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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P14061 HSD17B1 17-beta-hydroxysteroid dehydrogenase type 1 (17-beta-HSD … Homo sapiens (Human) 328 aa

Protein Details: P14061 (HSD17B1)

Protein Information
AccessionP14061
Protein Names17-beta-hydroxysteroid dehydrogenase type 1 (17-beta-HSD 1) (EC 1.1.1.51) (20 alpha-hydroxysteroid dehydrogenase) (20-alpha-HSD) (E2DH) (Estradiol 17-beta-dehydrogenase 1) (EC 1.1.1.62) (Placental 17-beta-hydroxysteroid dehydrogenase) (Short chain dehydrogenase/reductase family 28C member 1)
Gene SymbolHSD17B1
OrganismHomo sapiens (Human)
Length328 aa
IsoformsNo isoforms
Related PMIDs No related PMIDs
Database SourcesSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MARTVVLITG11CSSGIGLHLA21VRLASDPSQS31FKVYATLRDL41KTQGRLWEAA
51-10051RALACPPGSL61ETLQLDVRDS71KSVAAARERV81TEGRVDVLVC91NAGLGLLGPL
101-150101EALGEDAVAS111VLDVNVVGTV121RMLQAFLPDM131KRRGSGRVLV141TGSVGGLMGL
151-200151PFNDVYCASK161FALEGLCESL171AVLLLPFGVH181LSLIECGPVH191TAFMEKVLGS
201-250201PEEVLDRTDI211HTFHRFYQYL221AHSKQVFREA231AQNPEEVAEV241FLTALRAPKP
251-300251TLRYFTTERF261LPLLRMRLDD271PSGSNYVTAM281HREVFGDVPA291KAEAGAEAGG
301-328301GAGPGAEDEA311GRGAVGDPEL321GDPPAAPQ
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
11 NAD(P)-binding domain superfamily - -
GPS-Palm: 0.72
55 - - -
GPS-Palm: 0.89
90 - - -
GPS-Palm: 0.79
157 - - -
GPS-Palm: 0.71
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)
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
95 G → C 0.001887 SNP Missense Mutation UCEC
167 C → C 0.002545 SNP Silent GBM
177 F → C 0.001887 SNP Missense Mutation UCEC
186 C → C 0.002506 SNP Silent COAD