(Q24336008)

2

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Ai-Xin Song

3

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Yong-Gang Chang

4

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Xue-Chao Gao

5

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Nan Jiang

6

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Qi Zhang

7

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Hong-Yu Hu

Reexamination of the recognition preference of the specificity pocket of the Abl SH3 domain

8

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language of work or name

English

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publication date

December 2006

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published in

Structure

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volume

14

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page(s)

1755-65

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issue

12

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cites work

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Automated NOESY interpretation with ambiguous distance restraints: the refined NMR solution structure of the pleckstrin homology domain from beta-spectrin

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AQUA and PROCHECK-NMR: programs for checking the quality of protein structures solved by NMR

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NMR View: A computer program for the visualization and analysis of NMR data

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Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

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FBP11 regulates nuclear localization of N-WASP and inhibits N-WASP-dependent microspike formation

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Structural basis for APPTPPPLPP peptide recognition by the FBP11WW1 domain

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A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington's disease

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Huntington's disease: a synaptopathy?

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Highly efficient expression and purification system of small-size protein domains in Escherichia coli for biochemical characterization.

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Huntingtin-protein interactions and the pathogenesis of Huntington's disease

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Solution structure and ligand recognition of the WW domain pair of the yeast splicing factor Prp40

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How SH3 domains recognize proline

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Structure and function of the WW domain.

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Transcriptional abnormalities in Huntington disease

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Polyglutamines stop traffic: axonal transport as a common target in neurodegenerative diseases

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The WW domain: linking cell signalling to the membrane cytoskeleton

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New approaches to the dynamic interpretation and prediction of NMR relaxation data from proteins.

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The hunt for huntingtin function: interaction partners tell many different stories

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The three-dimensional structure of the HRDC domain and implications for the Werner and Bloom syndrome proteins

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SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates

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Topography for independent binding of alpha-helical and PPII-helical ligands to a peroxisomal SH3 domain

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Backbone dynamics of a free and phosphopeptide-complexed Src homology 2 domain studied by 15N NMR relaxation

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Protein backbone angle restraints from searching a database for chemical shift and sequence homology

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New applications of 2D filtered/edited NOESY for assignment and structure elucidation of RNA and RNA-protein complexes

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Huntingtin and the molecular pathogenesis of Huntington's disease. Fourth in molecular medicine review series

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Specificity and versatility of SH3 and other proline-recognition domains: structural basis and implications for cellular signal transduction

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Huntington's disease. Pathogenesis and management

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Effects of intracellular expression of anti-huntingtin antibodies of various specificities on mutant huntingtin aggregation and toxicity

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The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis

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SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexes

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Polyglutamine-expanded huntingtin promotes sensitization of N-methyl-D-aspartate receptors via post-synaptic density 95.

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The structure and dynamics of tandem WW domains in a negative regulator of notch signaling, Suppressor of deltex

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Regulation of WASP/WAVE proteins: making a long story short

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FBP WW domains and the Abl SH3 domain bind to a specific class of proline-rich ligands

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The peroxisomal membrane protein Pex13p shows a novel mode of SH3 interaction

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Diverse recognition of non-PxxP peptide ligands by the SH3 domains from p67(phox), Grb2 and Pex13p

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PACSIN 1 interacts with huntingtin and is absent from synaptic varicosities in presymptomatic Huntington's disease brains

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7 January 2021

Huntingtin interacts with a family of WW domain proteins

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Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis

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The importance of being proline: the interaction of proline-rich motifs in signaling proteins with their cognate domains

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Neuropathological classification of Huntington's disease

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Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

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The WW domain-containing proteins interact with the early spliceosome and participate in pre-mRNA splicing in vivo

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7 January 2021

Huntingtin bodies sequester vesicle-associated proteins by a polyproline-dependent interaction.

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NMR methods for the determination of protein-ligand dissociation constants

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