Results 51 to 60 of about 6,159,973 (405)

The Arabidopsis TOR Kinase Specifically Regulates the Expression of Nuclear Genes Coding for Plastidic Ribosomal Proteins and the Phosphorylation of the Cytosolic Ribosomal Protein S6

open access: yesFrontiers in Plant Science, 2016
Protein translation is an energy consuming process that has to be fine-tuned at both the cell and organism levels to match the availability of resources.
Thomas Dobrenel   +13 more
semanticscholar   +1 more source

Systematic identification of gene families for use as markers for phylogenetic and phylogeny- driven ecological studies of bacteria and archaea and their major subgroups [PDF]

open access: yes, 2013
With the astonishing rate that the genomic and metagenomic sequence data sets are accumulating, there are many reasons to constrain the data analyses.
Eisen, Jonathan A.   +2 more
core   +7 more sources

Fluorescent protein tagging confirms the presence of ribosomal proteins atDrosophilapolytene chromosomes [PDF]

open access: yes, 2013
\ud \ud Most ribosomal proteins (RPs) are stoichiometrically incorporated into ribosomal subunits and play essential roles in ribosome biogenesis and function.
Bischof   +27 more
core   +3 more sources

Sequential domain assembly of ribosomal protein S3 drives 40S subunit maturation

open access: yesNature Communications, 2016
Eukaryotic ribosomes assemble by association of ribosomal RNA with ribosomal proteins into nuclear precursor particles, which undergo a complex maturation pathway coordinated by non-ribosomal assembly factors.
Valentin Mitterer   +9 more
semanticscholar   +1 more source

When a ribosomal protein grows up – the ribosome assembly path of Rps3

open access: yesMicrobial Cell, 2017
The biogenesis of ribosomes is a central process in all dividing cells. Eukaryotic ribosomes are composed of a large 60S and a small 40S subunit, each comprising a complex assembly of ribosomal RNA (rRNA) and ribosomal proteins (r-proteins).
Brigitte Pertschy
doaj   +1 more source

Different domains cooperate to target the human ribosomal L7a protein to the nucleus and to the nucleoli. [PDF]

open access: yes, 1997
The human ribosomal protein L7a is a component of the major ribosomal subunit. We transiently expressed in HeLa cells L7a-β-galactosidase fusion proteins and studied their subcellular localization by indirect immunofluorescence staining with anti-β ...
Giulia RUSSO   +2 more
core   +1 more source

Bacterial protein interaction networks: connectivity is ruled by gene conservation, essentiality and function [PDF]

open access: yes, 2020
Protein-protein interaction (PPI) networks are the backbone of all processes in living cells. In this work we relate conservation, essentiality and functional repertoire of a gene to the connectivity $k$ of the corresponding protein in the PPI networks ...
Cimini, Giulio   +2 more
core   +2 more sources

Introns regulate the production of ribosomal proteins by modulating splicing of duplicated ribosomal protein genes

open access: yesNucleic Acids Research, 2016
Most budding yeast introns exist in the many duplicated ribosomal protein genes (RPGs) and it has been posited that they remain there to modulate the expression of RPGs and cell growth in response to stress.
Cyrielle Petibon   +3 more
semanticscholar   +1 more source

Ribosomal Protein S6 Phosphorylation in the Nervous System: From Regulation to Function

open access: yesFrontiers in Molecular Neuroscience, 2015
Since the discovery of the phosphorylation of the 40S ribosomal protein S6 (rpS6) about four decades ago, much effort has been made to uncover the molecular mechanisms underlying the regulation of this post-translational modification.
Anne Biever, E. Valjent, E. Puighermanal
semanticscholar   +1 more source

Ribosome-Inactivating and Related Proteins [PDF]

open access: yesToxins, 2015
Ribosome-inactivating proteins (RIPs) are toxins that act as N-glycosidases (EC 3.2.2.22). They are mainly produced by plants and classified as type 1 RIPs and type 2 RIPs. There are also RIPs and RIP related proteins that cannot be grouped into the classical type 1 and type 2 RIPs because of their different sizes, structures or functions. In addition,
Schrot, Joachim   +2 more
openaire   +5 more sources

Home - About - Disclaimer - Privacy