File:Protein-Translation-Enzyme-lysyl-tRNA-Synthetase-Presents-a-New-Target-for-Drug-Development-against-pntd.0005084.s003.ogv
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Size of this JPG preview of this OGG file: 800 × 488 pixels. Other resolutions: 320 × 195 pixels | 640 × 391 pixels | 1,024 × 625 pixels | 1,280 × 781 pixels | 2,560 × 1,563 pixels | 4,420 × 2,698 pixels.
Original file (Ogg Theora video file, length 8.1 s, 4,420 × 2,698 pixels, 17.17 Mbps, file size: 16.54 MB)
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[edit]DescriptionProtein-Translation-Enzyme-lysyl-tRNA-Synthetase-Presents-a-New-Target-for-Drug-Development-against-pntd.0005084.s003.ogv |
English: Morph movie for cladosporin (shown in yellow) binding to Pf KRS (shown in blue) is shown. In unbound state, Phe342 conformation disallows cladosporin stacking. Additionally, other active site residues are in an unfavorable non-binding conformation. Cladosporin selects for a conformation suitable for stacking and possibly induces rotameric adjustments in active site residues that together stabilize binding. |
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Source | S1 Movie from Sharma A, Sharma M, Yogavel M, Sharma A (2016). "Protein Translation Enzyme lysyl-tRNA Synthetase Presents a New Target for Drug Development against Causative Agents of Loiasis and Schistosomiasis". PLOS Neglected Tropical Diseases. DOI:10.1371/journal.pntd.0005084. PMID 27806050. PMC: 5091859. | ||
Author | Sharma A, Sharma M, Yogavel M, Sharma A | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 10:08, 31 January 2017 | 8.1 s, 4,420 × 2,698 (16.54 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Short title | Morph movie for cladosporin (shown in yellow) binding to Pf KRS (shown in blue) is shown. |
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Author | Sharma A, Sharma M, Yogavel M, Sharma A |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | In unbound state, Phe342 conformation disallows cladosporin stacking. Additionally, other active site residues are in an unfavorable non-binding conformation. Cladosporin selects for a conformation suitable for stacking and possibly induces rotameric adjustments in active site residues that together stabilize binding. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2016-11-02 |
Categories:
- Loa loa
- Schistosoma mansoni
- Videos of molecular biology
- Videos of molecular biology techniques
- Sequencing techniques
- Videos of sequence analysis
- Sequence motif analysis
- Energy-producing organelles
- Videos of cell biology
- Gene expression
- Translation (genetics)
- Videos of condensed matter physics
- Videos of solid state physics
- Parasitic protozoans
- Malarial parasites
- Post-translational modifications