Aberrant mobility phenomena of the DNA repair protein XPA
about
Structural basis of SUFU-GLI interaction in human Hedgehog signalling regulation.Lacritin and other new proteins of the lacrimal functional unitAn isoform of ZBP-89 predisposes the colon to colitisThe neuroendocrine protein 7B2 is intrinsically disorderedIdentification and characterization of Rhox13, a novel X-linked mouse homeobox geneUnderstanding protein non-folding.High-throughput characterization of intrinsic disorder in proteins from the Protein Structure Initiative.Dimerization of human XPA and formation of XPA2-RPA protein complex.Cooperative interaction of human XPA stabilizes and enhances specific binding of XPA to DNA damage.Phosphorylation of nucleotide excision repair factor xeroderma pigmentosum group A by ataxia telangiectasia mutated and Rad3-related-dependent checkpoint pathway promotes cell survival in response to UV irradiation.ATR-dependent checkpoint modulates XPA nuclear import in response to UV irradiationA filovirus-unique region of Ebola virus nucleoprotein confers aberrant migration and mediates its incorporation into virions.Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis.Differential splicing alters subcellular localization of the alpha but not beta isoform of the MIER1 transcriptional regulator in breast cancer cells.Molecular characterization and functional activity of an IL-15 antagonist MutIL-15/Fc human fusion protein.Intrinsic disorder in scaffold proteins: getting more from lessMultiple intrinsically disordered sequences alter DNA binding by the homeodomain of the Drosophila hox protein ultrabithoraxCold adaptation, ca2+ dependency and autolytic stability are related features in a highly active cold-adapted trypsin resistant to autoproteolysis engineered for biotechnological applications.Involvement of KDM1C histone demethylase-OTLD1 otubain-like histone deubiquitinase complexes in plant gene repression.Evolution and structural organization of the C proteins of paramyxovirinae.Human exonuclease 1 connects nucleotide excision repair (NER) processing with checkpoint activation in response to UV irradiation.Intrinsic disorder and functional proteomics.Plasticity in structural and functional interactions between the phosphoprotein and nucleoprotein of measles virus.Targeting intrinsically disordered proteins in neurodegenerative and protein dysfunction diseases: another illustration of the D(2) concept.Mammalian Bcnt/Cfdp1, a potential epigenetic factor characterized by an acidic stretch in the disordered N-terminal and Ser250 phosphorylation in the conserved C-terminal regions.Conservation of intrinsic disorder in protein domains and families: II. functions of conserved disorder.Another disordered chameleon: the Micro-Exon Gene 14 protein from Schistosomiasis.Functional anthology of intrinsic disorder. 2. Cellular components, domains, technical terms, developmental processes, and coding sequence diversities correlated with long disordered regions.Microarray based analysis of temperature and oxidative stress induced messenger RNA in Schistosoma mansoni.The mysterious unfoldome: structureless, underappreciated, yet vital part of any given proteome.Distribution and cluster analysis of predicted intrinsically disordered protein Pfam domains.Assessment of MS/MS search algorithms with parent-protein profiling.How disordered is my protein and what is its disorder for? A guide through the "dark side" of the protein universe.Human cytomegalovirus phosphoproteins are hypophosphorylated and intrinsically disordered.A novel four-amino acid determinant defines conformational freedom within chorionic gonadotropin beta-subunits.The C-terminus of ICln is natively disordered but displays local structural preformationInteraction between the C-terminal domains of measles virus nucleoprotein and phosphoprotein: a tight complex implying one binding site.A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis.Proteolytic processing of turnip yellow mosaic virus replication proteins and functional impact on infectivity.Development of a LytE-based high-density surface display system in Bacillus subtilis.
P2860
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P2860
Aberrant mobility phenomena of the DNA repair protein XPA
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Aberrant mobility phenomena of the DNA repair protein XPA
@ast
Aberrant mobility phenomena of the DNA repair protein XPA
@en
Aberrant mobility phenomena of the DNA repair protein XPA
@nl
type
label
Aberrant mobility phenomena of the DNA repair protein XPA
@ast
Aberrant mobility phenomena of the DNA repair protein XPA
@en
Aberrant mobility phenomena of the DNA repair protein XPA
@nl
prefLabel
Aberrant mobility phenomena of the DNA repair protein XPA
@ast
Aberrant mobility phenomena of the DNA repair protein XPA
@en
Aberrant mobility phenomena of the DNA repair protein XPA
@nl
P2093
P2860
P50
P356
P1433
P1476
Aberrant mobility phenomena of the DNA repair protein XPA
@en
P2093
A K Dunker
A L Kimzey
E J Ackerman
P2860
P304
P356
10.1110/PS.PS.40101
P407
P577
2001-07-01T00:00:00Z