scholarly article | Q13442814 |
P2093 | author name string | Masaru Tomita | |
Hiroshi Yanagawa | |||
Mitsuhiro Itaya | |||
Naoto Ohtani | |||
P2860 | cites work | Genome sequence of Halobacterium species NRC-1 | Q22066243 |
DNA sequence analysis: a general, simple and rapid method for sequencing large oligodeoxyribonucleotide fragments by mapping | Q24602115 | ||
Structural details of ribonuclease H from Escherichia coli as refined to an atomic resolution | Q27642055 | ||
Proposal for new catalytic roles for two invariant residues in Escherichia coli ribonuclease HI | Q27733938 | ||
Saccharomyces cerevisiae RNase H(35) functions in RNA primer removal during lagging-strand DNA synthesis, most efficiently in cooperation with Rad27 nuclease | Q27930354 | ||
The absence of ribonuclease H1 or H2 alters the sensitivity of Saccharomyces cerevisiae to hydroxyurea, caffeine and ethyl methanesulphonate: implications for roles of RNases H in DNA replication and repair | Q27931541 | ||
Isolation of RNase H genes that are essential for growth of Bacillus subtilis 168 | Q30657542 | ||
Isolation and characterization of a second RNase H (RNase HII) of Escherichia coli K-12 encoded by the rnhB gene | Q31022160 | ||
A Corynebacterium glutamicum rnhA recG double mutant showing lysozyme-sensitivity, temperature-sensitive growth, and UV-sensitivity | Q33195475 | ||
DNA sequence of the gene coding for Escherichia coli ribonuclease H | Q34254042 | ||
Overexpression of RNase H partially complements the growth defect of an Escherichia coli delta topA mutant: R-loop formation is a major problem in the absence of DNA topoisomerase I | Q34451557 | ||
Identification of the genes encoding Mn2+-dependent RNase HII and Mg2+-dependent RNase HIII from Bacillus subtilis: classification of RNases H into three families | Q34487534 | ||
Three-dimensional structure of ribonuclease H from E. coli | Q34566873 | ||
Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase | Q34577497 | ||
A common 40 amino acid motif in eukaryotic RNases H1 and caulimovirus ORF VI proteins binds to duplex RNAs | Q34661604 | ||
An unusual mechanism of self-primed reverse transcription requires the RNase H domain of reverse transcriptase to cleave an RNA duplex | Q36562838 | ||
Reconstitution in vitro of RNase H activity by using purified N-terminal and C-terminal domains of human immunodeficiency virus type 1 reverse transcriptase | Q37396397 | ||
Dispensability of glutamic acid 48 and aspartic acid 134 for Mn2+-dependent activity of Escherichia coli ribonuclease HI. | Q38356702 | ||
The spectrophotometric determination of tyrosine and tryptophan in proteins | Q39252126 | ||
Role of cysteine residues in ribonuclease H from Escherichia coli. Site-directed mutagenesis and chemical modification | Q41978100 | ||
Archaeoglobus fulgidus RNase HII in DNA replication: enzymological functions and activity regulation via metal cofactors | Q42658112 | ||
Purification and characterization of the RNase H domain of HIV-1 reverse transcriptase expressed in recombinant Escherichia coli | Q43449938 | ||
Mutating conserved residues in the ribonuclease H domain of Ty3 reverse transcriptase affects specialized cleavage events | Q43982347 | ||
Activation/attenuation model for RNase H. A one-metal mechanism with second-metal inhibition. | Q46245422 | ||
The putative substrate recognition loop of Escherichia coli ribonuclease H is not essential for activity | Q46401632 | ||
Molecular diversities of RNases H. | Q51336917 | ||
Far different levels of gene expression provided by an oriented cloning system inBacillus subtilisandEscherichia coli | Q53864068 | ||
Kinetic analysis of Escherichia coli ribonuclease HI using oligomeric DNA/RNA substrates suggests an alternative mechanism for the interaction between the enzyme and the substrate. | Q54607803 | ||
pH-dependent thermostabilization of Escherichia coli ribonuclease HI by histidine to alanine substitutions. | Q54661696 | ||
Importance of the positive charge cluster in Escherichia coli ribonuclease HI for the effective binding of the substrate. | Q54695492 | ||
Overproduction and preliminary crystallographic study of ribonuclease H from Escherichia coli. | Q54727290 | ||
Function of RNase H in DNA replication revealed by RNase H defective mutants of Escherichia coli | Q70186978 | ||
Substrate specificity of human RNase H1 and its role in excision repair of ribose residues misincorporated in DNA | Q70458178 | ||
Thermal stability of Escherichia coli ribonuclease HI and its active site mutants in the presence and absence of the Mg2+ ion. Proposal of a novel catalytic role for Glu48 | Q71859993 | ||
A novel strategy for stabilization of Escherichia coli ribonuclease HI involving a screen for an intragenic suppressor of carboxyl-terminal deletions | Q72724809 | ||
Creation and removal of embedded ribonucleotides in chromosomal DNA during mammalian Okazaki fragment processing | Q73648477 | ||
Characterization of ribonuclease HII from Escherichia coli overproduced in a soluble form | Q73731965 | ||
Cooperative regulation for Okazaki fragment processing by RNase HII and FEN-1 purified from a hyperthermophilic archaeon, Pyrococcus furiosus | Q73873899 | ||
Temporal coordination between initiation of HIV (+)-strand DNA synthesis and primer removal | Q77298456 | ||
P433 | issue | Pt 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 795-802 | |
P577 | publication date | 2004-08-01 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | Identification of the first archaeal Type 1 RNase H gene from Halobacterium sp. NRC-1: archaeal RNase HI can cleave an RNA-DNA junction | |
P478 | volume | 381 |
Q41772246 | A dual role of divalent metal ions in catalysis and folding of RNase H1 from extreme halophilic archaeon Halobacterium sp. NRC-1. |
Q37392491 | A phylogenetic view of bacterial ribonucleases |
Q34387980 | Acquisition of an Archaea-like ribonuclease H domain by plant L1 retrotransposons supports modular evolution |
Q34364175 | Cleavage of double-stranded RNA by RNase HI from a thermoacidophilic archaeon, Sulfolobus tokodaii 7. |
Q38908130 | Convergence of retrotransposons in oomycetes and plants. |
Q34458880 | Convergent evolution of ribonuclease h in LTR retrotransposons and retroviruses |
Q36459488 | Crystallization and preliminary crystallographic analysis of type 1 RNase H from the hyperthermophilic archaeon Sulfolobus tokodaii 7. |
Q35288330 | Divalent metal ion-induced folding mechanism of RNase H1 from extreme halophilic archaeon Halobacterium sp. NRC-1. |
Q38208817 | Diversity of the DNA replication system in the Archaea domain |
Q37848236 | Effect of the termini of RNase Hs from Chlamydophila pneumoniae on enzymatic biochemical characterization |
Q30832990 | Evolution of ribonuclease H genes in prokaryotes to avoid inheritance of redundant genes |
Q38853906 | Evolution of the archaeal and mammalian information processing systems: towards an archaeal model for human disease |
Q90455698 | Evolutionary history and activity of RNase H1-like proteins in Arabidopsis thaliana |
Q57103308 | Post-genomics of the model haloarchaeon Halobacterium sp. NRC-1 |
Q39162255 | Real time monitoring of junction ribonuclease activity of RNase H using chimeric molecular beacons |
Q34948257 | Ribonuclease H: molecular diversities, substrate binding domains, and catalytic mechanism of the prokaryotic enzymes |
Q26864225 | Ribonucleotides in bacterial DNA |
Q40395197 | Role of RNase H1 in DNA repair: removal of single ribonucleotide misincorporated into DNA in collaboration with RNase H2. |
Q41828496 | Structure-specific nuclease activities of Pyrococcus abyssi RNase HII. |
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