Results 51 to 60 of about 9,430 (262)
On The Local Edge Antimagic Coloring of Corona Product of Path and Cycle
Let be a nontrivial and connected graph of vertex set and edge set . A bijection is called a local edge antimagic labeling if for any two adjacent edges and , where for . Thus, the local edge antimagic labeling induces a proper edge coloring of G if
Siti Aisyah +4 more
doaj +1 more source
Tau acetylation at K331 has limited impact on tau pathology in vivo
We mapped tau post‐translational modifications in humanized MAPT knock‐in mice and in amyloid‐bearing double knock‐in mice. Acetylation within the repeat domain, particularly around K331, showed modest increases under amyloid pathology. To test functional relevance, we generated MAPTK331Q knock‐in mice.
Shoko Hashimoto +3 more
wiley +1 more source
Structural insights into an engineered feruloyl esterase with improved MHET degrading properties
A feruloyl esterase was engineered to mimic key features of MHETase, enhancing the degradation of PET oligomers. Structural and computational analysis reveal how a point mutation stabilizes the active site and reshapes the binding cleft, expading substrate scope.
Panagiota Karampa +5 more
wiley +1 more source
M2-Edge Colorings Of Cacti And Graph Joins
An edge coloring φ of a graph G is called an M2-edge coloring if |φ(v)| ≤ 2 for every vertex v of G, where φ(v) is the set of colors of edges incident with v. Let 𝒦2(G) denote the maximum number of colors used in an M2-edge coloring of G.
Czap Július +2 more
doaj +1 more source
Plasma membranes contain dynamic nanoscale domains that organize lipids and receptors. Because viruses operate at similar scales, this architecture shapes early infection steps, including attachment, receptor engagement, and entry. Using influenza A virus and HIV‐1 as examples, we highlight how receptor nanoclusters, multivalent glycan interactions ...
Jan Schlegel, Christian Sieben
wiley +1 more source
A note on compact and compact circular edge-colorings of graphs
In the paper we study two variants of edge-coloring of edge-weighted graphs, namely compact edge-coloring and circular compact edge-coloring. First, we discuss relations between these two coloring models.
Dariusz Dereniowski, Adam Nadolski
doaj
Ascidian Ciona larvae initially show strong clockwise tail twisting, which is largely corrected during development. However, a small residual twist remains. This study shows that organized helical myofibrils in tail muscles mechanically stabilize this residual asymmetry, preventing complete restoration of bilateral symmetry and revealing how embryos ...
Yuki S. Kogure +3 more
wiley +1 more source
Maximal edge colorings of graphs
For a graph $G$ of order $n$ a maximal edge coloring is a proper edge coloring with $χ'(K_n)$ colors such that adding any edge to $G$ in any color makes it improper. Meszka and Tyniec proved that for some values of the number of edges there are no graphs with a maximal edge coloring, while for some other values, they provided constructions of such ...
Sebastian Babinski, Andrzej Grzesik
openaire +6 more sources
Degradation mechanism of the von Willebrand factor A2 domain by nattokinase
Nattokinase, a natto‐derived protease, exhibits potent antithrombotic effects. This study demonstrates that nattokinase directly cleaves the von Willebrand factor (vWF) A2 domain in vitro. Unlike the native regulator ADAMTS13, nattokinase degrades folded vWF independently of shear stress.
Ryuichi Hyakumoto +3 more
wiley +1 more source
Modulation of Homer1 EVH1 domain internal dynamics by putative autism‐associated mutations
The putative autism‐associated M65I and S97L variants of the EVH1 domain of the postsynaptic scaffold protein Homer1 do not exhibit substantial changes in their overall structure or partner binding. Both of them, but especially the M65I variant, show altered internal dynamics relative to the wild‐type domain on the μs‐ms timescale, indicated by the ...
Fanni Farkas +6 more
wiley +1 more source

