<p>(<b>A</b>) Partial ribbon representation of a 3D model of myosin V 2DFS highlighting the Ile<sup>487</sup> amino acid residue, which is localised to the hinge region between the head and tail domains of the protein. (<b>B</b>) Schematic diagram showing superimposed images of the hinge region (<i>Myo7a<sup>+/+</sup></i> in red and the <i>Myo7a<sup>I487N/I487N</sup> ewaso</i> mutation in blue) after 4 ns of molecular dynamics simulation showing a conformational change in the hinge region close to the Ile<sup>487</sup> mutation site, showing the involvement of residues 670–673 around the hinge region causing the distortion.</p
AbstractMolecular dynamics calculations demonstrated the conformational change in the prion protein ...
<p>A) Domain organization of the IT4var60 PfEMP1 protein with underlined the construct used in this ...
AbstractA natural mutant of human lysozyme, D67H, causes hereditary systemic nonneuropathic amyloido...
<p>DFNA11/DFNB2/USH1B human mutations within close proximity to a reported <i>shaker</i> mutation ar...
<p>A) Amino acid sequence alignment (centered on Gly-345 of Myo2p) of a number of different myosins....
<p>(A) Overview of the predicted structure of myosin-VIIa (3–769) covering the majority of the myosi...
The β-cardiac myosin (β-MyHC) protein is a molecular motor fundamental to both the contractile and s...
<p>Congenital myopathy is a broad category of muscular diseases with symptoms appearing at the time ...
<p>The combined ribbon and stick-sphere representation indicate the predicted structure model of the...
<p>Actin and myosin amino acid numbers are according to human numbering <b>(A)</b> Backbone represen...
<p>Critical residues for each of the structure are red and were calculated independently. <b>A)</b> ...
<div><p>Src-homology regions 3 (SH3) domain is essential for the down-regulation of tyrosine kinase ...
<p>A: G25 in the wild-type protein has no side chain to interact with the His9 and Met59. B: The dis...
The knob-socket model is a novel approach to analyze and describe the tertiary packing of protein st...
Src-homology regions 3 (SH3) domain is essential for the down-regulation of tyrosine kinase activity...
AbstractMolecular dynamics calculations demonstrated the conformational change in the prion protein ...
<p>A) Domain organization of the IT4var60 PfEMP1 protein with underlined the construct used in this ...
AbstractA natural mutant of human lysozyme, D67H, causes hereditary systemic nonneuropathic amyloido...
<p>DFNA11/DFNB2/USH1B human mutations within close proximity to a reported <i>shaker</i> mutation ar...
<p>A) Amino acid sequence alignment (centered on Gly-345 of Myo2p) of a number of different myosins....
<p>(A) Overview of the predicted structure of myosin-VIIa (3–769) covering the majority of the myosi...
The β-cardiac myosin (β-MyHC) protein is a molecular motor fundamental to both the contractile and s...
<p>Congenital myopathy is a broad category of muscular diseases with symptoms appearing at the time ...
<p>The combined ribbon and stick-sphere representation indicate the predicted structure model of the...
<p>Actin and myosin amino acid numbers are according to human numbering <b>(A)</b> Backbone represen...
<p>Critical residues for each of the structure are red and were calculated independently. <b>A)</b> ...
<div><p>Src-homology regions 3 (SH3) domain is essential for the down-regulation of tyrosine kinase ...
<p>A: G25 in the wild-type protein has no side chain to interact with the His9 and Met59. B: The dis...
The knob-socket model is a novel approach to analyze and describe the tertiary packing of protein st...
Src-homology regions 3 (SH3) domain is essential for the down-regulation of tyrosine kinase activity...
AbstractMolecular dynamics calculations demonstrated the conformational change in the prion protein ...
<p>A) Domain organization of the IT4var60 PfEMP1 protein with underlined the construct used in this ...
AbstractA natural mutant of human lysozyme, D67H, causes hereditary systemic nonneuropathic amyloido...