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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
E9PLD0 RAB1B RAB1B, member RAS oncogene family Homo sapiens (Human) 169 aa

Protein Details: E9PLD0 (RAB1B)

Protein Information
AccessionE9PLD0
Protein NamesRAB1B, member RAS oncogene family
Gene SymbolRAB1B
OrganismHomo sapiens (Human)
Length169 aa
IsoformsNo isoforms
Related PMIDs 31251020 32944167
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MNPEYDYLFK11LLLIGDSGVG21KSCLLLRFAD31DTYTESYIST41IGVDFKIRTI
51-10051ELDGKTIKLQ61IESYANVKQW71LQEIDRYASE81NVNKLLVGNK91SDLTTKKVVD
101-150101NTTAKEFADS111LGIPFLETSA121KNATNVEQAF131MTMAAEIKKR141MGPGAASGGE
151-169151RPNLKIDSTP161VKPAGGGCC
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
23 SWISSPALM DBPTM CYSMODDB Ras family - -
Deep-Palm: 0.98
168 - - -
Deep-Palm: 0.03
169 - - -
Deep-Palm: 0.03
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)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.667
4
PC3
Specificity: 0.667
4/4 (100.0%)
2
LNCaP
Specificity: 0.333
2/2 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
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
88 Y → C 0.002141 SNP Missense Mutation SKCM
200 C → Y 0.002288 SNP Missense Mutation STAD
200 C → S 0.002033 SNP Missense Mutation LUSC