A key concept in template‐based modeling (TBM) is the high correlation between sequence and structural divergence, with the practical consequence that homologous proteins that are similar at the sequence level will also be similar at the structural level. However, conformational diversity of the native state will reduce the correlation between structural and sequence divergence, because structural variation can appear without sequence diversity. In this work, we explore the impact that conformational diversity has on the relationship between structural and sequence divergence. We find that the extent of conformational diversity can be as high as the maximum structural divergence among families. Also, as expected, conformational diversity im...
In this paper we describe a novel strategy for exploring the conformational space of proteins and sh...
Large-scale sequencing projects are widening the gap between the known protein universe and the frac...
The complex constraints imposed by protein structure and function result in varied rates of sequence...
The native state of proteins is composed of conformers in dynamical equilibrium. In this chapter, di...
It is well established that the conservation of protein structure during evolution constrains sequen...
Native state of proteins is better represented by an ensemble of conformers in equilibrium than by o...
Computational modeling of tertiary structures has become of standard use to study proteins that lack...
Major scientific challenges that are beyond the capability of individuals need to be addressed by mu...
<div><p>Computational modeling of tertiary structures has become of standard use to study proteins t...
Proteins' native structure is an ensemble of conformers in equilibrium, including all their respecti...
Protein motions are a key feature to understand biological function. Recently, a large-scale analysi...
Structural differences between conformers sustain protein biological function. Here, we studied in a...
CoDNaS (http://ufq.unq.edu.ar/codnas/) and CoDNaS-Q (http://ufq.unq.edu.ar/codnasq) are repositories...
Proteins are dynamic and can change conformation over time. We introduce a knowledge-based metric to...
In the absence of experimental structures, comparative modeling continues to be the chosen method fo...
In this paper we describe a novel strategy for exploring the conformational space of proteins and sh...
Large-scale sequencing projects are widening the gap between the known protein universe and the frac...
The complex constraints imposed by protein structure and function result in varied rates of sequence...
The native state of proteins is composed of conformers in dynamical equilibrium. In this chapter, di...
It is well established that the conservation of protein structure during evolution constrains sequen...
Native state of proteins is better represented by an ensemble of conformers in equilibrium than by o...
Computational modeling of tertiary structures has become of standard use to study proteins that lack...
Major scientific challenges that are beyond the capability of individuals need to be addressed by mu...
<div><p>Computational modeling of tertiary structures has become of standard use to study proteins t...
Proteins' native structure is an ensemble of conformers in equilibrium, including all their respecti...
Protein motions are a key feature to understand biological function. Recently, a large-scale analysi...
Structural differences between conformers sustain protein biological function. Here, we studied in a...
CoDNaS (http://ufq.unq.edu.ar/codnas/) and CoDNaS-Q (http://ufq.unq.edu.ar/codnasq) are repositories...
Proteins are dynamic and can change conformation over time. We introduce a knowledge-based metric to...
In the absence of experimental structures, comparative modeling continues to be the chosen method fo...
In this paper we describe a novel strategy for exploring the conformational space of proteins and sh...
Large-scale sequencing projects are widening the gap between the known protein universe and the frac...
The complex constraints imposed by protein structure and function result in varied rates of sequence...