GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
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:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:11309420
Myopalladin, a novel 145-kilodalton sarcomeric protein with multiple roles in Z-disc and I-band protein assemblies.
PMID:11353857
Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin.
PMID:16923132
Interactions between epiplakin and intermediate filaments.
PMID:20706999
Cytoskeletal scaffolding proteins interact with Lynch-Syndrome associated mismatch repair protein MLH1.
PMID:21135508
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscle.
PMID:23533145
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
PMID:23615443
Nebulin binding impedes mutant desmin filament assembly.
PMID:24200904
The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death.
PMID:24940650
Interaction of plectin with keratins 5 and 14: dependence on several plectin domains and keratin quaternary structure.
PMID:25394388
The toxic effect of R350P mutant desmin in striated muscle of man and mouse.
PMID:25416956
A proteome-scale map of the human interactome network.
PMID:25771144
A novel phosphorylation site, Serine 199, in the C-terminus of cardiac troponin I regulates calcium sensitivity and susceptibility to calpain-induced proteolysis.
PMID:26724190
Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect.
PMID:26816005
Homologous Transcription Factors DUX4 and DUX4c Associate with Cytoplasmic Proteins during Muscle Differentiation.
PMID:26871637
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
PMID:27107012
Pooled-matrix protein interaction screens using Barcode Fusion Genetics.
PMID:27733623
Nebulette is a powerful cytolinker organizing desmin and actin in mouse hearts.
PMID:28470624
αB-crystallin is a sensor for assembly intermediates and for the subunit topology of desmin intermediate filaments.
PMID:28514442
Architecture of the human interactome defines protein communities and disease networks.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:32814053
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
PMID:33961781
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
PMID:9415431
Spatial and temporal expression of the beta1D integrin during mouse development.
PMID:9697706
Missense mutations in desmin associated with familial cardiac and skeletal myopathy.
PMID:9736733
A dysfunctional desmin mutation in a patient with severe generalized myopathy.
Reactome:R-HSA-390593
ATP Hydrolysis By Myosin
Reactome:R-HSA-390595
Calcium Binds Troponin-C
Reactome:R-HSA-390597
Release Of ADP From Myosin
Reactome:R-HSA-390598
Myosin Binds ATP
PMID:26787680
Desmin enters the nucleus of cardiac stem cells and modulates Nkx2.5 expression by participating in transcription factor complexes that interact with the nkx2.5 gene.
PMID:35959657
Loss of Nuclear Envelope Integrity and Increased Oxidant Production Cause DNA Damage in Adult Hearts Deficient in PKP2: A Molecular Substrate of ARVC.
PMID:11732910
Ultrastructural and biochemical localization of N-RAP at the interface between myofibrils and intercalated disks in the mouse heart.
PMID:11694502
Association of syncoilin and desmin: linking intermediate filament proteins to the dystrophin-associated protein complex.
PMID:31822208
A Balance Between Intermediate Filaments and Microtubules Maintains Nuclear Architecture in the Cardiomyocyte.
file:human/DES/DES-source-evidence.yaml
DES source evidence and original-access notes