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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:NLK-KSR1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NLK-KSR1
FusionPDB ID: 59349
FusionGDB2.0 ID: 59349
HgeneTgene
Gene symbol

NLK

KSR1

Gene ID

51701

8844

Gene namenemo like kinasekinase suppressor of ras 1
Synonyms-KSR|RSU2
Cytomap

17q11.2

17q11.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase NLKkinase suppressor of Ras 1
Modification date2020031320200327
UniProtAcc

Q9UBE8

Main function of 5'-partner protein: FUNCTION: Serine/threonine-protein kinase that regulates a number of transcription factors with key roles in cell fate determination. Positive effector of the non-canonical Wnt signaling pathway, acting downstream of WNT5A, MAP3K7/TAK1 and HIPK2. Negative regulator of the canonical Wnt/beta-catenin signaling pathway. Binds to and phosphorylates TCF7L2/TCF4 and LEF1, promoting the dissociation of the TCF7L2/LEF1/beta-catenin complex from DNA, as well as the ubiquitination and subsequent proteolysis of LEF1. Together these effects inhibit the transcriptional activation of canonical Wnt/beta-catenin target genes. Negative regulator of the Notch signaling pathway. Binds to and phosphorylates NOTCH1, thereby preventing the formation of a transcriptionally active ternary complex of NOTCH1, RBPJ/RBPSUH and MAML1. Negative regulator of the MYB family of transcription factors. Phosphorylation of MYB leads to its subsequent proteolysis while phosphorylation of MYBL1 and MYBL2 inhibits their interaction with the coactivator CREBBP. Other transcription factors may also be inhibited by direct phosphorylation of CREBBP itself. Acts downstream of IL6 and MAP3K7/TAK1 to phosphorylate STAT3, which is in turn required for activation of NLK by MAP3K7/TAK1. Upon IL1B stimulus, cooperates with ATF5 to activate the transactivation activity of C/EBP subfamily members. Phosphorylates ATF5 but also stabilizes ATF5 protein levels in a kinase-independent manner (PubMed:25512613). {ECO:0000250|UniProtKB:O54949, ECO:0000269|PubMed:12482967, ECO:0000269|PubMed:14960582, ECO:0000269|PubMed:15004007, ECO:0000269|PubMed:15764709, ECO:0000269|PubMed:20061393, ECO:0000269|PubMed:20118921, ECO:0000269|PubMed:20874444, ECO:0000269|PubMed:21454679, ECO:0000269|PubMed:25512613}.

Q8IVT5

Main function of 5'-partner protein: FUNCTION: Part of a multiprotein signaling complex which promotes phosphorylation of Raf family members and activation of downstream MAP kinases (By similarity). Independently of its kinase activity, acts as MAP2K1/MEK1 and MAP2K2/MEK2-dependent allosteric activator of BRAF; upon binding to MAP2K1/MEK1 or MAP2K2/MEK2, dimerizes with BRAF and promotes BRAF-mediated phosphorylation of MAP2K1/MEK1 and/or MAP2K2/MEK2 (PubMed:29433126). Promotes activation of MAPK1 and/or MAPK3, both in response to EGF and to cAMP (By similarity). Its kinase activity is unsure (By similarity). Some protein kinase activity has been detected in vitro, however the physiological relevance of this activity is unknown (By similarity). {ECO:0000250|UniProtKB:Q61097, ECO:0000269|PubMed:29433126}.
Ensembl transtripts involved in fusion geneENST idsENST00000407008, ENST00000582037, 
ENST00000583517, 
ENST00000268763, 
ENST00000398988, ENST00000578981, 
ENST00000581975, ENST00000582410, 
ENST00000319524, ENST00000509603, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 10 X 9=162013 X 9 X 7=819
# samples 2012
** MAII scorelog2(20/1620*10)=-3.01792190799726
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/819*10)=-2.77082904603249
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NLK [Title/Abstract] AND KSR1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NLK [Title/Abstract] AND KSR1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NLK(26512291)-KSR1(25904518), # samples:1
Anticipated loss of major functional domain due to fusion event.NLK-KSR1 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.
NLK-KSR1 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.
NLK-KSR1 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.
NLK-KSR1 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
HgeneNLK

GO:0050821

protein stabilization

25512613

TgeneKSR1

GO:0000185

activation of MAPKKK activity

29433126



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/chr17:26512291/chr17:25904518)
- 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 NLK (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 KSR1 (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)
ENST00000407008NLKchr1726512291-ENST00000509603KSR1chr1725904518+4213195471842121165
ENST00000407008NLKchr1726512291-ENST00000319524KSR1chr1725904518+4653195471843531211

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
ENST00000407008ENST00000509603NLKchr1726512291-KSR1chr1725904518+0.244584430.7554156
ENST00000407008ENST00000319524NLKchr1726512291-KSR1chr1725904518+0.0078726320.9921274

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 NLK-KSR1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NLKchr1726512291KSR1chr17259045181954412AVHLLCRMLVFDPEIPRDLTLDALLE

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Potential FusionNeoAntigen Information of NLK-KSR1 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.
NLK-KSR1_26512291_25904518.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)
NLK-KSR1chr1726512291chr17259045181954HLA-A74:09LVFDPEIPR0.93340.5184817
NLK-KSR1chr1726512291chr17259045181954HLA-A74:11LVFDPEIPR0.93340.5184817
NLK-KSR1chr1726512291chr17259045181954HLA-A74:03LVFDPEIPR0.93340.5184817
NLK-KSR1chr1726512291chr17259045181954HLA-B13:02RMLVFDPEI0.36820.5574615
NLK-KSR1chr1726512291chr17259045181954HLA-B52:01RMLVFDPEI0.03740.9183615
NLK-KSR1chr1726512291chr17259045181954HLA-A31:02MLVFDPEIPR0.88720.593717
NLK-KSR1chr1726512291chr17259045181954HLA-A74:09MLVFDPEIPR0.87050.6191717
NLK-KSR1chr1726512291chr17259045181954HLA-A74:03MLVFDPEIPR0.87050.6191717
NLK-KSR1chr1726512291chr17259045181954HLA-A74:11MLVFDPEIPR0.87050.6191717
NLK-KSR1chr1726512291chr17259045181954HLA-B35:03DPEIPRDLTL0.74830.93411121
NLK-KSR1chr1726512291chr17259045181954HLA-B35:04DPEIPRDLTL0.61340.95521121
NLK-KSR1chr1726512291chr17259045181954HLA-B35:02DPEIPRDLTL0.61340.95521121
NLK-KSR1chr1726512291chr17259045181954HLA-A74:09RMLVFDPEIPR0.99340.5401617
NLK-KSR1chr1726512291chr17259045181954HLA-A74:11RMLVFDPEIPR0.99340.5401617
NLK-KSR1chr1726512291chr17259045181954HLA-A74:03RMLVFDPEIPR0.99340.5401617
NLK-KSR1chr1726512291chr17259045181954HLA-C04:10VFDPEIPRDL0.99970.7827919
NLK-KSR1chr1726512291chr17259045181954HLA-C04:07VFDPEIPRDL0.99960.8145919
NLK-KSR1chr1726512291chr17259045181954HLA-C04:14VFDPEIPRDL0.98640.8529919
NLK-KSR1chr1726512291chr17259045181954HLA-A31:01MLVFDPEIPR0.90170.5528717
NLK-KSR1chr1726512291chr17259045181954HLA-B39:10DPEIPRDLTL0.70010.87671121
NLK-KSR1chr1726512291chr17259045181954HLA-B35:12DPEIPRDLTL0.61340.95521121
NLK-KSR1chr1726512291chr17259045181954HLA-A74:01LVFDPEIPR0.93340.5184817
NLK-KSR1chr1726512291chr17259045181954HLA-B40:04PEIPRDLTL0.87480.65581221
NLK-KSR1chr1726512291chr17259045181954HLA-B41:03PEIPRDLTL0.17620.67391221
NLK-KSR1chr1726512291chr17259045181954HLA-C04:03VFDPEIPRDL0.99980.8458919
NLK-KSR1chr1726512291chr17259045181954HLA-C04:01VFDPEIPRDL0.99960.8145919
NLK-KSR1chr1726512291chr17259045181954HLA-C18:01VFDPEIPRDL0.99960.8239919
NLK-KSR1chr1726512291chr17259045181954HLA-C04:04VFDPEIPRDL0.98610.9265919
NLK-KSR1chr1726512291chr17259045181954HLA-C07:04VFDPEIPRDL0.9750.9254919
NLK-KSR1chr1726512291chr17259045181954HLA-A74:01MLVFDPEIPR0.87050.6191717
NLK-KSR1chr1726512291chr17259045181954HLA-B08:12DPEIPRDLTL0.75330.66991121
NLK-KSR1chr1726512291chr17259045181954HLA-B67:01DPEIPRDLTL0.66950.68031121
NLK-KSR1chr1726512291chr17259045181954HLA-B35:09DPEIPRDLTL0.61340.95521121
NLK-KSR1chr1726512291chr17259045181954HLA-B18:03DPEIPRDLTL0.17660.8851121
NLK-KSR1chr1726512291chr17259045181954HLA-A74:01RMLVFDPEIPR0.99340.5401617

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Potential FusionNeoAntigen Information of NLK-KSR1 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.
NLK-KSR1_26512291_25904518.msa

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)
NLK-KSR1chr1726512291chr17259045181954DRB1-0301CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0301RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0301LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0301LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0303RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0303CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0305CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0305RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0307RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0307CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0307LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0307LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0310CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0310RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0310LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0310LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0313CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0313RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0313LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0313LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0315CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0315RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0315LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0315LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0318CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0318RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0318LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0318LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0320RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0320CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0320LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0320LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0322CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0322RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0322LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0322LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0326RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0326CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0326LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0326LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0328CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0328RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0328LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0328LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0330CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0330RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0330LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0330LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0332CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0332RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0332LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0332LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0334CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0334RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0334LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0334LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0336CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0336RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0336LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0336LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0342CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0342RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0342LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0342LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0344CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0344RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0344LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0344LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0346CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0346RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0346LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0346LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0348CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0348RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0348LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0348LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0350CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0350RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0350LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0350LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0352CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0352RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0352LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0352LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-0354CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-0354RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-0354LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-0354LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-1107RMLVFDPEIPRDLTL621
NLK-KSR1chr1726512291chr17259045181954DRB1-1107CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-1107LCRMLVFDPEIPRDL419
NLK-KSR1chr1726512291chr17259045181954DRB1-1107LLCRMLVFDPEIPRD318
NLK-KSR1chr1726512291chr17259045181954DRB1-1476CRMLVFDPEIPRDLT520
NLK-KSR1chr1726512291chr17259045181954DRB1-1479CRMLVFDPEIPRDLT520

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Fusion breakpoint peptide structures of NLK-KSR1

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
8044RMLVFDPEIPRDLTNLKKSR1chr1726512291chr17259045181954

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NLK-KSR1

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-B14:023BVN8044RMLVFDPEIPRDLT-6.93863-7.05203
HLA-B14:023BVN8044RMLVFDPEIPRDLT-4.13527-5.17057
HLA-B52:013W398044RMLVFDPEIPRDLT-6.86405-6.97745
HLA-B52:013W398044RMLVFDPEIPRDLT-3.72209-4.75739
HLA-A24:025HGA8044RMLVFDPEIPRDLT-8.23297-9.26827
HLA-A24:025HGA8044RMLVFDPEIPRDLT-5.62477-5.73817
HLA-B27:056PYJ8044RMLVFDPEIPRDLT-5.8772-6.9125
HLA-B44:053DX88044RMLVFDPEIPRDLT-6.50682-6.62022
HLA-B44:053DX88044RMLVFDPEIPRDLT-4.20591-5.24121

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Vaccine Design for the FusionNeoAntigens of NLK-KSR1

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
NLK-KSR1chr1726512291chr17259045181121DPEIPRDLTLGATCCAGAGATCCCCCGAGACCTCACGCTG
NLK-KSR1chr1726512291chr17259045181221PEIPRDLTLCCAGAGATCCCCCGAGACCTCACGCTG
NLK-KSR1chr1726512291chr1725904518615RMLVFDPEIAGGATGTTGGTCTTTGATCCAGAGATC
NLK-KSR1chr1726512291chr1725904518617RMLVFDPEIPRAGGATGTTGGTCTTTGATCCAGAGATCCCCCGA
NLK-KSR1chr1726512291chr1725904518717MLVFDPEIPRATGTTGGTCTTTGATCCAGAGATCCCCCGA
NLK-KSR1chr1726512291chr1725904518817LVFDPEIPRTTGGTCTTTGATCCAGAGATCCCCCGA
NLK-KSR1chr1726512291chr1725904518919VFDPEIPRDLGTCTTTGATCCAGAGATCCCCCGAGACCTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
NLK-KSR1chr1726512291chr1725904518318LLCRMLVFDPEIPRDCTCCTTTGCAGGATGTTGGTCTTTGATCCAGAGATCCCCCGAGAC
NLK-KSR1chr1726512291chr1725904518419LCRMLVFDPEIPRDLCTTTGCAGGATGTTGGTCTTTGATCCAGAGATCCCCCGAGACCTC
NLK-KSR1chr1726512291chr1725904518520CRMLVFDPEIPRDLTTGCAGGATGTTGGTCTTTGATCCAGAGATCCCCCGAGACCTCACG
NLK-KSR1chr1726512291chr1725904518621RMLVFDPEIPRDLTLAGGATGTTGGTCTTTGATCCAGAGATCCCCCGAGACCTCACGCTG

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Information of the samples that have these potential fusion neoantigens of NLK-KSR1

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
STADNLK-KSR1chr1726512291ENST00000407008chr1725904518ENST00000319524TCGA-BR-4357-01A

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Potential target of CAR-T therapy development for NLK-KSR1

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 NLK-KSR1

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 NLK-KSR1

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