| scholarly article | Q13442814 |
| P356 | DOI | 10.1021/BI00193A013 |
| P698 | PubMed publication ID | 8031761 |
| P2093 | author name string | Corrie JE | |
| Webb MR | |||
| Hunter JL | |||
| Brune M | |||
| P433 | issue | 27 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 8262-8271 | |
| P577 | publication date | 1994-07-01 | |
| P1433 | published in | Biochemistry | Q764876 |
| P1476 | title | Direct, real-time measurement of rapid inorganic phosphate release using a novel fluorescent probe and its application to actomyosin subfragment 1 ATPase | |
| P478 | volume | 33 |
| Q36305732 | A Fluorescent, Reagentless Biosensor for ATP, Based on Malonyl-Coenzyme A Synthetase. |
| Q35574307 | A High-Throughput Enzyme-Coupled Assay for SAMHD1 dNTPase |
| Q97568612 | A STING-based biosensor affords broad cyclic dinucleotide detection within single living eukaryotic cells |
| Q37446066 | A biosensor for fluorescent determination of ADP with high time resolution |
| Q35743156 | A conserved histidine in switch-II of EF-G moderates release of inorganic phosphate |
| Q34444278 | A continuous enzyme-coupled assay for triphosphohydrolase activity of HIV-1 restriction factor SAMHD1 |
| Q37098377 | A continuous fluorescence assay for the characterization of Nudix hydrolases |
| Q36553774 | A continuous spectrophotometric enzyme-coupled assay for deoxynucleoside triphosphate triphosphohydrolases |
| Q34454125 | A fluorescent protein biosensor of myosin II regulatory light chain phosphorylation reports a gradient of phosphorylated myosin II in migrating cells. |
| Q54448843 | A function for the psi subunit in loading the Escherichia coli DNA polymerase sliding clamp. |
| Q44403091 | A generic assay for phosphate-consuming or -releasing enzymes coupled on-line to liquid chromatography for lead finding in natural products |
| Q27940293 | A histone acetylation switch regulates H2A.Z deposition by the SWR-C remodeling enzyme |
| Q27740637 | A low energy short hydrogen bond in very high resolution structures of protein receptor--phosphate complexes |
| Q27676444 | A metal switch for controlling the activity of molecular motor proteins |
| Q38316257 | A model for Escherichia coli DNA polymerase III holoenzyme assembly at primer/template ends. DNA triggers a change in binding specificity of the gamma complex clamp loader |
| Q44978572 | A model of myosin V processivity |
| Q34128944 | A new method for the time-resolved measurement of phosphate release in permeabilized muscle fibers |
| Q42030386 | A nonuniform stepping mechanism for E. coli UvrD monomer translocation along single-stranded DNA |
| Q37356238 | A novel analytical method for in vivo phosphate tracking |
| Q33883417 | A novel cross-talk in diacylglycerol signaling: the Rac-GAP beta2-chimaerin is negatively regulated by protein kinase Cdelta-mediated phosphorylation |
| Q36328820 | A novel mechanism of selectivity against AZT by the human mitochondrial DNA polymerase |
| Q30438509 | A rotor-stator cross-link in the F1-ATPase blocks the rate-limiting step of rotational catalysis |
| Q46858937 | A small-molecule modulator of cardiac myosin acts on multiple stages of the myosin chemomechanical cycle |
| Q28487419 | A subdomain interaction at the base of the lever allosterically tunes the mechanochemical mechanism of myosin 5a |
| Q33553288 | ADP but not P(i) dissociation contributes to rate limitation for Escherichia coli Rho. |
| Q30891612 | ATP consumption and efficiency of human single muscle fibers with different myosin isoform composition |
| Q27653383 | ATPase Cycle of the Nonmotile Kinesin NOD Allows Microtubule End Tracking and Drives Chromosome Movement |
| Q32060422 | ATPase and shortening rates in frog fast skeletal myofibrils by time-resolved measurements of protein-bound and free Pi. |
| Q28484131 | ATPase cycle and DNA unwinding kinetics of RecG helicase |
| Q36864113 | ATPase kinetics on activation of rabbit and frog permeabilized isometric muscle fibres: a real time phosphate assay |
| Q24650875 | ATPase mechanism of Eg5 in the absence of microtubules: insight into microtubule activation and allosteric inhibition by monastrol |
| Q37132080 | ATPase mechanism of the 5'-3' DNA helicase, RecD2: evidence for a pre-hydrolysis conformation change |
| Q24614286 | Active site opening and closure control translocation of multisubunit RNA polymerase |
| Q59289138 | Actomyosin energy turnover declines while force remains constant during isometric muscle contraction |
| Q41721480 | Advances in transient-state kinetics |
| Q36820177 | Allosteric mechanisms can be distinguished using structural mass spectrometry |
| Q40394857 | Alternating site ATPase pathway of rat conventional kinesin |
| Q43213979 | Amino acid transport in thermophiles: characterization of an arginine-binding protein in Thermotoga maritima. |
| Q44487517 | An elongation factor G-induced ribosome rearrangement precedes tRNA-mRNA translocation |
| Q90331317 | An integrated transport mechanism of the maltose ABC importer |
| Q45145779 | An intermediate form of ADP-F-actin |
| Q47602340 | Analyzing ATP utilization by DEAD-Box RNA helicases using kinetic and equilibrium methods |
| Q38332082 | Application of stopped-flow kinetics methods to investigate the mechanism of action of a DNA repair protein |
| Q40430116 | Arginines 29 and 59 of elongation factor G are important for GTP hydrolysis or translocation on the ribosome |
| Q43772608 | Assays for protein-tyrosine phosphatases |
| Q39656345 | Asymmetric ATP binding and hydrolysis activity of the Thermus aquaticus MutS dimer is key to modulation of its interactions with mismatched DNA. |
| Q34183559 | At Physiological Temperatures the ATPase Rates of Shortening Soleus and Psoas Myofibrils Are Similar |
| Q92751306 | Atomic view into Plasmodium actin polymerization, ATP hydrolysis, and fragmentation |
| Q34079096 | Bacterial ribosome requires multiple L12 dimers for efficient initiation and elongation of protein synthesis involving IF2 and EF-G. |
| Q35168355 | Biochemical assays for analyzing activities of ATP-dependent chromatin remodeling enzymes |
| Q37373801 | Biochemical characterization of hyperactive beta2-chimaerin mutants revealed an enhanced exposure of C1 and Rac-GAP domains |
| Q44394472 | Calcium functionally uncouples the heads of myosin VI. |
| Q36047360 | Calcium regulation of myosin-I tension sensing |
| Q30583292 | Cardiac myosin activation: a potential therapeutic approach for systolic heart failure |
| Q43920815 | Caught in the act: ATP hydrolysis of an ABC-multidrug transporter followed by real-time magic angle spinning NMR. |
| Q43996797 | Characterization of the cross-bridge force-generating step using inorganic phosphate and BDM in myofibrils from rabbit skeletal muscles |
| Q30721854 | Cloning, overexpression, and purification of functional human purine nucleoside phosphorylase |
| Q34592087 | Colicin E3 cleavage of 16S rRNA impairs decoding and accelerates tRNA translocation on Escherichia coli ribosomes |
| Q41886746 | Complex activities of the human Bloom's syndrome helicase are encoded in a core region comprising the RecA and Zn-binding domains. |
| Q59349283 | Conformationally Restricted Elongation Factor G Retains GTPase Activity but Is Inactive in Translocation on the Ribosome |
| Q36639569 | Construction of a fluorescent biosensor family |
| Q41996379 | Construction of a thiamin sensor from the periplasmic thiamin binding protein |
| Q42086975 | Control of phosphate release from elongation factor G by ribosomal protein L7/12. |
| Q35858223 | Conversion of a maltose receptor into a zinc biosensor by computational design |
| Q36731305 | Coupling of DNA unwinding to nucleotide hydrolysis in a ring-shaped helicase |
| Q96639915 | Crystal structures of SAMHD1 inhibitor complexes reveal the mechanism of water-mediated dNTP hydrolysis |
| Q48042595 | DNA synthesis from diphosphate substrates by DNA polymerases. |
| Q38689614 | Deconstruction of the Ras switching cycle through saturation mutagenesis |
| Q37098052 | Defining the roles of individual residues in the single-stranded DNA binding site of PcrA helicase |
| Q40113794 | Depletion of phosphate in active muscle fibers probes actomyosin states within the powerstroke |
| Q37972129 | Design strategies of fluorescent biosensors based on biological macromolecular receptors |
| Q36408188 | Design, total chemical synthesis, and binding properties of a [Leu-91-N1-methyl-7-azaTrp]Ras-binding domain of c-Raf-1. |
| Q78664498 | Determinants of relaxation rate in rabbit skinned skeletal muscle fibres |
| Q36543950 | Development of a Reagentless Biosensor for Inorganic Phosphate, Applicable over a Wide Concentration Range |
| Q35785839 | Dimeric Eg5 maintains processivity through alternating-site catalysis with rate-limiting ATP hydrolysis |
| Q30477237 | Dimerized Drosophila myosin VIIa: a processive motor |
| Q36820024 | Direct real-time detection of the actin-activated power stroke within the myosin catalytic domain |
| Q36306063 | Direct real-time detection of the structural and biochemical events in the myosin power stroke |
| Q41985630 | Directional transition from initiation to elongation in bacterial translation. |
| Q43141504 | Distinct functions of elongation factor G in ribosome recycling and translocation |
| Q45153686 | Does phosphate release limit the ATPases of soleus myofibrils? Evidence that (A)M. ADP.Pi states predominate on the cross-bridge cycle |
| Q35225761 | Domestication of the cardiac mitochondrion for energy conversion |
| Q35644681 | Drosophila Ncd reveals an evolutionarily conserved powerstroke mechanism for homodimeric and heterodimeric kinesin-14s. |
| Q46895770 | Drosophila myosin VIIA is a high duty ratio motor with a unique kinetic mechanism |
| Q41774372 | Dual function of Swc5 in SWR remodeling ATPase activation and histone H2A eviction. |
| Q40044638 | Dual use of GTP hydrolysis by elongation factor G on the ribosome |
| Q35218972 | Duplex unwinding and ATPase activities of the DEAD-box helicase eIF4A are coupled by eIF4G and eIF4B |
| Q36499592 | Dynamics of loading the Escherichia coli DNA polymerase processivity clamp |
| Q36228050 | EF-Tu dynamics during pre-translocation complex formation: EF-Tu·GDP exits the ribosome via two different pathways. |
| Q43146291 | Effect of phosphorylation in the motor domain of human myosin IIIA on its ATP hydrolysis cycle |
| Q34546970 | Effect of strain on actomyosin kinetics in isometric muscle fibers. |
| Q28366526 | Effects of substituting uridine triphosphate for ATP on the crossbridge cycle of rabbit muscle |
| Q37236546 | Electron transfer precedes ATP hydrolysis during nitrogenase catalysis. |
| Q89555093 | Elongation factor-Tu can repetitively engage aminoacyl-tRNA within the ribosome during the proofreading stage of tRNA selection |
| Q47585171 | Engineering a periplasmic binding protein for amino acid sensors with improved binding properties |
| Q43030049 | F1-ATPase changes its conformations upon phosphate release |
| Q35485376 | Fluorescence detection of GDP in real time with the reagentless biosensor rhodamine-ParM. |
| Q37694802 | Fluorescence tools to measure helicase activity in real time. |
| Q38237244 | Fluorescent biosensors: design and application to motor proteins |
| Q28346188 | Fluorescent coumarin-labeled nucleotides to measure ADP release from actomyosin |
| Q33585526 | Fluorescent probes for living cells |
| Q36899950 | Fluorescent single-stranded DNA binding protein as a probe for sensitive, real-time assays of helicase activity |
| Q73397040 | Force generation in muscle: time-resolved measurements of ATPase activity using a phosphate-sensitive fluorophore |
| Q30497272 | Functional adaptation of the switch-2 nucleotide sensor enables rapid processive translocation by myosin-5. |
| Q96576743 | GTP hydrolysis by Synechocystis IM30 does not decisively affect its membrane remodeling activity |
| Q91700786 | GTP hydrolysis promotes disassembly of the atlastin crossover dimer during ER fusion |
| Q36458411 | Glu257 in GroEL is a sensor involved in coupling polypeptide substrate binding to stimulation of ATP hydrolysis |
| Q38731413 | Glutathiolated Ras: characterization and implications for Ras activation |
| Q44900588 | GroEL mediates protein folding with a two successive timer mechanism. |
| Q61451189 | Hexameric assembly of the AAA+ protein McrB is necessary for GTPase activity |
| Q35862416 | High-throughput analysis and protein engineering using microcapillary arrays. |
| Q41999361 | Highly selective in vivo imaging of endogenous/exogenous phosphate ion over ATP and PPi. |
| Q27934508 | Histone modifications influence the action of Snf2 family remodelling enzymes by different mechanisms |
| Q33310247 | Human myosin Vc is a low duty ratio nonprocessive motor |
| Q46803460 | Human myosin Vc is a low duty ratio, nonprocessive molecular motor. |
| Q33513784 | Identification of distinct thiopeptide-antibiotic precursor lead compounds using translation machinery assays |
| Q46612883 | Influence of ionic strength on the time course of force development and phosphate release by dogfish muscle fibres |
| Q46150429 | Insights into the kinetics of Ca2+-regulated contraction and relaxation from myofibril studies |
| Q51175089 | Interdomain Communication of the Chd1 Chromatin Remodeler across the DNA Gyres of the Nucleosome. |
| Q92060490 | Investigation into the mechanism of thin filament regulation by transient kinetics and equilibrium binding: Is there a conflict? |
| Q30847789 | Kinesin Motor Enzymology: Chemistry, Structure, and Physics of Nanoscale Molecular Machines |
| Q37073544 | Kinesin's second step |
| Q41048804 | Kinetic adaptation of human Myo19 for active mitochondrial transport to growing filopodia tips |
| Q34066040 | Kinetic and equilibrium analysis of the myosin ATPase |
| Q37168421 | Kinetic characterization of the ATPase and actin-activated ATPase activities of Acanthamoeba castellanii myosin-2 |
| Q46665814 | Kinetic effects of kinesin switch I and switch II mutations |
| Q34577832 | Kinetic mechanism of human myosin IIIA. |
| Q27936457 | Kinetic model for the ATP-dependent translocation of Saccharomyces cerevisiae RSC along double-stranded DNA. |
| Q44133893 | Kinetic pathway of dTTP hydrolysis by hexameric T7 helicase-primase in the absence of DNA. |
| Q34171109 | Kinetics processivity and the direction of motion of Ncd. |
| Q34132131 | Knowledge-based design of reagentless fluorescent biosensors from recombinant antibodies |
| Q40387422 | Late events of translation initiation in bacteria: a kinetic analysis |
| Q28346229 | Link between the enzymatic kinetics and mechanical behavior in an actomyosin motor |
| Q38265817 | Load-dependent modulation of non-muscle myosin-2A function by tropomyosin 4.2. |
| Q46722180 | Maximal activation of skeletal muscle thin filaments requires both rigor myosin S1 and calcium |
| Q51538640 | Measuring In Vitro ATPase Activity for Enzymatic Characterization. |
| Q43153531 | Mechanism of RecQ helicase mechanoenzymatic coupling reveals that the DNA interactions of the ADP-bound enzyme control translocation run terminations. |
| Q40459823 | Mechanism of action of myosin X, a membrane-associated molecular motor. |
| Q38358899 | Mechanism of loading the Escherichia coli DNA polymerase III beta sliding clamp on DNA. Bona fide primer/templates preferentially trigger the gamma complex to hydrolyze ATP and load the clamp |
| Q44650487 | Mechanism of loading the Escherichia coli DNA polymerase III sliding clamp: I. Two distinct activities for individual ATP sites in the gamma complex. |
| Q34236866 | Mechanism of regulation of native cardiac muscle thin filaments by rigor cardiac myosin-S1 and calcium |
| Q34429702 | Mechanism of regulation of phosphate dissociation from actomyosin-ADP-Pi by thin filament proteins |
| Q47126896 | Mechanistic Insights into Autoinhibition of the Oncogenic Chromatin Remodeler ALC1. |
| Q42094494 | Mechanochemical coupling in muscle: attempts to measure simultaneously shortening and ATPase rates in myofibrils. |
| Q37201310 | Metal switch-controlled myosin II from Dictyostelium discoideum supports closure of nucleotide pocket during ATP binding coupled to detachment from actin filaments |
| Q35556373 | Millisecond-scale biochemical response to change in strain |
| Q93064723 | MoImd4 mediates crosstalk between MoPdeH-cAMP signalling and purine metabolism to govern growth and pathogenicity in Magnaporthe oryzae |
| Q88569420 | MoMip11, a MoRgs7-interacting protein, functions as a scaffolding protein to regulate cAMP signaling and pathogenicity in the rice blast fungus Magnaporthe oryzae |
| Q41433748 | Modeling of the actomyosin ATPase activity. Origin of the initial phosphate burst and implications of the phosphate release kinetics |
| Q41744309 | Molecular mechanism and energetics of clamp assembly in Escherichia coli. The role of ATP hydrolysis when gamma complex loads beta on DNA. |
| Q73614539 | Mycobacterial ABC transport system: structure of the primary phosphate receptor |
| Q46568450 | Myosin V from Drosophila reveals diversity of motor mechanisms within the myosin V family. |
| Q40391038 | Myosin VIIB from Drosophila is a high duty ratio motor |
| Q46551350 | Myosin X is a high duty ratio motor |
| Q40115854 | New findings on phosphodiesterases, MoPdeH and MoPdeL in Magnaporthe oryzae revealed by structure analysis. |
| Q43550150 | Optical determination of glutamine using a genetically engineered protein. |
| Q36553832 | P(I) Release Limits the Intrinsic and RNA-Stimulated ATPase Cycles of DEAD-Box Protein 5 (Dbp5) |
| Q24644762 | Pathway of ATP hydrolysis by monomeric kinesin Eg5 |
| Q35757837 | Pathway of processive ATP hydrolysis by kinesin. |
| Q38729141 | Performance and Limitations of Phosphate Quantification: Guidelines for Plant Biologists |
| Q36315665 | Phosphatase-triggered fusogenic liposomes for cytoplasmic delivery of cell-impermeable compounds. |
| Q33700162 | Phosphate release contributes to the rate-limiting step for unwinding by an RNA helicase |
| Q92715283 | Phosphate removal and recovery using immobilized phosphate binding proteins |
| Q35796953 | Phospho-dependent Regulation of SAMHD1 Oligomerisation Couples Catalysis and Restriction |
| Q93085445 | Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens |
| Q92882208 | Positive selection in dNTPase SAMHD1 throughout mammalian evolution |
| Q41992667 | Processive translocation mechanism of the human Bloom's syndrome helicase along single-stranded DNA. |
| Q74543210 | Protein engineering and the development of generic biosensors |
| Q39563501 | Protein phosphatases 2C regulate the activation of the Snf1-related kinase OST1 by abscisic acid in Arabidopsis |
| Q35864250 | Purification and in vitro functional analysis of the Arabidopsis thaliana regulator of G-protein signaling-1. |
| Q35996255 | Quantitative Microplate Assay for Real-Time Nuclease Kinetics |
| Q41047666 | ROS induced distribution of mitochondria to filopodia by Myo19 depends on a class specific tryptophan in the motor domain. |
| Q24318649 | RUTBC1 protein, a Rab9A effector that activates GTP hydrolysis by Rab32 and Rab33B proteins |
| Q28118044 | RUTBC2 protein, a Rab9A effector and GTPase-activating protein for Rab36 |
| Q28552639 | Rad51 Nucleoprotein Filament Disassembly Captured Using Fluorescent Plasmodium falciparum SSB as a Reporter for Single-Stranded DNA |
| Q46987199 | Rapid ribosomal translocation depends on the conserved 18-55 base pair in P-site transfer RNA. |
| Q34169363 | Rate of phosphate release after photoliberation of adenosine 5'-triphosphate in slow and fast skeletal muscle fibers |
| Q39253052 | Rate-limiting Pyrophosphate Release by HIV Reverse Transcriptase Improves Fidelity |
| Q44373982 | Reagentless optical sensing of glutamine using a dual-emitting glutamine-binding protein |
| Q33925519 | Real-time fluorescence assays to monitor duplex unwinding and ATPase activities of helicases |
| Q83937790 | Real-time in vitro measurement of intrinsic and Ras GAP-mediated GTP hydrolysis |
| Q42211959 | Real-time measurement of pyrophosphate release kinetics |
| Q24598928 | RecQ helicase translocates along single-stranded DNA with a moderate processivity and tight mechanochemical coupling |
| Q39805483 | Recent adaptations of fluorescence techniques for the determination of mechanistic parameters of helicases and translocases |
| Q39769965 | Recombination hotspots attenuate the coupled ATPase and translocase activities of an AddAB-type helicase-nuclease |
| Q36451514 | Redox regulation of Rac1 by thiol oxidation. |
| Q28184673 | Rnd proteins function as RhoA antagonists by activating p190 RhoGAP |
| Q36384866 | Role of a conserved glutamate residue in the Escherichia coli SecA ATPase mechanism |
| Q33719421 | Sequential allosteric mechanism of ATP hydrolysis by the CCT/TRiC chaperone is revealed through Arrhenius analysis |
| Q36967134 | Setting the chaperonin timer: the effects of K+ and substrate protein on ATP hydrolysis |
| Q52040647 | Simultaneous observation of individual ATPase and mechanical events by a single myosin molecule during interaction with actin. |
| Q35851112 | Single-stranded DNA translocation of E. coli UvrD monomer is tightly coupled to ATP hydrolysis |
| Q34611132 | Site-specific labeling of T7 DNA polymerase with a conformationally sensitive fluorophore and its use in detecting single-nucleotide polymorphisms. |
| Q41944771 | Small molecule-mediated refolding and activation of myosin motor function |
| Q42466475 | Stepping and stretching. How kinesin uses internal strain to walk processively |
| Q27932939 | Stepwise Histone Replacement by SWR1 Requires Dual Activation with Histone H2A.Z and Canonical Nucleosome |
| Q42120289 | Strand and nucleotide-dependent ATPase activity of gp16 of bacterial virus phi29 DNA packaging motor |
| Q39987218 | Streamlined determination of processive run length and mechanochemical coupling of nucleic acid motor activities. |
| Q39507689 | Strep-tag II Mutant Maltose-binding Protein for Reagentless Fluorescence Sensing |
| Q47121497 | Structural insights into the committed step of bacterial phospholipid biosynthesis. |
| Q30582092 | Structural prediction of a rhodamine-based biosensor and comparison with biophysical data. |
| Q27673803 | Structure of Streptomyces Maltosyltransferase GlgE, a Homologue of a Genetically Validated Anti-tuberculosis Target |
| Q24643436 | Structure, function, and evolution of bacterial ATP-binding cassette systems |
| Q41321762 | Studies of conformational changes of an arginine-binding protein from Thermotoga maritima in the presence and absence of ligand via molecular dynamics simulations with the coarse-grained UNRES force field |
| Q37319749 | Symmetric GroEL:GroES2 complexes are the protein-folding functional form of the chaperonin nanomachine |
| Q41329945 | Symmetry broken and rebroken during the ATP hydrolysis cycle of the mitochondrial Hsp90 TRAP1. |
| Q45309901 | Synthesis and characterization of cell-permeable caged phosphates that can be photolyzed by visible light or 800 nm two-photon photolysis |
| Q44121888 | T7 DNA helicase: a molecular motor that processively and unidirectionally translocates along single-stranded DNA. |
| Q33948559 | TBC-2 regulates RAB-5/RAB-7-mediated endosomal trafficking in Caenorhabditis elegans |
| Q28975624 | TBC1D13 is a RAB35 specific GAP that plays an important role in GLUT4 trafficking in adipocytes |
| Q36839886 | Temperature dependence of nucleotide association and kinetic characterization of myo1b |
| Q41791491 | Temporal correlation of DNA binding, ATP hydrolysis, and clamp release in the clamp loading reaction catalyzed by the Escherichia coli gamma complex |
| Q36608596 | The ATPase cycle mechanism of the DEAD-box rRNA helicase, DbpA |
| Q28189142 | The ATPase reaction cycle of yeast DNA topoisomerase II. Slow rates of ATP resynthesis and P(i) release |
| Q34723538 | The AddAB helicase-nuclease catalyses rapid and processive DNA unwinding using a single Superfamily 1A motor domain |
| Q41332148 | The Conserved Lysine-265 Allosterically Modulates Nucleotide- and Actin-binding Site Coupling in Myosin-2. |
| Q35726266 | The HRDC domain of E. coli RecQ helicase controls single-stranded DNA translocation and double-stranded DNA unwinding rates without affecting mechanoenzymatic coupling. |
| Q27678890 | The Legionella pneumophila GTPase Activating Protein LepB Accelerates Rab1 Deactivation by a Non-canonical Hydrolytic Mechanism |
| Q52312613 | The Mechanism of Acetyl Transfer Catalyzed by Mycobacterium tuberculosis GlmU. |
| Q41841294 | The MitCHAP-60 disease is due to entropic destabilization of the human mitochondrial Hsp60 oligomer |
| Q45073728 | The Shaker-1 Mouse Myosin VIIa Deafness Mutation Results in a Severely Reduced Rate of the ATP Hydrolysis Step |
| Q40165199 | The effect of inorganic phosphate on force generation in single myofibrils from rabbit skeletal muscle |
| Q40158546 | The effect of polyethylene glycol on the mechanics and ATPase activity of active muscle fibers |
| Q77841475 | The efficiency of contraction in rabbit skeletal muscle fibres, determined from the rate of release of inorganic phosphate |
| Q34187343 | The force exerted by a muscle cross-bridge depends directly on the strength of the actomyosin bond |
| Q46907779 | The kinetic mechanism of the SufC ATPase: the cleavage step is accelerated by SufB. |
| Q50114791 | The mechanism of smooth muscle caldesmon-tropomyosin inhibition of the elementary steps of the actomyosin ATPase |
| Q33885300 | The protease domain increases the translocation stepping efficiency of the hepatitis C virus NS3-4A helicase |
| Q36098943 | The rapid and direct determination of ATPase activity by ion exchange chromatography and the application to the activity of heat shock protein-90 |
| Q36130617 | The rational design of allosteric interactions in a monomeric protein and its applications to the construction of biosensors |
| Q41516548 | The tRNA-modifying function of MnmE is controlled by post-hydrolysis steps of its GTPase cycle |
| Q36526276 | The β sliding clamp closes around DNA prior to release by the Escherichia coli clamp loader γ complex |
| Q36426304 | Thiostrepton inhibits the turnover but not the GTPase of elongation factor G on the ribosome. |
| Q49388072 | Three mammalian tropomyosin isoforms have different regulatory effects on nonmuscle myosin-2B and filamentous β-actin in vitro |
| Q54612838 | Time resolved measurements show that phosphate release is the rate limiting step on myofibrillar ATPases. |
| Q30447524 | Time-resolved measurements of phosphate release by cycling cross-bridges in portal vein smooth muscle |
| Q38731418 | Timing and Reset Mechanism of GTP Hydrolysis-Driven Conformational Changes of Atlastin |
| Q64949400 | Transient Kinetic Analysis of SWR1C-Catalyzed H2A.Z Deposition Unravels the Impact of Nucleosome Dynamics and the Asymmetry of Histone Exchange. |
| Q54458808 | Transient kinetic investigation of GTP hydrolysis catalyzed by interferon-gamma-induced hGBP1 (human guanylate binding protein 1). |
| Q46968954 | Transient kinetics, fluorescence, and FRET in studies of initiation of translation in bacteria |
| Q35116428 | Uncoupling DNA translocation and helicase activity in PcrA: direct evidence for an active mechanism. |
| Q39912209 | Use of stopped-flow fluorescence and labeled nucleotides to analyze the ATP turnover cycle of kinesins |
| Q33223992 | Vertebrate myosin VIIb is a high duty ratio motor adapted for generating and maintaining tension |
| Q35580317 | Why choose myofibrils to study muscle myosin ATPase? |
| Q27932247 | Yeast Pif1 helicase exhibits a one-base-pair stepping mechanism for unwinding duplex DNA |
| Q34723572 | eIF4G stimulates the activity of the DEAD box protein eIF4A by a conformational guidance mechanism |
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