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Robuta

https://www.ncbi.nlm.nih.gov/gene/23347
SMCHD1 structural maintenance of chromosomes flexible hinge domain containing 1 [Homo sapiens...
structuralmaintenancechromosomesflexiblehinge
https://www.rcsb.org/structure/3PRP
RCSB PDB - 3PRP: Structural analysis of a viral OTU domain protease from the Crimean-Congo...
Structural analysis of a viral OTU domain protease from the Crimean-Congo Hemorrhagic Fever virus in complex with human ubiquitin
structural analysisrcsbpdbviralotu
https://www.ncbi.nlm.nih.gov/Structure/pdb/4Y1T
4Y1T: Structural basis for Ca2+-mediated interaction of the perforin C2 domain with lipid membranes
Perforin-1CALCIUM ION
mediated interactionstructuralbasisperforin
https://pubmed.ncbi.nlm.nih.gov/17085435/
Ligand-induced structural changes of the CD44 hyaluronan-binding domain revealed by NMR
CD44, a major cell surface receptor for hyaluronan (HA), contains a functional domain responsible for HA binding at its N terminus (residues 21-178)....
binding domainligandinducedstructuralchanges
https://www.rcsb.org/structure/2KMI
RCSB PDB - 2KMI: MESD(12-155), The Core Structural Domain of MESD that Is Essential for Proper...
MESD(12-155), The Core Structural Domain of MESD that Is Essential for Proper Folding of LRP5/6
the corestructural domainrcsbpdbmesd
https://www.rcsb.org/structure/4Y1S
RCSB PDB - 4Y1S: Structural basis for Ca2+-mediated interaction of the perforin C2 domain with...
Structural basis for Ca2+-mediated interaction of the perforin C2 domain with lipid membranes
mediated interactionrcsbpdbstructuralbasis
https://pubmed.ncbi.nlm.nih.gov/35394523/
Structural basis for the linkage specificity of ubiquitin-binding domain and deubiquitinase
Ubiquitination is a post-translational modification system essential for regulating a wide variety of biological processes in eukaryotes. Ubiquitin (Ub) itself...
ubiquitin binding domainstructuralbasislinkagespecificity
https://pubmed.ncbi.nlm.nih.gov/17609377/
Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the...
The chromatin-associated protein ATRX was originally identified because mutations in the ATRX gene cause a severe form of syndromal X-linked mental retardation...
in thestructuralconsequencesdiseasecausing