BAIT
KLHL41
KBTBD10, Krp1, NEM9, SARCOSIN
kelch-like family member 41
GO Process (6)
GO Function (1)
GO Component (8)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
IFRD1
PC4, TIS7
interferon-related developmental regulator 1
GO Process (1)
GO Function (0)
GO Component (0)
Gene Ontology Biological Process
Homo sapiens
Two-hybrid
Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.
Publication
Dysregulation of NRAP degradation by KLHL41 contributes to pathophysiology in Nemaline Myopathy.
Nemaline myopathy (NM) is the most common form of congenital myopathy that results in hypotonia and muscle weakness. This disease is clinically and genetically heterogeneous, but three recently discovered genes in NM encode for members of the Kelch family of proteins. Kelch proteins act as substrate-specific-adapters for CUL3 E3 ubiquitin ligase to regulate protein turn-over through the ubiquitin-proteasome machinery. Defects ... [more]
Hum. Mol. Genet. Apr. 15, 2019; (); [Pubmed: 30986853]
Throughput
- High Throughput
Curated By
- BioGRID