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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q86W47 KCNMB4 Calcium-activated potassium channel subunit beta-4 … Homo sapiens (Human) 210 aa

Protein Details: Q86W47 (KCNMB4)

Protein Information
Accession Q86W47
Protein Names Calcium-activated potassium channel subunit beta-4 (BK channel subunit beta-4) (BKbeta4) (Hbeta4) (Calcium-activated potassium channel, subfamily M subunit beta-4) (Charybdotoxin receptor subunit beta-4) (K(VCA)beta-4) (Maxi K channel subunit beta-4) (Slo-beta-4)
Gene Symbol KCNMB4
Organism Homo sapiens (Human)
Length 210 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
1-501MAKLRVAYEY11TEAEDKSIRL21GLFLIISGVV31SLFIFGFCWL41SPALQDLQAT
51-10051EANCTVLSVQ61QIGEVFECTF71TCGADCRGTS81QYPCVQVYVN91NSESNSRALL
101-150101HSDEHQLLTN111PKCSYIPPCK121RENQKNLESV131MNWQQYWKDE141IGSQPFTCYF
151-200151NQHQRPDDVL161LHRTHDEIVL171LHCFLWPLVT181FVVGVLIVVL191TICAKSLAVK
201-210201AEAMKKRKFS
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
54 Prediction (Low) - -
119 Prediction (Low) - -
193 DBPTM SWISSPALM Prediction (High) Calcium-activated potassium channel beta subunit -
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
39 W → C 0.001969 SNP Missense Mutation HNSC
76 C → Y 0.005618 SNP Missense Mutation PAAD
146 F → C 0.001887 SNP Missense Mutation UCEC
149 Y → C 0.002427 SNP Missense Mutation BLCA
163 R → C 0.001969 SNP Missense Mutation HNSC
163 R → C 0.002141 SNP Missense Mutation SKCM
207 R → C 0.001969 SNP Missense Mutation HNSC
207 R → C 0.001887 SNP Missense Mutation UCEC