scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Kathleen Sandman | Q58829071 |
P2093 | author name string | J. N. Reeve | |
C. J. Daniels | |||
P2860 | cites work | Complete Genome Sequence of the Methanogenic Archaeon, Methanococcus jannaschii | Q22065564 |
RNA polymerase II transcription initiation: a structural view | Q24614755 | ||
NMR structure of HMfB from the hyperthermophile, Methanothermus fervidus, confirms that this archaeal protein is a histone | Q27732536 | ||
The crystal structure of a hyperthermophilic archaeal TATA-box binding protein | Q27734618 | ||
HMf, a DNA-binding protein isolated from the hyperthermophilic archaeon Methanothermus fervidus, is most closely related to histones | Q33718187 | ||
The histone fold: a ubiquitous architectural motif utilized in DNA compaction and protein dimerization | Q33761918 | ||
Transcription in archaea: similarity to that in eucarya | Q34058138 | ||
Interaction of the histone (H3-H4)2 tetramer of the nucleosome with positively supercoiled DNA minicircles: Potential flipping of the protein from a left- to a right-handed superhelical form | Q37427611 | ||
More than just "histone-like" proteins | Q37826709 | ||
DNA binding and nuclease protection by the HMf histones from the hyperthermophilic archaeon Methanothermus fervidus | Q38346174 | ||
In vivo definition of an archaeal promoter | Q39836228 | ||
Genetic and topological analyses of the bop promoter of Halobacterium halobium: stimulation by DNA supercoiling and non-B-DNA structure | Q39840175 | ||
Chromosomal structure of the halophilic archaebacterium Halobacterium salinarium | Q39939665 | ||
DNA stability and DNA binding proteins. | Q41100270 | ||
Chromatin architectural proteins and transcription factors: a structural connection | Q41130996 | ||
Identification of a minimal set of proteins that is sufficient for accurate initiation of transcription by RNA polymerase II. | Q42505514 | ||
Antisense RNA mediates transcriptional processing in an archaebacterium, indicating a novel kind of RNase activity | Q43022366 | ||
Histone-like transcription factors in eukaryotes | Q73070825 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 999-1002 | |
P577 | publication date | 1997-06-01 | |
1997-06-27 | |||
P1433 | published in | Cell | Q655814 |
P1476 | title | Archaeal histones, nucleosomes, and transcription initiation | |
Archaeal Histones, Nucleosomes, and Transcription Initiation | |||
P478 | volume | 89 |
Q33701756 | A Phenomenological Model for Predicting Melting Temperatures of DNA Sequences |
Q24561954 | A new biology for a new century |
Q48385584 | A novel member of the bacterial-archaeal regulator family is a nonspecific dna-binding protein and induces positive supercoiling |
Q34301047 | A pursuit of lineage-specific and niche-specific proteome features in the world of archaea |
Q33736568 | A statistical thermodynamic model for investigating the stability of DNA sequences from oligonucleotides to genomes |
Q33991360 | An Lrp-like protein of the hyperthermophilic archaeon Sulfolobus solfataricus which binds to its own promoter |
Q27634967 | An ancestral nuclear protein assembly: Crystal structure of theMethanopyrus kandlerihistone |
Q46566637 | An archaeal SET domain protein exhibits distinct lysine methyltransferase activity towards DNA-associated protein MC1-alpha |
Q27642106 | An extended winged helix domain in general transcription factor E/IIE alpha |
Q32001511 | Archaea and the cell cycle |
Q24643523 | Archaea and the prokaryote-to-eukaryote transition |
Q41703450 | Archaea: what can we learn from their sequences? |
Q37631446 | Archaeal genome guardians give insights into eukaryotic DNA replication and damage response proteins. |
Q39494153 | Archaeal nucleosome positioning by CTG repeats |
Q22066190 | Archaeal nucleosomes |
Q33658157 | Archaebacteria then ... Archaes now (are there really no archaeal pathogens?) |
Q77063246 | Basal and regulated transcription in archaea |
Q77373839 | Both DNA and histone fold sequences contribute to archaeal nucleosome stability |
Q24676592 | Complete genome sequence of Methanobacterium thermoautotrophicum deltaH: functional analysis and comparative genomics |
Q38288227 | DNA bending, compaction and negative supercoiling by the architectural protein Sso7d of Sulfolobus solfataricus |
Q41728287 | DNA binding within the nucleosome core |
Q33836594 | DNA repeats and archaeal nucleosome positioning |
Q34025418 | Deletion of switch 3 results in an archaeal RNA polymerase that is defective in transcript elongation |
Q33966689 | Effects of histone tail domains on the rate of transcriptional elongation through a nucleosome |
Q47756900 | Eubacterial origin of nuclear genes for chloroplast and cytosolic glucose-6-phosphate isomerase from spinach: sampling eubacterial gene diversity in eukaryotic chromosomes through symbiosis. |
Q34654528 | Evidence for an early prokaryotic origin of histones H2A and H4 prior to the emergence of eukaryotes |
Q22162489 | Evolution in the laboratory: The genome of Halobacterium salinarum strain R1 compared to that of strain NRC-1 |
Q30873629 | Evolution of domain families |
Q47931317 | Expression and heat-responsive regulation of a TFIIB homologue from the archaeon Haloferax volcanii. |
Q82548023 | Formation and positioning of nucleosomes: effect of sequence-dependent long-range correlated structural disorder |
Q34708554 | Functional analysis of archaeal MBF1 by complementation studies in yeast |
Q42078850 | GlpR represses fructose and glucose metabolic enzymes at the level of transcription in the haloarchaeon Haloferax volcanii |
Q48039898 | Heat shock inducibility of an archaeal TATA-like promoter is controlled by adjacent sequence elements. |
Q27759004 | High-resolution structure of an archaeal zinc ribbon defines a general architectural motif in eukaryotic RNA polymerases |
Q39726785 | Histone stoichiometry and DNA circularization in archaeal nucleosomes |
Q51763123 | Histone tail cleavage as a novel epigenetic regulatory mechanism for gene expression. |
Q28144638 | Homologous gene knockout in the archaeon Halobacterium salinarum with ura3 as a counterselectable marker |
Q30978559 | Identification and properties of the crenarchaeal single-stranded DNA binding protein from Sulfolobus solfataricus |
Q33229362 | In silico functional characterization of a double histone fold domain from the Heliothis zea virus 1. |
Q46284251 | Insights into Epigenome Evolution from Animal and Plant Methylomes |
Q63647644 | Investigating the Origins of Membrane Phospholipid Biosynthesis Genes Using Outgroup-Free Rooting |
Q42460454 | Isolation and structure of repressor-like proteins from the archaeon Sulfolobus solfataricus. Co-purification of RNase A with Sso7c |
Q47928962 | Isolation of TBP-interacting protein (TIP) from a hyperthermophilic archaeon that inhibits the binding of TBP to TATA-DNA. |
Q39847300 | Methanogenesis: genes, genomes, and who's on first? |
Q33993711 | Mutational analysis of differences in thermostability between histones from mesophilic and hyperthermophilic archaea |
Q47228932 | Mutational analysis of genes encoding chromatin proteins in the archaeon Methanococcus voltae indicates their involvement in the regulation of gene expression |
Q33888142 | Negative constrained DNA supercoiling in archaeal nucleosomes |
Q38074821 | Nucleosomal composition at the centromere: a numbers game |
Q24675851 | On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells |
Q36698728 | Orientation of the transcription preinitiation complex in archaea |
Q40695732 | Physical and functional interaction of the archaeal single-stranded DNA-binding protein SSB with RNA polymerase |
Q24548562 | Protein phylogenies and signature sequences: A reappraisal of evolutionary relationships among archaebacteria, eubacteria, and eukaryotes |
Q39499941 | Purification and characterization of Sa-lrp, a DNA-binding protein from the extreme thermoacidophilic archaeon Sulfolobus acidocaldarius homologous to the bacterial global transcriptional regulator Lrp. |
Q35125953 | RNA polymerase switch in transcription of yeast rDNA: role of transcription factor UAF (upstream activation factor) in silencing rDNA transcription by RNA polymerase II. |
Q42472724 | RNA polymerase-specific nucleosome disruption by transcription in vivo |
Q33965781 | Role of histone N-terminal tails and their acetylation in nucleosome dynamics |
Q33334155 | Stress genes and proteins in the archaea |
Q47276084 | Subtracting the sequence bias from partially digested MNase-seq data reveals a general contribution of TFIIS to nucleosome positioning. |
Q34405654 | Supplementing with non-glycoside hydrolase proteins enhances enzymatic deconstruction of plant biomass |
Q39502898 | TFE, an archaeal transcription factor in Methanobacterium thermoautotrophicum related to eucaryal transcription factor TFIIEalpha |
Q33574111 | Temperature, template topology, and factor requirements of archaeal transcription |
Q81575857 | The Archaeal Concept and the World it Lives in: A Retrospective |
Q42692692 | The DNA binding protein Tfx from Methanobacterium thermoautotrophicum: structure, DNA binding properties and transcriptional regulation |
Q42246217 | The archaeal TFIIEalpha homologue facilitates transcription initiation by enhancing TATA-box recognition |
Q31032209 | The archaeal histone-fold protein HMf organizes DNA into bona fide chromatin fibers |
Q22066249 | The complete genome of the crenarchaeon Sulfolobus solfataricus P2 |
Q24522494 | The final cut. The importance of tRNA 3'-processing. |
Q41681259 | The origin and utility of histone deacetylases. |
Q58835264 | The origin of eukaryotes and their relationship with the Archaea: are we at a phylogenomic impasse? |
Q74424658 | The switch in the helical handedness of the histone (H3-H4)2 tetramer within a nucleoprotein particle requires a reorientation of the H3-H3 interface |
Q32048214 | The tRNA(guanine-26,N2-N2) methyltransferase (Trm1) from the hyperthermophilic archaeon Pyrococcus furiosus: cloning, sequencing of the gene and its expression in Escherichia coli. |
Q33671277 | Transcription in Archaea |
Q33592579 | Transcription initiation in Archaea: facts, factors and future aspects |
Q33590089 | Transcriptional control by two leucine-responsive regulatory proteins in Halobacterium salinarum R1. |
Q33632460 | Transcriptional regulation in Archaea |
Q44908633 | Translation initiation with GUC codon in the archaeon Halobacterium salinarum: implications for translation of leaderless mRNA and strict correlation between translation initiation and presence of mRNA. |
Q37713544 | Well-positioned nucleosomes punctuate polycistronic pol II transcription units and flank silent VSG gene arrays in Trypanosoma brucei. |
Q28769102 | What archaea have to tell biologists |
Q34751832 | What are archaebacteria: life's third domain or monoderm prokaryotes related to gram-positive bacteria? A new proposal for the classification of prokaryotic organisms |
Q24804610 | Where does DNA replication start in archaea? |
Search more.