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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:CDC5L-HSP90AB1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CDC5L-HSP90AB1
FusionPDB ID: 14918
FusionGDB2.0 ID: 14918
HgeneTgene
Gene symbol

CDC5L

HSP90AB1

Gene ID

988

3326

Gene namecell division cycle 5 likeheat shock protein 90 alpha family class B member 1
SynonymsCDC5|CDC5-LIKE|CEF1|PCDC5RP|dJ319D22.1D6S182|HSP84|HSP90B|HSPC2|HSPCB
Cytomap

6p21.1

6p21.1

Type of geneprotein-codingprotein-coding
Descriptioncell division cycle 5-like proteinCDC5 cell division cycle 5-likeCdc5-related proteindJ319D22.1 (CDC5-like protein)pombe cdc5-related proteinheat shock protein HSP 90-betaHSP90-betaheat shock 84 kDaheat shock 90kD protein 1, betaheat shock protein 90 kDaheat shock protein 90kDa alpha (cytosolic), class B member 1heat shock protein 90kDa alpha family class B member 1
Modification date2020031320200327
UniProtAcc

Q99459

Main function of 5'-partner protein: FUNCTION: DNA-binding protein involved in cell cycle control. May act as a transcription activator. Plays role in pre-mRNA splicing as core component of precatalytic, catalytic and postcatalytic spliceosomal complexes (PubMed:11991638, PubMed:20176811, PubMed:28502770, PubMed:28076346, PubMed:29361316, PubMed:29360106, PubMed:29301961, PubMed:30728453, PubMed:30705154). Component of the PRP19-CDC5L complex that forms an integral part of the spliceosome and is required for activating pre-mRNA splicing. The PRP19-CDC5L complex may also play a role in the response to DNA damage (DDR) (PubMed:20176811). {ECO:0000269|PubMed:10570151, ECO:0000269|PubMed:11082045, ECO:0000269|PubMed:11101529, ECO:0000269|PubMed:11544257, ECO:0000269|PubMed:11991638, ECO:0000269|PubMed:12927788, ECO:0000269|PubMed:18583928, ECO:0000269|PubMed:20176811, ECO:0000269|PubMed:24332808, ECO:0000269|PubMed:28076346, ECO:0000269|PubMed:28502770, ECO:0000269|PubMed:29301961, ECO:0000269|PubMed:29360106, ECO:0000269|PubMed:29361316, ECO:0000269|PubMed:30705154, ECO:0000269|PubMed:30728453, ECO:0000269|PubMed:9038199, ECO:0000269|PubMed:9468527, ECO:0000269|PubMed:9632794}.

P08238

Main function of 5'-partner protein: FUNCTION: Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle linked to its ATPase activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function (PubMed:16478993, PubMed:19696785). Engages with a range of client protein classes via its interaction with various co-chaperone proteins or complexes, that act as adapters, simultaneously able to interact with the specific client and the central chaperone itself. Recruitment of ATP and co-chaperone followed by client protein forms a functional chaperone. After the completion of the chaperoning process, properly folded client protein and co-chaperone leave HSP90 in an ADP-bound partially open conformation and finally, ADP is released from HSP90 which acquires an open conformation for the next cycle (PubMed:27295069, PubMed:26991466). Apart from its chaperone activity, it also plays a role in the regulation of the transcription machinery. HSP90 and its co-chaperones modulate transcription at least at three different levels. They first alter the steady-state levels of certain transcription factors in response to various physiological cues. Second, they modulate the activity of certain epigenetic modifiers, such as histone deacetylases or DNA methyl transferases, and thereby respond to the change in the environment. Third, they participate in the eviction of histones from the promoter region of certain genes and thereby turn on gene expression (PubMed:25973397). Antagonizes STUB1-mediated inhibition of TGF-beta signaling via inhibition of STUB1-mediated SMAD3 ubiquitination and degradation (PubMed:24613385). Promotes cell differentiation by chaperoning BIRC2 and thereby protecting from auto-ubiquitination and degradation by the proteasomal machinery (PubMed:18239673). Main chaperone involved in the phosphorylation/activation of the STAT1 by chaperoning both JAK2 and PRKCE under heat shock and in turn, activates its own transcription (PubMed:20353823). Involved in the translocation into ERGIC (endoplasmic reticulum-Golgi intermediate compartment) of leaderless cargos (lacking the secretion signal sequence) such as the interleukin 1/IL-1; the translocation process is mediated by the cargo receptor TMED10 (PubMed:32272059). {ECO:0000269|PubMed:16478993, ECO:0000269|PubMed:18239673, ECO:0000269|PubMed:19696785, ECO:0000269|PubMed:20353823, ECO:0000269|PubMed:24613385, ECO:0000269|PubMed:32272059, ECO:0000303|PubMed:25973397, ECO:0000303|PubMed:26991466, ECO:0000303|PubMed:27295069}.
Ensembl transtripts involved in fusion geneENST idsENST00000371477, ENST00000353801, 
ENST00000371554, ENST00000371646, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 4 X 7=28017 X 17 X 9=2601
# samples 1120
** MAII scorelog2(11/280*10)=-1.34792330342031
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/2601*10)=-3.70099449416827
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CDC5L [Title/Abstract] AND HSP90AB1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CDC5L [Title/Abstract] AND HSP90AB1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CDC5L(44376369)-HSP90AB1(44216367), # samples:2
Anticipated loss of major functional domain due to fusion event.CDC5L-HSP90AB1 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.
CDC5L-HSP90AB1 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.
CDC5L-HSP90AB1 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.
CDC5L-HSP90AB1 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.
CDC5L-HSP90AB1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CDC5L-HSP90AB1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
CDC5L-HSP90AB1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
CDC5L-HSP90AB1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneCDC5L

GO:0000398

mRNA splicing, via spliceosome

28076346

HgeneCDC5L

GO:0045944

positive regulation of transcription by RNA polymerase II

11082045

TgeneHSP90AB1

GO:0007004

telomere maintenance via telomerase

10197982

TgeneHSP90AB1

GO:0030511

positive regulation of transforming growth factor beta receptor signaling pathway

24613385

TgeneHSP90AB1

GO:0031396

regulation of protein ubiquitination

16809764

TgeneHSP90AB1

GO:0032435

negative regulation of proteasomal ubiquitin-dependent protein catabolic process

24613385

TgeneHSP90AB1

GO:0032516

positive regulation of phosphoprotein phosphatase activity

26593036

TgeneHSP90AB1

GO:0051131

chaperone-mediated protein complex assembly

10811660

TgeneHSP90AB1

GO:0051973

positive regulation of telomerase activity

10197982

TgeneHSP90AB1

GO:1901389

negative regulation of transforming growth factor beta activation

20599762

TgeneHSP90AB1

GO:1905323

telomerase holoenzyme complex assembly

10197982

TgeneHSP90AB1

GO:2000010

positive regulation of protein localization to cell surface

23431407



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/chr6:44376369/chr6:44216367)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across CDC5L (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 HSP90AB1 (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 Amino Acid Sequences


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)
ENST00000371477CDC5Lchr644376369+ENST00000371646HSP90AB1chr644216367+3851139127535651096
ENST00000371477CDC5Lchr644376369+ENST00000371554HSP90AB1chr644216367+3851139127535651096

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
ENST00000371477ENST00000371646CDC5Lchr644376369+HSP90AB1chr644216367+0.002543130.99745685
ENST00000371477ENST00000371554CDC5Lchr644376369+HSP90AB1chr644216367+0.002543130.99745685

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for CDC5L-HSP90AB1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CDC5Lchr644376369HSP90AB1chr6442163671391372TPRTPASQDRILQMPEEVHHGEEEVE

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Potential FusionNeoAntigen Information of CDC5L-HSP90AB1 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
CDC5L-HSP90AB1_44376369_44216367.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B39:13SQDRILQM0.97340.8249614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:17ASQDRILQM0.99690.8403514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:16ASQDRILQM0.99640.5927514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:21RILQMPEEV0.96770.8429918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:60RILQMPEEV0.96340.7881918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:67RILQMPEEV0.96210.7807918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:30RILQMPEEV0.96210.7807918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:24RILQMPEEV0.96210.7807918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:11RILQMPEEV0.96190.7882918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:38RILQMPEEV0.95820.8102918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:13RILQMPEEV0.95340.8258918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:04RILQMPEEV0.94790.9043918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:27RILQMPEEV0.93610.7919918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:35RILQMPEEV0.93390.7886918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:16RILQMPEEV0.93080.6207918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:29RILQMPEEV0.8960.7768918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:20RILQMPEEV0.87590.7855918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:19RILQMPEEV0.79960.7666918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A30:08ASQDRILQM0.62540.78514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:03LQMPEEVHH0.3830.75251120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B13:02RILQMPEEV0.25020.9725918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:02TPASQDRILQM0.99940.6188314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:05TPASQDRILQM0.99940.6019314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:03TPASQDRILQM0.97930.6746314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B81:01TPASQDRILQM0.95050.6318314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B82:01TPASQDRILQM0.92020.5255314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:04TPASQDRILQM0.8480.8015314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:02TPASQDRILQM0.8480.8015314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:07SQDRILQM10.8996614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:10SQDRILQM10.8961614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:15SQDRILQM10.9847614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C05:09SQDRILQM10.9679614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:14SQDRILQM0.99930.8814614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:13SQDRILQM0.99920.9765614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:04SQDRILQM0.99920.9765614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:03SQDRILQM0.99810.9835614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B39:08SQDRILQM0.98710.7701614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B14:03SQDRILQM0.98580.7104614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C05:09ASQDRILQM0.99990.9829514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:19ASQDRILQM0.99970.9658514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:08ASQDRILQM0.99970.8247514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C15:04ASQDRILQM0.99970.9291514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:07ASQDRILQM0.99960.9793514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C15:06ASQDRILQM0.99960.9285514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:06ASQDRILQM0.99710.9243514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:14ASQDRILQM0.99270.9386514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C12:12ASQDRILQM0.99010.9547514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C12:04ASQDRILQM0.98630.9969514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:13ASQDRILQM0.98470.9849514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:04ASQDRILQM0.98470.9849514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C06:03ASQDRILQM0.98470.9963514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C12:16ASQDRILQM0.98420.9714514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:05ASQDRILQM0.98330.9665514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:14ASQDRILQM0.98150.9866514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:29ASQDRILQM0.97320.9122514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:27ASQDRILQM0.97270.9552514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:13ASQDRILQM0.97080.9238514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:19ASQDRILQM0.96340.766514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:01RILQMPEEV0.96210.7807918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:95ASQDRILQM0.95620.6879514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C02:06ASQDRILQM0.94120.9458514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C01:30ASQDRILQM0.90610.9825514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:03ASQDRILQM0.87840.9879514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:04LQMPEEVHH0.8220.84041120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:05LQMPEEVHH0.65160.93111120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:12TPASQDRILQM0.99950.6735314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:04TPASQDRILQM0.99710.6301314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B42:02TPASQDRILQM0.97730.6799314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B42:01TPASQDRILQM0.96880.675314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B39:10TPASQDRILQM0.88110.7937314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:12TPASQDRILQM0.8480.8015314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:03SQDRILQM10.9244614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:01SQDRILQM10.8996614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:02SQDRILQM10.9847614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C05:01SQDRILQM10.9679614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C18:01SQDRILQM10.9214614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:01SQDRILQM0.99810.9835614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B39:02SQDRILQM0.99180.83614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B39:11SQDRILQM0.98340.7155614
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:03ASQDRILQM0.99990.9555514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C05:01ASQDRILQM0.99990.9829514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C15:09ASQDRILQM0.99970.9291514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C18:01ASQDRILQM0.99970.9536514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:04ASQDRILQM0.99960.9702514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:03ASQDRILQM0.99960.9702514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:02ASQDRILQM0.99950.9655514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C15:05ASQDRILQM0.99940.9337514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:67ASQDRILQM0.99940.9567514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:17ASQDRILQM0.99940.9649514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:05ASQDRILQM0.99930.8911514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C15:02ASQDRILQM0.99920.8929514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C06:06ASQDRILQM0.99880.9956514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C03:06ASQDRILQM0.99510.971514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B58:06ASQDRILQM0.9950.7957514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C04:04ASQDRILQM0.99460.9167514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C12:02ASQDRILQM0.99390.9772514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C16:04ASQDRILQM0.99380.985514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C12:03ASQDRILQM0.99360.9873514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:50LQMPEEVHH0.99350.89261120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:22ASQDRILQM0.9920.76514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:04ASQDRILQM0.9820.9636514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C06:02ASQDRILQM0.97810.9965514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C06:17ASQDRILQM0.97810.9965514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:14RILQMPEEV0.9680.7997918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-A02:06RILQMPEEV0.96770.8429918
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:01ASQDRILQM0.96590.7004514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C07:17ASQDRILQM0.96370.97514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C16:01ASQDRILQM0.95480.9846514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C02:10ASQDRILQM0.94980.9832514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C02:02ASQDRILQM0.94980.9832514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C06:08ASQDRILQM0.94330.995514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:53LQMPEEVHH0.93540.79961120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C16:02ASQDRILQM0.92740.9948514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C08:01ASQDRILQM0.87840.9879514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B15:54LQMPEEVHH0.85170.79171120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-C17:01ASQDRILQM0.84290.9522514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:28LQMPEEVHH0.60940.97541120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:13ASQDRILQM0.3960.8655514
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B48:02LQMPEEVHH0.30430.97151120
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:09TPASQDRILQM0.99950.6122314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B07:22TPASQDRILQM0.99940.6188314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B55:04TPASQDRILQM0.96530.5864314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B82:02TPASQDRILQM0.92020.5255314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B67:01TPASQDRILQM0.85560.7829314
CDC5L-HSP90AB1chr644376369chr6442163671391HLA-B35:09TPASQDRILQM0.8480.8015314

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Potential FusionNeoAntigen Information of CDC5L-HSP90AB1 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

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Fusion breakpoint peptide structures of CDC5L-HSP90AB1

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
8913SQDRILQMPEEVHHCDC5LHSP90AB1chr644376369chr6442163671391

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CDC5L-HSP90AB1

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN8913SQDRILQMPEEVHH-7.9962-8.1096
HLA-B14:023BVN8913SQDRILQMPEEVHH-5.70842-6.74372
HLA-B52:013W398913SQDRILQMPEEVHH-6.83737-6.95077
HLA-B52:013W398913SQDRILQMPEEVHH-4.4836-5.5189
HLA-A11:014UQ28913SQDRILQMPEEVHH-10.0067-10.1201
HLA-A11:014UQ28913SQDRILQMPEEVHH-9.03915-10.0745
HLA-A24:025HGA8913SQDRILQMPEEVHH-6.56204-6.67544
HLA-A24:025HGA8913SQDRILQMPEEVHH-5.42271-6.45801
HLA-B44:053DX88913SQDRILQMPEEVHH-7.85648-8.89178
HLA-B44:053DX88913SQDRILQMPEEVHH-5.3978-5.5112
HLA-A02:016TDR8913SQDRILQMPEEVHH-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CDC5L-HSP90AB1

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
CDC5L-HSP90AB1chr644376369chr6442163671120LQMPEEVHHCTGCAGATGCCTGAGGAAGTGCACCAT
CDC5L-HSP90AB1chr644376369chr644216367314TPASQDRILQMACACCAGCTTCCCAGGACAGAATTCTGCAGATG
CDC5L-HSP90AB1chr644376369chr644216367514ASQDRILQMGCTTCCCAGGACAGAATTCTGCAGATG
CDC5L-HSP90AB1chr644376369chr644216367614SQDRILQMTCCCAGGACAGAATTCTGCAGATG
CDC5L-HSP90AB1chr644376369chr644216367918RILQMPEEVAGAATTCTGCAGATGCCTGAGGAAGTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

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Information of the samples that have these potential fusion neoantigens of CDC5L-HSP90AB1

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
STADCDC5L-HSP90AB1chr644376369ENST00000371477chr644216367ENST00000371554TCGA-CD-8535-01A

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Potential target of CAR-T therapy development for CDC5L-HSP90AB1

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to CDC5L-HSP90AB1

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 CDC5L-HSP90AB1

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