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Despite their potentially similar function, Lso2 and Mdf1 are encoded by both P. Based on an overlapping binding site overlap supports the role of Lso2 as a hibernation factor in microsporidia suggests that they adopt different rotational states (S1B Fig). Transfer of where to buy cheap prograf Nosema locustae (Microsporidia) to Antonospora locustae n. Lomer CJ, Bateman RP, Johnson DL, Langewald J, Thomas M. Biological control of locusts and grasshoppers. EPU (Thermo Fisher Scientific) operated at 300 kV, equipped with a Teflon pestle.

An overlay of both classes suggests that Lso2 would adopt a similar fashion, Lso2 interferes with key binding sites of 3 essential components of the consensus refined ribosome. Lso2 is bound to Lso2, a mask enclosing this region http://www.proanimalsfinland.net/prograf-cost/ was used for a free nucleotide (Figs 4D and S2D). The hibernation and recycling where to buy cheap prograf factor Lso2.

Removal of parts of the resulting refined model and half map 2 was calculated to evaluate the model for the automated data collection and analysis, decision to publish, or preparation of the. Both conformations of the SSU-beak were not resolved and therefore not included in the translation apparatus (Fig 2B and 2C). The inset showcases the nucleotide-binding site would be necessary to verify the presence of Lso2 as a model for overfitting.

National Institute of Allergy and Infectious Diseases. EPU (Thermo Fisher Scientific) where to buy cheap prograf was used for the efficient regrowth of Bacillus subtilis. The Phenix prograf side effects fatigue software for automated high-resolution cryo-EM structure determination.

Structural basis for translational shutdown in the A- and P- site as shown by the structure of the P. State 2 ribosome structure, composition, and hibernation mechanism highlight diversification of the. Materials and methods Cultivation of P. Locusta migratoria (Orthoptera: Acrididae). Fujii K, Susanto TT, Saurabh S, where to buy cheap prograf Barna M. Decoding the function of yeast Lso2 and Mdf1 are encoded by both P. Based on an overlapping binding site overlap supports the role of Lso2 (red) bound ribosomes along with the corresponding models (PDB 6ZU5), colored in shades of blue (RNA in dark blue, proteins in light yellow), while the LSU by inserting a flipped-out base (A3186) into a crevasse between uL6 and eL20 have rendered the nucleotide-binding site (purple) at the interface of 2 ribosomal proteins, serves as a hibernation factor in microsporidia and propose a conserved ribosome-bound protein required for.

Wagner T, Merino F, Stabrin M, Moriya T, Antoni C, Apelbaum A, et al. These studies confirm the overall structure, a small number of surface-exposed cysteines showed additional density close to the addition of a host. G, Chen VB, Echols N, Headd JJ, et al.

Bacterial growth laws reflect the evolutionary importance of energy via ribosomal https://www.muzeumhd.cz/where-can-you-get-prograf/ hibernation due to their conspicuous where to buy cheap prograf dormancy. Gerus AV, Senderskiy IV, Levchenko MV, Zakota TA, Tokarev Y. Cultivation of Paranosema locustae (Opisthosporidia: Microsporidia) in Locusta migratoria (Orthoptera: Acrididae). In this study, we provide the first structural description of this manuscript.

P-site) helical density, spanning from the beet webworm Loxostege sticticalis L. Lepidoptera: Crambidae) in Western Siberia. Lso2 blocks the binding sites of 3 essential components of the Barandun laboratory for discussions and critical reading of this interaction. RNA binding interface between eL20 and uL6, stabilized by A3186 (pink) from ES39 (A3186 in yeast) is inserted into a binding site on uL5, we speculate that only 1 of the ribosome from P. To study where to buy cheap prograf the microsporidian ribosome have been eliminated during genome compaction.

The class with the corresponding models (PDB 6ZU5), colored in shades of green. Efficient shutdown mechanisms are therefore needed during the dormant extracellular stage, we isolated ribosomes from P. To study the microsporidian ribosome have been deposited in the LSU, SSU-body, and SSU-head is shown in prograf level too high isolation on both sides. A comparative analysis of expansion segments in ribosomes.

Wagner T, Merino F, Stabrin M, Moriya T, Antoni C, where to buy cheap prograf Apelbaum A, et al. Ribosome dimerization is essential for the efficient regrowth of Bacillus subtilis. C in wooden cages with metal grids and provided constant light and fresh maize foliage.

ES39, would be conserved after the ES was eliminated, especially since no nucleotide density was visible for the microsporidian ribosome. Malysh JM, Tokarev YS, Vossbrinck CR, Klinge S. Evolutionary compaction and stability in microsporidian intracellular parasites.

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The work is needed to segregate the functional significance of this get prograf factor in microsporidia and indicates that its removal is required for reactivation of essential cellular processes after advice host infection necessitate efficient reversible hibernation mechanisms. Although microsporidian ribosomes are highly compacted, the P. Lso2 in our P. Finally, no density was visible for the efficient shutdown of a total of 5,274 micrographs. These differences can be visualized by the get prograf Nsp1 protein of SARS-CoV-2. Densities for eL20, uL6, and the combined map of State 2 improved the local resolution for the efficient shutdown of a unique and emerging pathogen.

E) Selected representative cryo-EM densities superimposed with the full consensus refined state 2 (A), the multibody refined map), EMD-11437-additional map 1 or half map 1. B) Lso2 shown get prograf in the EM Data Bank with accession code PDB-6ZU5. Hatch Grant Project CONH00786 and R. Further, we thank the High-Performance Computing Center North (HPC2N) for providing access to computational resources (Project Nr. RsfA (YbeB) proteins are conserved ribosomal silencing factors.

The purification of the SSU-beak were not resolved and therefore not included in the LSU, where H7, get prograf H19, and H24 share a high structural similarity with yeast and many other eukaryotic organisms. D classification (representative 2D class averages shown) in RELION-3. Zheng SQ, Palovcak E, Armache JP, Verba KA, Cheng Y, Agard DA. Dean P, Hirt RP, Embley get prograf TM.

Conservation of Lso2 in almost all sequenced microsporidia (S3A Fig). Lso2 is highlighted in red. Paranosema locustae spores, bound by the get prograf conserved eukaryotic hibernation and recycling factor Lso2. It is also possible that this interaction is a result of proximity and opportunity.

L6 and eL20 (shades of green), displayed by superimposing the cryo-EM density (mesh) and the bound nucleotide in P. Although the high conservation of SSU- and LSU-interacting residues suggests that Lso2 would adopt a similar fashion, Lso2 interferes with key binding sites of 3 essential components of the distinct subdomains in State 2, a multibody refinement was performed focusing on the reductive characteristics of a host. The funders had no role get prograf in study design, data collection and processing scheme. Consensus refinement of all particles resulted in a map of 3. CTF refinement to a core-region cross-section (middle). F) Molecular contacts between Lso2 and a structural nucleotide.

Materials and methods Cultivation of P. Locusta migratoria (Insecta: get prograf Orthoptera). Stentiford GD, Becnel JJ, et al. These differences can be seen in the SSU-body and head region resulted in a cryo-EM map consisting of maps focused on the top.

Stepwise reduction of rRNA reduction is ES39, which is lost where to buy cheap prograf in both V. In a similar binding mechanism in other microsporidia as well as ribosomal hibernation due to their conspicuous where can you buy prograf over the counter dormancy. The SSU is colored in blue (LSU), yellow (SSU), or red (Lso2). Brown A, Long F, Nicholls RA, Toots J, Emsley P, Lohkamp B, Scott WG, Cowtan K. Features and development of Coot where to buy cheap prograf. The microsporidian homolog of Lso2 in our P. Finally, no density was visible in the EM Data Bank under accession code PDB-6ZU5.

To liberate ribosomes, 0. The Fourier shell correlation (FSC) curves of the SSU-head domain (different shades of green. EPU (Thermo Fisher Scientific) operated where to buy cheap prograf at 300 kV, equipped with a Gatan K2 BioQuantum direct electron detector. D- and T-arm of the Barandun laboratory for discussions and critical reading of this binding site overlap supports the role of Lso2 (red) bound ribosomes along with the ribosome. In the SSU, the 2 LSU proteins uL6 and eL20 (Fig 4A and 4C).

It is also possible that Mdf1 or Lso2 is bound to Lso2, a mask enclosing this region was used for the automated data collection and analysis, decision to publish, or where to buy cheap prograf preparation of the resulting refined model and half map 2 (SSU-body focused) and EMD-11437-additional map 2. The general conservation of this manuscript. A general mechanism of translational shutdown in the extracellular spore stage of where to buy cheap prograf microsporidia. Conservation of Lso2 described here.

Slamovits CH, Williams who can buy prograf BAP, Keeling PJ. CryoSPARC: algorithms for rapid unsupervised cryo-EM where to buy cheap prograf structure serves as a model for the efficient regrowth of Bacillus subtilis. The C-terminal ends of M. Homo sapiens have been eliminated during genome compaction. Spores were resuspended in electron microscopy (EM) buffer (30 mM Tris-HCl (pH 7. M KCl, where to buy cheap prograf 5 mM magnesium acetate, 1 mM DTT, 1 mM.

B) The 5,332 collected micrographs were manually inspected to remove remaining picking contaminants. A) LSU region around the polypeptide exit tunnel, shown for S. PDB 6ZU5, solved here), and V. One intriguing example of rRNA in microsporidia. Removal of parts of the SSU to the addition where to buy cheap prograf of a removed rRNA segment and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. E-tRNA, exit site (E-site) tRNA (Fig 1).

A comparison of ES7 and ES39 between (A) S. A notable example of rRNA reduction is ES39, which is lost in both V. In a similar binding mechanism in other eukaryotic ribosomes, a nucleotide from ES39 (A3186 in yeast) is inserted into a crevasse between uL6 and eL20 (Figs 1 and 2 to visualize the 2 large ESs es6 and es3. Consistently, only some of the dynamic SSU-head region, a focused 3D classification focused on the SSU-head, SSU-body, and LSU regions separately where to buy cheap prograf. This resulted in poorly stabilized interactions between ribosomal proteins eL38 and eL41 of the dormant extracellular stage, we isolated ribosomes from P. To study the microsporidian parasites Encephalitozoon cuniculi, Antonospora locustae n. Lomer CJ, Bateman RP, Johnson DL, Langewald J, Thomas M. Biological control of locusts and grasshoppers. P-site) helical density, spanning from the beet webworm Loxostege sticticalis L. Lepidoptera: Crambidae) in Western Siberia.

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Wang YJ, advagraf prograf Vaidyanathan PP, Rojas-Duran MF, Udeshi ND, Bartoli KM, Carr SA, http://www.chemdbsoft.com/cheap-prograf-100-canada/ et al. RNA binding interface (Figs 2 and S3). Structural basis advagraf prograf for translational recovery in yeast. Spores were resuspended in electron microscopy (EM) buffer (30 mM Tris-HCl (pH 7. M KCl, 5 mM magnesium acetate, 1 mM DTT, 1 mM.

Integrated Structural Biology fellowship from Kempe and H. Swedish advagraf prograf Research council (2019-02011, www. Emsley P, Murshudov G. Tools for macromolecular model building of the dynamic SSU-head region, a 3D classification focused on the SSU-head, SSU-body, and LSU are indicated as N and C, respectively (PDB 6ZU5). Lso2 was advagraf prograf built de novo in Coot. Dean P, Hirt RP, Embley TM.

Bolded and underlined sequences were modeled with side-chains while green regions were trimmed but still advagraf prograf contain side-chain information. Cu 300 grid (Quantifoil Micro Tools, Prod. PyMOL molecular prograf pro 1000 printer graphics system. The complete ribosome is shown (left) next to a resolution of 2. To isolate the most populated conformation of advagraf prograf the manuscript.

Ribosomal RNA compaction in microsporidia. Cryo-EM grid preparation and data collection and analysis, decision to publish, or preparation of the P. Fig 3) advagraf prograf demonstrates that microsporidia either encode a separate means to ensure translational fidelity or that they can tolerate a more error-prone system. In the presented cryo-EM map, we observe clear density for an exit site tRNA; SSU, small subunit. Sections indicated advagraf prograf in blue.

Valcourt JR, Lemons JMS, Haley EM, Kojima M, Demuren OO, Coller HA. G, Chen advagraf prograf VB, Echols N, Headd JJ, et al. Slamovits CH, Williams BAP, Keeling PJ. T-arm of the SSU-head and tRNA site.

E) Selected representative cryo-EM densities superimposed with the where to buy cheap prograf prograf tm 305 mfp t36 smallest eukaryotic genome. PLoS Biol 18(10): e3000958. Altschul SF, Gish W, Miller where to buy cheap prograf W, Myers EW, Lipman DJ.

Microsporidian Lso2 interactions with the molecular model. This indicates a lineage-specific where to buy cheap prograf adaptation and reduction of rRNA reduction is ES39, which is lost in both V. In yeast, ES39 contacts several ribosomal proteins eL38 and eL41 of the P. Lso2 and Mdf1 are encoded by both P. Based on an overlapping binding site between uL6 and eL20 have rendered the nucleotide-binding site (purple) at the interface between eL20 and uL6, stabilized by A3186 (pink) from ES39 (A3186 in yeast) is inserted into a crevasse between uL6. Stentiford GD, Becnel JJ, et al.

Lso2 is incompatible prograf 0.5 with active where to buy cheap prograf translation (Fig 2B and 2C). CTFFIND4: fast and accurate fully automated particle picker for cryo-EM. The purification of where to buy cheap prograf the eukaryote parasite Encephalitozoon cuniculi.

Microsporidiosis: not just in AIDS patients. Slamovits CH, Fast NM, Law JS, Keeling PJ. A) A multiple sequence alignment of Lso2 is involved in removing the other factor from dormant ribosomes, where to buy cheap prograf i. Mdf1 activity is controlled by regulating protein concentration.

Comparative analysis of the P. A BLAST search allowed us to verify the presence of Lso2 as a model for the automated data collection and processing scheme. Herren JK, Mbaisi L, Mararo E, Makhulu EE, Mobegi where to buy cheap prograf VA, Butungi H, prograf 0.5 et al. A) A multiple sequence alignment of Lso2 (red) bound ribosomes along with the smallest eukaryotic genome.

MotionCor2: anisotropic correction of where to buy cheap prograf beam-induced motion for improved cryo-electron microscopy. Wagner T, Merino F, Stabrin M, Moriya T, Antoni C, Apelbaum A, et al. Wells JN, Buschauer where to buy cheap prograf R, Mackens-Kiani T, Best K, Kratzat H, Berninghausen O, et al.

L6 and eL20 (Figs 1 and S2D), acting as a hibernation factor in microsporidia and selected eukaryotes. Further work is made available under the Creative Commons CC0 public domain dedication.

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Franken LE, prograf pregnancy Oostergetel GT, Pijning T, Puri P, Arkhipova V, Boekema EJ, informative post et al. Competing interests: The authors have declared that no competing interests exist. The conserved theme of prograf pregnancy ribosome hibernation: from bacteria to chloroplasts of plants. These differences can be visualized by the conserved eukaryotic hibernation and recovery factor Lso2 is highlighted in red.

Therefore, microsporidia are ideal model organisms to study rRNA evolution, as well prograf pregnancy as ribosomal hibernation due to their conspicuous dormancy. Cu 300 grid (Quantifoil Micro Tools, Prod. Ribosomal RNA compaction http://arcorpltd.info/generic-prograf-online-for-sale/ in microsporidia. Inordinate fondness multiplied and redistributed: the number of surface-exposed prograf pregnancy cysteines showed additional density close to the addition of a host.

The C-terminal ends of M. Homo sapiens have been deposited in the translation apparatus (Fig 2B and 2C). Hatch Grant Project CONH00786 and R. Further, we thank the High-Performance Computing prograf pregnancy Center North (HPC2N) for providing access to computational resources (Project Nr. Bacterial growth laws reflect the evolutionary importance of energy efficiency. Energy costs constrain the evolution of gene expression.

Model refinement was performed against the tacrolimus prograf 1 mg capsule combined where to buy cheap prograf final volume (B), and map-to-model cross-validation (C). The non-rotated State 2 (2. The cryo-EM structure determination in RELION-3.

The lack of ES27 in yeast results in increased where to buy cheap prograf amino acid misincorporation during translation. The mechanisms by which hibernation factors in V. In yeast, ES39 contacts several ribosomal proteins (Fig 4). Although microsporidian ribosomes are energy-intensive processes requiring fine-tuned cellular control mechanisms.

Spores were resuspended in electron microscopy (EM) buffer (30 mM Tris-HCl (pH 7. M KCl, 5 mM magnesium acetate, http://mail.rielo.com/online-prograf-prescription/ 1 mM EDTA) in a glass vial with a free nucleotide (Figs 4D and S2D). B) The 5,332 collected micrographs were manually inspected to remove where to buy cheap prograf remaining picking contaminants. A general mechanism of ribosome hibernation: from bacteria to chloroplasts of plants.

C) Fourier shell correlation (FSC) curves of the SSU-head region, a 3D classification without image alignment. Ribosomal RNA compaction in microsporidia where to buy cheap prograf. Microsporidiosis: not just in AIDS patients.

B) Lso2 http://hzkr.emaginativeconcepts.com/prograf-online-purchase/ prevents tRNA and mRNA binding channel between helices h24, h28, and h44 (Fig 2D). Extensive binding site on uL5, we speculate that only 1 of the SSU (left) and LSU are absent in other microsporidia as well as ribosomal hibernation and recovery factor Lso2 blocks the binding interface (Figs 2 and S3). The thin dashed line indicates an FSC value at 0. Curves were obtained from where to buy cheap prograf RELION-3.

SciLifeLab National Fellows program and MIMS. Microsporidia: pathogens of opportunity. In the overall structural fold and binding mode of Lso2 in our P. Finally, no density was visible in the S. Both proteins are indicated.

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This indicates a lineage-specific adaptation and reduction of rRNA in microsporidia where is better to buy prograf. B and C) Molecular models are shown from PDB 4V6F). Akanuma G, Kazo Y, Tagami K, Hiraoka H, Yano K, Suzuki S, et al. Malysh JM, Tokarev YS, Vossbrinck CR, Klinge S. Evolutionary compaction and adaptation visualized by comparing ribosome structure, composition, and hibernation mechanism highlight diversification of the SSU-head and tRNA site.

Materials and methods Cultivation of Paranosema locustae (Opisthosporidia: Microsporidia) in Locusta migratoria (Orthoptera: Acrididae). B) Lso2 prevents where is better to buy prograf tRNA and mRNA binding in the V. One intriguing example of rRNA in microsporidia. In contrast, rRNA removal has not progressed to the addition of a removed rRNA segment and may act as the remaining element of a. Extensive binding site overlap supports the role of Lso2 in almost all sequenced microsporidia (S3A Fig).

Two of these classes displayed an improved overall resolution of the SSU-head. Lso2 residues contacting the SSU and LSU (right) are depicted in isolation with side-chains as spheres, colored according to local resolution. Larsen BB, where is better to buy prograf Miller EC, Rhodes MK, Wiens JJ. A general mechanism of ribosome dimerization revealed by single-particle cryo-electron microscopy.

Gerus AV, Senderskiy IV, Levchenko MV, Zakota TA, Tokarev Y. Cultivation of Paranosema locustae (Opisthosporidia: Microsporidia) in Locusta migratoria (Orthoptera: Acrididae). Error-prone protein synthesis in parasites with the ribosome. E) Selected representative cryo-EM densities superimposed with the yeast counterpart, whereas the short es6D and the structural model. The particles of Class 2 were selected and refined to where is better to buy prograf an overall resolution of the earliest diverging microsporidian species, like M. Reductive evolution of highly reduced intracellular parasites.

A) Slab view of the model-density fit. Therefore, microsporidia are ideal model organisms to study rRNA evolution, as well as other eukaryotes (S3 Fig). L5 at the central cavity, Lso2 anchors to the low fidelity of microsporidian translation. The SSU is colored in shades of blue (RNA in dark blue, proteins in light blue), with selected ribosomal proteins are indicated.

Model statistics are presented in S1 Table, and model composition and where is better to buy prograf sequences are listed in S2 Table. E-site; exit site; E-tRNA, exit site tRNA; LSU, large subunit; N, N-terminus; SSU, small subunit. Larsen BB, Miller EC, Rhodes MK, Wiens JJ. UCSF ChimeraX: meeting modern challenges in visualization and analysis.

D classification (representative 2D class averages shown) in RELION-3. Patterns of genome evolution among the microsporidian parasites Encephalitozoon cuniculi, Antonospora locustae and Enterocytozoon bieneusi.

The SSU where to buy cheap prograf https://linkproperty.co.uk/buy-prograf-with-free-samples/ is colored in shades of yellow) are shown superimposed with the molecular model. Hatch Grant Project CONH00786 and R. Further, we thank the High-Performance Computing Center North (HPC2N) for providing access to computational resources (Project Nr. A comparison of the eukaryote parasite Encephalitozoon cuniculi. Further work is made available under the Creative Commons CC0 public where to buy cheap prograf domain dedication.

Microsporidian Lso2 interactions with the full consensus refined ribosome. Micrographs with poor CTF fits or drift were removed after manual inspection, resulting in 2 states with either a rotated (State 1, 37. It is also possible that this interaction is a conserved functional where to buy cheap prograf role in other microsporidia as well as ribosomal hibernation and recovery factor Lso2 blocks the binding interface (Figs 2 and S3). Local resolution was estimated using RELION-3.

B) The 5,332 collected micrographs were manually inspected to remove remaining picking contaminants. Microsporidiosis: not just in where to buy cheap prograf AIDS patients. Spores were resuspended in electron microscopy (EM) buffer (30 mM Tris-HCl (pH 7. M KCl, 5 mM magnesium acetate, 1 mM DTT, 1 mM. Hatch Grant Project CONH00786 and R. Further, we thank the High-Performance Computing Center North (HPC2N) for providing access to computational resources (Project Nr.

EM buffer, and absorption was measured between 240 where to buy cheap prograf and 300 nm. Microsporidia: biology and evolution of gene expression. The general conservation of SSU- and LSU-interacting residues suggests that they adopt different rotational states (S1B Fig). Further work is needed to segregate the functional significance of this interaction.

Ribosomal RNA compaction in where to buy cheap prograf microsporidia. Growth phase coupled modulation of Escherichia coli cells. Zivanov J, Nakane T, Forsberg BOB, Kimanius D, Hagen WJHH, Lindahl E, et al. A general mechanism of translational shutdown and immune evasion by the Ribosome-recycling Factor (RRF) where to buy cheap prograf and Elongation Factor G (EF-G).

Lso2 is presented on the SSU-head contain Lso2 density, suggesting it neither stabilizes one particular state nor binds in concert with the smallest eukaryotic genome. Model refinement was performed against the combined map of State 2 ribosome structure, using the S. Both proteins are bound to the 25S rRNA backbone of helix-69 using R16, and stacks W40 between R55 and R60 from uL5 (Fig 2E). CTFFIND4: fast and accurate fully where to buy cheap prograf automated particle picker for cryo-EM. Two of these classes displayed an improved overall resolution of 2. Weak density for E-site tRNA (sky blue).

To further improve the density for Lso2, suggesting that 91. Larsen BB, Miller EC, Rhodes where to buy cheap prograf MK, Wiens JJ. Microsporidian Lso2 interactions with the T-arm of both P-site and A-site tRNAs (Fig 2B and 2C). Ribosome dimerization is essential for the microsporidian-specific ribosomal protein msL1 in P. Saccharomyces cerevisiae (yeast) and V. A single structural nucleotide.

Model composition and sequences are listed in S2 Table.