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Fusion Protein:AKAP6-EGLN3 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: AKAP6-EGLN3 | FusionPDB ID: 3350 | FusionGDB2.0 ID: 3350 | Hgene | Tgene | Gene symbol | AKAP6 | EGLN3 | Gene ID | 9472 | 112399 |
Gene name | A-kinase anchoring protein 6 | egl-9 family hypoxia inducible factor 3 | |
Synonyms | ADAP100|ADAP6|AKAP100|PRKA6|mAKAP | HIFP4H3|HIFPH3|PHD3 | |
Cytomap | 14q12 | 14q13.1 | |
Type of gene | protein-coding | protein-coding | |
Description | A-kinase anchor protein 6A kinase (PRKA) anchor protein 6A-kinase anchor protein 100 kDaAKAP 100AKAP-6protein kinase A anchoring protein 6 | egl nine homolog 3HIF-PH3HIF-prolyl hydroxylase 3HPH-1HPH-3egl nine-like protein 3 isoformhypoxia-inducible factor prolyl hydroxylase 3prolyl hydroxylase domain-containing protein 3 | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | Q13023 | Q9H6Z9 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000554449, ENST00000280979, ENST00000557272, ENST00000557354, | ENST00000250457, ENST00000553215, ENST00000547327, ENST00000557521, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 9 X 8 X 4=288 | 5 X 4 X 3=60 |
# samples | 9 | 5 | |
** MAII score | log2(9/288*10)=-1.67807190511264 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/60*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: AKAP6 [Title/Abstract] AND EGLN3 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | AKAP6(32903023)-EGLN3(34400421), # samples:4 | ||
Anticipated loss of major functional domain due to fusion event. | AKAP6-EGLN3 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. AKAP6-EGLN3 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. AKAP6-EGLN3 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. AKAP6-EGLN3 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 | AKAP6 | GO:0060306 | regulation of membrane repolarization | 11299204 |
Hgene | AKAP6 | GO:0071320 | cellular response to cAMP | 11299204 |
Hgene | AKAP6 | GO:1901381 | positive regulation of potassium ion transmembrane transport | 11299204 |
Hgene | AKAP6 | GO:1902261 | positive regulation of delayed rectifier potassium channel activity | 11299204 |
Tgene | EGLN3 | GO:0018126 | protein hydroxylation | 19584355 |
Tgene | EGLN3 | GO:0018401 | peptidyl-proline hydroxylation to 4-hydroxy-L-proline | 11598268 |
![]() * 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 | GBM | TCGA-06-5413-01A | AKAP6 | chr14 | 32903023 | - | EGLN3 | chr14 | 34400421 | - |
ChimerDB4 | GBM | TCGA-06-5413-01A | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - |
ChimerDB4 | GBM | TCGA-06-5413 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - |
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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) |
ENST00000280979 | AKAP6 | chr14 | 32903023 | + | ENST00000250457 | EGLN3 | chr14 | 34400421 | - | 2517 | 494 | 170 | 856 | 228 |
ENST00000280979 | AKAP6 | chr14 | 32903023 | + | ENST00000553215 | EGLN3 | chr14 | 34400421 | - | 1349 | 494 | 170 | 856 | 228 |
ENST00000557354 | AKAP6 | chr14 | 32903023 | + | ENST00000250457 | EGLN3 | chr14 | 34400421 | - | 2446 | 423 | 99 | 785 | 228 |
ENST00000557354 | AKAP6 | chr14 | 32903023 | + | ENST00000553215 | EGLN3 | chr14 | 34400421 | - | 1278 | 423 | 99 | 785 | 228 |
ENST00000557272 | AKAP6 | chr14 | 32903023 | + | ENST00000250457 | EGLN3 | chr14 | 34400421 | - | 2390 | 367 | 43 | 729 | 228 |
ENST00000557272 | AKAP6 | chr14 | 32903023 | + | ENST00000553215 | EGLN3 | chr14 | 34400421 | - | 1222 | 367 | 43 | 729 | 228 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000280979 | ENST00000250457 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000540768 | 0.9994592 |
ENST00000280979 | ENST00000553215 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000511528 | 0.9994885 |
ENST00000557354 | ENST00000250457 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000451088 | 0.99954885 |
ENST00000557354 | ENST00000553215 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000475411 | 0.9995246 |
ENST00000557272 | ENST00000250457 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000511596 | 0.99948835 |
ENST00000557272 | ENST00000553215 | AKAP6 | chr14 | 32903023 | + | EGLN3 | chr14 | 34400421 | - | 0.000512735 | 0.9994873 |
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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 >3350_3350_1_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000280979_EGLN3_chr14_34400421_ENST00000250457_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- >3350_3350_2_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000280979_EGLN3_chr14_34400421_ENST00000553215_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- >3350_3350_3_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000557272_EGLN3_chr14_34400421_ENST00000250457_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- >3350_3350_4_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000557272_EGLN3_chr14_34400421_ENST00000553215_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- >3350_3350_5_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000557354_EGLN3_chr14_34400421_ENST00000250457_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- >3350_3350_6_AKAP6-EGLN3_AKAP6_chr14_32903023_ENST00000557354_EGLN3_chr14_34400421_ENST00000553215_length(amino acids)=228AA_BP=108 MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr14:32903023/chr14:34400421) - 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 |
AKAP6 | EGLN3 |
FUNCTION: Binds to type II regulatory subunits of protein kinase A and anchors/targets them to the nuclear membrane or sarcoplasmic reticulum. May act as an adapter for assembling multiprotein complexes. | FUNCTION: Prolyl hydroxylase that mediates hydroxylation of proline residues in target proteins, such as PKM, TELO2, ATF4 and HIF1A (PubMed:19584355, PubMed:21620138, PubMed:21483450, PubMed:22797300, PubMed:20978507, PubMed:21575608). Target proteins are preferentially recognized via a LXXLAP motif. Cellular oxygen sensor that catalyzes, under normoxic conditions, the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins (PubMed:11595184, PubMed:12181324). Hydroxylates a specific proline found in each of the oxygen-dependent degradation (ODD) domains (N-terminal, NODD, and C-terminal, CODD) of HIF1A (PubMed:11595184, PubMed:12181324). Also hydroxylates HIF2A (PubMed:11595184, PubMed:12181324). Has a preference for the CODD site for both HIF1A and HIF2A (PubMed:11595184, PubMed:12181324). Hydroxylation on the NODD site by EGLN3 appears to require prior hydroxylation on the CODD site (PubMed:11595184, PubMed:12181324). Hydroxylated HIFs are then targeted for proteasomal degradation via the von Hippel-Lindau ubiquitination complex (PubMed:11595184, PubMed:12181324). Under hypoxic conditions, the hydroxylation reaction is attenuated allowing HIFs to escape degradation resulting in their translocation to the nucleus, heterodimerization with HIF1B, and increased expression of hypoxy-inducible genes (PubMed:11595184, PubMed:12181324). ELGN3 is the most important isozyme in limiting physiological activation of HIFs (particularly HIF2A) in hypoxia. Also hydroxylates PKM in hypoxia, limiting glycolysis (PubMed:21620138, PubMed:21483450). Under normoxia, hydroxylates and regulates the stability of ADRB2 (PubMed:19584355). Regulator of cardiomyocyte and neuronal apoptosis. In cardiomyocytes, inhibits the anti-apoptotic effect of BCL2 by disrupting the BAX-BCL2 complex (PubMed:20849813). In neurons, has a NGF-induced proapoptotic effect, probably through regulating CASP3 activity (PubMed:16098468). Also essential for hypoxic regulation of neutrophilic inflammation (PubMed:21317538). Plays a crucial role in DNA damage response (DDR) by hydroxylating TELO2, promoting its interaction with ATR which is required for activation of the ATR/CHK1/p53 pathway (PubMed:22797300). Also mediates hydroxylation of ATF4, leading to decreased protein stability of ATF4 (Probable). {ECO:0000269|PubMed:11595184, ECO:0000269|PubMed:12181324, ECO:0000269|PubMed:16098468, ECO:0000269|PubMed:19584355, ECO:0000269|PubMed:20849813, ECO:0000269|PubMed:20978507, ECO:0000269|PubMed:21317538, ECO:0000269|PubMed:21483450, ECO:0000269|PubMed:21575608, ECO:0000269|PubMed:21620138, ECO:0000269|PubMed:22797300, ECO:0000305|PubMed:17684156}. |
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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 |
Tgene | EGLN3 | chr14:32903023 | chr14:34400421 | ENST00000250457 | 0 | 5 | 116_214 | 119.0 | 240.0 | Domain | Fe2OG dioxygenase |
- 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 | AKAP6 | chr14:32903023 | chr14:34400421 | ENST00000280979 | + | 2 | 14 | 1560_1701 | 108.0 | 2779.3333333333335 | Compositional bias | Note=Ser-rich |
Hgene | AKAP6 | chr14:32903023 | chr14:34400421 | ENST00000280979 | + | 2 | 14 | 2063_2076 | 108.0 | 2779.3333333333335 | Region | Note=PKA-RII subunit binding domain |
Hgene | AKAP6 | chr14:32903023 | chr14:34400421 | ENST00000280979 | + | 2 | 14 | 1036_1150 | 108.0 | 2779.3333333333335 | Repeat | Note=Spectrin 2 |
Hgene | AKAP6 | chr14:32903023 | chr14:34400421 | ENST00000280979 | + | 2 | 14 | 762_848 | 108.0 | 2779.3333333333335 | Repeat | Note=Spectrin 1 |
Tgene | EGLN3 | chr14:32903023 | chr14:34400421 | ENST00000250457 | 0 | 5 | 62_73 | 119.0 | 240.0 | Region | Beta(2)beta(3) 'finger-like' loop |
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Fusion Protein Structures |
![]() * Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format. |
Fusion protein PDB link (fusion AA seq ID in FusionPDB) | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | AA seq | Len(AA seq) |
PDB file >>>348_AKAP6_32903023_EGLN3_34400421_ranked_0.pdb | AKAP6 | 32903023 | 32903023 | ENST00000553215 | EGLN3 | chr14 | 34400421 | - | MLTMSVTLSPLRSQDLDPMATDASPMAINMTPTVEQGEGEEAMKDMDSDQQYEKPPPLHTGADWKIVLHLPEIETWLRMTSERVRDLTYS VQQDSDSKHVDVHLVQLKAMVACYPGNGTGYVRHVDNPNGDGRCITCIYYLNKNWDAKLHGGILRIFPEGKSFIADVEPIFDRLLFFWSD | 228 |
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pLDDT score distribution |
![]() * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
AKAP6_pLDDT.png![]() |
EGLN3_pLDDT.png![]() |
![]() * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
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Ramachandran Plot of Fusion Protein Structure |
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Fusion AA seq ID in FusionPDB and their Ramachandran plots |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
AKAP6 | |
EGLN3 |
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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 AKAP6-EGLN3 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to AKAP6-EGLN3 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |