scholarly article | Q13442814 |
P50 | author | Edward H Egelman | Q44068749 |
Xiong Yu | Q62505736 | ||
Margaret S VanLoock | Q63023382 | ||
P2093 | author name string | Shixin Yang | |
Maria J Jezewska | |||
Wlodzimierz Bujalowski | |||
P2860 | cites work | Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes | Q24635818 |
Improved methods for building protein models in electron density maps and the location of errors in these models | Q26776980 | ||
NMR structure of the N-terminal domain of E. coli DnaB helicase: implications for structure rearrangements in the helicase hexamer | Q27619049 | ||
Crystal structure of the N-terminal domain of the DnaB hexameric helicase | Q27619052 | ||
Crystal structure of T7 gene 4 ring helicase indicates a mechanism for sequential hydrolysis of nucleotides | Q27625337 | ||
Crystal structure of the hexameric replicative helicase RepA of plasmid RSF1010 | Q27629602 | ||
Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria | Q27730864 | ||
Crystal structure of a DExx box DNA helicase | Q27733946 | ||
The RecA hexamer is a structural homologue of ring helicases | Q27734778 | ||
Structure of the hepatitis C virus RNA helicase domain | Q27739123 | ||
The crystal structure of the nucleotide-free alpha 3 beta 3 subcomplex of F1-ATPase from the thermophilic Bacillus PS3 is a symmetric trimer | Q27741925 | ||
Major domain swiveling revealed by the crystal structures of complexes of E. coli Rep helicase bound to single-stranded DNA and ADP | Q27742867 | ||
Crystal structure of the RNA-binding domain from transcription termination factor rho | Q27757526 | ||
Multiple-step kinetic mechanism of DNA-independent ATP binding and hydrolysis by Escherichia coli replicative helicase DnaB protein: quantitative analysis using the rapid quench-flow method | Q73149334 | ||
Precise limits of the N-terminal domain of DnaB helicase determined by NMR spectroscopy | Q73154939 | ||
Does single-stranded DNA pass through the inner channel of the protein hexamer in the complex with the Escherichia coli DnaB Helicase? Fluorescence energy transfer studies | Q74465581 | ||
Three-dimensional reconstructions from cryoelectron microscopy images reveal an intimate complex between helicase DnaB and its loading partner DnaC | Q74486176 | ||
Mechanism of DnaB helicase of Escherichia coli: structural domains involved in ATP hydrolysis, DNA binding, and oligomerization | Q78166172 | ||
The NMR structure of the RNA binding domain of E. coli rho factor suggests possible RNA-protein interactions | Q27757597 | ||
SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields | Q27860560 | ||
Further additions to MolScript version 1.4, including reading and contouring of electron-density maps | Q27860974 | ||
Systematic identification, classification, and characterization of the open reading frames which encode novel helicase-related proteins in Saccharomyces cerevisiae by gene disruption and Northern analysis | Q27937685 | ||
DNA is bound within the central hole to one or two of the six subunits of the T7 DNA helicase | Q28288465 | ||
Three-dimensional reconstruction of transcription termination factor rho: orientation of the N-terminal domain and visualization of an RNA-binding site. | Q30305807 | ||
The primase active site is on the outside of the hexameric bacteriophage T7 gene 4 helicase-primase ring | Q30307816 | ||
SV40 large T antigen hexamer structure: domain organization and DNA-induced conformational changes | Q30309106 | ||
Structure and function of hexameric helicases. | Q34019405 | ||
Bacteriophage T7 helicase/primase proteins form rings around single-stranded DNA that suggest a general structure for hexameric helicases | Q34387475 | ||
The DnaB.DnaC complex: a structure based on dimers assembled around an occluded channel. | Q34584666 | ||
Helicases: a unifying structural theme? | Q34746482 | ||
A ring-opening mechanism for DNA binding in the central channel of the T7 helicase-primase protein | Q35114392 | ||
Harmonic analysis of electron microscope images with rotational symmetry. | Q36563823 | ||
A structural model for the Escherichia coli DnaB helicase based on electron microscopy data. | Q36693128 | ||
A 7-kDa region of the bacteriophage T7 gene 4 protein is required for primase but not for helicase activity | Q37482283 | ||
DNA helicases | Q37886473 | ||
Biochemical and electron microscopic image analysis of the hexameric E1 helicase. | Q38328578 | ||
Mapping protein-protein interactions within a stable complex of DNA primase and DnaB helicase from Bacillus stearothermophilus. | Q38642649 | ||
Large T-antigen double hexamers imaged at the simian virus 40 origin of replication | Q39449950 | ||
A functional interaction between the putative primosomal protein DnaI and the main replicative DNA helicase DnaB in Bacillus | Q39530817 | ||
Characterisation of Bacillus stearothermophilus PcrA helicase: evidence against an active rolling mechanism | Q39723941 | ||
Polymorphic quaternary organization of the Bacillus subtilis bacteriophage SPP1 replicative helicase (G40 P). | Q42685118 | ||
E. coli Rep oligomers are required to initiate DNA unwinding in vitro | Q43655291 | ||
Organization and evolution of bacterial and bacteriophage primase-helicase systems | Q44080673 | ||
Six molecules of SV40 large T antigen assemble in a propeller-shaped particle around a channel. | Q52266893 | ||
Global conformational transitions in Escherichia coli primary replicative helicase DnaB protein induced by ATP, ADP, and single-stranded DNA binding. Multiple conformational states of the helicase hexamer. | Q52310280 | ||
Three-dimensional reconstruction of single particles embedded in ice | Q52430878 | ||
Interactions of Escherichia coli primary replicative helicase DnaB protein with single-stranded DNA. The nucleic acid does not wrap around the protein hexamer. | Q54608569 | ||
Structure and function of Escherichia coli DnaB protein: role of the N-terminal domain in helicase activity. | Q54627242 | ||
Negative cooperativity in the binding of nucleotides to Escherichia coli replicative helicase DnaB protein. Interactions with fluorescent nucleotide analogs. | Q54655984 | ||
Helicases: amino acid sequence comparisons and structure-function relationships | Q56657141 | ||
The 3′-tail of a forked-duplex sterically determines whether one or two DNA strands pass through the central channel of a replication-fork helicase 1 1Edited by M. Gottesman | Q56928642 | ||
The HexamericE. coliDnaB Helicase can Exist in Different Quarternary States | Q56937904 | ||
pH-controlled quaternary states of hexameric DnaB helicase | Q58660211 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 839-849 | |
P577 | publication date | 2002-08-01 | |
P1433 | published in | Journal of Molecular Biology | Q925779 |
P1476 | title | Flexibility of the rings: structural asymmetry in the DnaB hexameric helicase | |
P478 | volume | 321 |
Q37339766 | A method for the alignment of heterogeneous macromolecules from electron microscopy |
Q35580268 | An integrative approach to the study of filamentous oligomeric assemblies, with application to RecA. |
Q33928683 | Architecture of the bacteriophage T4 primosome: electron microscopy studies of helicase (gp41) and primase (gp61). |
Q33525212 | Automated multi-model reconstruction from single-particle electron microscopy data |
Q37065777 | Biochemical Characterization of the Human Mitochondrial Replicative Twinkle Helicase: SUBSTRATE SPECIFICITY, DNA BRANCH MIGRATION, AND ABILITY TO OVERCOME BLOCKADES TO DNA UNWINDING. |
Q41955522 | Conserved residues of the C-terminal p16 domain of primase are involved in modulating the activity of the bacterial primosome. |
Q27485475 | Cross-correlation of common lines: A novel approach for single-particle reconstruction of a structure containing a flexible domain |
Q40458920 | DNA Helicases. |
Q24794720 | DNA binding and helicase actions of mouse MCM4/6/7 helicase |
Q47603277 | DnaC, the indispensable companion of DnaB helicase, controls the accessibility of DnaB helicase by primase |
Q40969310 | DnaG interacts with a linker region that joins the N- and C-domains of DnaB and induces the formation of 3-fold symmetric rings |
Q43203582 | In the Bacillus stearothermophilus DnaB-DnaG complex, the activities of the two proteins are modulated by distinct but overlapping networks of residues |
Q42687923 | Lactococcal phage p2 ORF35-Sak3 is an ATPase involved in DNA recombination and AbiK mechanism. |
Q38216120 | Loading strategies of ring-shaped nucleic acid translocases and helicases |
Q43154731 | Mcm subunits can assemble into two different active unwinding complexes |
Q27937246 | Mcm4,6,7 uses a "pump in ring" mechanism to unwind DNA by steric exclusion and actively translocate along a duplex. |
Q34769234 | Mechanism of NTP hydrolysis by the Escherichia coli primary replicative helicase DnaB protein. 2. Nucleotide and nucleic acid specificities. |
Q26827264 | Mechanisms for initiating cellular DNA replication |
Q83232691 | Mechanisms of opening and closing of the bacterial replicative helicase |
Q41986081 | Multiple global conformational states of the hexameric RepA helicase of plasmid RSF1010 with different ssDNA-binding capabilities are induced by different numbers of bound nucleotides. Analytical ultracentrifugation and dynamic light scattering stud |
Q43037770 | Nucleic acid unwinding by hepatitis C virus and bacteriophage t7 helicases is sensitive to base pair stability |
Q27681112 | Nucleotide and Partner-Protein Control of Bacterial Replicative Helicase Structure and Function |
Q34288492 | Organization, developmental dynamics, and evolution of plastid nucleoids. |
Q33999043 | Regulation of bacterial priming and daughter strand synthesis through helicase-primase interactions |
Q41343446 | Replication Initiation in Bacteria |
Q33940331 | Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex |
Q38601246 | Replisome Dynamics during Chromosome Duplication |
Q38327850 | Solution structure of the helicase-interaction domain of the primase DnaG: a model for helicase activation. |
Q24547949 | Structural insights into the assembly of the type III secretion needle complex. |
Q27648844 | Structure of hexameric DnaB helicase and its complex with a domain of DnaG primase |
Q36744600 | Substitutions of Conserved Residues in the C-terminal Region of DnaC Cause Thermolability in Helicase Loading |
Q52656083 | The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery. |
Q36895278 | The bacterial DnaC helicase loader is a DnaB ring breaker |
Q36153494 | The bacterial helicase-primase interaction: a common structural/functional module. |
Q42105879 | The clamp-loader-helicase interaction in Bacillus. Atomic force microscopy reveals the structural organisation of the DnaB-tau complex in Bacillus |
Q27646527 | The crystal structure of the Thermus aquaticus DnaB helicase monomer |
Q27649417 | The structure of a DnaB-family replicative helicase and its interactions with primase |
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