Search Results - "Menon, Rajesh P"
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The role of interruptions in polyQ in the pathology of SCA1
Published in PLoS genetics (01-07-2013)“…At least nine dominant neurodegenerative diseases are caused by expansion of CAG repeats in coding regions of specific genes that result in abnormal elongation…”
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2
Myosin IIa Promotes Antibody Responses by Regulating B Cell Activation, Acquisition of Antigen, and Proliferation
Published in Cell reports (Cambridge) (22-05-2018)“…B cell responses are regulated by antigen acquisition, processing, and presentation to helper T cells. These functions are thought to depend on contractile…”
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3
Josephin domain of ataxin-3 contains two distinct ubiquitin-binding sites
Published in Biopolymers (01-12-2009)“…Joseph‐Machado is an incurable neurodegenerative disease caused by toxic aggregation of ataxin‐3, a ubiquitin‐specific cysteine protease, involved in the…”
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Protein-protein interactions as a strategy towards protein-specific drug design: the example of ataxin-1
Published in PloS one (14-10-2013)“…A main challenge for structural biologists is to understand the mechanisms that discriminate between molecular interactions and determine function. Here, we…”
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The Solution Structure of the Josephin Domain of Ataxin-3: Structural Determinants for Molecular Recognition
Published in Proceedings of the National Academy of Sciences - PNAS (26-07-2005)“…The Josephin domain plays an important role in the cellular functions of ataxin-3, the protein responsible for the neurodegenerative Machado-Joseph disease. We…”
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Phosphorylation of S776 and 14-3-3 binding modulate ataxin-1 interaction with splicing factors
Published in PloS one (23-12-2009)“…Ataxin-1 (Atx1), a member of the polyglutamine (polyQ) expanded protein family, is responsible for spinocerebellar ataxia type 1. Requirements for developing…”
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The importance of serine 776 in Ataxin-1 partner selection: A FRET Analysis
Published in Scientific reports (04-12-2012)“…Anomalous expansion of a polymorphic tract in Ataxin-1 causes the autosomal dominant spinocerebellar ataxia type 1. In addition to polyglutamine expansion,…”
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Structural basis for Fc receptor recognition of immunoglobulin M
Published in Nature structural & molecular biology (01-07-2023)“…Immunoglobulin Fc receptors are cell surface transmembrane proteins that bind to the Fc constant region of antibodies and play critical roles in regulating…”
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Domain architecture of the polyglutamine protein ataxin-3: a globular domain followed by a flexible tail
Published in FEBS letters (14-08-2003)“…Anomalous expansion of a polyglutamine (polyQ) tract in the protein ataxin-3 causes spinocerebellar ataxia type 3, an autosomal dominant neurodegenerative…”
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Mapping the self-association domains of ataxin-1: identification of novel non overlapping motifs
Published in PeerJ (San Francisco, CA) (25-03-2014)“…The neurodegenerative disease spinocerebellar ataxia type 1 (SCA1) is caused by aggregation and misfolding of the ataxin-1 protein. While the pathology…”
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Allosteric regulation of deubiquitylase activity through ubiquitination
Published in Frontiers in molecular biosciences (05-02-2015)“…Ataxin-3, the protein responsible for spinocerebellar ataxia type-3, is a cysteine protease that specifically cleaves poly-ubiquitin chains and participates in…”
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Characterization of the Structure and the Amyloidogenic Properties of the Josephin Domain of the Polyglutamine-containing Protein Ataxin-3
Published in Journal of molecular biology (03-12-2004)“…Expansion of the polyglutamine (polyQ) region in the protein ataxin-3 is associated with spinocerebellar ataxia type 3, an inherited neurodegenerative disorder…”
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The C Terminus of Fragile X Mental Retardation Protein Interacts with the Multi-domain Ran-binding Protein in the Microtubule-organising Centre
Published in Journal of molecular biology (08-10-2004)“…Absence of the fragile X mental retardation protein (FMRP) causes fragile X syndrome, the most common form of hereditary mental retardation. FMRP is a mainly…”
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Polyglutamine is Not All: The Functional Role of the AXH Domain in the Ataxin-1 Protein
Published in Journal of molecular biology (09-12-2005)“…A family of neurodegenerative diseases is associated with anomalous expansion of a polyglutamine tract in the coding region of the corresponding proteins. The…”
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Specificity of interactions of galectin-3 with Chrp, a cysteine- and histidine-rich cytoplasmic protein
Published in Biochimie (01-01-2003)“…Earlier work described the cloning of a gene from murine 3T3 cells encoding a cytoplasmic protein Chrp containing a cysteine- and histidine-rich motif…”
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Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1
Published in Human molecular genetics (01-09-2007)“…Ataxin 1 (Atxn1) is a protein of unknown function associated with spinocerebellar ataxia type 1 (SCA1), a neurodegenerative disease of late onset with variable…”
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Chemical shift assignment of the ataxin-1 AXH domain in complex with a CIC ligand peptide
Published in Biomolecular NMR assignments (01-10-2014)“…Ataxin-1 is the protein responsible for the genetically-inherited neurodegenerative disease spinocerebellar ataxia type-1 linked to the expansion of a…”
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Structural bases for recognition of Anp32/LANP proteins
Published in The FEBS journal (01-05-2008)“…The leucine-rich repeat acidic nuclear protein (Anp32a/LANP) belongs to a family of evolutionarily-conserved phosphoproteins involved in a complex network of…”
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The AXH domain adopts alternative folds the solution structure of HBP1 AXH
Published in Structure (London) (01-05-2005)“…AXH is a protein module identified in two unrelated families that comprise the transcriptional repressor HBP1 and ataxin-1 (ATX1), the protein responsible for…”
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Enzymatic production of mono-ubiquitinated proteins for structural studies: The example of the Josephin domain of ataxin-3
Published in FEBS open bio (01-01-2013)“…Protein ubiquitination occurs through formation of an isopeptide bond between the C-terminal glycine of ubiquitin (Ub) and the ɛ-amino group of a substrate…”
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