Three-dimensional density maps of biological specimens from cryo-electron microscopy (cryo-EM) can be interpreted in the form of atomic models that are modeled into the density, or they can be compared to known atomic structures. When the central axis of a helix is detectable in a cryo-EM density map, it is possible to quantify the agreement between this central axis and a central axis calculated from the atomic model or structure. We propose a novel arc-length association method to compare the two axes reliably. This method was applied to 79 helices in simulated density maps and six case studies using cryo-EM maps at 6.4-7.7 Å resolution. The arc-length association method is then compared to three existing measures that evaluate the separa...
SummaryMajor secondary structure elements such as α helices and β sheets can be computationally dete...
Background: De novo protein modeling approaches utilize 3-dimensional (3D) images derived from elect...
Although atomic structures have been determined directly from cryo-EM density maps with high resolut...
Three-dimensional density maps of biological specimens from cryo-electron microscopy (cryo-EM) can b...
Three-dimensional density maps of biological specimens from cryo-electron microscopy (cryo- EM) can ...
Cryo-electron microscopy is an emerging biophysical technique for structural determination of large ...
Cryo-electron microscopy (cryo-EM) density maps at medium resolution (5-10 Å) reveal secondary struc...
Cryo-electron microscopy density maps at medium resolutions (5-10Å) offer insights about secondary s...
Background De novo protein modeling approaches utilize 3-dimensional (3D) images derived from electr...
Background: De novo protein modeling approaches utilize 3-dimensional (3D) images derived from elect...
We are describing best practices and assessment strategies for the atomic interpretation of cryo-ele...
Cryo-electron microscopy (cryo-EM) has produced density maps of various resolutions. Although ά-heli...
Cryo-electron microscopy (cryo-EM) is a structure determination method for large molecular complexes...
Major secondary structure elements such as α helices and β sheets can be computationally detected fr...
Electron cryomicroscopy (cryo-EM) has been used to determine the atomic coordinates (models) from de...
SummaryMajor secondary structure elements such as α helices and β sheets can be computationally dete...
Background: De novo protein modeling approaches utilize 3-dimensional (3D) images derived from elect...
Although atomic structures have been determined directly from cryo-EM density maps with high resolut...
Three-dimensional density maps of biological specimens from cryo-electron microscopy (cryo-EM) can b...
Three-dimensional density maps of biological specimens from cryo-electron microscopy (cryo- EM) can ...
Cryo-electron microscopy is an emerging biophysical technique for structural determination of large ...
Cryo-electron microscopy (cryo-EM) density maps at medium resolution (5-10 Å) reveal secondary struc...
Cryo-electron microscopy density maps at medium resolutions (5-10Å) offer insights about secondary s...
Background De novo protein modeling approaches utilize 3-dimensional (3D) images derived from electr...
Background: De novo protein modeling approaches utilize 3-dimensional (3D) images derived from elect...
We are describing best practices and assessment strategies for the atomic interpretation of cryo-ele...
Cryo-electron microscopy (cryo-EM) has produced density maps of various resolutions. Although ά-heli...
Cryo-electron microscopy (cryo-EM) is a structure determination method for large molecular complexes...
Major secondary structure elements such as α helices and β sheets can be computationally detected fr...
Electron cryomicroscopy (cryo-EM) has been used to determine the atomic coordinates (models) from de...
SummaryMajor secondary structure elements such as α helices and β sheets can be computationally dete...
Background: De novo protein modeling approaches utilize 3-dimensional (3D) images derived from elect...
Although atomic structures have been determined directly from cryo-EM density maps with high resolut...