GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000108
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
PMID:12690205
Human chromosome 7: DNA sequence and biology.
PMID:12853948
The DNA sequence of human chromosome 7.
PMID:14702039
Complete sequencing and characterization of 21,243 full-length human cDNAs.
PMID:15489334
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PMID:16897187
The potential role of DFNA5, a hearing impairment gene, in p53-mediated cellular response to DNA damage.
PMID:18223688
Aberrant promoter methylation and tumor suppressive activity of the DFNA5 gene in colorectal carcinoma.
PMID:19690332
Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
PMID:19911014
Evidence for a founder mutation causing DFNA5 hearing loss in East Asians.
PMID:21269460
Initial characterization of the human central proteome.
PMID:21522185
The DFNA5 gene, responsible for hearing loss and involved in cancer, encodes a novel apoptosis-inducing protein.
PMID:22814378
N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
PMID:24506266
A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing loss.
PMID:26236191
The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways.
PMID:27281216
Pore-forming activity and structural autoinhibition of the gasdermin family.
PMID:28045099
Cleavage of DFNA5 by caspase-3 during apoptosis mediates progression to secondary necrotic/pyroptotic cell death.
PMID:28459430
Chemotherapy drugs induce pyroptosis through caspase-3 cleavage of a gasdermin.
PMID:30976076
Gasdermin pores permeabilize mitochondria to augment caspase-3 activation during apoptosis and inflammasome activation.
PMID:31953257
Gasdermin E-mediated target cell pyroptosis by CAR T cells triggers cytokine release syndrome.
PMID:32188940
Gasdermin E suppresses tumour growth by activating anti-tumour immunity.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:32820063
Succination inactivates gasdermin D and blocks pyroptosis.
PMID:33852854
Gasdermin E permits interleukin-1 beta release in distinct sublytic and pyroptotic phases.
PMID:35594856
Human NLRP1 is a sensor of pathogenic coronavirus 3CL proteases in lung epithelial cells.
PMID:35972780
Zika virus causes placental pyroptosis and associated adverse fetal outcomes by activating GSDME.
PMID:36607699
USP48 Stabilizes Gasdermin E to Promote Pyroptosis in Cancer.
PMID:38599239
ROS-dependent S-palmitoylation activates cleaved and intact gasdermin D.
PMID:39673710
SARS-CoV-2 3CL(pro) (main protease) regulates caspase activation of gasdermin-D/E pores leading to secretion and extracellular activity of 3CL(pro).
PMID:9523727
Characterization of a gene that is inversely correlated with estrogen receptor expression (ICERE-1) in breast carcinomas.
PMID:9771715
Nonsyndromic hearing impairment is associated with a mutation in DFNA5.
Reactome:R-HSA-9647632
CASP3 cleaves GSDME
Reactome:R-HSA-9647660
GSDME (1-270) binds PIPs
Reactome:R-HSA-9710254
GSDME oligomerizes
Reactome:R-HSA-9710263
GZMB cleaves GSDME
Reactome:R-HSA-9710306
GSDME expression mediated by TP53, TP63
Reactome:R-HSA-9710354
GSDME (1-270) binds cardiolipin
Reactome:R-HSA-9710468
GSDME variant does not bind PIPs
UniProtKB:O60443
UniProtKB O60443 (GSDME_HUMAN) record
file:human/GSDME/GSDME-source-evidence.json
Independent GSDME source records, target paths and ontology comparisons