SCUBA

ZDHHC20 — Zinc finger DHHC-type palmitoyltransferase 20

ZDHHC20 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

ZDHHC20's module in each cell type

Cell typeModuleShares the module with
EndothelialIntegrin-Actin Adhesion
migration & adhesion
APP, CHD3, CTNNA1, DAG1, DOCK6, FKBP9, FMNL3, ITGA9 +6 moreView in SCUBA
Gamma-delta T cellsHypoxia Stress Response
Stress
ARIH2, BNIP2, C9orf78, CHD4, FBXO7, HIF1A, HNRNPH1, JADE1 +16 more
MacrophagesHypoxia-driven Activation
Inflammatory
ACVR1B, ADAM10, ADAM9, ALCAM, ANO6, B3GNT2, BTG1, C5AR1 +33 moreView in SCUBA
NeutrophilsUbiquitin-Proteasome Turnover
Housekeeping
BLTP3B, CACUL1, CLIP1, FBXL20, FBXO33, FGD3, IL18RAP, KIF13A +10 more
PericytesBMP Receptor Signaling
Developmental
BMPR2, CRK, LRRC8C, PLEKHG1, PTPRN2, RBMS2, RPS6KA2, SNAP23 +1 moreView in SCUBA

About the gene

SynonymsDHHC20, FLJ25952
Chromosome13: 21348784-21459370
Predicted locationMembrane
Essential geneNo
Protein classEnzymes, Metabolic proteins, Predicted membrane proteins, Transporters
Molecular functionAcyltransferase, Transferase
Biological processHost-virus interaction

Function

Palmitoyltransferase that could catalyze the addition of palmitate onto various protein substrates. Catalyzes palmitoylation of Cys residues in the cytoplasmic C-terminus of EGFR, and modulates the duration of EGFR signaling by modulating palmitoylation-dependent EGFR internalization and degradation. Has a preference for acyl-CoA with C16 fatty acid chains. Can also utilize acyl-CoA with C14 and C18 fatty acid chains. May palmitoylate CALHM1 subunit of gustatory voltage-gated ion channels and modulate channel gating and kinetics. (Microbial infection) Dominant palmitoyltransferase responsible for lipidation of SARS coronavirus-2/SARS-CoV-2 spike protein. Through a sequential action with ZDHHC9, rapidly and efficiently palmitoylates spike protein following its synthesis in the endoplasmic reticulum (ER). In the infected cell, promotes spike biogenesis by protecting it from premature ER degradation, increases half-life and controls the lipid organization of its immediate membrane environment. Once the virus has formed, spike palmitoylation controls fusion with the target cell

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.