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UniProt ID Gene Symbol Protein Name Organism Length Action
Q10589-2 BST2 Bone marrow stromal antigen 2 … Homo sapiens (Human) 180 aa

Protein Details: Q10589-2 (BST2)

Protein Information
AccessionQ10589-2
Protein NamesBone marrow stromal antigen 2 (BST-2) (HM1.24 antigen) (Tetherin) (CD antigen CD317)
Gene SymbolBST2
OrganismHomo sapiens (Human)
Length180 aa
Isoforms
Related PMIDs 32651440 33636221 36430497
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MASTSYDYCR11VPMEDGDKRC21KLLLGIGILV31LLIIVILGVP41LIIFTIKANS
51-10051EACRDGLRAV61MECRNVTHLL71QQELTEAQKG81FQDVEAQAAT91CNHTVMALMA
101-150101SLDAEKAQGQ111KKVEELEGEI121TTLNHKLQDA131SAEVERLRRE141NQVLSVRIAD
151-180151KKYYPSSQDS161SSAAAPQLLI171VLLGLSALLQ
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
9 - - -
Deep-Palm: 0.03
20 - - -
Deep-Palm: 0.97
53 - - -
Deep-Palm: 0.82
63 - - -
Deep-Palm: 0.87
91 - - -
Deep-Palm: 0.85
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
cerebral cortex
Specificity: 0.667
4/4 (100.0%)
1
Jurkat T cell
Specificity: 0.167
1/1 (100.0%)
1
heart
Specificity: 0.167
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.
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
64 R → C 0.001887 SNP Missense Mutation UCEC
? ? → ? 0.001764 SNP Nonsense Mutation LUAD