The structural basis of ribosome activity in peptide bond synthesis.
By P. Nissen, Jeffrey Hansen, N. Ban, P. Moore, T. Steitz. Science, 2000
2,223 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/86586d2e52615d5bc7b54d21f828c12c31869d80
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In Genetics
- James J. Collins
- Michael A. Kohanski
- Xiang-Jun Lu
- Kalle Kipper
- Wilma K. Olson
- Gernot G. Presting
- M. Siomi
- A. Ishizuka
In Molecular Biology
- Xiang-Jun Lu
- Wilma K. Olson
- James J. Collins
- Michael A. Kohanski
- Daniel J. Dwyer
- H. Siomi
- F. Hartl
- Kalle Kipper
Citations in the corpus
- Studies on the structure-function relationship of the bacterial ribosome (2004, background): “This means that the tetrahedral intermediate analogue, which was used in the co-crystallization of the 50S subunits (Nissen et al. 2000a), is not a realistic creation, and that the A2451 cannot act as a general acid in proton donation.”
- Identification of conserved regions in the plastid genome: implications for DNA barcoding and biological function (2006, background): “Indeed, p23SrV_r contains the putative peptidyl transferase activity (Nissen et al. 2000), which is stabilized by five complex three-strand interactions (Lee et al.”
- A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins. (2002, background): “L5 and L11 are eukaryotic counterparts of bacterial ribosomal proteins L18 and L5, respectively, both of which are shown to locate on the surface of the 50S large ribosomal subunit along with 5S rRNA (Nissen et al. 2000).”
- Ribosome assembly in eukaryotes. (2003, background): “Two main features are associated with modified nucleotides: (i) none of them seems important individually but globally they are believed to play a general role in RNA conformation and stabilization, (ii) they tend to be concentrated in functional rRNA regions and to fine-tune ribosome activity in tr”
- 3DNA: a software package for the analysis, rebuilding and visualization of three-dimensional nucleic acid structures. (2003, background): “The remaining ®ve examples come from other, less well-resolved ribosomal structures, rr0014 (62), rr0020 (63), rr0025 (64) and rr0052 (65), and from the 2.”
- Chapter 1. General introduction (2015, neutral): “…books Built by scientists, for scientists 12.2% 117,000 130M TOP 1%154 4,400 Chapter 1 General Introduction: Advances in Hepatic Surgery J.H.M.B. Stoot, R.J.S. Coelen, J.L.A. van Vugt and C.H.C. Dejong Additional information is available at the end of the chapter http://dx.doi.org/10.5772/54710”
- RNAmmer: consistent and rapid annotation of ribosomal RNA genes (2007, neutral): “16S 1172 (299) 1146 (299) 22 (12) 4 (4) 1237 (320) 91 (34) 23S 1197 (297) 1154 (291) 22 (13) 21 (12) 1248 (313) 94 (36) Eukaryotes (n1⁄4 13) 5S 65 (7) 46 (6) 19 (1) 0 (0) 324 (9) 278 (5) 18S 13 (4) 6 (4) 0 (0) 7 (2) 13 (6) 7 (3) 28S 13 (5) 12 (4) 0 (0) 1 (1) 19 (7) 7 (3)”
- Studies on the role of helix 69 of 23S rRNA in the factor-dependent stages of translation initiation, elongation, and termination (2011, background): “Puromycin is a mimic of the acceptor end of aminoacyl-tRNA to which a peptidyl group (or its analogue) can be transferred in the transpeptidylation reaction (Monro 1967; Monro and Marcker 1967; Green and Noller 1996; Nissen et al. 2000).”