| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2004PNAS..101.4373C |
| P356 | DOI | 10.1073/PNAS.0400968101 |
| P932 | PMC publication ID | 384754 |
| P698 | PubMed publication ID | 15070725 |
| P5875 | ResearchGate publication ID | 8630497 |
| P50 | author | Charles C. Richardson | Q56420957 |
| P2093 | author name string | Donald E Johnson | |
| Donald J Crampton | |||
| Shenyuan Guo | |||
| P2860 | cites work | The Ras-RasGAP Complex: Structural Basis for GTPase Activation and Its Loss in Oncogenic Ras Mutants | Q24317051 |
| Structure at 1.65 A of RhoA and its GTPase-activating protein in complex with a transition-state analogue | Q24319143 | ||
| Crystal structure of a small G protein in complex with the GTPase-activating protein rhoGAP | Q24324015 | ||
| Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold | Q24556499 | ||
| DNA binding mediates conformational changes and metal ion coordination in the active site of PcrA helicase | Q27618867 | ||
| Crystal structure of the helicase domain from the replicative helicase-primase of bacteriophage T7 | Q27620078 | ||
| Crystal structure of T7 gene 4 ring helicase indicates a mechanism for sequential hydrolysis of nucleotides | Q27625337 | ||
| Nucleotide-dependent binding of the gene 4 protein of bacteriophage T7 to single-stranded DNA | Q69865305 | ||
| Characterization of strand displacement synthesis catalyzed by bacteriophage T7 DNA polymerase | Q70158810 | ||
| Structural and functional dissections of transcription termination factor rho by random mutagenesis | Q71588097 | ||
| A preformed, topologically stable replication fork. Characterization of leading strand DNA synthesis catalyzed by T7 DNA polymerase and T7 gene 4 protein | Q71829738 | ||
| Myosin active-site trapping with vanadate ion | Q71958560 | ||
| DNA-dependent nucleoside 5'-triphosphatase activity of the gene 4 protein of bacteriophage T7 | Q72566898 | ||
| Importance of F1-ATPase residue alpha-Arg-376 for catalytic transition state stabilization | Q73201387 | ||
| Bacteriophage T7 DNA helicase binds dTTP, forms hexamers, and binds DNA in the absence of Mg2+. The presence of dTTP is sufficient for hexamer formation and DNA binding | Q77387679 | ||
| Structure and mechanism of the RuvB Holliday junction branch migration motor | Q27633740 | ||
| Crystal structure of the SF3 helicase from adeno-associated virus type 2 | Q27641803 | ||
| Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria | Q27730864 | ||
| X-ray structure of the magnesium(II).ADP.vanadate complex of the Dictyostelium discoideum myosin motor domain to 1.9 A resolution | Q27732650 | ||
| DNA is bound within the central hole to one or two of the six subunits of the T7 DNA helicase | Q28288465 | ||
| Confirmation of the arginine-finger hypothesis for the GAP-stimulated GTP-hydrolysis reaction of Ras | Q28646214 | ||
| Structure and function of hexameric helicases. | Q34019405 | ||
| Interaction of adjacent primase domains within the hexameric gene 4 helicase-primase of bacteriophage T7. | Q34189392 | ||
| The gene 4 protein of bacteriophage T7. Characterization of helicase activity | Q34255123 | ||
| Bacteriophage T7 helicase/primase proteins form rings around single-stranded DNA that suggest a general structure for hexameric helicases | Q34387475 | ||
| Template recognition sequence for RNA primer synthesis by gene 4 protein of bacteriophage T7 | Q35303298 | ||
| Roles of bacteriophage T7 gene 4 proteins in providing primase and helicase functions in vivo | Q37291070 | ||
| DNA helicases | Q37886473 | ||
| A Domain of the Gene 4 Helicase/Primase of Bacteriophage T7 Required for the Formation of an Active Hexamer | Q38292397 | ||
| The K318A mutant of bacteriophage T7 DNA primase-helicase protein is deficient in helicase but not primase activity and inhibits primase-helicase protein wild-type activities by heterooligomer formation | Q38306925 | ||
| The nucleotide binding site of the helicase/primase of bacteriophage T7. Interaction of mutant and wild-type proteins | Q38313252 | ||
| Interactions of bacteriophage T7 DNA primase/helicase protein with single-stranded and double-stranded DNAs | Q38314172 | ||
| The linker region between the helicase and primase domains of the bacteriophage T7 gene 4 protein is critical for hexamer formation | Q38319669 | ||
| Vanadate inhibits the ATPase activity and DNA binding capability of bacterial MutS. A structural model for the vanadate-MutS interaction at the Walker A motif | Q38361436 | ||
| Nucleotide binding studies of bacteriophage T7 DNA helicase-primase protein | Q39656366 | ||
| Gene 4 protein of bacteriophage T7. Purification physical properties, and stimulation of T7 DNA polymerase during the elongation of polynucleotide chains | Q40838839 | ||
| Mechanisms of helicase-catalyzed DNA unwinding | Q41114786 | ||
| Organization and evolution of bacterial and bacteriophage primase-helicase systems | Q44080673 | ||
| T7 DNA helicase: a molecular motor that processively and unidirectionally translocates along single-stranded DNA. | Q44121888 | ||
| Molecular mechanisms of the functional coupling of the helicase (gp41) and polymerase (gp43) of bacteriophage T4 within the DNA replication fork | Q44365798 | ||
| Probing the mechanism of ATP hydrolysis on F-actin using vanadate and the structural analogs of phosphate BeF-3 and A1F-4. | Q52548964 | ||
| A built-in arginine finger triggers the self-stimulatory GTPase-activating activity of rho family GTPases. | Q52567908 | ||
| Aluminum fluoride associates with the small guanine nucleotide binding proteins. | Q54565581 | ||
| Cooperative interactions of nucleotide ligands are linked to oligomerization and DNA binding in bacteriophage T7 gene 4 helicases. | Q54637121 | ||
| Mutational replacements of conserved amino acid residues in the alpha subunit change the catalytic properties of Escherichia coli F1-ATPase. | Q54734582 | ||
| Bacteriophage T7: minimal requirements for the replication of a duplex DNA molecule. | Q55062506 | ||
| Novel Insights into the Chemical Mechanism of ATP Synthase | Q57206185 | ||
| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bacteriophage | Q165028 |
| P304 | page(s) | 4373-4378 | |
| P577 | publication date | 2004-03-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | The arginine finger of bacteriophage T7 gene 4 helicase: role in energy coupling | |
| P478 | volume | 101 |
| Q34608172 | A specific scenario for the origin of life and the genetic code based on peptide/oligonucleotide interdependence |
| Q33908440 | Bacterial RadA is a DnaB-type helicase interacting with RecA to promote bidirectional D-loop extension |
| Q46983567 | Complementation of one RecA protein point mutation by another. Evidence for trans catalysis of ATP hydrolysis |
| Q35310624 | Coupling dTTP hydrolysis with DNA unwinding by the DNA helicase of bacteriophage T7. |
| Q42426538 | Defective dissociation of a "slow" RecA mutant protein imparts an Escherichia coli growth defect |
| Q57976550 | Disorder-order folding transitions underlie catalysis in the helicase motor of SecA |
| Q47939773 | Hybrid Methods Reveal Multiple Flexibly Linked DNA Polymerases within the Bacteriophage T7 Replisome. |
| Q33809000 | It takes two to tango: defining an essential second active site in pyridoxal 5'-phosphate synthase |
| Q36578943 | Mechanisms of a ring shaped helicase |
| Q34181409 | Molecular Basis for Recognition of Nucleoside Triphosphate by Gene 4 Helicase of Bacteriophage T7 |
| Q36341536 | Multimeric BLM is dissociated upon ATP hydrolysis and functions as monomers in resolving DNA structures |
| Q39574927 | Multiple active centers of multi-subunit RNA polymerases |
| Q37105913 | On helicases and other motor proteins |
| Q36855814 | Physiological and biochemical defects in carboxyl-terminal mutants of mitochondrial DNA helicase |
| Q41851634 | Promiscuous usage of nucleotides by the DNA helicase of bacteriophage T7: determinants of nucleotide specificity |
| Q24294274 | Structural and functional analyses of disease-causing missense mutations in Bloom syndrome protein |
| Q93367206 | Structural basis for adPEO-causing mutations in the mitochondrial TWINKLE helicase |
| Q27649210 | Structural basis of mechanochemical coupling in a hexameric molecular motor |
| Q27648844 | Structure of hexameric DnaB helicase and its complex with a domain of DnaG primase |
| Q42048581 | Structure of the hexameric HerA ATPase reveals a mechanism of translocation-coupled DNA-end processing in archaea. |
| Q36168680 | The arginine finger of the Bloom syndrome protein: its structural organization and its role in energy coupling. |
| Q35067767 | The glutamate switch of bacteriophage T7 DNA helicase: role in coupling nucleotide triphosphate (NTP) and DNA binding to NTP hydrolysis |
| Q34607601 | The hepatitis C virus NS3 protein: a model RNA helicase and potential drug target |
| Q27673737 | The hexameric helicase DnaB adopts a nonplanar conformation during translocation. |
| Q36447325 | Understanding helicases as a means of virus control. |
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