGAGESGKSTIVKQMKIIH KNGYSEQECMEFKAVIYSNTLQSILAIVKAMTTLGIDYVNPRSAEDQRQLYAMANTLEDGGMTPQLAEVIKRLWRDPGIQACFERASEYQ LNDSAAYYLNDLDRITASGYVPNEQDVLHSRVKTTGIIETQFSFKDLHFRMFDVGGQRSERKKWIHCFEGVTCIIFCAALSAYDMVLVED EEVNRMHESLHLFNSICNHKYFSTTSIVLFLNKKDIFQEKVTKVHLSICFPEYTGPNTFEDAGNYIKNQFLDLNLKKEDKEIYSHMTCAT -------------------------------------------------------------- >44711_44711_2_LIMK1-GNAT3_LIMK1_chr7_73530288_ENST00000418310_GNAT3_chr7_80123963_ENST00000398291_length(amino acids)=869AA_BP=554 MPMSSILELSTSRQGVPPSVLDWTTQFLWTLDSAQTRAPSRTLGRAAPAPGSELPVCASCGQRIYDGQYLQALNADWHADCFRCCDCSAS LSHQYYEKDGQLFCKKDYWARYGESCHGCSEQITKGLVMVAGELKYHPECFICLTCGTFIGDGDTYTLVEHSKLYCGHCYYQTVVTPVIE QILPDSPGSHLPHTVTLVSIPASSHGKRGLSVSIDPPHGPPGCGTEHSHTVRVQGVDPGCMSPDVKNSIHVGDRILEINGTPIRNVPLDE IDLLIQETSRLLQLTLEHDPHDTLGHGLGPETSPLSSPAYTPSGEAGSSARQKPVLRSCSIDRSPGAGSLGSPASQRKDLGRSESLRVVC RPHRIFRPSDLIHGEVLGKGCFGQAIKVTHRETGEVMVMKELIRFDEETQRTFLKEVKVMRCLEHPNVLKFIGVLYKDKRLNFITEYIKG GTLRGIIKSMDSQYPWSQRVSFAKDIASGMAYLHSMNIIHRDLNSHNCLVRENKNVVVADFGLARLMVDEKTQPEGLRSLKKPDRKKRYT VVGNPYWMAPEMINGAGESGKSTIVKQMKIIHKNGYSEQECMEFKAVIYSNTLQSILAIVKAMTTLGIDYVNPRSAEDQRQLYAMANTLE DGGMTPQLAEVIKRLWRDPGIQACFERASEYQLNDSAAYYLNDLDRITASGYVPNEQDVLHSRVKTTGIIETQFSFKDLHFRMFDVGGQR SERKKWIHCFEGVTCIIFCAALSAYDMVLVEDEEVNRMHESLHLFNSICNHKYFSTTSIVLFLNKKDIFQEKVTKVHLSICFPEYTGPNT -------------------------------------------------------------- >44711_44711_3_LIMK1-GNAT3_LIMK1_chr7_73530288_ENST00000538333_GNAT3_chr7_80123963_ENST00000398291_length(amino acids)=803AA_BP=488 MLLASAPRRRRFLQRAKCCDCSASLSHQYYEKDGQLFCKKDYWARYGESCHGCSEQITKGLVMVAGELKYHPECFICLTCGTFIGDGDTY TLVEHSKLYCGHCYYQTVVTPVIEQILPDSPGSHLPHTVTLVSIPASSHGKRGLSVSIDPPHGPPGCGTEHSHTVRVQGVDPGCMSPDVK NSIHVGDRILEINGTPIRNVPLDEIDLLIQETSRLLQLTLEHDPHDTLGHGLGPETSPLSSPAYTPSGEAGSSARQKPVLRSCSIDRSPG AGSLGSPASQRKDLGRSESLRVVCRPHRIFRPSDLIHGEVLGKGCFGQAIKVTHRETGEVMVMKELIRFDEETQRTFLKEVKVMRCLEHP NVLKFIGVLYKDKRLNFITEYIKGGTLRGIIKSMDSQYPWSQRVSFAKDIASGMAYLHSMNIIHRDLNSHNCLVRENKNVVVADFGLARL MVDEKTQPEGLRSLKKPDRKKRYTVVGNPYWMAPEMINGAGESGKSTIVKQMKIIHKNGYSEQECMEFKAVIYSNTLQSILAIVKAMTTL GIDYVNPRSAEDQRQLYAMANTLEDGGMTPQLAEVIKRLWRDPGIQACFERASEYQLNDSAAYYLNDLDRITASGYVPNEQDVLHSRVKT TGIIETQFSFKDLHFRMFDVGGQRSERKKWIHCFEGVTCIIFCAALSAYDMVLVEDEEVNRMHESLHLFNSICNHKYFSTTSIVLFLNKK -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr7:73530288/chr7:80123963) - 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. |
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Hgene | Tgene |
LIMK1 | . |
FUNCTION: Serine/threonine-protein kinase that plays an essential role in the regulation of actin filament dynamics. Acts downstream of several Rho family GTPase signal transduction pathways (PubMed:10436159, PubMed:11832213, PubMed:12807904, PubMed:15660133, PubMed:16230460, PubMed:18028908, PubMed:22328514, PubMed:23633677). Activated by upstream kinases including ROCK1, PAK1 and PAK4, which phosphorylate LIMK1 on a threonine residue located in its activation loop (PubMed:10436159). LIMK1 subsequently phosphorylates and inactivates the actin binding/depolymerizing factors cofilin-1/CFL1, cofilin-2/CFL2 and destrin/DSTN, thereby preventing the cleavage of filamentous actin (F-actin), and stabilizing the actin cytoskeleton (PubMed:11832213, PubMed:15660133, PubMed:16230460, PubMed:23633677). In this way LIMK1 regulates several actin-dependent biological processes including cell motility, cell cycle progression, and differentiation (PubMed:11832213, PubMed:15660133, PubMed:16230460, PubMed:23633677). Phosphorylates TPPP on serine residues, thereby promoting microtubule disassembly (PubMed:18028908). Stimulates axonal outgrowth and may be involved in brain development (PubMed:18028908). {ECO:0000269|PubMed:10436159, ECO:0000269|PubMed:11832213, ECO:0000269|PubMed:12807904, ECO:0000269|PubMed:15660133, ECO:0000269|PubMed:16230460, ECO:0000269|PubMed:18028908, ECO:0000269|PubMed:22328514, ECO:0000269|PubMed:23633677}.; FUNCTION: [Isoform 3]: Has a dominant negative effect on actin cytoskeletal changes. Required for atypical chemokine receptor ACKR2-induced phosphorylation of cofilin (CFL1). {ECO:0000269|PubMed:10196227}. | FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. |
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- Retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000336180 | + | 13 | 16 | 165_258 | 522.3333333333334 | 648.0 | Domain | PDZ |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000336180 | + | 13 | 16 | 25_75 | 522.3333333333334 | 648.0 | Domain | LIM zinc-binding 1 |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000336180 | + | 13 | 16 | 84_137 | 522.3333333333334 | 648.0 | Domain | LIM zinc-binding 2 |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000538333 | + | 12 | 15 | 165_258 | 488.3333333333333 | 614.0 | Domain | PDZ |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000538333 | + | 12 | 15 | 25_75 | 488.3333333333333 | 614.0 | Domain | LIM zinc-binding 1 |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000538333 | + | 12 | 15 | 84_137 | 488.3333333333333 | 614.0 | Domain | LIM zinc-binding 2 |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000336180 | + | 13 | 16 | 345_353 | 522.3333333333334 | 648.0 | Nucleotide binding | ATP |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000538333 | + | 12 | 15 | 345_353 | 488.3333333333333 | 614.0 | Nucleotide binding | ATP |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 175_181 | 39.333333333333336 | 355.0 | Nucleotide binding | GTP | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 200_204 | 39.333333333333336 | 355.0 | Nucleotide binding | GTP | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 269_272 | 39.333333333333336 | 355.0 | Nucleotide binding | GTP | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 40_47 | 39.333333333333336 | 355.0 | Nucleotide binding | GTP | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 173_181 | 39.333333333333336 | 355.0 | Region | G2 motif | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 196_205 | 39.333333333333336 | 355.0 | Region | G3 motif | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 265_272 | 39.333333333333336 | 355.0 | Region | G4 motif | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 324_329 | 39.333333333333336 | 355.0 | Region | G5 motif |
- Not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000336180 | + | 13 | 16 | 339_604 | 522.3333333333334 | 648.0 | Domain | Protein kinase |
Hgene | LIMK1 | chr7:73530288 | chr7:80123963 | ENST00000538333 | + | 12 | 15 | 339_604 | 488.3333333333333 | 614.0 | Domain | Protein kinase |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 32_354 | 39.333333333333336 | 355.0 | Domain | G-alpha | |
Tgene | GNAT3 | chr7:73530288 | chr7:80123963 | ENST00000398291 | 0 | 8 | 35_48 | 39.333333333333336 | 355.0 | Region | G1 motif |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
LIMK1 | |
GNAT3 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to LIMK1-GNAT3 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to LIMK1-GNAT3 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |