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  1. Structural Activation of DNA Unwinding by MCM8/9/HROB
  2. Response Factor Correction for Quantitative Determination of Homooligomeric Sso SSB Binding to ssDNA by Native Mass Spectrometry
  3. MCM8/9 and FANCD2 interact within a shared pathway in response to replication stress caused by DNA crosslinks
  4. Residues in the little finger domain of the Y-family Dpo4 DNA polymerase communicate to restrict synthesis past 8-oxoguanine lesions
  5. Response Factor Correction for Quantitative Determination of Homooligomeric Protein Binding to DNA by Native Protein Mass Spectrometry
  6. MCM8/9 and FANCD2 interact within a shared pathway in response to replication stress caused by DNA crosslinks
  7. Tau-mediated coupling between Pol III synthesis and DnaB helicase unwinding helps maintain genomic stability
  8. Dysregulated DnaB unwinding induces replisome decoupling and daughter strand gaps that are countered by RecA polymerization
  9. Gas-phase stability and thermodynamics of ligand-bound, binary complexes of chloramphenicol acetyltransferase reveal negative cooperativity
  10. Dysregulated DnaB unwinding induces replisome decoupling and daughter strand gaps that are countered by RecA polymerization
  11. Activity, substrate preference and structure of the HsMCM8/9 helicase
  12. A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress
  13. In vivo fluorescent TUNEL detection of single stranded DNA gaps and breaks induced by dnaB helicase mutants in Escherichia coli
  14. A novel multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress
  15. Targeted chromosomal Escherichia coli:dnaB exterior surface residues regulate DNA helicase behavior to maintain genomic stability and organismal fitness
  16. Division of Chemical Toxicology Program at the American Chemical Society National Meeting: Celebrating 25 Years!
  17. A Unifying Framework for Understanding Biological Structures and Functions Across Levels of Biological Organization
  18. Targeted chromosomal Escherichia coli:dnaB exterior surface residues regulate DNA helicase behavior to maintain genomic stability and organismal fitness
  19. Motifs of the C-terminal domain of MCM9 direct localization to sites of mitomycin-C damage for RAD51 recruitment
  20. A hand-off of DNA between archaeal polymerases allows high-fidelity replication to resume at a discrete intermediate three bases past 8-oxoguanine
  21. Motifs of the C-terminal Domain of MCM9 Direct Localization to Sites of Mitomycin-C Damage for RAD51 Recruitment
  22. A hand-off of DNA between archaeal polymerases allows high-fidelity replication to resume at a discrete intermediate three bases past 8-oxoguanine
  23. Amidst multiple binding orientations on fork DNA, Saccharolobus MCM helicase proceeds N-first for unwinding
  24. Fine-tuning of the replisome: Mcm10 regulates fork progression and regression
  25. The MCM8/9 complex: A recent recruit to the roster of helicases involved in genome maintenance
  26. Contacts and context that regulate DNA helicase unwinding and replisome progression
  27. Control of Hexamerization, Assembly, and Excluded Strand Specificity for the Sulfolobus solfataricus MCM Helicase
  28. Bacterial DnaB helicase interacts with the excluded strand to regulate unwinding
  29. Coordination and Substitution of DNA Polymerases in Response to Genomic Obstacles
  30. Mechanistic insights into how CMG helicase facilitates replication past DNA roadblocks
  31. Biochemical Characterization of the Human Mitochondrial Replicative Twinkle Helicase
  32. DNA Interactions Probed by H/D Exchange FT-ICR Mass Spectrometry Confirm External Binding Sites on the MCM Helicase
  33. The excluded DNA strand is SEW important for hexameric helicase unwinding
  34. Structural Mechanisms of Hexameric Helicase Loading, Assembly, and Unwinding
  35. Crystal Structure of a Transcribing RNA Polymerase II Complex Reveals a Complete Transcription Bubble
  36. Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability
  37. MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability
  38. Corrigendum to “Identification, quantification, and evolutionary analysis of a novel isoform of MCM9” [Gene 519 (2013) 41–49]
  39. Structure of a Highly Conserved Domain of Rock1 Required for Shroom-Mediated Regulation of Cell Morphology
  40. Assembly and Distributive Action of an Archaeal DNA Polymerase Holoenzyme
  41. A clamp-like biohybrid catalyst for DNA oxidation
  42. Novel Interaction of the Bacterial-Like DnaG Primase with the MCM Helicase in Archaea
  43. Identification, quantification, and evolutionary analysis of a novel isoform of MCM9
  44. Biochemistry: Molecular hurdles cleared with ease
  45. Differential Temperature-Dependent Multimeric Assemblies of Replication and Repair Polymerases on DNA Increase Processivity
  46. Structure of Shroom domain 2 reveals a three-segmented coiled-coil required for dimerization, Rock binding, and apical constriction
  47. Kinetics and Fidelity of Polymerization by DNA Polymerase III from Sulfolobus solfataricus
  48. Strand Annealing and Terminal Transferase Activities of a B-family DNA Polymerase
  49. Steric exclusion and wrapping of the excluded DNA strand occurs along discrete external binding paths during MCM helicase unwinding
  50. Characterization of a Functional DnaG-Type Primase in Archaea: Implications for a Dual-Primase System
  51. A trimeric DNA polymerase complex increases the native replication processivity
  52. MCM Forked Substrate Specificity Involves Dynamic Interaction with the 5'-Tail
  53. Correction
  54. Organization of the archaeal MCM complex on DNA and implications for the helicase mechanism
  55. Identification and Mapping of Protein−Protein Interactions by a Combination of Cross-Linking, Cleavage, and Proteomics
  56. Architecture of the bacteriophage T4 primosome: Electron microscopy studies of helicase (gp41) and primase (gp61)
  57. Assembly of the bacteriophage T4 primosome: Single-molecule and ensemble studies
  58. On the Solution Structure of the T4 Sliding Clamp (gp45) †
  59. 'Screw-cap' clamp loader proteins that thread
  60. Molecular biology: The loader of the rings
  61. The dynamic processivity of the T4 DNA polymerase during replication
  62. The Application of a Minicircle Substrate in the Study of the Coordinated T4 DNA Replication
  63. Dissociative Properties of the Proteins within the Bacteriophage T4 Replisome
  64. Examination of the Role of the Clamp-loader and ATP Hydrolysis in the Formation of the Bacteriophage T4 Polymerase Holoenzyme
  65. Protein-Protein Interactions in the Bacteriophage T4 Replisome: THE LEADING STRAND HOLOENZYME IS PHYSICALLY LINKED TO THE LAGGING STRAND HOLOENZYME AND THE PRIMOSOME
  66. Intricacies in ATP-Dependent Clamp Loading
  67. Dynamic protein interactions in the bacteriophage T4 replisome
  68. Building a Replisome Solution Structure by Elucidation of Protein-Protein Interactions in the Bacteriophage T4 DNA Polymerase Holoenzyme
  69. Creating a dynamic picture of the sliding clamp during T4 DNA polymerase holoenzyme assembly by using fluorescence resonance energy transfer
  70. Faculty of 1000 evaluation for A Major Role of DNA Polymerase δ in Replication of Both the Leading and Lagging DNA Strands.
  71. Faculty of 1000 evaluation for CMG helicase and DNA polymerase ε form a functional 15-subunit holoenzyme for eukaryotic leading-strand DNA replication.
  72. Faculty of 1000 evaluation for Dynamic look at DNA unwinding by a replicative helicase.
  73. Faculty of 1000 evaluation for Structures of human primase reveal design of nucleotide elongation site and mode of Pol α tethering.
  74. Faculty of 1000 evaluation for Ribonucleotides misincorporated into DNA act as strand-discrimination signals in eukaryotic mismatch repair.
  75. Faculty of 1000 evaluation for The Bacterial DnaC Helicase Loader Is a DnaB Ring Breaker.