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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q8WZ55 BSND Barttin Homo sapiens (Human) 320 aa

Protein Details: Q8WZ55 (BSND)

Protein Information
AccessionQ8WZ55
Protein NamesBarttin
Gene SymbolBSND
OrganismHomo sapiens (Human)
Length320 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
1-501MADEKTFRIG11FIVLGLFLLA21LGTFLMSHDR31PQVYGTFYAM41GSVMVIGGII
51-10051WSMCQCYPKI61TFVPADSDFQ71GILSPKAMGL81LENGLAAEMK91SPSPQPPYVR
101-150101LWEEAAYDQS111LPDFSHIQMK121VMSYSEDHRS131LLAPEMGQPK141LGTSDGGEGG
151-200151PGDVQAWMEA161AVVIHKGSDE171SEGERRLTQS181WPGPLACPQG191PAPLASFQDD
201-250201LDMDSSEGSS211PNASPHDREE221ACSPQQEPQG231CRCPLDRFQD241FALIDAPTLE
251-300251DEPQEGQQWE261IALPNNWQRY271PRTKVEEKEA281SDTGGEEPEK291EEEDLYYGLP
301-320301DGAGDLLPDK311ELGFEPDTQG
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
54 DBPTM SWISSPALM Bartter syndrome infantile with sensorineural deafness (Barttin) - -
GPS-Palm: 0.90
Deep-Palm: 0.12
56 DBPTM SWISSPALM Bartter syndrome infantile with sensorineural deafness (Barttin) - -
GPS-Palm: 0.84
Deep-Palm: 0.19
187 - - -
Deep-Palm: 0.93
222 - - -
Deep-Palm: 0.20
231 - - -
Deep-Palm: 0.34
233 - - -
Deep-Palm: 0.47
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
129 R → C 0.001887 SNP Missense Mutation UCEC
176 R → C 0.002506 SNP Missense Mutation COAD
176 R → C 0.002033 SNP Missense Mutation LUSC
? ? → ? 0.002141 SNP Missense Mutation SKCM