Related references
Note: Only part of the references are listed.The π-helix translates structure into function
Todd M. Weaver
PROTEIN SCIENCE (2010)
Intrinsically disordered proteins in human diseases: Introducing the D-2 concept
Vladimir N. Uversky et al.
ANNUAL REVIEW OF BIOPHYSICS (2008)
Hofmeister salts and potential therapeutic compounds accelerate in vitro fibril formation of the N-terminal domain of PABPN1 containing a disease-causing alanine extension
Grit Lodderstedt et al.
BIOCHEMISTRY (2008)
The unfoldomics decade: an update on intrinsically disordered proteins
A. Keith Dunker et al.
BMC GENOMICS (2008)
Features of trinucleotide repeat instability in vivo
Irina V. Kovtun et al.
CELL RESEARCH (2008)
Chaperones in control of protein disaggregation
Krzysztof Liberek et al.
EMBO JOURNAL (2008)
3′ end mRNA processing:: molecular mechanisms and implications for health and disease
Sven Danckwardt et al.
EMBO JOURNAL (2008)
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expression
Arnaud F. Klein et al.
EXPERIMENTAL CELL RESEARCH (2008)
Monitoring fibril formation of the N-terminal domain of PABPN1 carrying an alanine repeat by tryptophan fluorescence and real-time NMR
Julia Rohrberg et al.
FEBS LETTERS (2008)
Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1
Helene Catoire et al.
HUMAN MOLECULAR GENETICS (2008)
Promiscuous modification of the nuclear poly(A)-binding protein by multiple protein-arginine methyltransferases does not affect the aggregation behavior
Katharina Fronz et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Structural basis for RNA recognition by a type II poly(A)-binding protein
Jikui Song et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Crystal structure and possible dimerization of the single RRM of human PABPN1
Honghua Ge et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2008)
Polyglutamine diseases: emerging concepts in pathogenesis and therapy
Jieya Shao et al.
HUMAN MOLECULAR GENETICS (2007)
Regulation of the nuclear poly(A)-binding protein by arginine methylation in fission yeast
Audrey Perreault et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
AGGRESCAN:: a server for the prediction and evaluation of hot spots of aggregation in polypeptides
Oscar Conchillo-Sole et al.
BMC BIOINFORMATICS (2007)
A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1
Aymeric Chartier et al.
EMBO JOURNAL (2006)
Molecular chaperones and protein quality control
Bernd Bukau et al.
CELL (2006)
Asymmetric arginine dimethylation of heterogeneous nuclear ribonucleoprotein K by protein-arginine methyltransferase 1 inhibits its interaction with c-Src
A Ostareck-Lederer et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
GROMACS: Fast, flexible, and free
D Van der Spoel et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2005)
Repeat instability: Mechanisms of dynamic mutations
CE Pearson et al.
NATURE REVIEWS GENETICS (2005)
Heat shock response modulators as therapeutic tools for diseases of protein conformation
SD Westerheide et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
IUPred:: web server for the prediction of intrinsically unstructured regions of proteins based on estimated energy content
Z Dosztányi et al.
BIOINFORMATICS (2005)
The other trinucleotide repeat: polyalanine expansion disorders
A Albrecht et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2005)
In vivo aggregation properties of the nuclear poly(A)-binding protein PABPN1
JP Tavanez et al.
RNA (2005)
Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in normal magnocellular neurosecretory neurons of the hypothalamus
MT Berciano et al.
HUMAN MOLECULAR GENETICS (2004)
Polyalanine expansions in human
J Amiel et al.
HUMAN MOLECULAR GENETICS (2004)
Reduced amino acid alphabet is sufficient to accurately recognize intrinsically disordered protein
EA Weathers et al.
FEBS LETTERS (2004)
Alanine tracts: the expanding story of human illness and trinucleotide repeats
LY Brown et al.
TRENDS IN GENETICS (2004)
Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains
H Lavoie et al.
HUMAN MOLECULAR GENETICS (2003)
Stimulation of poly(A) polymerase through a direct interaction with the nuclear poly(A) binding protein allosterically regulated by RNA
Y Kerwitz et al.
EMBO JOURNAL (2003)
DSSPcont: continuous secondary structure assignments for proteins
P Carter et al.
NUCLEIC ACIDS RESEARCH (2003)
Nuclear poly(A)-binding protein PABPN1 is associated with RNA polymerase II during transcription and accompanies the released transcript to the nuclear pore
DG Bear et al.
EXPERIMENTAL CELL RESEARCH (2003)
The RNA binding domains of the nuclear poly(A)-binding protein
U Kühn et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
What does it mean to be natively unfolded?
VN Uversky
EUROPEAN JOURNAL OF BIOCHEMISTRY (2002)
The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression
YJ Kim et al.
HUMAN MOLECULAR GENETICS (2001)
Arginine N-methyltransferase 1 is required for early postimplantation mouse development, but cells deficient in the enzyme are viable
MR Pawlak et al.
MOLECULAR AND CELLULAR BIOLOGY (2000)
Protein-arginine methyltransferase I, the predominant protein-arginine methyltransferase in cells, interacts with and is regulated by interleukin enhancer-binding factor 3
J Tang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
The nuclear poly(A) binding protein, PABP2, forms an oligomeric particle covering the length of the poly(A) tail
RW Keller et al.
JOURNAL OF MOLECULAR BIOLOGY (2000)