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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
O95999 BCL10 B-cell lymphoma/leukemia 10 (B-cell CLL/lymphoma … Homo sapiens (Human) 233 aa

Protein Details: O95999 (BCL10)

Protein Information
AccessionO95999
Protein NamesB-cell lymphoma/leukemia 10 (B-cell CLL/lymphoma 10) (Bcl-10) (CARD-containing molecule enhancing NF-kappa-B) (CARD-like apoptotic protein) (hCLAP) (CED-3/ICH-1 prodomain homologous E10-like regulator) (CIPER) (Cellular homolog of vCARMEN) (cCARMEN) (Cellular-E10) (c-E10) (Mammalian CARD-containing adapter molecule E10) (mE10)
Gene SymbolBCL10
OrganismHomo sapiens (Human)
Length233 aa
IsoformsNo isoforms
Related PMIDs No related PMIDs
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MEPTAPSLTE11EDLTEVKKDA21LENLRVYLCE31KIIAERHFDH41LRAKKILSRE
51-10051DTEEISCRTS61SRKRAGKLLD71YLQENPKGLD81TLVESIRREK91TQNFLIQKIT
101-150101DEVLKLRNIK111LEHLKGLKCS121SCEPFPDGAT131NNLSRSNSDE141SNFSEKLRAS
151-200151TVMYHPEGES161STTPFFSTNS171SLNLPVLEVG181RTENTIFSST191TLPRPGDPGA
201-233201PPLPPDLQLE211EEGTCANSSE221MFLPLRSRTV231SRQ
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
29 SWISSPALM DBPTM CYSMODDB Death-like domain superfamily Caspase recruitment domain B-cell lymphoma/leukemia 10/E10 CARD domain - -
Deep-Palm: 0.95
57 - - -
GPS-Palm: 0.81
Deep-Palm: 0.96
119 - - -
GPS-Palm: 0.78
Deep-Palm: 0.94
122 - - -
GPS-Palm: 0.74
Deep-Palm: 0.85
215 - - -
Deep-Palm: 0.97
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
42 R → C 0.001887 SNP Missense Mutation UCEC
228 R → C 0.001014 SNP Missense Mutation BRCA
228 R → C 0.003460 SNP Missense Mutation CESC
215* C → ? 0.027027 SNP Nonsense Mutation DLBC