scholarly article | Q13442814 |
P356 | DOI | 10.1038/NSB0797-553 |
P698 | PubMed publication ID | 9228948 |
P50 | author | Jennifer Doudna | Q56068 |
P2093 | author name string | J H Cate | |
R L Hanna | |||
P2860 | cites work | Defining the chemical groups essential for Tetrahymena group I intron function by nucleotide analog interference mapping | Q24569590 |
Are buried salt bridges important for protein stability and conformational specificity? | Q27730229 | ||
Three-dimensional structure of a hammerhead ribozyme | Q27730774 | ||
Crystal structure of a group I ribozyme domain: principles of RNA packing | Q27733326 | ||
Capturing the structure of a catalytic RNA intermediate: the hammerhead ribozyme | Q27734150 | ||
The CCP4 suite: programs for protein crystallography | Q27861090 | ||
Ribozymes: A Distinct Class of Metalloenzymes | Q28315324 | ||
Dominant forces in protein folding | Q29616390 | ||
Modelling of the three-dimensional architecture of group I catalytic introns based on comparative sequence analysis | Q29616731 | ||
Visualizing the higher order folding of a catalytic RNA molecule | Q30449417 | ||
An independently folding domain of RNA tertiary structure within the Tetrahymena ribozyme | Q30464666 | ||
GAAA tetraloop and conserved bulge stabilize tertiary structure of a group I intron domain | Q30466318 | ||
RNA tertiary structure mediation by adenosine platforms | Q30469007 | ||
Metal-binding sites in the major groove of a large ribozyme domain | Q34408837 | ||
Catalytic activity is retained in the Tetrahymena group I intron despite removal of the large extension of element P5. | Q35948736 | ||
RNA - ligand interactions:(I) magnesium binding sites in yeast tRNAPhe | Q36184432 | ||
Do salt bridges stabilize proteins? A continuum electrostatic analysis. | Q36278616 | ||
Crystallization of ribozymes and small RNA motifs by a sparse matrix approach | Q36492163 | ||
Stability constants of magnesium and cadmium complexes of adenine nucleotides and thionucleotides and rate constants for formation and dissociation of magnesium-ATP and magnesium-ADP | Q36599356 | ||
Reconstitution of a group I intron self-splicing reaction with an activator RNA. | Q37362138 | ||
Bond order and charge localization in nucleoside phosphorothioates | Q39493502 | ||
The P9.1-P9.2 peripheral extension helps guide folding of the Tetrahymena ribozyme | Q39715684 | ||
Absolute configuration of Rp-uridine 3',5'-cyclic phosphorothioate | Q40388724 | ||
A crystallographic study of metal-binding to yeast phenylalanine transfer RNA | Q40774280 | ||
A nuclear magnetic resonance study of secondary and tertiary structure in yeast tRNAPhe | Q40826564 | ||
DNA and RNA sequence determination based on phosphorothioate chemistry | Q43693032 | ||
Metal coordination sites that contribute to structure and catalysis in the group I intron from Tetrahymena | Q52225074 | ||
Analysis of the role of phosphate oxygens in the group I intron from Tetrahymena | Q52228932 | ||
Thermal unfolding of a group I ribozyme: the low-temperature transition is primarily disruption of tertiary structure. | Q52517201 | ||
New loop-loop tertiary interactions in self-splicing introns of subgroup IC and ID: a complete 3D model of the Tetrahymena thermophila ribozyme | Q67426634 | ||
Melting and chemical modification of a cyclized self-splicing group I intron: similarity of structures in 1 M Na+, in 10 mM Mg2+, and in the presence of substrate | Q68649225 | ||
Conformational changes of transfer ribonucleic acid. Equilibrium phase diagrams | Q69209943 | ||
Disulfide determinants of calcium-induced packing in alpha-lactalbumin | Q70862469 | ||
Protein stabilization by removal of unsatisfied polar groups: computational approaches and experimental tests | Q71165654 | ||
Kinetic intermediates in RNA folding | Q72112171 | ||
P433 | issue | 7 | |
P921 | main subject | magnesium | Q660 |
P304 | page(s) | 553-558 | |
P577 | publication date | 1997-07-01 | |
P1433 | published in | Nature structural biology | Q26842658 |
P1476 | title | A magnesium ion core at the heart of a ribozyme domain | |
P478 | volume | 4 |
Q27765139 | A 1.3-A resolution crystal structure of the HIV-1 trans-activation response region RNA stem reveals a metal ion-dependent bulge conformation |
Q33653378 | A chemogenetic approach to RNA function/structure analysis |
Q27639113 | A compact RNA tertiary structure contains a buried backbone-K+ complex |
Q37215335 | A recurrent magnesium-binding motif provides a framework for the ribosomal peptidyl transferase center |
Q41912492 | A short fragment of 23S rRNA containing the binding sites for two ribosomal proteins, L24 and L4, is a key element for rRNA folding during early assembly |
Q77530280 | A specific monovalent metal ion integral to the AA platform of the RNA tetraloop receptor |
Q27625449 | A water channel in the core of the vitamin B(12) RNA aptamer |
Q27764890 | A zipper-like duplex in DNA: the crystal structure of d(GCGAAAGCT) at 2.1 A resolution |
Q34366723 | Accessibility of 18S rRNA in human 40S subunits and 80S ribosomes at physiological magnesium ion concentrations--implications for the study of ribosome dynamics |
Q62763957 | All-atom MD indicates ion-dependent behavior of therapeutic DNA polymer |
Q30306960 | An early transition state for folding of the P4-P6 RNA domain |
Q36542678 | An optimal Mg(2+) concentration for kinetic folding of the tetrahymena ribozyme |
Q34362691 | An unconventional origin of metal-ion rescue and inhibition in the Tetrahymena group I ribozyme reaction |
Q34282416 | Beyond kinetic traps in RNA folding |
Q34497381 | Bidentate RNA-magnesium clamps: on the origin of the special role of magnesium in RNA folding |
Q35115810 | Binding of Europium(III) ions to RNA stem loops: Role of the primary hydration sphere in complex formation |
Q34553023 | Biography of Jennifer A. Doudna |
Q36684846 | Cation-dependent folding of 3' cap-independent translation elements facilitates interaction of a 17-nucleotide conserved sequence with eIF4G |
Q42266431 | Characterizing riboswitch function: identification of Mg2+ binding site in T box antiterminator RNA |
Q42412663 | Charge density of divalent metal cations determines RNA stability |
Q37619599 | Cobalt hexammine induced tautomeric shift in Z-DNA: the structure of d(CGCGCA)*d(TGCGCG) in two crystal forms |
Q41819265 | Comparison of interactions of diamine and Mg²⁺ with RNA tertiary structures: similar versus differential effects on the stabilities of diverse RNA folds |
Q37686061 | Conformational entropy of the RNA phosphate backbone and its contribution to the folding free energy |
Q27679196 | Crystal structure of 3WJ core revealing divalent ion-promoted thermostability and assembly of the Phi29 hexameric motor pRNA |
Q24540022 | Crystal structure of a model branchpoint-U2 snRNA duplex containing bulged adenosines |
Q34037316 | DNA-dependent divalent cation binding in the nucleosome core particle |
Q36972871 | Deletion of the P5abc peripheral element accelerates early and late folding steps of the Tetrahymena group I ribozyme |
Q43950191 | Design, construction, and analysis of a novel class of self-folding RNA. |
Q27629997 | Detection of alkali metal ions in DNA crystals using state-of-the-art X-ray diffraction experiments |
Q41950806 | Determining the Mg2+ stoichiometry for folding an RNA metal ion core |
Q33749946 | Dissecting electrostatic screening, specific ion binding, and ligand binding in an energetic model for glycine riboswitch folding |
Q40848247 | Distinct sites of phosphorothioate substitution interfere with folding and splicing of the Anabaena group I intron |
Q33635820 | Divalent ion competition reveals reorganization of an RNA ion atmosphere upon folding |
Q36425977 | Effects of Mg2+ on the free energy landscape for folding a purine riboswitch RNA. |
Q34361485 | Effects of polyvalent cations on the folding of an rRNA three-way junction and binding of ribosomal protein S15 |
Q41648625 | Emerging themes in RNA folding |
Q37300652 | Energy barriers, pathways, and dynamics during folding of large, multidomain RNAs |
Q41687485 | Enhanced RNA binding of dimerized aminoglycosides |
Q40305001 | Entropy-driven folding of an RNA helical junction: an isothermal titration calorimetric analysis of the hammerhead ribozyme. |
Q36420588 | Evidence for a thermodynamically distinct Mg2+ ion associated with formation of an RNA tertiary structure |
Q80306650 | Evidence for ditopic coordination of phosphate diesters to [Mg(15-crown-5)]2+. Implications for magnesium biocoordination chemistry |
Q28199046 | Exposing the kinetic traps in RNA folding |
Q27679537 | Fluoride ion encapsulation by Mg2+ ions and phosphates in a fluoride riboswitch |
Q36968465 | Folding of a universal ribozyme: the ribonuclease P RNA. |
Q39094727 | Folding of the group I intron ribozyme from the 26S rRNA gene of Candida albicans |
Q36228464 | Folding path of P5abc RNA involves direct coupling of secondary and tertiary structures |
Q35035429 | Formation of a GNRA tetraloop in P5abc can disrupt an interdomain interaction in the Tetrahymena group I ribozyme |
Q24812515 | Functional identification of catalytic metal ion binding sites within RNA. |
Q64259209 | Further Probing of Cu-Dependent PNAzymes Acting as Artificial RNA Restriction Enzymes |
Q34362552 | Helix P4 is a divalent metal ion binding site in the conserved core of the ribonuclease P ribozyme |
Q52347706 | Hidden Structural Modules in a Cooperative RNA Folding Transition. |
Q36841288 | Hinge stiffness is a barrier to RNA folding |
Q27660714 | Identification and characterization of anion binding sites in RNA |
Q43206276 | Identification by modification-interference of purine N-7 and ribose 2'-OH groups critical for catalysis by bacterial ribonuclease P. |
Q39258358 | Identification of a GUAAY Pentaloop Sequence Involved in a Novel RNA Loop-Helix Interaction |
Q47632628 | Inner-Sphere Coordination of Divalent Metal Ion with Nucleobase in Catalytic RNA. |
Q27666944 | Insights into Metalloregulation by M-box Riboswitch RNAs via Structural Analysis of Manganese-Bound Complexes |
Q74251949 | Interstrand disulfide cross-linking of internal sugar residues in duplex RNA |
Q39959277 | Inverse thio effects in the hepatitis delta virus ribozyme reveal that the reaction pathway is controlled by metal ion charge density |
Q38379384 | Ion binding to biological macromolecules |
Q34711836 | Ion distributions around left- and right-handed DNA and RNA duplexes: a comparative study |
Q37213759 | Kinetic and thermodynamic framework for P4-P6 RNA reveals tertiary motif modularity and modulation of the folding preferred pathway |
Q37173101 | Kinetic barriers and the role of topology in protein and RNA folding |
Q77456678 | Leaving group stabilization by metal ion coordination and hydrogen bond donation is an evolutionarily conserved feature of group I introns |
Q42144239 | Low specificity of metal ion binding in the metal ion core of a folded RNA. |
Q34363194 | Magnesium ions mediate contacts between phosphoryl oxygens at positions 2122 and 2176 of the 23S rRNA and ribosomal protein L1. |
Q37199348 | Magnesium-dependent folding of self-splicing RNA: exploring the link between cooperativity, thermodynamics, and kinetics |
Q42093680 | Metal ion dependence of cooperative collapse transitions in RNA |
Q43206321 | Metal ion probing of rRNAs: evidence for evolutionarily conserved divalent cation binding pockets. |
Q38299358 | Metal-ion binding and metal-ion induced folding of the adenine-sensing riboswitch aptamer domain |
Q42155694 | Metal-ion rescue revisited: biochemical detection of site-bound metal ions important for RNA folding |
Q27748294 | Metals, motifs, and recognition in the crystal structure of a 5S rRNA domain |
Q39808443 | Microenvironment analysis and identification of magnesium binding sites in RNA |
Q24555115 | Modelling ion binding to AA platform motifs in RNA: a continuum solvent study including conformational adaptation |
Q41721465 | Modern methods for probing RNA structure. |
Q39319421 | Modulation of RNA metal binding by flanking bases: 15N NMR evaluation of GC, tandem GU, and tandem GA sites |
Q38352124 | Multiple metal-binding cores are required for metalloregulation by M-box riboswitch RNAs |
Q36076703 | Native secondary structure formation in RNA may be a slave to tertiary folding |
Q28487403 | Nuclear localization and in situ DNA damage by Mycobacterium tuberculosis nucleoside-diphosphate kinase |
Q58589393 | Nucleobase carbonyl groups are poor Mg inner-sphere binders but excellent monovalent ion binders - A critical PDB survey |
Q42837216 | Nucleobases Undergo Dynamic Rearrangements during RNA Tertiary Folding |
Q30472826 | Peptidyl-transferase ribozymes: trans reactions, structural characterization and ribosomal RNA-like features |
Q33928709 | Phosphorothioate modification of RNA for stereochemical and interference analyses |
Q33299471 | Prediction of RNA pseudoknots using heuristic modeling with mapping and sequential folding |
Q36539995 | Probing the kinetic and thermodynamic consequences of the tetraloop/tetraloop receptor monovalent ion-binding site in P4-P6 RNA by smFRET. |
Q30304561 | Quantifying the energetic interplay of RNA tertiary and secondary structure interactions |
Q39597487 | Quantitative studies of Mn(2+)-promoted specific and non-specific cleavages of a large RNA: Mn(2+)-GAAA ribozymes and the evolution of small ribozymes |
Q47756940 | Quantitative tests of a reconstitution model for RNA folding thermodynamics and kinetics |
Q35769969 | RNA and its ionic cloud: solution scattering experiments and atomically detailed simulations. |
Q33879873 | RNA bulges as architectural and recognition motifs |
Q46726319 | RNA catalysis |
Q28484063 | RNA folding and catalysis mediated by iron (II) |
Q36313074 | RNA folding causes secondary structure rearrangement |
Q33879864 | RNA folding: beyond Watson-Crick pairs |
Q36774903 | RNA folding: conformational statistics, folding kinetics, and ion electrostatics. |
Q28139993 | RNA folds: insights from recent crystal structures |
Q77530243 | RNA shows its metal |
Q74782081 | RNA structure |
Q41595272 | RNA structure comes of age. |
Q58952040 | RNA switches function |
Q50972828 | RNA with iron(II) as a cofactor catalyses electron transfer. |
Q73958586 | Rearrangement of a stable RNA secondary structure during VS ribozyme catalysis |
Q35011079 | Removal of covalent heterogeneity reveals simple folding behavior for P4-P6 RNA. |
Q28205184 | Ribozyme structures and mechanisms |
Q34019400 | Ribozyme structures and mechanisms |
Q36697486 | Role of ion valence in the submillisecond collapse and folding of a small RNA domain |
Q39628690 | Roles of long-range tertiary interactions in limiting dynamics of the Tetrahymena group I ribozyme |
Q35687704 | Selecting rRNA binding sites for the ribosomal proteins L4 and L6 from randomly fragmented rRNA: application of a method called SERF |
Q34663762 | Short unligated sticky ends enable the observation of circularised DNA by atomic force and electron microscopies |
Q35234470 | Single-molecule transition-state analysis of RNA folding |
Q34364582 | Specific phosphorothioate substitutions probe the active site of Bacillus subtilis ribonuclease P. |
Q57260333 | Structural Requirement for Mg2+ Binding in the Group I Intron Core |
Q27631000 | Structural basis of the enhanced stability of a mutant ribozyme domain and a detailed view of RNA--solvent interactions |
Q36670098 | Structural inference of native and partially folded RNA by high-throughput contact mapping |
Q27638009 | Structural insights into group II intron catalysis and branch-site selection |
Q36128803 | Structural metals in the group I intron: a ribozyme with a multiple metal ion core |
Q41457306 | Structure of stem-loop IV of Tetrahymena telomerase RNA. |
Q35269518 | Structure-function analysis from the outside in: long-range tertiary contacts in RNA exhibit distinct catalytic roles |
Q28769589 | Tertiary structure formation in the hairpin ribozyme monitored by fluorescence resonance energy transfer |
Q27635370 | The 1.19 A X-ray structure of 2'-O-Me(CGCGCG)(2) duplex shows dehydrated RNA with 2-methyl-2,4-pentanediol in the minor groove |
Q41982240 | The P15-loop of Escherichia coli RNase P RNA is an autonomous divalent metal ion binding domain. |
Q38314751 | The P5abc peripheral element facilitates preorganization of the tetrahymena group I ribozyme for catalysis |
Q57054050 | The Story of RNA Folding, as Told in Epochs |
Q39698136 | The bulge region of HIV-1 TAR RNA binds metal ions in solution. |
Q41876011 | The chemical basis of adenosine conservation throughout the Tetrahymena ribozyme |
Q34365980 | The contribution of metal ions to the structural stability of the large ribosomal subunit |
Q42538862 | The electrostatic characteristics of G.U wobble base pairs |
Q42995296 | The hepatitis C virus internal ribosome entry site adopts an ion-dependent tertiary fold |
Q73522859 | The ion core in RNA folding |
Q74546400 | The parallel universe of RNA folding |
Q34064701 | The rate-limiting step in the folding of a large ribozyme without kinetic traps |
Q46758030 | The role of intramolecular hydrogen bonding on nucleobase acidification following metal coordination: possible implications of an "indirect" role of metals in acid-base catalysis of nucleic acids |
Q35773278 | Thermodynamic examination of 1- to 5-nt purine bulge loops in RNA and DNA constructs |
Q38677817 | Thermodynamics and kinetics of RNA tertiary structure formation in the junctionless hairpin ribozyme |
Q34362185 | Thiophilic metal ion rescue of phosphorothioate interference within the Tetrahymena ribozyme P4-P6 domain |
Q28315032 | Three metal ions at the active site of the Tetrahymena group I ribozyme |
Q27627193 | Two crystal forms of helix II of Xenopus laevis 5S rRNA with a cytosine bulge |
Q26822427 | Understanding nucleic acid-ion interactions |
Q85194981 | Using Analytical Ultracentrifugation (AUC) to Measure Global Conformational Changes Accompanying Equilibrium Tertiary Folding of RNA Molecules |
Q27674728 | Visualizing Group II Intron Catalysis through the Stages of Splicing |
Q74450662 | Visualizing metal-ion-binding sites in group I introns by iron(II)-mediated Fenton reactions |