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UniProt ID Gene Symbol Protein Name Organism Length Action
P62910 RPL32 Large ribosomal subunit protein eL32 … Homo sapiens (Human) 135 aa

Protein Details: P62910 (RPL32)

Protein Information
AccessionP62910
Protein NamesLarge ribosomal subunit protein eL32 (60S ribosomal protein L32)
Gene SymbolRPL32
OrganismHomo sapiens (Human)
Length135 aa
IsoformsNo isoforms
Related PMIDs 29733200
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MAALRPLVKP11KIVKKRTKKF21IRHQSDRYVK31IKRNWRKPRG41IDNRVRRRFK
51-10051GQILMPNIGY61GSNKKTKHML71PSGFRKFLVH81NVKELEVLLM91CNKSYCAEIA
101-135101HNVSSKNRKA111IVERAAQLAI121RVTNPNARLR131SEENE
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
91 - -
Unknown (32651440)
GPS-Palm: 0.66
Deep-Palm: 0.93
96 SWISSPALM DBPTM CYSMODDB Ribosomal protein L32
SW480 cell line (26865113)
-
GPS-Palm: 0.80
Deep-Palm: 0.93
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): 0.500
1
HAP1 cell
Specificity: 0.500
1/1 (100.0%)
1
293T cell
Specificity: 0.500
1/1 (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.
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
130 R → C 0.001969 SNP Missense Mutation LGG