SummaryThis paper explores the structural continuum in CATH and the extent to which superfamilies adopt distinct folds. Although most superfamilies are structurally conserved, in some of the most highly populated superfamilies (4% of all superfamilies) there is considerable structural divergence. While relatives share a similar fold in the evolutionary conserved core, diverse elaborations to this core can result in significant differences in the global structures. Applying similar protocols to examine the extent to which structural overlaps occur between different fold groups, it appears this effect is confined to just a few architectures and is largely due to small, recurring super-secondary motifs (e.g., αβ-motifs, α-hairpins). Although 2...
We report the latest release (version 3.0) of the CATH protein domain database (). There has been a ...
Deep-learning (DL) methods like DeepMind's AlphaFold2 (AF2) have led to substantial improvements in ...
A comparison of protein backbones makes clear that not more than approximately 1400 different folds ...
SummaryThis paper explores the structural continuum in CATH and the extent to which superfamilies ad...
This paper explores the structural continuum in CATH and the extent to which superfamilies adopt dis...
This paper explores the structural continuum in CATH and the extent to which superfamilies adopt dis...
The latest version of CATH (class, architecture, topology, homology) (version 3.2), released in July...
We have used GRATH, a graph-based structure comparison algorithm, to map the similarities between th...
CATH version 3.5 (Class, Architecture, Topology, Homology, available at http://www.cathdb.info/) con...
Many protein classification systems capture homologous relationships by grouping domains into famili...
CATH version 3.3 (class, architecture, topology, homology) contains 128,688 domains, 2386 homologous...
Many protein classification systems capture homologous relationships by grouping domains into famili...
AbstractThis article presents a historical review of the protein structure classification database C...
The spatial arrangements of secondary structures in proteins, irrespective of their connectivity, de...
Understanding how protein structures evolve is essential for deciphering relationships between homol...
We report the latest release (version 3.0) of the CATH protein domain database (). There has been a ...
Deep-learning (DL) methods like DeepMind's AlphaFold2 (AF2) have led to substantial improvements in ...
A comparison of protein backbones makes clear that not more than approximately 1400 different folds ...
SummaryThis paper explores the structural continuum in CATH and the extent to which superfamilies ad...
This paper explores the structural continuum in CATH and the extent to which superfamilies adopt dis...
This paper explores the structural continuum in CATH and the extent to which superfamilies adopt dis...
The latest version of CATH (class, architecture, topology, homology) (version 3.2), released in July...
We have used GRATH, a graph-based structure comparison algorithm, to map the similarities between th...
CATH version 3.5 (Class, Architecture, Topology, Homology, available at http://www.cathdb.info/) con...
Many protein classification systems capture homologous relationships by grouping domains into famili...
CATH version 3.3 (class, architecture, topology, homology) contains 128,688 domains, 2386 homologous...
Many protein classification systems capture homologous relationships by grouping domains into famili...
AbstractThis article presents a historical review of the protein structure classification database C...
The spatial arrangements of secondary structures in proteins, irrespective of their connectivity, de...
Understanding how protein structures evolve is essential for deciphering relationships between homol...
We report the latest release (version 3.0) of the CATH protein domain database (). There has been a ...
Deep-learning (DL) methods like DeepMind's AlphaFold2 (AF2) have led to substantial improvements in ...
A comparison of protein backbones makes clear that not more than approximately 1400 different folds ...