نتایج جستجو برای: polyalanine

تعداد نتایج: 385  

Journal: :Human molecular genetics 2004
Jeanne Amiel Delphine Trochet Mathieu Clément-Ziza Arnold Munnich Stanislas Lyonnet

Beside the well-known polyglutamine expansions involved in several neurodegenerative disorders, convergent recent findings pointed to the expansion of polyalanine stretches as a disease mechanism in congenital malformations, skeletal dysplasia and nervous system anomalies. Polyalanine stretches have been predicted in roughly 500 human proteins among which nine have been ascribed to disease phen...

Journal: :Acta crystallographica. Section D, Biological crystallography 1999
N M Glykos M Kokkinidis

Conventional refinement methods, when applied to even correctly positioned polyalanine models of a target structure, result in a systematic distortion of the molecular geometry and to a concomitant increase in the mean phase difference from the correct phase set. Here, it is shown that iterative rigid-body simulated-annealing refinement of polyalanine models employing successively fewer residue...

2013
Crystal L. Wilcox Natalie A. Terry Catherine Lee May

ARX/Arx is a homeodomain-containing transcription factor necessary for the specification and early maintenance of pancreatic endocrine α-cells. Many transcription factors important to pancreas development, including ARX/Arx, are also crucial for proper brain development. Although null mutations of ARX in human patients result in the severe neurologic syndrome XLAG (X-linked lissencephaly associ...

Journal: :Journal of the American Chemical Society 2004
Sanford A Asher Alexander V Mikhonin Sergei Bykov

We examined the 204-nm UV Raman spectra of the peptide XAO, which was previously found by Shi et al.'s NMR study to occur in aqueous solution in a polyproline II (PPII) conformation. The UV Raman spectra of XAO are essentially identical to the spectra of small peptides such as ala(5) and to the large 21-residue predominantly Ala peptide, AP. We conclude that the non-alpha-helical conformations ...

2011
Chun-rong Qin Ji-long Yao Wen-jie Zhu Wei-qing Wu Jian-sheng Xie

BACKGROUND FOXE1 is one of the candidate genes for genetic predisposition to premature ovarian failure (POF) and it contains an alanine tract. Our purpose is to assess the influence of length of the alanine tract of FOXE1 on genetic susceptibility to POF. METHODS The group studied consisted of 110 Chinese patients with idiopathic POF and 110 women from normal controls. The polyalanine tract a...

Journal: :Biophysical journal 2005
Dalit Shental-Bechor Safak Kirca Nir Ben-Tal Turkan Haliloglu

Folding simulations of polyalanine peptides were carried out using an off-lattice Monte Carlo simulation technique. The peptide was represented as a chain of residues, each of which contains two interaction sites: one corresponding to the C(alpha) atom and the other to the side chain. A statistical potential was used to describe the interaction between these sites. The preferred conformations o...

Journal: :Biophysical journal 2007
Jian Zhou Ian F Thorpe Sergey Izvekov Gregory A Voth

A systematic new approach to derive multiscale coarse-grained (MS-CG) models has been recently developed. The approach employs information from atomistically detailed simulations to derive CG forces and associated effective potentials. In this work, the MS-CG methodology is extended to study two peptides representing distinct structural motifs, alpha-helical polyalanine and the beta-hairpin V(5...

Journal: :Human Molecular Genetics 2004

Journal: :Proteins 2004
Alex Kentsis Mihaly Mezei Tatyana Gindin Roman Osman

Definition of the unfolded state of proteins is essential for understanding their stability and folding on biological timescales. Here, we find that under near physiological conditions the configurational ensemble of the unfolded state of the simplest protein structure, polyalanine alpha-helix, cannot be described by the commonly used Flory random coil model, in which configurational probabilit...

Journal: :American journal of respiratory and critical care medicine 2006
Elizabeth M Berry-Kravis Lili Zhou Casey M Rand Debra E Weese-Mayer

RATIONALE Congenital central hypoventilation syndrome (CCHS), a unique disorder of respiratory control associated with Hirschsprung disease (HSCR) and tumors of neural crest origin, results from polyalanine repeat expansion mutations in the paired-like homeobox (PHOX)2B gene in more than 90% of cases, and alternative PHOX2B mutations in remaining cases. OBJECTIVES To characterize CCHS-associa...

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