The complexes of Zn II 2,2′-bipyridine diacetate with salen (LH2) and salophen (L′H2) have been characterized in which complex with L′H2 in DMSO has yielded a novel one-dimensional molecular architecture of micrometer length.
In contrast, the relative abundance of KR sites at the other embryonic enhancers from the BX-C may provide an explanation for the fact that no gain-of-function mutations have ever been characterized in the complex outside of IAB5 and IAB2.
Here we report a study on three newly synthesized Smac mimetics, which have been characterized in their complexes with XIAP BIR3 domain through X-ray crystallography and molecular modelling/docking simulations.
Ribonucleoprotein foci of repeated CUG, CCUG, CGG, CAG, AUUCU and UGGAA motifs present in different human tissues, cultured cells and several model organisms have been characterized in detail providing a complex picture of foci morphology, abundance and molecular composition and their detection method.
MADS-box family genes have been thoroughly studied in its close relative Arabidopsis, but have not been characterized in the relatively large and complex genome of B. rapa.
Although α-type subunits of the SnRK1 complex have been characterized in several plant species, the biological function of β-type and γ-type subunits remains largely unknown.
The structure of the cNTnC−cTnI complex has been characterized in several studies.
The role for the Bur and Ctk complexes has been characterized, in part, by their genetic interactions with other components of the transcription apparatus.
A range of bioinorganic Ni II -complexes have beeNi II -complexesin order to study thavenzymatic mechanism of Ni(II)-ARD [141–144].
So far, two protein translocation complexes have been characterized in the outer and inner envelope (IE) membrane: Toc and Tic (Translocon at the outer/ inner envelope membrane of chloroplasts) [ 3, 4].
