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Fusion Protein:FOXK1-SDK1 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: FOXK1-SDK1 | FusionPDB ID: 31090 | FusionGDB2.0 ID: 31090 | Hgene | Tgene | Gene symbol | FOXK1 | SDK1 | Gene ID | 221937 | 221935 |
Gene name | forkhead box K1 | sidekick cell adhesion molecule 1 | |
Synonyms | FOXK1L | - | |
Cytomap | 7p22.1 | 7p22.2 | |
Type of gene | protein-coding | protein-coding | |
Description | forkhead box protein K1MNFmyocyte nuclear factor | protein sidekick-1sidekick homolog 1, cell adhesion molecule | |
Modification date | 20200313 | 20200320 | |
UniProtAcc | P85037 | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000328914, ENST00000446823, | ENST00000466611, ENST00000389531, ENST00000404826, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 6 X 4 X 5=120 | 21 X 21 X 9=3969 |
# samples | 7 | 23 | |
** MAII score | log2(7/120*10)=-0.777607578663552 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(23/3969*10)=-4.10906979605546 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: FOXK1 [Title/Abstract] AND SDK1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | FOXK1(4722499)-SDK1(4247731), # samples:2 FOXK1(4722499)-SDK1(3861082), # samples:2 SDK1(3861215)-FOXK1(4794089), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | FOXK1-SDK1 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. FOXK1-SDK1 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. FOXK1-SDK1 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. FOXK1-SDK1 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. FOXK1-SDK1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. FOXK1-SDK1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF. SDK1-FOXK1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. SDK1-FOXK1 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted 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 | FOXK1 | GO:0001678 | cellular glucose homeostasis | 29861159|30700909 |
Hgene | FOXK1 | GO:0010507 | negative regulation of autophagy | 25402684 |
Hgene | FOXK1 | GO:0010906 | regulation of glucose metabolic process | 29861159|30700909 |
Hgene | FOXK1 | GO:0042594 | response to starvation | 25402684 |
Hgene | FOXK1 | GO:0045892 | negative regulation of transcription, DNA-templated | 17670796|25402684 |
Hgene | FOXK1 | GO:0045893 | positive regulation of transcription, DNA-templated | 29861159|30700909 |
Hgene | FOXK1 | GO:0061621 | canonical glycolysis | 30700909 |
![]() * 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 | BRCA | TCGA-C8-A12L-01A | FOXK1 | chr7 | 4722499 | + | SDK1 | chr7 | 4247731 | + |
ChimerDB4 | PRAD | TCGA-CH-5751-01A | FOXK1 | chr7 | 4722499 | + | SDK1 | chr7 | 3861082 | + |
ChimerDB4 | PRAD | TCGA-CH-5751 | FOXK1 | chr7 | 4722499 | + | SDK1 | chr7 | 3861082 | + |
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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) |
ENST00000328914 | FOXK1 | chr7 | 4722499 | + | ENST00000404826 | SDK1 | chr7 | 3861082 | + | 10105 | 560 | 0 | 6488 | 2162 |
ENST00000328914 | FOXK1 | chr7 | 4722499 | + | ENST00000389531 | SDK1 | chr7 | 3861082 | + | 7453 | 560 | 0 | 6428 | 2142 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000328914 | ENST00000404826 | FOXK1 | chr7 | 4722499 | + | SDK1 | chr7 | 3861082 | + | 0.000863214 | 0.99913687 |
ENST00000328914 | ENST00000389531 | FOXK1 | chr7 | 4722499 | + | SDK1 | chr7 | 3861082 | + | 0.001900389 | 0.9980996 |
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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 >31090_31090_1_FOXK1-SDK1_FOXK1_chr7_4722499_ENST00000328914_SDK1_chr7_3861082_ENST00000389531_length(amino acids)=2142AA_BP=187 MAEVGEDSGARALLALRSAPCSPVLCAAAAAAAFPAAAPPPAPAQPQPPPGPPPPPPPPLPPGAIAGAGSSGGSSGVSGDSAVAGAAPAL VAAAAASVRQSPGPALARLEGREFEFLMRQPSVTIGRNSSQGSVDLSMGLSSFISRRHLQLSFQEPHFYLRCLGKNGVFVDGAFQRRGAP ALQLPKQAITLENQLVILATTTSDAGAYYVQAVNEKNGENKTSPFIHLSIARDVGTPETMAPTIVVPPGNRSVVAGSSETTLECIASARP VEDLSVTWKRNGVRITSGLHSFGRRLTISNPTSADTGPYVCEAALPGSAFEPARATAFLFIIEPPYFTAEPESRISAEVEETVDIGCQAM GVPLPTLQWYKDAISISRLQNPRYKVLASGGLRIQKLRPEDSGIFQCFASNEGGEIQTHTYLDVTNIAPVFTQRPVDTTVTDGMTAILRC EVSGAPKPAITWKRENHILASGSVRIPRFMLLESGGLQIAPVFIQDAGNYTCYAANTEGSLNASATLTVWNRTSIVHPPEDHVVIKGTTA TLHCGATHDPRVSLRYVWKKDNVALTPSSTSRIVVEKDGSLLISQTWSGDIGDYSCEIVSEGGNDSRMARLEVIELPHSPQNLLVSPNSS HSHAVVLSWVRPFDGNSPILYYIVELSENNSPWKVHLSNVGPEMTGVTVSGLTPARTYQFRVCAVNEVGRGQYSAETSRLMLPEEPPSAP PKNIVASGRTNQSIMVQWQPPPETEHNGVLRGYILRYRLAGLPGEYQQRNITSPEVNYCLVTDLIIWTQYEIQVAAYNGAGLGVFSRAVT EYTLQGVPTAPPQNVQTEAVNSTTIQFLWNPPPQQFINGINQGYKLLAWPADAPEAVTVVTIAPDFHGVHHGHITNLKKFTAYFTSVLCF TTPGDGPPSTPQLVWTQEDKPGAVGHLSFTEILDTSLKVSWQEPLEKNGIITGYQISWEVYGRNDSRLTHTLNSTTHEYKIQGLSSLTTY TIDVAAVTAVGTGLVTSSTISSGVPPDLPGAPSNLVISNISPRSATLQFRPGYDGKTSISRWIVEGQVGAIGDEEEWVTLYEEENEPDAQ MLEIPNLTPYTHYRFRMKQVNIVGPSPYSPSSRVIQTLQAPPDVAPTSVTVRTASETSLRLRWVPLPDSQYNGNPESVGYRIKYWRSDLQ SSAVAQVVSDRLEREFTIEELEEWMEYELQMQAFNAVGAGPWSEVVRGRTRESVPSAAPENVSAEAVSSTQILLTWTSVPEQDQNGLILG YKILFRAKDLDPEPRSHIVRGNHTQSALLAGLRKFVLYELQVLAFTRIGNGVPSTPLILERTKDDAPGPPVRLVFPEVRLTSVRIVWQPP EEPNGIILGYQIAYRLASSSPHTFTTVEVGATVRQFTATDLAPESAYIFRLSAKTRQGWGEPLEATVITTEKRERPAPPRELLVPQAEVT ARSLRLQWVPGSDGASPIRYFTMQVRELPRGEWQTYSSSISHEATACVVDRLRPFTSYKLRLKATNDIGDSDFSSETEAVTTLQDVPGEP PGSVSATPHTTSSVLIQWQPPRDESLNGLLQGYRIYYRELEYEAGSGTEAKTLKNPIALHAELTDLKKYRRYEVIMTAYNIIGESPASAP VEVFVGEAAPAMAPQNVQVTPLTASQLEVTWDPPPPESQNGNIQGYKIYYWEADSQNETEKMKVLFLPEPVVRLKNLTSHTKYLVSISAF NAAGDGPKSDPQQGRTHQAAPGAPSFLAFSEITSTTLNVSWGEPAAANGILQGYRVVYEPLAPVQGVSKVVTVEVRGNWQRWLKVRDLTK GVTYFFRVQARTITYGPELQANITAGPAEGSPGSPRDVLVTKSASELTLQWTEGHSGDTPTTGYVIEARPSDEGLWDMFVKDIPRSATSY TLSLDKLRQGVTYEFRVVAVNEAGYGEPSNPSTAVSAQVEAPFYEEWWFLLVMALSSLIVILLVVFALVLHGQNKKYKNCSTGKGISTME ESVTLDNGGFAALELSSRHLNVKSTFSKKNGTRSPPRPSPGGLHYSDEDICNKYNGAVLTESVSLKEKSADASESEATDSDYEDALPKHS -------------------------------------------------------------- >31090_31090_2_FOXK1-SDK1_FOXK1_chr7_4722499_ENST00000328914_SDK1_chr7_3861082_ENST00000404826_length(amino acids)=2162AA_BP=187 MAEVGEDSGARALLALRSAPCSPVLCAAAAAAAFPAAAPPPAPAQPQPPPGPPPPPPPPLPPGAIAGAGSSGGSSGVSGDSAVAGAAPAL VAAAAASVRQSPGPALARLEGREFEFLMRQPSVTIGRNSSQGSVDLSMGLSSFISRRHLQLSFQEPHFYLRCLGKNGVFVDGAFQRRGAP ALQLPKQAITLENQLVILATTTSDAGAYYVQAVNEKNGENKTSPFIHLSIARDVGTPETMAPTIVVPPGNRSVVAGSSETTLECIASARP VEDLSVTWKRNGVRITSGLHSFGRRLTISNPTSADTGPYVCEAALPGSAFEPARATAFLFIIEPPYFTAEPESRISAEVEETVDIGCQAM GVPLPTLQWYKDAISISRLQNPRYKVLASGGLRIQKLRPEDSGIFQCFASNEGGEIQTHTYLDVTNIAPVFTQRPVDTTVTDGMTAILRC EVSGAPKPAITWKRENHILASGSVRIPRFMLLESGGLQIAPVFIQDAGNYTCYAANTEGSLNASATLTVWNRTSIVHPPEDHVVIKGTTA TLHCGATHDPRVSLRYVWKKDNVALTPSSTSRIVVEKDGSLLISQTWSGDIGDYSCEIVSEGGNDSRMARLEVIELPHSPQNLLVSPNSS HSHAVVLSWVRPFDGNSPILYYIVELSENNSPWKVHLSNVGPEMTGVTVSGLTPARTYQFRVCAVNEVGRGQYSAETSRLMLPEEPPSAP PKNIVASGRTNQSIMVQWQPPPETEHNGVLRGYILRYRLAGLPGEYQQRNITSPEVNYCLVTDLIIWTQYEIQVAAYNGAGLGVFSRAVT EYTLQGVPTAPPQNVQTEAVNSTTIQFLWNPPPQQFINGINQGYKLLAWPADAPEAVTVVTIAPDFHGVHHGHITNLKKFTAYFTSVLCF TTPGDGPPSTPQLVWTQEDKPGAVGHLSFTEILDTSLKVSWQEPLEKNGIITGYQISWEVYGRNDSRLTHTLNSTTHEYKIQGLSSLTTY TIDVAAVTAVGTGLVTSSTISSGVPPDLPGAPSNLVISNISPRSATLQFRPGYDGKTSISRWIVEGQVGAIGDEEEWVTLYEEENEPDAQ MLEIPNLTPYTHYRFRMKQVNIVGPSPYSPSSRVIQTLQAPPDVAPTSVTVRTASETSLRLRWVPLPDSQYNGNPESVGYRIKYWRSDLQ SSAVAQVVSDRLEREFTIEELEEWMEYELQMQAFNAVGAGPWSEVVRGRTRESVPSAAPENVSAEAVSSTQILLTWTSVPEQDQNGLILG YKILFRAKDLDPEPRSHIVRGNHTQSALLAGLRKFVLYELQVLAFTRIGNGVPSTPLILERTKDDAPGPPVRLVFPEVRLTSVRIVWQPP EEPNGIILGYQIAYRLASSSPHTFTTVEVGATVRQFTATDLAPESAYIFRLSAKTRQGWGEPLEATVITTEKRERPAPPRELLVPQAEVT ARSLRLQWVPGSDGASPIRYFTMQVRELPRGEWQTYSSSISHEATACVVDRLRPFTSYKLRLKATNDIGDSDFSSETEAVTTLQDVPGEP PGSVSATPHTTSSVLIQWQPPRDESLNGLLQGYRIYYRELEYEAGSGTEAKTLKNPIALHAELTAQSSFKTVNSSSTSTMCELTHLKKYR RYEVIMTAYNIIGESPASAPVEVFVGEAAPAMAPQNVQVTPLTASQLEVTWDPPPPESQNGNIQGYKIYYWEADSQNETEKMKVLFLPEP VVRLKNLTSHTKYLVSISAFNAAGDGPKSDPQQGRTHQAAPGAPSFLAFSEITSTTLNVSWGEPAAANGILQGYRVVYEPLAPVQGVSKV VTVEVRGNWQRWLKVRDLTKGVTYFFRVQARTITYGPELQANITAGPAEGSPGSPRDVLVTKSASELTLQWTEGHSGDTPTTGYVIEARP SDEGLWDMFVKDIPRSATSYTLSLDKLRQGVTYEFRVVAVNEAGYGEPSNPSTAVSAQVEAPFYEEWWFLLVMALSSLIVILLVVFALVL HGQNKKYKNCSTGKGISTMEESVTLDNGGFAALELSSRHLNVKSTFSKKNGTRSPPRPSPGGLHYSDEDICNKYNGAVLTESVSLKEKSA DASESEATDSDYEDALPKHSFVNHYMSDPTYYNSWKRRAQGRAPAPHRYEAVAGSEAGAQLHPVITTQSAGGVYTPAGPGARTPLTGFSS -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr7:4722499/chr7:4247731) - 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 |
FOXK1 | . |
FUNCTION: Transcriptional regulator involved in different processes such as glucose metabolism, aerobic glycolysis, muscle cell differentiation and autophagy (By similarity). Recognizes and binds the forkhead DNA sequence motif (5'-GTAAACA-3') and can both act as a transcription activator or repressor, depending on the context (PubMed:17670796). Together with FOXK2, acts as a key regulator of metabolic reprogramming towards aerobic glycolysis, a process in which glucose is converted to lactate in the presence of oxygen (By similarity). Acts by promoting expression of enzymes for glycolysis (such as hexokinase-2 (HK2), phosphofructokinase, pyruvate kinase (PKLR) and lactate dehydrogenase), while suppressing further oxidation of pyruvate in the mitochondria by up-regulating pyruvate dehydrogenase kinases PDK1 and PDK4 (By similarity). Probably plays a role in gluconeogenesis during overnight fasting, when lactate from white adipose tissue and muscle is the main substrate (By similarity). Involved in mTORC1-mediated metabolic reprogramming: in response to mTORC1 signaling, translocates into the nucleus and regulates the expression of genes associated with glycolysis and downstream anabolic pathways, such as HIF1A, thereby regulating glucose metabolism (By similarity). Together with FOXK2, acts as a negative regulator of autophagy in skeletal muscle: in response to starvation, enters the nucleus, binds the promoters of autophagy genes and represses their expression, preventing proteolysis of skeletal muscle proteins (By similarity). Acts as a transcriptional regulator of the myogenic progenitor cell population in skeletal muscle (By similarity). Binds to the upstream enhancer region (CCAC box) of myoglobin (MB) gene, regulating the myogenic progenitor cell population (By similarity). Promotes muscle progenitor cell proliferation by repressing the transcriptional activity of FOXO4, thereby inhibiting myogenic differentiation (By similarity). Involved in remodeling processes of adult muscles that occur in response to physiological stimuli (By similarity). Required to correct temporal orchestration of molecular and cellular events necessary for muscle repair (By similarity). Represses myogenic differentiation by inhibiting MEFC activity (By similarity). Positively regulates Wnt/beta-catenin signaling by translocating DVL into the nucleus (PubMed:25805136). Reduces virus replication, probably by binding the interferon stimulated response element (ISRE) to promote antiviral gene expression (PubMed:25852164). {ECO:0000250|UniProtKB:P42128, ECO:0000269|PubMed:17670796, ECO:0000269|PubMed:25805136, ECO:0000269|PubMed:25852164}. | 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 | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000328914 | + | 1 | 9 | 10_96 | 186.66666666666666 | 734.0 | Compositional bias | Ala-rich |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000328914 | + | 1 | 9 | 35_62 | 186.66666666666666 | 734.0 | Compositional bias | Pro-rich |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000328914 | + | 1 | 9 | 123_175 | 186.66666666666666 | 734.0 | Domain | FHA |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1072_1171 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 5 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1176_1274 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 6 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1279_1376 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 7 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1380_1474 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 8 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1479_1576 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 9 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1581_1699 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 10 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1704_1800 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 11 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1804_1899 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 12 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 1902_2000 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 13 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 293_378 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 3 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 386_476 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 4 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 480_569 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 5 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 574_663 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 6 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 670_766 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 1 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 771_867 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 2 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 872_970 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 3 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 974_1068 | 237.66666666666666 | 2214.0 | Domain | Fibronectin type-III 4 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 2207_2213 | 237.66666666666666 | 2214.0 | Motif | PDZ-binding | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 2031_2213 | 237.66666666666666 | 2214.0 | Topological domain | Cytoplasmic | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 2010_2030 | 237.66666666666666 | 2214.0 | Transmembrane | Helical |
- 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 | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000446823 | + | 1 | 12 | 10_96 | 0 | 571.0 | Compositional bias | Ala-rich |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000446823 | + | 1 | 12 | 35_62 | 0 | 571.0 | Compositional bias | Pro-rich |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000328914 | + | 1 | 9 | 305_400 | 186.66666666666666 | 734.0 | DNA binding | Fork-head |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000446823 | + | 1 | 12 | 305_400 | 0 | 571.0 | DNA binding | Fork-head |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000446823 | + | 1 | 12 | 123_175 | 0 | 571.0 | Domain | FHA |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 19_58 | 237.66666666666666 | 2214.0 | Compositional bias | Note=Pro-rich | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 104_186 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 1 | |
Tgene | SDK1 | chr7:4722499 | chr7:3861082 | ENST00000404826 | 3 | 45 | 191_277 | 237.66666666666666 | 2214.0 | Domain | Note=Ig-like C2-type 2 |
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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) |
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pLDDT score distribution |
![]() * AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. |
FOXK1_pLDDT.png![]() |
SDK1_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 |
FOXK1 | |
SDK1 |
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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 |
Hgene | FOXK1 | chr7:4722499 | chr7:3861082 | ENST00000446823 | + | 1 | 12 | 2_40 | 0 | 571.0 | SIN3A and SIN3B |
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Related Drugs to FOXK1-SDK1 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to FOXK1-SDK1 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |