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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P07306 ASGR1 Asialoglycoprotein receptor 1 (ASGP-R 1) … Homo sapiens (Human) 291 aa

Protein Details: P07306 (ASGR1)

Protein Information
AccessionP07306
Protein NamesAsialoglycoprotein receptor 1 (ASGP-R 1) (ASGPR 1) (C-type lectin domain family 4 member H1) (Hepatic lectin H1) (HL-1)
Gene SymbolASGR1
OrganismHomo sapiens (Human)
Length291 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
1-501MTKEYQDLQH11LDNEESDHHQ21LRKGPPPPQP31LLQRLCSGPR41LLLLSLGLSL
51-10051LLLVVVCVIG61SQNSQLQEEL71RGLRETFSNF81TASTEAQVKG91LSTQGGNVGR
101-150101KMKSLESQLE111KQQKDLSEDH121SSLLLHVKQF131VSDLRSLSCQ141MAALQGNGSE
151-200151RTCCPVNWVE161HERSCYWFSR171SGKAWADADN181YCRLEDAHLV191VVTSWEEQKF
201-250201VQHHIGPVNT211WMGLHDQNGP221WKWVDGTDYE231TGFKNWRPEQ241PDDWYGHGLG
251-291251GGEDCAHFTD261DGRWNDDVCQ271RPYRWVCETE281LDKASQEPPL291L
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
36 DBPTM SWISSPALM Hepatic lectin, N-terminal domain Hepatic lectin N-terminal domain - -
GPS-Palm: 0.85
Deep-Palm: 0.99
57 - - -
GPS-Palm: 0.67
Deep-Palm: 0.98
139 - - -
GPS-Palm: 0.72
Deep-Palm: 0.87
153 - - -
Deep-Palm: 0.05
154 - - -
Deep-Palm: 0.06
165 - - -
Deep-Palm: 0.07
182 - - -
GPS-Palm: 0.74
Deep-Palm: 0.41
255 - - -
Deep-Palm: 0.04
269 - - -
Deep-Palm: 0.10
277 - - -
Deep-Palm: 0.44
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
40 R → C 0.002020 SNP Missense Mutation PRAD
158 W → C 0.002033 SNP Missense Mutation LUSC
200 F → C 0.002747 SNP Missense Mutation LIHC
211 W → C 0.001887 SNP Missense Mutation UCEC
255* C → ? 0.002545 SNP Nonsense Mutation GBM