| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1045376961 |
| P356 | DOI | 10.1038/NATURE04943 |
| P698 | PubMed publication ID | 16855583 |
| P5875 | ResearchGate publication ID | 6929468 |
| P50 | author | Leemor Joshua-Tor | Q25358110 |
| P2093 | author name string | Eric J Enemark | |
| P2860 | cites work | Interactions of bacteriophage T7 DNA primase/helicase protein with single-stranded and double-stranded DNAs | Q38314172 |
| Biochemical and electron microscopic image analysis of the hexameric E1 helicase. | Q38328578 | ||
| Chaperone proteins abrogate inhibition of the human papillomavirus (HPV) E1 replicative helicase by the HPV E2 protein | Q39681443 | ||
| Simian virus 40 T-antigen DNA helicase is a hexamer which forms a binary complex during bidirectional unwinding from the viral origin of DNA replication | Q40063919 | ||
| Recruitment and loading of the E1 initiator protein: an ATP-dependent process catalysed by a transcription factor | Q42662203 | ||
| DnaB drives DNA branch migration and dislodges proteins while encircling two DNA strands. | Q44199583 | ||
| Asymmetric interactions of hexameric bacteriophage T7 DNA helicase with the 5'- and 3'-tails of the forked DNA substrate. | Q44224411 | ||
| Backbone tracking by the SF2 helicase NPH-II. | Q44898061 | ||
| Mechanisms of conformational change for a replicative hexameric helicase of SV40 large tumor antigen | Q45082909 | ||
| Mechanochemistry of t7 DNA helicase. | Q46540594 | ||
| Assembly of a double hexameric helicase | Q46802326 | ||
| Crystal structure of T7 gene 4 ring helicase indicates a mechanism for sequential hydrolysis of nucleotides | Q27625337 | ||
| Crystal structures of two intermediates in the assembly of the papillomavirus replication initiation complex | Q27638318 | ||
| Structure of the replicative helicase of the oncoprotein SV40 large tumour antigen | Q27641342 | ||
| Solution structure of the origin DNA-binding domain of SV40 T-antigen | Q27734074 | ||
| Raster3D Version 2.0. A program for photorealistic molecular graphics | Q27860485 | ||
| An extensively modified version of MolScript that includes greatly enhanced coloring capabilities | Q27860594 | ||
| Likelihood-enhanced fast translation functions | Q27860634 | ||
| DNA replication in eukaryotic cells | Q28131747 | ||
| DNA-induced switch from independent to sequential dTTP hydrolysis in the bacteriophage T7 DNA helicase | Q28292888 | ||
| Clamp loaders and sliding clamps | Q31048743 | ||
| The papillomavirus E1 protein forms a DNA-dependent hexameric complex with ATPase and DNA helicase activities | Q33783679 | ||
| Sequential and ordered assembly of E1 initiator complexes on the papillomavirus origin of DNA replication generates progressive structural changes related to melting | Q34325784 | ||
| Bacteriophage T7 helicase/primase proteins form rings around single-stranded DNA that suggest a general structure for hexameric helicases | Q34387475 | ||
| Replicative helicase loaders: ring breakers and ring makers | Q35195270 | ||
| Induction of structural changes in the bovine papillomavirus type 1 origin of replication by the viral E1 and E2 proteins | Q35750818 | ||
| Binding and unwinding: SF3 viral helicases | Q36046459 | ||
| Bovine papilloma virus (BPV)-encoded E1 protein contains multiple activities required for BPV DNA replication | Q36068854 | ||
| The E1 protein of bovine papilloma virus 1 is an ATP-dependent DNA helicase | Q36336279 | ||
| The X-ray structure of the papillomavirus helicase in complex with its molecular matchmaker E2. | Q37480430 | ||
| P433 | issue | 7100 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 270-275 | |
| P577 | publication date | 2006-07-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Mechanism of DNA translocation in a replicative hexameric helicase | |
| P478 | volume | 442 |
| Q43161101 | A DNA-binding activity in BPV initiator protein E1 required for melting duplex ori DNA but not processive helicase activity initiated on partially single-stranded DNA. |
| Q37273634 | A biochemically active MCM-like helicase in Bacillus cereus |
| Q41812141 | A common feature from different subunits of a homomeric AAA+ protein contacts three spatially distinct transcription elements |
| Q27649681 | A common mechanism for the ATP-DnaA-dependent formation of open complexes at the replication origin |
| Q27682741 | A conserved MCM single-stranded DNA binding element is essential for replication initiation |
| Q41840185 | A conserved regulatory module at the C terminus of the papillomavirus E1 helicase domain controls E1 helicase assembly |
| Q42587602 | A flexible brace maintains the assembly of a hexameric replicative helicase during DNA unwinding |
| Q43535639 | A helicase staircase |
| Q92513029 | A processive rotary mechanism couples substrate unfolding and proteolysis in the ClpXP degradation machinery |
| Q48831196 | A stepwise 2'-hydroxyl activation mechanism for the bacterial transcription termination factor Rho helicase |
| Q38069696 | A structural framework for replication origin opening by AAA+ initiation factors. |
| Q37500135 | ATP binding and hydrolysis by Mcm2 regulate DNA binding by Mcm complexes |
| Q42119457 | ATP-dependent minor groove recognition of TA base pairs is required for template melting by the E1 initiator protein |
| Q38671672 | ATP-induced helicase slippage reveals highly coordinated subunits. |
| Q42292719 | Action of CMG with strand-specific DNA blocks supports an internal unwinding mode for the eukaryotic replicative helicase. |
| Q91198457 | Active DNA unwinding and transport by a membrane-adapted helicase nanopore |
| Q35991585 | Active DNA unwinding dynamics during processive DNA replication. |
| Q27680547 | Altered Intersubunit Communication Is the Molecular Basis for Functional Defects of Pathogenic p97 Mutants |
| Q83227442 | Amidst multiple binding orientations on fork DNA, MCM helicase proceeds N-first for unwinding |
| Q41050732 | An Atypical AAA+ ATPase Assembly Controls Efficient Transposition through DNA Remodeling and Transposase Recruitment |
| Q28251784 | An asymmetric interface between the regulatory and core particles of the proteasome |
| Q27940248 | An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases |
| Q35185890 | Analyses of the interaction between the origin binding domain from simian virus 40 T antigen and single-stranded DNA provide insights into DNA unwinding and initiation of DNA replication |
| Q27675607 | Analysis of the Costructure of the Simian Virus 40 T-Antigen Origin Binding Domain with Site I Reveals a Correlation between GAGGC Spacing and Spiral Assembly |
| Q35176524 | Analysis of the crystal structure of an active MCM hexamer |
| Q26779724 | Archaeal MCM Proteins as an Analog for the Eukaryotic Mcm2-7 Helicase to Reveal Essential Features of Structure and Function |
| Q50233460 | Architecture of the Saccharomyces cerevisiae Replisome |
| Q36187419 | Assembly and subunit stoichiometry of the functional helicase-primase (primosome) complex of bacteriophage T4. |
| Q38964718 | Assessing heterogeneity in oligomeric AAA+ machines. |
| Q57754548 | Bacterial and Eukaryotic Replisome Machines |
| Q39738711 | Bacteriophage T5 gene D10 encodes a branch-migration protein |
| Q35861018 | Binding of Substrates to the Central Pore of the Vps4 ATPase Is Autoinhibited by the Microtubule Interacting and Trafficking (MIT) Domain and Activated by MIT Interacting Motifs (MIMs). |
| Q28546970 | Biochemical Characterization of a Mycobacteriophage Derived DnaB Ortholog Reveals New Insight into the Evolutionary Origin of DnaB Helicases |
| Q36631415 | Biological Nanomotors with a Revolution, Linear, or Rotation Motion Mechanism |
| Q37142304 | Biophysics of viral infectivity: matching genome length with capsid size. |
| Q42612859 | Bovine papillomavirus type 1 E2 protein heterodimer is functional in papillomavirus DNA replication in vivo. |
| Q42653767 | Breaking symmetry in multimeric ATPase motors. |
| Q42410390 | Bypass of a protein barrier by a replicative DNA helicase. |
| Q36978987 | CK2 phosphorylation inactivates DNA binding by the papillomavirus E1 and E2 proteins. |
| Q42557562 | Catalytic turnover triggers exchange of subunits of the magnesium chelatase AAA+ motor unit |
| Q35031537 | Cdc45 (cell division cycle protein 45) guards the gate of the Eukaryote Replisome helicase stabilizing leading strand engagement. |
| Q36881426 | Cell cycle regulation of DNA replication. |
| Q42420204 | Chance, destiny, and the inner workings of ClpXP. |
| Q28481495 | Characterization and whole genome analysis of human papillomavirus type 16 e1-1374^63nt variants |
| Q41968624 | Characterization of papillomavirus E1 helicase mutants defective for interaction with the SUMO-conjugating enzyme Ubc9. |
| Q41883688 | Chemical modifications of DNA for study of helicase mechanisms |
| Q33736472 | Common mechanisms of DNA translocation motors in bacteria and viruses using one-way revolution mechanism without rotation |
| Q36752413 | Communication between subunits critical to DNA binding by hexameric helicase of bacteriophage T7. |
| Q28257212 | Complete subunit architecture of the proteasome regulatory particle |
| Q38430334 | Conformational plasticity of RepB, the replication initiator protein of promiscuous streptococcal plasmid pMV158. |
| Q28292908 | Conformational switching of the 26S proteasome enables substrate degradation |
| Q91851435 | Controlling the Revolving and Rotating Motion Direction of Asymmetric Hexameric Nanomotor by Arginine Finger and Channel Chirality |
| Q35698731 | Cooperative base pair melting by helicase and polymerase positioned one nucleotide from each other |
| Q38180431 | Coordination and control inside simple biomolecular machines |
| Q50995389 | Covalently linked HslU hexamers support a probabilistic mechanism that links ATP hydrolysis to protein unfolding and translocation. |
| Q38944970 | Cryo-EM of dynamic protein complexes in eukaryotic DNA replication |
| Q46428907 | Cryo-EM structure of Mcm2-7 double hexamer on DNA suggests a lagging-strand DNA extrusion model. |
| Q59060928 | Cryo-EM structures and dynamics of substrate-engaged human 26S proteasome |
| Q27332117 | Cryo-EM structures of the eukaryotic replicative helicase bound to a translocation substrate |
| Q33615630 | Crystal structure of 2C helicase from enterovirus 71 |
| Q24600725 | Crystal structure of the dynein motor domain |
| Q38308257 | Crystal structure of the human AAA+ protein RuvBL1. |
| Q41779921 | Crystallization and X-ray structure determination of an RNA-dependent hexameric helicase |
| Q37066451 | DNA Interactions Probed by Hydrogen-Deuterium Exchange (HDX) Fourier Transform Ion Cyclotron Resonance Mass Spectrometry Confirm External Binding Sites on the Minichromosomal Maintenance (MCM) Helicase |
| Q35176517 | DNA binding polarity, dimerization, and ATPase ring remodeling in the CMG helicase of the eukaryotic replisome. |
| Q41807172 | DNA replication: making two forks from one prereplication complex |
| Q27674672 | DNA stretching by bacterial initiators promotes replication origin opening |
| Q33480968 | DNA structure modulates the oligomerization properties of the AAV initiator protein Rep68. |
| Q42637956 | DNA translocation activity of the multifunctional replication protein ORF904 from the archaeal plasmid pRN1. |
| Q91902302 | DNA translocation mechanism of the MCM complex and implications for replication initiation |
| Q89531922 | DNA unwinding mechanism of a eukaryotic replicative CMG helicase |
| Q36536393 | Design principles of a universal protein degradation machine |
| Q35592783 | Discovering new medicines targeting helicases: challenges and recent progress |
| Q43151994 | Diverse pore loops of the AAA+ ClpX machine mediate unassisted and adaptor-dependent recognition of ssrA-tagged substrates. |
| Q34590765 | DnaB helicase activity is modulated by DNA geometry and force |
| Q38231539 | Do the same traffic rules apply? Directional chromosome segregation by SpoIIIE and FtsK. |
| Q40116810 | Domain Organization of Vaccinia Virus Helicase-Primase D5. |
| Q26998987 | Dynamic coupling between the motors of DNA replication: hexameric helicase, DNA polymerase, and primase |
| Q37628012 | Dynamic look at DNA unwinding by a replicative helicase. |
| Q89490013 | Dynamic structural insights into the molecular mechanism of DNA unwinding by the bacteriophage T7 helicase |
| Q64260618 | Dynamics of the Eukaryotic Replicative Helicase at Lagging-Strand Protein Barriers Support the Steric Exclusion Model |
| Q33826988 | Effect of ATP binding and hydrolysis on dynamics of canine parvovirus NS1 |
| Q33608503 | Eukaryotic Replicative Helicase Subunit Interaction with DNA and Its Role in DNA Replication |
| Q36845840 | Evidence for a structural relationship between BRCT domains and the helicase domains of the replication initiators encoded by the Polyomaviridae and Papillomaviridae families of DNA tumor viruses. |
| Q38829896 | Evolution of replication machines |
| Q40797637 | Finding of widespread viral and bacterial revolution dsDNA translocation motors distinct from rotation motors by channel chirality and size |
| Q37699568 | Fitting CRISPR-associated Cas3 into the helicase family tree |
| Q30495859 | Foot-and-mouth disease virus 2C is a hexameric AAA+ protein with a coordinated ATP hydrolysis mechanism |
| Q54452598 | FtsK: a groovy helicase. |
| Q42146996 | Functional roles of the pre-sensor I insertion sequence in an AAA+ bacterial enhancer binding protein |
| Q28299219 | Functions and mechanics of dynein motor proteins |
| Q28066287 | Fundamental Characteristics of AAA+ Protein Family Structure and Function |
| Q39226842 | Helicase and polymerase move together close to the fork junction and copy DNA in one-nucleotide steps |
| Q79375530 | Helicase: mystery of progression |
| Q61451189 | Hexameric assembly of the AAA+ protein McrB is necessary for GTPase activity |
| Q61807894 | Hexameric helicase G40P unwinds DNA in single base pair steps |
| Q33795674 | Hexameric helicase deconstructed: interplay of conformational changes and substrate coupling |
| Q36840758 | High degree of coordination and division of labor among subunits in a homomeric ring ATPase |
| Q89975997 | History of DNA Helicases |
| Q37065911 | How Aromatic Compounds Block DNA Binding of HcaR Catabolite Regulator |
| Q27676381 | How a DNA Polymerase Clamp Loader Opens a Sliding Clamp |
| Q36537688 | Identification of a nuclear export signal sequence for bovine papillomavirus E1 protein |
| Q28281309 | Insights into the MCM functional mechanism: lessons learned from the archaeal MCM complex |
| Q42854097 | Interactions between the RepB initiator protein of plasmid pMV158 and two distant DNA regions within the origin of replication. |
| Q37078991 | Intersubunit allosteric communication mediated by a conserved loop in the MCM helicase |
| Q30489077 | Intersubunit coordination in a homomeric ring ATPase |
| Q47983792 | Katanin spiral and ring structures shed light on power stroke for microtubule severing |
| Q34503714 | Keeping up to speed with the transcription termination factor Rho motor |
| Q33876054 | Kinetic mechanism for DNA unwinding by multiple molecules of Dda helicase aligned on DNA. |
| Q36344950 | Lessons learned from UvrD helicase: mechanism for directional movement |
| Q46573086 | Limited proteolysis of E. coli ATP-dependent protease Lon - a unified view of the subunit architecture and characterization of isolated enzyme fragments |
| Q34778227 | Linked domain architectures allow for specialization of function in the FtsK/SpoIIIE ATPases of ESX secretion systems |
| Q37993607 | Loading mechanisms of ring helicases at replication origins. |
| Q38216120 | Loading strategies of ring-shaped nucleic acid translocases and helicases |
| Q36559777 | Low-resolution structure of vaccinia virus DNA replication machinery |
| Q37625067 | Marching to the beat of the ring: polypeptide translocation by AAA+ proteases. |
| Q43154731 | Mcm subunits can assemble into two different active unwinding complexes |
| Q41062701 | Mcm10 promotes rapid isomerization of CMG-DNA for replisome bypass of lagging strand DNA blocks. |
| Q27931022 | Mcm2 phosphorylation and the response to replicative stress |
| Q33595796 | Mechanical operation and intersubunit coordination of ring-shaped molecular motors: insights from single-molecule studies |
| Q27677146 | Mechanism of Origin DNA Recognition and Assembly of an Initiator-Helicase Complex by SV40 Large Tumor Antigen |
| Q35372059 | Mechanism of substrate translocation by a ring-shaped ATPase motor at millisecond resolution |
| Q39017132 | Mechanisms and regulation of DNA replication initiation in eukaryotes |
| Q83232691 | Mechanisms of opening and closing of the bacterial replicative helicase |
| Q38963413 | Mechanistic analysis of local ori melting and helicase assembly by the papillomavirus E1 protein |
| Q38629844 | Meiotic Clade AAA ATPases: Protein Polymer Disassembly Machines |
| Q33919887 | Methodology for the Simulation of Molecular Motors at Different Scales |
| Q38772212 | Mini review: ATP-dependent proteases in bacteria |
| Q35857324 | Model for T-antigen-dependent melting of the simian virus 40 core origin based on studies of the interaction of the beta-hairpin with DNA. |
| Q41892646 | Modeling of the SV40 DNA Replication Machine |
| Q93101116 | Molecular Basis for ATP-Hydrolysis-Driven DNA Translocation by the CMG Helicase of the Eukaryotic Replisome |
| Q34181409 | Molecular Basis for Recognition of Nucleoside Triphosphate by Gene 4 Helicase of Bacteriophage T7 |
| Q34222628 | Molecular architecture of a multifunctional MCM complex |
| Q24681607 | Molecular architecture of the human GINS complex. |
| Q93159431 | Molecular dynamics simulations of nucleotide release from the circadian clock protein KaiC reveal atomic-resolution functional insights |
| Q39903122 | Molecular mechanics of RNA translocases |
| Q99706572 | Molecular mechanisms of eukaryotic origin initiation, replication fork progression, and chromatin maintenance |
| Q37473805 | Molecular mechanisms of substrate-controlled ring dynamics and substepping in a nucleic acid-dependent hexameric motor |
| Q48269447 | Monitoring ssDNA Binding to the DnaB Helicase from Helicobacter pylori by Solid-State NMR Spectroscopy. |
| Q36341536 | Multimeric BLM is dissociated upon ATP hydrolysis and functions as monomers in resolving DNA structures |
| Q34103581 | Mutations altering the interplay between GkDnaC helicase and DNA reveal an insight into helicase unwinding |
| Q37252727 | Mutations in DNA binding and transactivation domains affect the dynamics of parvovirus NS1 protein |
| Q42132331 | Mutations in Sensor 1 and Walker B in the bovine papillomavirus E1 initiator protein mimic the nucleotide-bound state |
| Q30484551 | Novel mechanism of hexamer ring assembly in protein/RNA interactions revealed by single molecule imaging |
| Q28740849 | Nuclear accumulation of the papillomavirus E1 helicase blocks S-phase progression and triggers an ATM-dependent DNA damage response |
| Q43037770 | Nucleic acid unwinding by hepatitis C virus and bacteriophage t7 helicases is sensitive to base pair stability |
| Q27677748 | Nucleotide Binding and Conformational Switching in the Hexameric Ring of a AAA+ Machine |
| Q27680618 | Nucleotide-induced asymmetry within ATPase activator ring drives 54-RNAP interaction and ATP hydrolysis |
| Q37105913 | On helicases and other motor proteins |
| Q36248529 | Origin DNA Melting-An Essential Process with Divergent Mechanisms |
| Q37792588 | Origin DNA melting and unwinding in DNA replication |
| Q36473565 | P53 represses human papillomavirus type 16 DNA replication via the viral E2 protein |
| Q37367646 | Papillomavirus DNA replication - from initiation to genomic instability |
| Q27648329 | Papillomavirus E1 helicase assembly maintains an asymmetric state in the absence of DNA and nucleotide cofactors |
| Q27655468 | Plasmid replication initiator RepB forms a hexamer reminiscent of ring helicases and has mobile nuclease domains |
| Q27489840 | Poliovirus 2C Protein Forms Homo-oligomeric Structures Required for ATPase Activity |
| Q41923324 | Polypeptide translocation by the AAA+ ClpXP protease machine. |
| Q43218186 | Pore loops of the AAA+ ClpX machine grip substrates to drive translocation and unfolding |
| Q38568949 | Preparing to unwind |
| Q35904077 | Processive ATP-driven substrate disassembly by the N-ethylmaleimide-sensitive factor (NSF) molecular machine |
| Q41851634 | Promiscuous usage of nucleotides by the DNA helicase of bacteriophage T7: determinants of nucleotide specificity |
| Q37826501 | Proteasome activators |
| Q99557412 | RCSB Protein Data Bank tools for 3D structure-guided cancer research: human papillomavirus (HPV) case study |
| Q37921468 | RNA helicases and remodeling proteins |
| Q41597556 | Ratchet-like polypeptide translocation mechanism of the AAA+ disaggregase Hsp104. |
| Q24669910 | Real-time observation of bacteriophage T4 gp41 helicase reveals an unwinding mechanism |
| Q26738716 | Recent advances in the structural biology of the 26S proteasome |
| Q37406494 | Reconstitution of the 26S proteasome reveals functional asymmetries in its AAA+ unfoldase |
| Q35257872 | Regulated protein turnover: snapshots of the proteasome in action |
| Q41912774 | Regulatory ATPase sites of cytoplasmic dynein affect processivity and force generation |
| Q41343446 | Replication Initiation in Bacteria |
| Q35150925 | Replication and partitioning of papillomavirus genomes |
| Q34209486 | Replication initiation at the Escherichia coli chromosomal origin |
| Q37522596 | Replication interference between human papillomavirus types 16 and 18 mediated by heterologous E1 helicases. |
| Q27647690 | Replication origin recognition and deformation by a heterodimeric archaeal Orc1 complex |
| Q37450024 | Replisome structure and conformational dynamics underlie fork progression past obstacles |
| Q36736558 | Requirement for the E1 Helicase C-Terminal Domain in Papillomavirus DNA Replication In Vivo |
| Q33859399 | Residues in the central beta-hairpin of the DNA helicase of bacteriophage T7 are important in DNA unwinding |
| Q34594659 | Reverse-chaperoning activity of an AAA+ protein. |
| Q38751208 | Review: The lord of the rings: Structure and mechanism of the sliding clamp loader |
| Q38304700 | Role of the hydrophilic channels of simian virus 40 T-antigen helicase in DNA replication |
| Q26861945 | Roles of DNA helicases in the maintenance of genome integrity |
| Q43986161 | Rolling circle replication of human papillomavirus type 16 DNA in epithelial cell extracts. |
| Q27658029 | Running in Reverse: The Structural Basis for Translocation Polarity in Hexameric Helicases |
| Q38964959 | Selective bypass of a lagging strand roadblock by the eukaryotic replicative DNA helicase. |
| Q51529163 | Sending protein aggregates into a downward spiral. |
| Q40508567 | Separating speed and ability to displace roadblocks during DNA translocation by FtsK |
| Q34377632 | Sequence-specific assembly of FtsK hexamers establishes directional translocation on DNA |
| Q41961062 | Simian virus 40 large T antigen can specifically unwind the central palindrome at the origin of DNA replication |
| Q30487475 | Simulating the electrostatic guidance of the vectorial translocations in hexameric helicases and translocases |
| Q34313069 | Simultaneous binding to the tracking strand, displaced strand and the duplex of a DNA fork enhances unwinding by Dda helicase |
| Q34394106 | Single-molecule FRET studies of HIV TAR-DNA hairpin unfolding dynamics. |
| Q37706259 | Single-molecule fluorescence reveals the unwinding stepping mechanism of replicative helicase. |
| Q38626003 | Single-molecule perspectives on helicase mechanisms and functions. |
| Q24642351 | Single-molecule studies reveal dynamics of DNA unwinding by the ring-shaped T7 helicase |
| Q35107717 | Small molecule inhibitors of human papillomavirus protein - protein interactions |
| Q34978255 | Specific genomic sequences of E. coli promote replicational initiation by directly reactivating ADP-DnaA. |
| Q90623818 | Stairway to translocation: AAA+ motor structures reveal the mechanisms of ATP-dependent substrate translocation |
| Q37313838 | Staphylococcal SCCmec elements encode an active MCM-like helicase and thus may be replicative. |
| Q35174785 | Steric exclusion and wrapping of the excluded DNA strand occurs along discrete external binding paths during MCM helicase unwinding. |
| Q43507564 | Stochastic detection of motor protein-RNA complexes by single-channel current recording |
| Q35886711 | Structural Based Analyses of the JC Virus T-Antigen F258L Mutant Provides Evidence for DNA Dependent Conformational Changes in the C-Termini of Polyomavirus Origin Binding Domains |
| Q27681178 | Structural Basis for the Interaction of a Hexameric Replicative Helicase with the Regulatory Subunit of Human DNA Polymerase -Primase |
| Q33634058 | Structural Elements Regulating AAA+ Protein Quality Control Machines |
| Q26766086 | Structural Mechanisms of Hexameric Helicase Loading, Assembly, and Unwinding |
| Q27650348 | Structural analysis of the Sulfolobus solfataricus MCM protein N-terminal domain |
| Q102220223 | Structural asymmetry governs the assembly and GTPase activity of McrBC restriction complexes |
| Q38935107 | Structural basis for DNA strand separation by a hexameric replicative helicase |
| Q96110646 | Structural basis for distinct operational modes and protease activation in AAA+ protease Lon |
| Q27649210 | Structural basis of mechanochemical coupling in a hexameric molecular motor |
| Q42289897 | Structural basis of protein translocation by the Vps4-Vta1 AAA ATPase. |
| Q37603329 | Structural biology of MCM helicases |
| Q38081952 | Structural biology of the proteasome |
| Q43231579 | Structural biology: Steps in the right direction |
| Q37223884 | Structural frameworks for considering microbial protein- and nucleic acid-dependent motor ATPases |
| Q33263880 | Structural mechanism of RPA loading on DNA during activation of a simple pre-replication complex |
| Q89522106 | Structural studies reveal a ring-shaped architecture of deep-sea vent phage NrS-1 polymerase |
| Q35895531 | Structure and mechanism of the ATPase that powers viral genome packaging |
| Q64231635 | Structure and mechanism of the ESCRT pathway AAA+ ATPase Vps4 |
| Q59801443 | Structure of DNA-CMG-Pol epsilon elucidates the roles of the non-catalytic polymerase modules in the eukaryotic replisome |
| Q41598312 | Structure of a AAA+ unfoldase in the process of unfolding substrate. |
| Q27679984 | Structure of a helicase–helicase loader complex reveals insights into the mechanism of bacterial primosome assembly |
| Q37626173 | Structure of eukaryotic CMG helicase at a replication fork and implications to replisome architecture and origin initiation |
| Q27701671 | Structure of the eukaryotic MCM complex at 3.8 Å |
| Q27310160 | Structure of the eukaryotic replicative CMG helicase suggests a pumpjack motion for translocation |
| Q42048581 | Structure of the hexameric HerA ATPase reveals a mechanism of translocation-coupled DNA-end processing in archaea. |
| Q45325699 | Structure of the large terminase from a hyperthermophilic virus reveals a unique mechanism for oligomerization and ATP hydrolysis |
| Q48373223 | Structure of the mitochondrial inner membrane AAA+ protease YME1 gives insight into substrate processing. |
| Q35222255 | Structure of the origin-binding domain of simian virus 40 large T antigen bound to DNA. |
| Q91809478 | Structure-based mechanism for activation of the AAA+ GTPase McrB by the endonuclease McrC |
| Q40339706 | Structure-based mutational analysis of the bovine papillomavirus E1 helicase domain identifies residues involved in the nonspecific DNA binding activity required for double trimer formation |
| Q61908508 | Structures and operating principles of the replisome |
| Q27658178 | Structures of asymmetric ClpX hexamers reveal nucleotide-dependent motions in a AAA+ protein-unfolding machine |
| Q33564505 | Study of SV40 large T antigen nucleotide specificity for DNA unwinding |
| Q37404660 | Substrate interactions and promiscuity in a viral DNA packaging motor |
| Q57477239 | Substrate-engaged 26 proteasome structures reveal mechanisms for ATP-hydrolysis-driven translocation |
| Q58024045 | Substrate-engaged 26S proteasome structures reveal mechanisms for ATP-hydrolysis–driven translocation |
| Q41881445 | Subunit organization of Mcm2-7 and the unequal role of active sites in ATP hydrolysis and viability. |
| Q36769543 | Switching from single-stranded to double-stranded DNA limits the unwinding processivity of ring-shaped T7 DNA helicase |
| Q47161924 | The AAA ATPase Vps4 binds ESCRT-III substrates through a repeating array of dipeptide-binding pockets. |
| Q35680285 | The Cell Cycle Timing of Human Papillomavirus DNA Replication |
| Q27643659 | The Crystal Structure of the SV40 T-Antigen Origin Binding Domain in Complex with DNA |
| Q37262962 | The E1 proteins |
| Q27677343 | The Elongator subcomplex Elp456 is a hexameric RecA-like ATPase |
| Q50190654 | The Eukaryotic CMG Helicase at the Replication Fork: Emerging Architecture Reveals an Unexpected Mechanism |
| Q26752772 | The Eukaryotic Replisome Goes Under the Microscope |
| Q52656083 | The Macromolecular Machines that Duplicate the Escherichia coli Chromosome as Targets for Drug Discovery. |
| Q37451513 | The Mcm complex: unwinding the mechanism of a replicative helicase. |
| Q27655502 | The Mechanism of ATP-Dependent Primer-Template Recognition by a Clamp Loader Complex |
| Q27680464 | The Oligomeric State of the Active Vps4 AAA ATPase |
| Q35070043 | The PS1 hairpin of Mcm3 is essential for viability and for DNA unwinding in vitro |
| Q42777752 | The RNA-mediated, asymmetric ring regulatory mechanism of the transcription termination Rho helicase decrypted by time-resolved nucleotide analog interference probing (trNAIP). |
| Q35826233 | The amino acid linker between the endonuclease and helicase domains of adeno-associated virus type 5 Rep plays a critical role in DNA-dependent oligomerization |
| Q60921857 | The conformational changes coupling ATP hydrolysis and translocation in a bacterial DnaB helicase |
| Q27653133 | The crystal structure of a replicative hexameric helicase DnaC and its complex with single-stranded DNA |
| Q27646527 | The crystal structure of the Thermus aquaticus DnaB helicase monomer |
| Q30444766 | The domain structure of Helicobacter pylori DnaB helicase: the N-terminal domain can be dispensable for helicase activity whereas the extreme C-terminal region is essential for its function |
| Q33699332 | The effects of oligomerization on Saccharomyces cerevisiae Mcm4/6/7 function |
| Q37028396 | The eukaryotic CMG helicase pumpjack and integration into the replisome |
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