The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Ribozyme speed limits
Open accessAbstract
The speed at which RNA molecules decompose is a critical determinant of many biological processes, including those directly involved in the storage and expression of genetic information. One mechanism for RNA cleavage involves internal phosphoester transfer, wherein the 2′-oxygen atom carries out an S N 2-like nucleophilic attack on the adjacent phosphorus center (transesterification). In this article, we discuss fundamental principles of RNA transesterification and define a conceptual framework that can be used to assess the catalytic power of enzymes that cleave RNA. We deduce that certain ribozymes and deoxyribozymes, like their protein enzyme counterparts, can bring about enormous rate enhancements.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“All of these tasks might be performed by RNA (Narlikar and Herschlag 1997;Emilsson et al. 2003), acting either alone (Strobel and Ortoleva-Donnelly 1999) or with the help of a suitably positioned metal cation or other cofactor (Shan et al. 1999(Shan et al. , 2001)).”
From Protocells and RNA Self-Replication (2018) · cites this paper as Emilsson et al. 2003
Citations
Cites
Catalysis in chemistry and enzymology
Jencks, W. P. (1969) · Medical Entomology and Zoology · Cited by 3,217
Structure and Mechanism in Protein Science
Fersht, A. (2017) · WORLD SCIENTIFIC eBooks · doi:10.1142/10574 · Cited by 2,053
Westheimer, F. H. (1987) · Science · doi:10.1126/science.2434996 · Cited by 1,711 · cited 2×
“Both the stability of phosphate esters and their chemical pliability have been suggested as foremost reasons why a phosphate ester has emerged as the backbone of choice for the molecules responsible for genetic information storage and transfer (Westheimer 1987).”
BackgroundA general purpose RNA-cleaving DNA enzyme
Santoro, S. W., & Joyce, G. F. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.9.4262 · Cited by 1,546
In Vitro Selection of Functional Nucleic Acids
Wilson, D. S., & Szostak, J. W. (1999) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.68.1.611 · Cited by 1,217
A general two-metal-ion mechanism for catalytic RNA
Steitz, T. A., & Steitz, J. A. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.14.6498 · Cited by 1,171
Raines, R. T. (1998) · Chemical Reviews · doi:10.1021/cr960427h · Cited by 938
Pseudo-rotation in the hydrolysis of phosphate esters
Westheimer, F. H. (1968) · Accounts of Chemical Research · doi:10.1021/ar50003a002 · Cited by 772
Li, Y., & Breaker, R. R. (1999) · Journal of the American Chemical Society · doi:10.1021/ja990592p · Cited by 587
Self-citationRelationship between internucleotide linkage geometry and the stability of RNA
Soukup, G. A., & Breaker, R. R. (1999) · RNA · doi:10.1017/s1355838299990891 · Cited by 549
Self-citation
Flagged first, then by citations
Research works printed but not linked: 5
- Carlson, W.D. 1976. “X-ray diffraction studies of bovine pancreatic ribonuclease-S and E. coli alkaline phosphatase.” Ph.D. thesis, Yale University, New Haven, CT.
- 1996, Angew. Chem. Int. Ed. Engl., 35, 707
- 1995, J. Chem. Soc. Perkin Trans., 2, 1203
- March, J. 1992. Acids and bases. In Advanced organic chemistry, 4th ed., pp. 248–272. John Wiley & Sons, New York.
- 1997, RNA, 3, 914
Cited by
Sorted by citations
Items 101–200 of 216
RNA targeting and cleavage by the type III-Dv CRISPR effector complex
Schwartz, E. A., Bravo, J. P. K., Ahsan, M., Macias, L. A., McCafferty, C. L., Dangerfield, T. L., Walker, J. N., Brodbelt, J. S., Palermo, G., Fineran, P. C., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47506-y · Cited by 30
Influence of Cleavage Site on Global Folding of an RNA‐Cleaving DNAzyme
Lam, J. C. F., & Li, Y. (2010) · ChemBioChem · doi:10.1002/cbic.201000144 · Cited by 29
Effect of Ribose Conformation on RNA Cleavage via Internal Transesterification
Guo, F., Yue, Z.-K., Trajkovski, M., Zhou, X., Cao, D., Li, Q., Wang, B., Wen, X., Plavec, J., Peng, Q., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b06313 · Cited by 30
Mechanistic Debris Generated by Twister Ribozymes
Breaker, R. R. (2017) · ACS Chemical Biology · doi:10.1021/acschembio.7b00010 · Cited by 28
Self-citationBreaker, R. R. (2020) · ACS Chemical Biology · doi:10.1021/acschembio.0c00214 · Cited by 28
Self-citationDNAzyme-mediated catalysis with only guanosine and cytidine nucleotides
Schlosser, K., & Li, Y. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn930 · Cited by 27
The Mechanism of RNA Strand Scission: An Experimental Measure of the Brønsted Coefficient, βnuc
Ye, J., Li, N., Dai, Q., & Piccirilli, J. A. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200605124 · Cited by 28
He, J., Zhang, D., Wang, Q., Wei, X., Cheng, M., & Liu, K. (2011) · Organic & Biomolecular Chemistry · doi:10.1039/c1ob05065f · Cited by 26
Min, D., Xue, S., Li, H., & Yang, W. Y. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm394 · Cited by 24
Kostenbader, K., & York, D. M. (2019) · RNA · doi:10.1261/rna.071944.119 · Cited by 23
Coupling of Fast and Slow Modes in the Reaction Pathway of the Minimal Hammerhead Ribozyme Cleavage
Radhakrishnan, R. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.104661 · Cited by 23
Studying the Key Intermediate of RNA Autohydrolysis by Cryogenic Gas‐Phase Infrared Spectroscopy
Greis, K., Kirschbaum, C., Taccone, M. I., Götze, M., Gewinner, S., Schöllkopf, W., Meijer, G., von Helden, G., & Pagel, K. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202115481 · Cited by 22
Cleavage of RNA by an amphiphilic compound lacking traditional catalytic groups
Kovalev, N. A., Medvedeva, D. A., Аркадьевна, З. М., & Vlassov, V. V. (2007) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2007.10.003 · Cited by 22
Nucleic Acid Enzymes (Ribozymes and Deoxyribozymes): In Vitro Selection and Application
Silverman, S. K. (2008) · Wiley eBooks · doi:10.1002/9780470048672.wecb406 · Cited by 25
Mechanisms of catalytic RNA molecules
Alonso, D., & Mondragón, A. (2021) · Biochemical Society Transactions · doi:10.1042/bst20200465 · Cited by 21
Weinberg, C. E., Weinberg, Z., & Breaker, R. R. (2016) · RNA Biology · doi:10.1080/15476286.2016.1251002 · Cited by 21
Self-citationScaling Catalytic Contributions of Small Self‐Cleaving Ribozymes
Egger, M., Bereiter, R., Mair, S., & Micura, R. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202207590 · Cited by 20
Photooxidation of Nucleic Acids on Metal Oxides: Physicochemical and Astrobiological Perspectives
Shkrob, I. A., Marin, T. W., Adhikary, A., & Sevilla, M. D. (2011) · The Journal of Physical Chemistry C · doi:10.1021/jp110682c · Cited by 23
Early evolution of efficient enzymes and genome organization
Szilágyi, A., Kun, Á., & Szathmáry, E. (2012) · Biology Direct · doi:10.1186/1745-6150-7-38 · Cited by 18
Link, K. H., Guo, L., & Breaker, R. R. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl643 · Cited by 19
Self-citationAnalysis on a Cooperative Pathway Involving Multiple Cations in Hammerhead Reactions
Takagi, Y., Inoue, A., & Taira, K. (2004) · Journal of the American Chemical Society · doi:10.1021/ja031991u · Cited by 18
Model for the Functional Active State of the TS Ribozyme from Molecular Simulation
Gaines, C. S., & York, D. M. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201705608 · Cited by 17
Cas6 processes tight and relaxed repeat RNA via multiple mechanisms: A hypothesis
Sefcikova, J., Roth, M. O., Yu, G., & Li, H. (2017) · BioEssays · doi:10.1002/bies.201700019 · Cited by 17
Probing Metal-Dependent Phosphate Binding for the Catalysis of the 17E DNAzyme
Moon, W. J., Huang, P. J., & Liu, J. (2021) · Biochemistry · doi:10.1021/acs.biochem.1c00091 · Cited by 17
Cellular Small Molecules Contribute to Twister Ribozyme Catalysis
Messina, K. J., & Bevilacqua, P. C. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b06065 · Cited by 16
Hydrated metal ion as a general acid in the catalytic mechanism of the 8–17 DNAzyme
Cortés-Guajardo, C., Rojas-Hernández, F., Paillao-Bustos, R., & Cepeda‐Plaza, M. (2021) · Organic & Biomolecular Chemistry · doi:10.1039/d1ob00366f · Cited by 16
Lain, L., Lönnberg, H., & Lönnberg, T. (2013) · Chemistry - A European Journal · doi:10.1002/chem.201301711 · Cited by 16
The Ribosome: A Molecular Machine Powered by RNA
Trappl, K., & Polacek, N. (2011) · Royal Society of Chemistry eBooks · doi:10.1039/9781849732512-00253 · Cited by 16
Cleavage mediated by the P15 domain of bacterial RNase P RNA
Kikovska, E., Wu, S., Mao, G., & Kirsebom, L. A. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1001 · Cited by 15
Theoretical Examination of Two Opposite Mechanisms Proposed for Hepatitis Delta Virus Ribozyme
Wei, K., Liu, L., Yuhui Cheng, A., Fu, Y., & Guo, Q. (2007) · The Journal of Physical Chemistry B · doi:10.1021/jp070120u · Cited by 15
Harp, J. M., Lybrand, T. P., Pallan, P. S., Coates, L., Sullivan, B., & Egli, M. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac577 · Cited by 14
Dissociative Transition State in Hepatitis Delta Virus Ribozyme Catalysis
Weissman, B. P., Ekesan, Ş., Lin, H.-C., Gardezi, S., Li, N., Giese, T. J., McCarthy, E., Harris, M. E., York, D. M., & Piccirilli, J. A. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c10079 · Cited by 14
Activation of the glmS Ribozyme Nucleophile via Overdetermined Hydrogen Bonding
Bingaman, J. L., Gonzalez, I. Y., Wang, B., & Bevilacqua, P. C. (2017) · Biochemistry · doi:10.1021/acs.biochem.7b00662 · Cited by 14
Non-Enzymatic Template-Directed Recombination of RNAs
Nechaev, S. Y., Lutay, A., Vlassov, V. V., & Аркадьевна, З. М. (2009) · International Journal of Molecular Sciences · doi:10.3390/ijms10041788 · Cited by 14
Srinivas, K. A., Chiuman, W., & Li, Y. (2006) · Chemical Communications · doi:10.1039/b604682g · Cited by 14
Probing the Catalytic Triad of an Archaeal RNA Splicing Endonuclease
Calvin, K., Xue, S., Ellis, C. D., Mitchell, M., & Li, H. (2008) · Biochemistry · doi:10.1021/bi801141q · Cited by 13
The Universal Plausibility Metric (UPM) & Principle (UPP)
Abel, D. L. (2009) · Theoretical Biology and Medical Modelling · doi:10.1186/1742-4682-6-27 · Cited by 13
Staroseletz, Y., Miroshnichenko, S. K., Patutina, O., Bichenkova, E. V., Amirloo, B., Heyman, T., Chiglintseva, D., & Аркадьевна, З. М. (2021) · Molecules · doi:10.3390/molecules26061732 · Cited by 14
Pioneering role of RNA in the early evolution of life
Muñoz‐Velasco, I., Cruz-González, A., Hernández-Morales, R., Campillo-Balderas, J. A., Cottom-Salas, W., Jácome, R., & Vázquez-Salazar, A. (2024) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2024-0028 · Cited by 12
DNA-catalyzed glycosylation using aryl glycoside donors
Hesser, A. R., Brandsen, B. M., Walsh, S. M., Wang, P., & Silverman, S. K. (2016) · Chemical Communications · doi:10.1039/c6cc04329a · Cited by 11
Understanding in-line probing experiments by modeling cleavage of nonreactive RNA nucleotides
Mlýnský, V., & Bussi, G. (2017) · RNA · doi:10.1261/rna.060442.116 · Cited by 11
Trujillo, A. J., Myers, J. M., Fayazi, Z. S., Butler, M. C., & Sullivan, J. M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-27378-1_20 · Cited by 11
Lihanova, Y., & Weinberg, C. E. (2021) · RNA Biology · doi:10.1080/15476286.2021.1874706 · Cited by 11
Non-enzymatic recombination of RNA: Ligation in loops
Staroseletz, Y., Nechaev, S., Bichenkova, E. V., Bryce, R. A., Watson, C., Vlassov, V. V., & Аркадьевна, З. М. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.10.019 · Cited by 12
White, N. A., Sumita, M., Márquez, V. E., & Hoogstraten, C. G. (2018) · RNA · doi:10.1261/rna.067579.118 · Cited by 11
An Integrated Picture of HDV Ribozyme Catalysis
Golden, B. L., Hammes‐Schiffer, S., CAREY, P. R., & Bevilacqua, P. C. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4954-6_8 · Cited by 10
Ren, M., Cheng, Y., Duan, Q., & Zhou, C. (2019) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.9b00059 · Cited by 10
Kirsebom, L. A., & Ciesiołka, J. (2014) · doi:10.1002/9783527647064.ch13 · Cited by 10
Kläge, D., Müller, E., & Hartig, J. S. (2023) · RNA Biology · doi:10.1080/15476286.2023.2296203 · Cited by 9
Energy landscapes of homopolymeric RNAs revealed by deep unsupervised learning
Ramachandran, V., & Potoyan, D. A. (2024) · Biophysical Journal · doi:10.1016/j.bpj.2024.04.003 · Cited by 10
Catalytic mechanisms of the 8–17 and 10–23 DNAzymes: shared mechanistic strategies
Muñoz-González, M., Silva-Galleguillos, V., Parra-Meneses, V., Aguilar, R., & Cepeda‐Plaza, M. (2025) · Organic & Biomolecular Chemistry · doi:10.1039/d5ob00387c · Cited by 8
Investigation of the pKa of the Nucleophilic O2′ of the Hairpin Ribozyme
Veenis, A. J., Li, P., Soudackov, A. V., Hammes‐Schiffer, S., & Bevilacqua, P. C. (2021) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.1c06546 · Cited by 7
The Small Ribozymes: Common and Diverse Features Observed Through the FRET Lens
Walter, N. G., & Perumal, S. (2008) · Springer series in biophysics · doi:10.1007/978-3-540-70840-7_5 · Cited by 8
Olzog, V. J., Gärtner, C., Stadler, P. F., Fallmann, J., & Weinberg, C. E. (2021) · RNA Biology · doi:10.1080/15476286.2021.1999105 · Cited by 8
Who stole the proton? Suspect general base guanine found with a smoking gun in the pistol ribozyme
Ekesan, Ş., & York, D. M. (2022) · Organic & Biomolecular Chemistry · doi:10.1039/d2ob00234e · Cited by 8
The role of Na + in catalysis by the 8–17 DNAzyme
Parra-Meneses, V., Rojas-Hernández, F., & Cepeda‐Plaza, M. (2022) · Organic & Biomolecular Chemistry · doi:10.1039/d2ob01075e · Cited by 8
Pb 2+ ‐induced Cleavage of RNA
Kirsebom, L. A., & Ciesiołka, J. (2005) · doi:10.1002/9783527619504.ch13 · Cited by 8
Model for the Functional Active State of the TS Ribozyme from Molecular Simulation
Gaines, C. S., & York, D. M. (2017) · Angewandte Chemie · doi:10.1002/ange.201705608 · Cited by 7
Lönnberg, H. (2022) · The Chemical Record · doi:10.1002/tcr.202200141 · Cited by 8
Kersten, C., Archambault, P., & Köhler, L. P. (2024) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.4c00520 · Cited by 7
Emerging Mechanisms of Metal-Catalyzed RNA and DNA Modifications
Ahsan, M., Pindi, C., & Palermo, G. (2025) · Annual Review of Physical Chemistry · doi:10.1146/annurev-physchem-082423-030241 · Cited by 9
Takeuchi, K., Yanagisawa, H., Kurosawa, Y., Iida, Y., Kawai, K., & Fujimaki, S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264541 · Cited by 7
Lakin, M. R., Brown, C. W., Horwitz, E. K., Fanning, M. L., West, H. E., Stefanović, D., & Graves, S. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110986 · Cited by 7
Elucidating the underlying mechanism of mechanical stress-induced impact on mRNA-LNP structure
Jensen, E. L., Chi, Y., Edwards, R., Wang, H. L., Matthessen, R., Goffin, B., Hees, S. V., Friese, O. V., & Pottelberge, R. V. (2025) · Scientific Reports · doi:10.1038/s41598-025-21880-z · Cited by 6
Pottelberge, R. V., Matthessen, R., Salem, S., Goffin, B., Oien, N. L., Bharti, P., & Ripley, D. (2024) · Journal of Pharmaceutical Sciences · doi:10.1016/j.xphs.2024.10.012 · Cited by 6
The Role of snRNAs in Spliceosomal Catalysis
Valadkhan, S. (2013) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-381286-5.00006-8 · Cited by 6
Rapid Kinetics of Pistol Ribozyme: Insights into Limits to RNA Catalysis
Yoon, S., Ollie, E. W., York, D. M., Piccirilli, J. A., & Harris, M. E. (2023) · Biochemistry · doi:10.1021/acs.biochem.3c00160 · Cited by 6
Prediction of hammerhead ribozyme intracellular activity with the catalytic core fingerprint
Gabryelska, M., Wyszko, E., Szymański, M., Popenda, M., & Barciszewski, J. (2013) · Biochemical Journal · doi:10.1042/bj20121761 · Cited by 6
SYBR green one-step qRT-PCR for the detection of SARS-CoV-2 RNA in salivaPreprint
Ganguly, D. R., Rottet, S., Yee, S., Hee, W. Y., Smith, A., Khin, N. C., Millar, A. A., & Fahrer, A. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.29.109702 · Cited by 5
Enhanced hammerhead ribozyme turnover rates: Reevaluating therapeutic space for small catalytic RNAs
Myers, J. M., & Sullivan, J. M. (2024) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2024.102431 · Cited by 5
Lain, L., Lönnberg, H., & Lönnberg, T. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob00400d · Cited by 5
Mapping the Chemical Space of the RNA Cleavage and Its Implications for Ribozyme Catalysis
Mlýnský, V., Kührová, P., Jurečka, P., Šponer, J., Otyepka, M., & Banáš, P. (2017) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.7b09129 · Cited by 5
Joseph, N. N., Roy, R. N., & Steitz, T. A. (2020) · Journal of Computational Chemistry · doi:10.1002/jcc.26179 · Cited by 5
Mammalian Self-Cleaving Ribozymes
Lupták, A., & Szostak, J. W. (2007) · Royal Society of Chemistry eBooks · doi:10.1039/9781847557988-00123 · Cited by 5
Small Molecule Rescue and Glycosidic Conformational Analysis of the Twister Ribozyme
Messina, K. J., Kierzek, R., Tracey, M. P., & Bevilacqua, P. C. (2019) · Biochemistry · doi:10.1021/acs.biochem.9b00742 · Cited by 5
Inhibition of HIV-1 gp41 expression with hammerhead ribozymes
Fedoruk‐Wyszomirska, A., Szymański, M., Głodowicz, P., Gabryelska, M., Wyszko, E., Estrin, W. J., & Barciszewski, J. (2015) · Biochemical Journal · doi:10.1042/bj20150398 · Cited by 4
Long-Term Room Temperature Storage of Dry Ribonucleic Acid for Use in RNA-Seq Analysis
Li, Q., Wang, X., Liu, X., Liao, Q., Sun, J., He, X., Yang, T., Yin, J., Jia, J., Li, X., et al. (2017) · Biopreservation and Biobanking · doi:10.1089/bio.2017.0024 · Cited by 4
The Mechanism of RNA Strand Scission: An Experimental Measure of the Brønsted Coefficient, βnuc
Ye, J., Li, N., Dai, Q., & Piccirilli, J. A. (2007) · Angewandte Chemie · doi:10.1002/ange.200605124 · Cited by 4
Structure and Mechanism of the glmS Ribozyme
Strauss-Soukup, J. K., & Soukup, G. A. (2008) · Springer series in biophysics · doi:10.1007/978-3-540-70840-7_6 · Cited by 4
Kavita, K., Narunsky, A., Mohsen, J. J., Mahadeshwar, I., Mohsen, M. G., Chang, Y.-S., & Breaker, R. R. (2025) · Nature Communications · doi:10.1038/s41467-025-62815-6 · Cited by 3
Self-citationTheoretical Studies of the Self Cleavage Pistol Ribozyme Mechanism
Serrano-Aparicio, N., Świderek, K., Tuñón, I., Moliner, V., & Bertrán, J. (2021) · Topics in Catalysis · doi:10.1007/s11244-021-01494-1 · Cited by 3
Small Interfering RNA Drug Delivery System in Cancer
Nayak, P., & Charyulu, R. (2024) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/2847 · Cited by 3
Yau, E. H., Taggart, R. T., Zuber, M., Trujillo, A. J., Fayazi, Z. S., Butler, M. C., Sheflin, L. G., Breen, J. B., Yu, D., & Sullivan, J. M. (2019) · Translational Vision Science & Technology · doi:10.1167/tvst.8.6.28 · Cited by 2
Recombination: RNA — A Powerful Tool for Recombination and Regulated Expression of Genes
Müller, D., & Ståhl, U. (2005) · Springer eBooks · doi:10.1007/3-540-27043-4_2 · Cited by 3
Computational Modeling Methods for 3D Structure Prediction of Ribozymes
Ghosh, P., Nithin, C., Joshi, A., Stefaniak, F., Wirecki, T. K., & Bujnicki, J. M. (2021) · Wiley eBooks · doi:10.1002/9783527814527.ch33 · Cited by 3
Harnessing thiophilic cadmium to enhance 8–17 DNAzyme activity in cascade oligo biosensors
Sadraeian, M., Maleki, R., Fu, L., Lin, G., Zhou, J., Jin, D., & Reimers, J. R. (2025) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2025.117816 · Cited by 2
Nonenzymatic and Metal-Ion-Dependent RNA Cleavage, and RNase Models
Lönnberg, H. (2011) · Nucleic acids and molecular biology · doi:10.1007/978-3-642-21078-5_14 · Cited by 2
Catalytic Mechanism of the HDV Ribozyme
Koo, S. C., Novak, T., & Piccirilli, J. A. (2007) · Royal Society of Chemistry eBooks · doi:10.1039/9781847557988-00092 · Cited by 2
The glmS Ribozyme and Its Multifunctional Coenzyme Glucosamine‐6‐phosphate
Strauss-Soukup, J. K. (2021) · doi:10.1002/9783527814527.ch4 · Cited by 2
Hipotetyczna rola autokatalitycznych właściwości kwasów nukleinowych w procesie biogenezy
Adamala, K. P., & Pikuła, S. (2004) · Cited by 1
Roy, S. (2008) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont) · Cited by 1
Yoon, S., & Harris, M. E. (2021) · Biochemistry · doi:10.1021/acs.biochem.1c00489 · Cited by 1
Elucidation of Ribozyme Mechanisms at the Example of the Pistol Ribozyme
Falschlunger, C., Leiter, J. M. E., & Micura, R. (2021) · doi:10.1002/9783527814527.ch29 · Cited by 1
Ramachandran, V., & Potoyan, D. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.10.561750 · Cited by 1
Kang, T.-W. P. (2009) · OhioLink ETD Center (Ohio Library and Information Network)
Functional quality control for human blood-based gene expression products
Frahm, S. (2012) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3dn442f
The Structure and Action of glmS Ribozymes
Link, K. H., & Breaker, R. R. (2007) · Royal Society of Chemistry eBooks · doi:10.1039/9781847557988-00134
Self-citationKellerman, D. L. (2016) · OhioLink ETD Center (Ohio Library and Information Network)
Phosphoryl‐Transfer Reaction in RNA under Alkaline Conditions
Acosta‐Silva, C., Bertrán, J., Branchadell, V., & Oliva, A. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201802332
Metadata
- Authors
- EMILSSON, G. M., NAKAMURA, S., ROTH, A., & BREAKER, R. R.
- Affiliations
- Yale University (US)
- Corresponding author
- BREAKER, RONALD R.
- Venue
- RNA
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2003-07-17
- Volume
- 9
- Issue
- 8
- Pages
- 907-918
- ISSN
- 1355-8382 (ISSN-L)
- 1469-9001
- PMC
- PMC1370456
- OpenAlex
- W2160498409
- Cited by
- 216
- References
- 70
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 11 · 2023: 6 · 2022: 11 · 2021: 18 · 2020: 7 · 2019: 16 · 2018: 9 · 2017: 16 · 2016: 8 · 2015: 6 · 2014: 5 · 2013: 10 · 2012: 5
- FWCI
- 0.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- RNA (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- David and Lucile Packard Foundation
- National Institutes of Health (5r01gm057500-03)
- National Institute of General Medical Sciences (GM559343, GM57500)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Physical Sciences › Chemistry › Organic Chemistry › Physical Organic Chemistry and Reaction Kinetics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Keywords
- ribozymes, deoxyribozymes, RNA cleavage, catalytic rate enhancement
- MeSH terms
- Esterification, Hydrolysis, Oxygen, RNA, RNA, Catalytic, Hydroxyl Radical
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review