The observed crystallographic B-factors (left) and the predicted B-factors from the Seq-GNM superimposed on the structure. The three proteins selected–2JAO, 1F2J, and 1UMK–are high-resolution structures better than 2.0 Å. The B-factors are color-coded according to their B-factor profile on a spectrum of blue–white–red where blue represents the lowest B-factors (less mobility) and red represents the highest B-factors (more mobility). The B-factor scores are converted to a percentile rank so that they can be compared across different proteins. Each protein is also rotated 180° so that both sides can be visualized and compared. Moreover, the proteins are selected so that they have a variety of secondary structure components–2JAO contains prima...
(a) Overview of CYP1B1 wild type protein in ribbon-presentation (b-l) In-silico protein prediction r...
The accuracy of B factors in protein crystal structures has been determined by comparing the same at...
<p>TM-score for folded segments of the protein structures for different runs at Q = 0.8, 0.4, 0.2 fr...
<p>B-factors were calculated from the three first modes of NMA (blue), and EDA (orange) and plotted ...
A ribbon diagram for two human enzymes, human lysozyme (a) and cytochrome reductase (b) colored acco...
B-factors are shown on the respective structures for (a) 5'(3')-deoxyribonucleotidase (2JAO) and (b)...
<p>For each property, colored lines represent proteins of different age: orphans (red), genus orphan...
<p>Only the protein backbone is shown in ribbon presentation. α-helices in blue, β-sheets in red, tu...
<p>Two scores were computed for the native structures of all 740 proteins chains in BLC-NEW using th...
<p>The green bar above the ribbon diagrams represents protein sequences with their corresponding ami...
BACKGROUND:Protein crystal structures are potentially over-interpreted since they are routinely refi...
BACKGROUND:Protein crystal structures are potentially over-interpreted since they are routinely refi...
Background: Protein crystal structures are potentially over-interpreted since they are routinely ref...
A. Topology of Esp1 (top) and Esp2 (bottom) shown in rainbow coloring, with similar coloring of the ...
The topology of most experimentally determined protein domains is defined by the relative arrangemen...
(a) Overview of CYP1B1 wild type protein in ribbon-presentation (b-l) In-silico protein prediction r...
The accuracy of B factors in protein crystal structures has been determined by comparing the same at...
<p>TM-score for folded segments of the protein structures for different runs at Q = 0.8, 0.4, 0.2 fr...
<p>B-factors were calculated from the three first modes of NMA (blue), and EDA (orange) and plotted ...
A ribbon diagram for two human enzymes, human lysozyme (a) and cytochrome reductase (b) colored acco...
B-factors are shown on the respective structures for (a) 5'(3')-deoxyribonucleotidase (2JAO) and (b)...
<p>For each property, colored lines represent proteins of different age: orphans (red), genus orphan...
<p>Only the protein backbone is shown in ribbon presentation. α-helices in blue, β-sheets in red, tu...
<p>Two scores were computed for the native structures of all 740 proteins chains in BLC-NEW using th...
<p>The green bar above the ribbon diagrams represents protein sequences with their corresponding ami...
BACKGROUND:Protein crystal structures are potentially over-interpreted since they are routinely refi...
BACKGROUND:Protein crystal structures are potentially over-interpreted since they are routinely refi...
Background: Protein crystal structures are potentially over-interpreted since they are routinely ref...
A. Topology of Esp1 (top) and Esp2 (bottom) shown in rainbow coloring, with similar coloring of the ...
The topology of most experimentally determined protein domains is defined by the relative arrangemen...
(a) Overview of CYP1B1 wild type protein in ribbon-presentation (b-l) In-silico protein prediction r...
The accuracy of B factors in protein crystal structures has been determined by comparing the same at...
<p>TM-score for folded segments of the protein structures for different runs at Q = 0.8, 0.4, 0.2 fr...