Search Database

Select Protein (1 found)

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

Protein Details: Q8WZ55 (BSND)

Protein Information
Accession Q8WZ55
Protein Names Barttin
Gene Symbol BSND; BART
Organism Homo sapiens (Human)
Length 320 aa
Isoforms No isoforms
Related PMIDs No related PMIDs
Database Sources dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MADEKTFRIG11FIVLGLFLLA21LGTFLMSHDR31PQVYGTFYAM41GSVMVIGGII
51-10051WSMCQCYPKI61TFVPADSDFQ71GILSPKAMGL81LENGLAAEMK91SPSPQPPYVR
101-150101LWEEAAYDQS111LPDFSHIQMK121VMSYSEDHRS131LLAPEMGQPK141LGTSDGGEGG
151-200151PGDVQAWMEA161AVVIHKGSDE171SEGERRLTQS181WPGPLACPQG191PAPLASFQDD
201-250201LDMDSSEGSS211PNASPHDREE221ACSPQQEPQG231CRCPLDRFQD241FALIDAPTLE
251-300251DEPQEGQQWE261IALPNNWQRY271PRTKVEEKEA281SDTGGEEPEK291EEEDLYYGLP
301-320301DGAGDLLPDK311ELGFEPDTQG
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
54 DBPTM SWISSPALM Prediction (High) Bartter syndrome infantile with sensorineural deafness (Barttin) -
56 DBPTM SWISSPALM Prediction (Medium) Bartter syndrome infantile with sensorineural deafness (Barttin) -
Conservation Scores
PhyloP
PhastCons
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