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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:ABR-NXN

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ABR-NXN
FusionPDB ID: 556
FusionGDB2.0 ID: 556
HgeneTgene
Gene symbol

ABR

NXN

Gene ID

29

64359

Gene nameABR activator of RhoGEF and GTPasenucleoredoxin
SynonymsMDBNRX|RRS2|TRG-4
Cytomap

17p13.3

17p13.3

Type of geneprotein-codingprotein-coding
Descriptionactive breakpoint cluster region-related proteinABR, RhoGEF and GTPase activating proteinactive BCR-relatednucleoredoxinnucleoredoxin 1
Modification date2020031320200327
UniProtAcc

Q15018

.
Ensembl transtripts involved in fusion geneENST idsENST00000291107, ENST00000302538, 
ENST00000536794, ENST00000544583, 
ENST00000574437, ENST00000543210, 
ENST00000572441, ENST00000573895, 
ENST00000537628, ENST00000575801, 
ENST00000577098, ENST00000538650, 
ENST00000336868, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score23 X 15 X 14=483017 X 15 X 5=1275
# samples 3620
** MAII scorelog2(36/4830*10)=-3.74595437739346
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/1275*10)=-2.6724253419715
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ABR [Title/Abstract] AND NXN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NXN(882559)-ABR(916404), # samples:5
ABR(953290)-NXN(729318), # samples:2
Anticipated loss of major functional domain due to fusion event.ABR-NXN 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.
ABR-NXN 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.
ABR-NXN 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.
ABR-NXN 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.
NXN-ABR 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.
NXN-ABR 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.
ABR-NXN seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
ABR-NXN seems lost the major protein functional domain in Tgene partner, which is a essential gene 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)

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

GO:0090630

activation of GTPase activity

7479768


check buttonFusion gene breakpoints across ABR (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 NXN (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
ChimerDB4BRCATCGA-OL-A66P-01AABRchr17

953290

-NXNchr17

729318

-
ChimerDB4LUADTCGA-91-6836-01AABRchr17

1082961

-NXNchr17

729318

-
ChimerDB4SKCMTCGA-D3-A3CC-06AABRchr17

953290

-NXNchr17

729318

-


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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)
ENST00000302538ABRchr17953290-ENST00000336868NXNchr17729318-452219381472885912
ENST00000574437ABRchr17953290-ENST00000336868NXNchr17729318-470221181233065980
ENST00000291107ABRchr17953290-ENST00000336868NXNchr17729318-42961712322659875
ENST00000536794ABRchr17953290-ENST00000336868NXNchr17729318-400814241402371743
ENST00000302538ABRchr171082961-ENST00000336868NXNchr17729318-27922082981155285

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
ENST00000302538ENST00000336868ABRchr17953290-NXNchr17729318-0.001393780.99860626
ENST00000574437ENST00000336868ABRchr17953290-NXNchr17729318-0.0021883150.99781173
ENST00000291107ENST00000336868ABRchr17953290-NXNchr17729318-0.0029501570.9970498
ENST00000536794ENST00000336868ABRchr17953290-NXNchr17729318-0.0100140150.989986
ENST00000302538ENST00000336868ABRchr171082961-NXNchr17729318-0.0028109580.9971891

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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

>556_556_1_ABR-NXN_ABR_chr17_1082961_ENST00000302538_NXN_chr17_729318_ENST00000336868_length(amino acids)=285AA_BP=
MLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSE
ESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLV
LFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLFFVAGEDDMTDSLRDYTNLPEAAPLLTILDMSARAKYVMDVEEITPAIVEA

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

>556_556_2_ABR-NXN_ABR_chr17_953290_ENST00000291107_NXN_chr17_729318_ENST00000336868_length(amino acids)=875AA_BP=0
MEEEEEAIGLLDKVLEDEDVFLLEECELGTPTSPGSGSPFLVAVKVEAGKGLEMRKLVLSGFLASEEIYINQLEALLLPMKPLKATATTS
QPVLTIQQIETIFYKIQDIYEIHKEFYDNLCPKVQQWDSQVTMGHLFQKLASQLGVYKAFVDNYKVALETAEKCSQSNNQFQKISEELKV
KGPKDSKDSHTSVTMEALLYKPIDRVTRSTLVLHDLLKHTPVDHPDYPLLQDALRISQNFLSSINEDIDPRRTAVTTPKGETRQLVKDGF
LVEVSESSRKLRHVFLFTDVLLCAKLKKTSAGKHQQYDCKWYIPLADLVFPSPEESEASPQVHPFPDHELEDMKMKISALKSEIQKEKAN
KGQSRAIERLKKKMFENEFLLLLNSPTIPFRIHNRNGKSYLFLLSSDYERSEWREAIQKLQKKDLQAFVLSSVELQVLTGSCFKLRTVHN
IPVTSNKDDDESPGLYGFLHVIVHSAKGFKQSANLYCTLEVDSFGYFVSKAKTRVFRDTAEPKWDEEFEIELEGSQSLRILCYEKCYDKT
KVNKDNNEIVDKIMGKGQIQLKLWNKYRISNIPSLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSS
LEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIM
LDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLF

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

>556_556_3_ABR-NXN_ABR_chr17_953290_ENST00000302538_NXN_chr17_729318_ENST00000336868_length(amino acids)=912AA_BP=0
MEPLSHRGLPRLSWIDTLYSNFSYGTDEYDGEGNEEQKGPPEGSETMPYIDESPTMSPQLSARSQGGGDGVSPTPPEGLAPGVEAGKGLE
MRKLVLSGFLASEEIYINQLEALLLPMKPLKATATTSQPVLTIQQIETIFYKIQDIYEIHKEFYDNLCPKVQQWDSQVTMGHLFQKLASQ
LGVYKAFVDNYKVALETAEKCSQSNNQFQKISEELKVKGPKDSKDSHTSVTMEALLYKPIDRVTRSTLVLHDLLKHTPVDHPDYPLLQDA
LRISQNFLSSINEDIDPRRTAVTTPKGETRQLVKDGFLVEVSESSRKLRHVFLFTDVLLCAKLKKTSAGKHQQYDCKWYIPLADLVFPSP
EESEASPQVHPFPDHELEDMKMKISALKSEIQKEKANKGQSRAIERLKKKMFENEFLLLLNSPTIPFRIHNRNGKSYLFLLSSDYERSEW
REAIQKLQKKDLQAFVLSSVELQVLTGSCFKLRTVHNIPVTSNKDDDESPGLYGFLHVIVHSAKGFKQSANLYCTLEVDSFGYFVSKAKT
RVFRDTAEPKWDEEFEIELEGSQSLRILCYEKCYDKTKVNKDNNEIVDKIMGKGQIQLKLWNKYRISNIPSLIFLDATTGKVVCRNGLLV
IRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSEESF
KQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLVLFV
DSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLFFVAGEDDMTDSLRDYTNLPEAAPLLTILDMSARAKYVMDVEEITPAIVEAFVN

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

>556_556_4_ABR-NXN_ABR_chr17_953290_ENST00000536794_NXN_chr17_729318_ENST00000336868_length(amino acids)=743AA_BP=1
MLEEHSGAAARCWSPCGSISKVAEWPGCWWAPGSLERWLHAPAAGTEAAMEILLIIRFCCNCTYALLYKPIDRVTRSTLVLHDLLKHTPV
DHPDYPLLQDALRISQNFLSSINEDIDPRRTAVTTPKGETRQLVKDGFLVEVSESSRKLRHVFLFTDVLLCAKLKKTSAGKHQQYDCKWY
IPLADLVFPSPEESEASPQVHPFPDHELEDMKMKISALKSEIQKEKANKGQSRAIERLKKKMFENEFLLLLNSPTIPFRIHNRNGKSYLF
LLSSDYERSEWREAIQKLQKKDLQAFVLSSVELQVLTGSCFKLRTVHNIPVTSNKDDDESPGLYGFLHVIVHSAKGFKQSANLYCTLEVD
SFGYFVSKAKTRVFRDTAEPKWDEEFEIELEGSQSLRILCYEKCYDKTKVNKDNNEIVDKIMGKGQIQLKLWNKYRISNIPSLIFLDATT
GKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIAGPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEII
FVSADRSEESFKQYFSEMPWLAVPYTDEARRSRLNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQ
LNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKIIAKYKAKEEEAPLLFFVAGEDDMTDSLRDYTNLPEAAPLLTILDMSARAKYVMDVEE

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

>556_556_5_ABR-NXN_ABR_chr17_953290_ENST00000574437_NXN_chr17_729318_ENST00000336868_length(amino acids)=980AA_BP=1
MTCSSSGSNSRAAPPRLPAAPERAGPGACWLSPAPHQAQAPAQPPPGPGVDGAAGAMAAGGRRRRPLRYQSLAALVEDSQWPFLFLVSDF
SYGTDEYDGEGNEEQKGPPEGSETMPYIDESPTMSPQLSARSQGGGDGVSPTPPEGLAPGVEAGKGLEMRKLVLSGFLASEEIYINQLEA
LLLPMKPLKATATTSQPVLTIQQIETIFYKIQDIYEIHKEFYDNLCPKVQQWDSQVTMGHLFQKLASQLGVYKAFVDNYKVALETAEKCS
QSNNQFQKISEELKVKGPKDSKDSHTSVTMEALLYKPIDRVTRSTLVLHDLLKHTPVDHPDYPLLQDALRISQNFLSSINEDIDPRRTAV
TTPKGETRQLVKDGFLVEVSESSRKLRHVFLFTDVLLCAKLKKTSAGKHQQYDCKWYIPLADLVFPSPEESEASPQVHPFPDHELEDMKM
KISALKSEIQKEKANKGQSRAIERLKKKMFENEFLLLLNSPTIPFRIHNRNGKSYLFLLSSDYERSEWREAIQKLQKKDLQAFVLSSVEL
QVLTGSCFKLRTVHNIPVTSNKDDDESPGLYGFLHVIVHSAKGFKQSANLYCTLEVDSFGYFVSKAKTRVFRDTAEPKWDEEFEIELEGS
QSLRILCYEKCYDKTKVNKDNNEIVDKIMGKGQIQLKLWNKYRISNIPSLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIA
GPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSR
LNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKI

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

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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/chr17:882559/chr17:916404)
- 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
ABR

Q15018

.
FUNCTION: Component of the BRISC complex, a multiprotein complex that specifically cleaves 'Lys-63'-linked polyubiquitin, leaving the last ubiquitin chain attached to its substrates (PubMed:19214193, PubMed:20032457, PubMed:20656690, PubMed:24075985). May act as a central scaffold protein that assembles the various components of the BRISC complex and retains them in the cytoplasm (PubMed:20656690). Plays a role in regulating the onset of apoptosis via its role in modulating 'Lys-63'-linked ubiquitination of target proteins (By similarity). Required for normal mitotic spindle assembly and microtubule attachment to kinetochores via its role in deubiquitinating NUMA1 (PubMed:26195665). Plays a role in interferon signaling via its role in the deubiquitination of the interferon receptor IFNAR1; deubiquitination increases IFNAR1 activities by enhancing its stability and cell surface expression (PubMed:24075985, PubMed:26344097). Down-regulates the response to bacterial lipopolysaccharide (LPS) via its role in IFNAR1 deubiquitination (PubMed:24075985). Required for normal induction of p53/TP53 in response to DNA damage (PubMed:25283148). Independent of the BRISC complex, promotes interaction between USP7 and p53/TP53, and thereby promotes deubiquitination of p53/TP53, preventing its degradation and resulting in increased p53/TP53-mediated transcription regulation and p53/TP53-dependent apoptosis in response to DNA damage (PubMed:25283148). {ECO:0000250|UniProtKB:Q3TCJ1, ECO:0000269|PubMed:19214193, ECO:0000269|PubMed:20032457, ECO:0000269|PubMed:20656690, ECO:0000269|PubMed:24075985, ECO:0000269|PubMed:25283148}.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
HgeneABRchr17:953290chr17:729318ENST00000291107-1522417_420560.0823.0Compositional biasNote=Poly-Leu
HgeneABRchr17:953290chr17:729318ENST00000302538-1623417_420597.0860.0Compositional biasNote=Poly-Leu
HgeneABRchr17:953290chr17:729318ENST00000544583-1623417_420551.0814.0Compositional biasNote=Poly-Leu
HgeneABRchr17:953290chr17:729318ENST00000574437-1522417_420551.0814.0Compositional biasNote=Poly-Leu
HgeneABRchr17:953290chr17:729318ENST00000291107-1522301_459560.0823.0DomainPH
HgeneABRchr17:953290chr17:729318ENST00000291107-152291_284560.0823.0DomainDH
HgeneABRchr17:953290chr17:729318ENST00000302538-1623301_459597.0860.0DomainPH
HgeneABRchr17:953290chr17:729318ENST00000302538-162391_284597.0860.0DomainDH
HgeneABRchr17:953290chr17:729318ENST00000544583-1623301_459551.0814.0DomainPH
HgeneABRchr17:953290chr17:729318ENST00000544583-162391_284551.0814.0DomainDH
HgeneABRchr17:953290chr17:729318ENST00000574437-1522301_459551.0814.0DomainPH
HgeneABRchr17:953290chr17:729318ENST00000574437-152291_284551.0814.0DomainDH
TgeneNXNchr17:1082961chr17:729318ENST0000033686808167_321120.0436.0DomainThioredoxin
TgeneNXNchr17:1082961chr17:729318ENST0000053762808167_3210187.0DomainThioredoxin
TgeneNXNchr17:1082961chr17:729318ENST0000057580108167_32112.0328.0DomainThioredoxin
TgeneNXNchr17:953290chr17:729318ENST0000033686808167_321120.0436.0DomainThioredoxin
TgeneNXNchr17:953290chr17:729318ENST0000053762808167_3210187.0DomainThioredoxin
TgeneNXNchr17:953290chr17:729318ENST0000057580108167_32112.0328.0DomainThioredoxin

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneABRchr17:1082961chr17:729318ENST00000291107-122417_4200823.0Compositional biasNote=Poly-Leu
HgeneABRchr17:1082961chr17:729318ENST00000302538-123417_42020.333333333333332860.0Compositional biasNote=Poly-Leu
HgeneABRchr17:1082961chr17:729318ENST00000543210-18417_4200311.0Compositional biasNote=Poly-Leu
HgeneABRchr17:1082961chr17:729318ENST00000544583-123417_4200814.0Compositional biasNote=Poly-Leu
HgeneABRchr17:1082961chr17:729318ENST00000574437-122417_4200814.0Compositional biasNote=Poly-Leu
HgeneABRchr17:953290chr17:729318ENST00000543210-18417_4200311.0Compositional biasNote=Poly-Leu
HgeneABRchr17:1082961chr17:729318ENST00000291107-122301_4590823.0DomainPH
HgeneABRchr17:1082961chr17:729318ENST00000291107-122484_6130823.0DomainC2
HgeneABRchr17:1082961chr17:729318ENST00000291107-122647_8450823.0DomainRho-GAP
HgeneABRchr17:1082961chr17:729318ENST00000291107-12291_2840823.0DomainDH
HgeneABRchr17:1082961chr17:729318ENST00000302538-123301_45920.333333333333332860.0DomainPH
HgeneABRchr17:1082961chr17:729318ENST00000302538-123484_61320.333333333333332860.0DomainC2
HgeneABRchr17:1082961chr17:729318ENST00000302538-123647_84520.333333333333332860.0DomainRho-GAP
HgeneABRchr17:1082961chr17:729318ENST00000302538-12391_28420.333333333333332860.0DomainDH
HgeneABRchr17:1082961chr17:729318ENST00000543210-18301_4590311.0DomainPH
HgeneABRchr17:1082961chr17:729318ENST00000543210-18484_6130311.0DomainC2
HgeneABRchr17:1082961chr17:729318ENST00000543210-18647_8450311.0DomainRho-GAP
HgeneABRchr17:1082961chr17:729318ENST00000543210-1891_2840311.0DomainDH
HgeneABRchr17:1082961chr17:729318ENST00000544583-123301_4590814.0DomainPH
HgeneABRchr17:1082961chr17:729318ENST00000544583-123484_6130814.0DomainC2
HgeneABRchr17:1082961chr17:729318ENST00000544583-123647_8450814.0DomainRho-GAP
HgeneABRchr17:1082961chr17:729318ENST00000544583-12391_2840814.0DomainDH
HgeneABRchr17:1082961chr17:729318ENST00000574437-122301_4590814.0DomainPH
HgeneABRchr17:1082961chr17:729318ENST00000574437-122484_6130814.0DomainC2
HgeneABRchr17:1082961chr17:729318ENST00000574437-122647_8450814.0DomainRho-GAP
HgeneABRchr17:1082961chr17:729318ENST00000574437-12291_2840814.0DomainDH
HgeneABRchr17:953290chr17:729318ENST00000291107-1522484_613560.0823.0DomainC2
HgeneABRchr17:953290chr17:729318ENST00000291107-1522647_845560.0823.0DomainRho-GAP
HgeneABRchr17:953290chr17:729318ENST00000302538-1623484_613597.0860.0DomainC2
HgeneABRchr17:953290chr17:729318ENST00000302538-1623647_845597.0860.0DomainRho-GAP
HgeneABRchr17:953290chr17:729318ENST00000543210-18301_4590311.0DomainPH
HgeneABRchr17:953290chr17:729318ENST00000543210-18484_6130311.0DomainC2
HgeneABRchr17:953290chr17:729318ENST00000543210-18647_8450311.0DomainRho-GAP
HgeneABRchr17:953290chr17:729318ENST00000543210-1891_2840311.0DomainDH
HgeneABRchr17:953290chr17:729318ENST00000544583-1623484_613551.0814.0DomainC2
HgeneABRchr17:953290chr17:729318ENST00000544583-1623647_845551.0814.0DomainRho-GAP
HgeneABRchr17:953290chr17:729318ENST00000574437-1522484_613551.0814.0DomainC2
HgeneABRchr17:953290chr17:729318ENST00000574437-1522647_845551.0814.0DomainRho-GAP


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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 >>>1781_ABR_953290_NXN_729318_ranked_0.pdbABR1082961953290ENST00000336868NXNchr17729318-
MTCSSSGSNSRAAPPRLPAAPERAGPGACWLSPAPHQAQAPAQPPPGPGVDGAAGAMAAGGRRRRPLRYQSLAALVEDSQWPFLFLVSDF
SYGTDEYDGEGNEEQKGPPEGSETMPYIDESPTMSPQLSARSQGGGDGVSPTPPEGLAPGVEAGKGLEMRKLVLSGFLASEEIYINQLEA
LLLPMKPLKATATTSQPVLTIQQIETIFYKIQDIYEIHKEFYDNLCPKVQQWDSQVTMGHLFQKLASQLGVYKAFVDNYKVALETAEKCS
QSNNQFQKISEELKVKGPKDSKDSHTSVTMEALLYKPIDRVTRSTLVLHDLLKHTPVDHPDYPLLQDALRISQNFLSSINEDIDPRRTAV
TTPKGETRQLVKDGFLVEVSESSRKLRHVFLFTDVLLCAKLKKTSAGKHQQYDCKWYIPLADLVFPSPEESEASPQVHPFPDHELEDMKM
KISALKSEIQKEKANKGQSRAIERLKKKMFENEFLLLLNSPTIPFRIHNRNGKSYLFLLSSDYERSEWREAIQKLQKKDLQAFVLSSVEL
QVLTGSCFKLRTVHNIPVTSNKDDDESPGLYGFLHVIVHSAKGFKQSANLYCTLEVDSFGYFVSKAKTRVFRDTAEPKWDEEFEIELEGS
QSLRILCYEKCYDKTKVNKDNNEIVDKIMGKGQIQLKLWNKYRISNIPSLIFLDATTGKVVCRNGLLVIRDDPEGLEFPWGPKPFREVIA
GPLLRNNGQSLESSSLEGSHVGVYFSAHWCPPCRSLTRVLVESYRKIKEAGQNFEIIFVSADRSEESFKQYFSEMPWLAVPYTDEARRSR
LNRLYGIQGIPTLIMLDPQGEVITRQGRVEVLNDEDCREFPWHPKPVLELSDSNAAQLNEGPCLVLFVDSEDDGESEAAKQLIQPIAEKI
980


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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.
ABR_pLDDT.png
all structure
all structure
NXN_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
ABR
NXN


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 ABR-NXN


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 ABR-NXN


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