نتایج جستجو برای: rnase

تعداد نتایج: 8269  

Journal: :Genetics 2008
Eunkyoung Shin Hayoung Go Ji-Hyun Yeom Miae Won Jeehyeon Bae Seung Hyun Han Kook Han Younghoon Lee Nam-Chul Ha Christopher J Moore Björn Sohlberg Stanley N Cohen Kangseok Lee

RNase E is an essential Escherichia coli endoribonuclease that plays a major role in the decay and processing of a large fraction of RNAs in the cell. To better understand the molecular mechanisms of RNase E action, we performed a genetic screen for amino acid substitutions in the catalytic domain of the protein (N-Rne) that knock down the ability of RNase E to support survival of E. coli. Comp...

Journal: :Acta medicinae Okayama 1962
T KIMOTO K HAYASHI H MONDEN

Activities of intracellular RNase of the liver cytoplasm, normal liver cells exposed to 3’Me-DAB and heaptoma cells, have been studied in correlation with the contents of RNA and DNA and morphologic changes of the cells with or without treating RNase. The data showed that in hepatoma cells the intracellular acid RNase activity decreases with the decrease of RNA and unchanged DNA contents and al...

Journal: :The Journal of biological chemistry 2003
Ryohei Ishii Osamu Nureki Shigeyuki Yokoyama

RNase PH is one of the exoribonucleases that catalyze the 3' end processing of tRNA in bacteria. RNase PH removes nucleotides following the CCA sequence of tRNA precursors by phosphorolysis and generates mature tRNAs with amino acid acceptor activity. In this study, we determined the crystal structure of Aquifex aeolicus RNase PH bound with a phosphate, a co-substrate, in the active site at 2.3...

Journal: :Medecine sciences : M/S 2008
Catherine Bisbal Tamim Salehzada

The 2-5A/RNase L pathway is one of the first cellular defences against viruses. RNase L is an unusual endoribonuclease which activity is strictly regulated by its binding to a small oligonucleotide, 2-5A. 2-5A itself is very unusual, consisting of a series of 5'- triphosphorylated oligoadenylates with 2'-5' bonds. But RNase L activity is not limited to viral RNA cleavage. RNase L plays a centra...

Journal: :Biomolecules 2015
Merel Derksen Vicky Mertens Ger J M Pruijn

The RNA cleavage activity of RNase P can be employed to decrease the levels of specific RNAs and to study their function or even to eradicate pathogens. Two different technologies have been developed to use RNase P as a tool for RNA knockdown. In one of these, an external guide sequence, which mimics a tRNA precursor, a well-known natural RNase P substrate, is used to target an RNA molecule for...

Journal: :The Plant cell 1997
D. P. Matton O. Maes G. Laublin Q. Xike C. Bertrand D. Morse M. Cappadocia

Self-incompatibility (SI) in angiosperms is a genetic mechanism that promotes outcrossing through rejection of self-pollen. In the Solanaceae, SI is determined by a multiallelic S locus whose only known product is an S RNase. S RNases show a characteristic pattern of five conserved and two hypervariable regions. These are thought to be involved in the catalytic function and in allelic specifici...

2010
Monika P. Rychlik Hyongi Chon Susana M. Cerritelli Paulina Klimek Robert J. Crouch Marcin Nowotny

Two classes of RNase H hydrolyze RNA of RNA/DNA hybrids. In contrast to RNase H1 that requires four ribonucleotides for cleavage, RNase H2 can nick duplex DNAs containing a single ribonucleotide, suggesting different in vivo substrates. We report here the crystal structures of a type 2 RNase H in complex with substrates containing a (5')RNA-DNA(3') junction. They revealed a unique mechanism of ...

2013
Anthony Gobert Franziska Pinker Olivier Fuchsbauer Bernard Gutmann René Boutin Pierre Roblin Claude Sauter Philippe Giegé

RNase P is the essential activity removing 5'-leader sequences from transfer RNA precursors. RNase P was always associated with ribonucleoprotein complexes before the discovery of protein-only RNase P enzymes called PRORPs (PROteinaceous RNase P) in eukaryotes. Here we provide biophysical and functional data to understand the mode of action of PRORP enzymes. Activity assays and footprinting exp...

Journal: :Structure 2005
Jianhua Gan Joseph E Tropea Brian P Austin Donald L Court David S Waugh Xinhua Ji

Bacterial ribonuclease III (RNase III) can affect RNA structure and gene expression in either of two ways: as a processing enzyme that cleaves double-stranded (ds) RNA, or as a binding protein that binds but does not cleave dsRNA. We previously proposed a model of the catalytic complex of RNase III with dsRNA based on three crystal structures, including the endonuclease domain of RNase III with...

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