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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P35070 BTC Probetacellulin [Cleaved into: Betacellulin (BTC)] Homo sapiens (Human) 178 aa

Protein Details: P35070 (BTC)

Protein Information
AccessionP35070
Protein NamesProbetacellulin [Cleaved into: Betacellulin (BTC)]
Gene SymbolBTC
OrganismHomo sapiens (Human)
Length178 aa
IsoformsNo isoforms
Related PMIDs No related PMIDs
Database SourcesdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MDRAARCSGA11SSLPLLLALA21LGLVILHCVV31ADGNSTRSPE41TNGLLCGDPE
51-10051ENCAATTTQS61KRKGHFSRCP71KQYKHYCIKG81RCRFVVAEQT91PSCVCDEGYI
101-150101GARCERVDLF111YLRGDRGQIL121VICLIAVMVV131FIILVIGVCT141CCHPLRKRRK
151-178151RKKKEEEMET161LGKDITPINE171DIEETNIA
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
7 - - -
GPS-Palm: 0.85
Deep-Palm: 0.87
28 - - -
GPS-Palm: 0.71
Deep-Palm: 0.98
46 - - -
Deep-Palm: 0.72
53 - - -
GPS-Palm: 0.67
Deep-Palm: 0.69
69 - - -
Deep-Palm: 0.08
77 - - -
GPS-Palm: 0.71
Deep-Palm: 0.05
82 - - -
Deep-Palm: 0.02
93 - - -
Deep-Palm: 0.19
95 - - -
Deep-Palm: 0.26
104 - - -
GPS-Palm: 0.75
Deep-Palm: 0.28
123 - - -
GPS-Palm: 0.67
Deep-Palm: 0.71
139 DBPTM SWISSPALM - - -
GPS-Palm: 0.96
Deep-Palm: 0.93
141 DBPTM SWISSPALM - - -
GPS-Palm: 0.97
Deep-Palm: 0.96
142 DBPTM SWISSPALM - - -
GPS-Palm: 0.97
Deep-Palm: 0.94
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
77 C → C 0.001887 SNP Silent UCEC
149 R → C 0.002506 SNP Missense Mutation COAD
149 R → C 0.002141 SNP Missense Mutation SKCM