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Center for Computational Systems Medicine level2
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:HS2ST1-SH3GLB1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HS2ST1-SH3GLB1
FusionPDB ID: 37593
FusionGDB2.0 ID: 37593
HgeneTgene
Gene symbol

HS2ST1

SH3GLB1

Gene ID

9653

51100

Gene nameheparan sulfate 2-O-sulfotransferase 1SH3 domain containing GRB2 like, endophilin B1
SynonymsdJ604K5.2Bif-1|CGI-61|PPP1R70|dJ612B15.2
Cytomap

1p22.3

1p22.3

Type of geneprotein-codingprotein-coding
Descriptionheparan sulfate 2-O-sulfotransferase 12-O-sulfotransferase2OSTendophilin-B1Bax-interacting factor 1SH3 domain-containing GRB2-like protein B1SH3-containing protein SH3GLB1SH3-domain GRB2 like endophilin B1protein phosphatase 1, regulatory subunit 70testicular tissue protein Li 172
Modification date2020031320200313
UniProtAcc

Q7LGA3

.
Ensembl transtripts involved in fusion geneENST idsENST00000370550, ENST00000370551, 
ENST00000356813, 
ENST00000482504, 
ENST00000535010, ENST00000370558, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 5 X 7=3854 X 4 X 3=48
# samples 124
** MAII scorelog2(12/385*10)=-1.68182403997375
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*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: HS2ST1 [Title/Abstract] AND SH3GLB1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HS2ST1(87380843)-SH3GLB1(87185190), # samples:3
Anticipated loss of major functional domain due to fusion event.HS2ST1-SH3GLB1 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.
HS2ST1-SH3GLB1 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.
HS2ST1-SH3GLB1 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.
HS2ST1-SH3GLB1 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneSH3GLB1

GO:0031334

positive regulation of protein complex assembly

19074440


check buttonFusion gene breakpoints across HS2ST1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across SH3GLB1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4LIHCTCGA-DD-AAEG-01AHS2ST1chr1

87380843

-SH3GLB1chr1

87185190

+
ChimerDB4LIHCTCGA-DD-AAEG-01AHS2ST1chr1

87380843

+SH3GLB1chr1

87185190

+
ChimerDB4LIHCTCGA-DD-AAEGHS2ST1chr1

87380843

+SH3GLB1chr1

87185190

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000370551HS2ST1chr187380843+ENST00000370558SH3GLB1chr187185190+63465133891396335
ENST00000370550HS2ST1chr187380843+ENST00000370558SH3GLB1chr187185190+63204873631370335

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000370551ENST00000370558HS2ST1chr187380843+SH3GLB1chr187185190+0.000250370.9997496
ENST00000370550ENST00000370558HS2ST1chr187380843+SH3GLB1chr187185190+0.0002488920.99975115

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>37593_37593_1_HS2ST1-SH3GLB1_HS2ST1_chr1_87380843_ENST00000370550_SH3GLB1_chr1_87185190_ENST00000370558_length(amino acids)=335AA_BP=33
MGLLRIMMPPKLQLLAVVAFAVAMLFLENQIQKLEESRSKLDARIEEFVYEKLDRKAPSRINNPELLGQYMIDAGTEFGPGTAYGNALIK
CGETQKRIGTADRELIQTSALNFLTPLRNFIEGDYKTIAKERKLLQNKRLDLDAAKTRLKKAKAAETRNSSEQELRITQSEFDRQAEITR
LLLEGISSTHAHHLRCLNDFVEAQMTYYAQCYQYMLDLQKQLGSFPSNYLSNNNQTSVTPVPSVLPNAIGSSAMASTSGLVITSPSNLSD

--------------------------------------------------------------

>37593_37593_2_HS2ST1-SH3GLB1_HS2ST1_chr1_87380843_ENST00000370551_SH3GLB1_chr1_87185190_ENST00000370558_length(amino acids)=335AA_BP=33
MGLLRIMMPPKLQLLAVVAFAVAMLFLENQIQKLEESRSKLDARIEEFVYEKLDRKAPSRINNPELLGQYMIDAGTEFGPGTAYGNALIK
CGETQKRIGTADRELIQTSALNFLTPLRNFIEGDYKTIAKERKLLQNKRLDLDAAKTRLKKAKAAETRNSSEQELRITQSEFDRQAEITR
LLLEGISSTHAHHLRCLNDFVEAQMTYYAQCYQYMLDLQKQLGSFPSNYLSNNNQTSVTPVPSVLPNAIGSSAMASTSGLVITSPSNLSD

--------------------------------------------------------------

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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/chr1:87380843/chr1:87185190)
- 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
HS2ST1

Q7LGA3

.
FUNCTION: Catalyzes the transfer of sulfate to the C2-position of selected hexuronic acid residues within the maturing heparan sulfate (HS). 2-O-sulfation within HS, particularly of iduronate residues, is essential for HS to participate in a variety of high-affinity ligand-binding interactions and signaling processes. Mediates 2-O-sulfation of both L-iduronyl and D-glucuronyl residues (By similarity). {ECO:0000250}.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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370550+171_1141.333333333333336357.0Topological domainCytoplasmic
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370551+151_1141.333333333333336230.0Topological domainCytoplasmic
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370550+1712_2841.333333333333336357.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370551+1512_2841.333333333333336230.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneSH3GLB1chr1:87380843chr1:87185190ENST0000037055819155_19571.33333333333333366.0Coiled coilOntology_term=ECO:0000255
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000482504111155_19571.33333333333333387.0Coiled coilOntology_term=ECO:0000255
TgeneSH3GLB1chr1:87380843chr1:87185190ENST0000053501008155_1950266.0Coiled coilOntology_term=ECO:0000255
TgeneSH3GLB1chr1:87380843chr1:87185190ENST0000037055819305_36571.33333333333333366.0DomainSH3
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000482504111305_36571.33333333333333387.0DomainSH3
TgeneSH3GLB1chr1:87380843chr1:87185190ENST000005350100827_2610266.0DomainBAR
TgeneSH3GLB1chr1:87380843chr1:87185190ENST0000053501008305_3650266.0DomainSH3
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000535010081_300266.0RegionNote=Membrane-binding amphipathic helix
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000535010081_370266.0RegionRequired for membrane binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370550+1729_35641.333333333333336357.0Topological domainLumenal
HgeneHS2ST1chr1:87380843chr1:87185190ENST00000370551+1529_35641.333333333333336230.0Topological domainLumenal
TgeneSH3GLB1chr1:87380843chr1:87185190ENST000003705581927_26171.33333333333333366.0DomainBAR
TgeneSH3GLB1chr1:87380843chr1:87185190ENST0000048250411127_26171.33333333333333387.0DomainBAR
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000370558191_3071.33333333333333366.0RegionNote=Membrane-binding amphipathic helix
TgeneSH3GLB1chr1:87380843chr1:87185190ENST00000370558191_3771.33333333333333366.0RegionRequired for membrane binding
TgeneSH3GLB1chr1:87380843chr1:87185190ENST000004825041111_3071.33333333333333387.0RegionNote=Membrane-binding amphipathic helix
TgeneSH3GLB1chr1:87380843chr1:87185190ENST000004825041111_3771.33333333333333387.0RegionRequired for membrane binding


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* 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)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>631_HS2ST1_87380843_SH3GLB1_87185190_ranked_0.pdbHS2ST18738084387380843ENST00000370558SH3GLB1chr187185190+
MGLLRIMMPPKLQLLAVVAFAVAMLFLENQIQKLEESRSKLDARIEEFVYEKLDRKAPSRINNPELLGQYMIDAGTEFGPGTAYGNALIK
CGETQKRIGTADRELIQTSALNFLTPLRNFIEGDYKTIAKERKLLQNKRLDLDAAKTRLKKAKAAETRNSSEQELRITQSEFDRQAEITR
LLLEGISSTHAHHLRCLNDFVEAQMTYYAQCYQYMLDLQKQLGSFPSNYLSNNNQTSVTPVPSVLPNAIGSSAMASTSGLVITSPSNLSD
335


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
HS2ST1_pLDDT.png
all structure
all structure
SH3GLB1_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
HS2ST1
SH3GLB1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to HS2ST1-SH3GLB1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to HS2ST1-SH3GLB1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource