Category:Videos of protein structures

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Subcategories

This category has the following 6 subcategories, out of 6 total.

D

Videos of protein domains‎ (1 C, 38 F)

G

Media from Gill 2014 - 10.1371/journal.pone.0087354‎ (21 F)

Q

Videos of quaternary protein structure‎ (76 F)

S

Videos of secondary protein structure‎ (79 F)

T

Videos of tertiary protein structure‎ (273 F)

V

Videos with ribbon diagrams of Escherichia coli proteins‎ (24 F)

Media in category "Videos of protein structures"

The following 200 files are in this category, out of 237 total.

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-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s002.ogv 40 s, 426 × 240; 1.54 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s003.ogv 40 s, 426 × 240; 2.19 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s004.ogv 40 s, 426 × 240; 1.8 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s005.ogv 40 s, 426 × 240; 2.02 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s006.ogv 40 s, 426 × 240; 1.16 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s007.ogv 40 s, 426 × 240; 2.07 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s008.ogv 40 s, 426 × 240; 1.86 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s009.ogv 40 s, 426 × 240; 1.71 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s010.ogv 40 s, 426 × 240; 2.21 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s011.ogv 40 s, 426 × 240; 1.93 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s012.ogv 40 s, 426 × 240; 2.14 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s013.ogv 40 s, 426 × 240; 2.04 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s014.ogv 40 s, 426 × 240; 1.92 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s015.ogv 40 s, 426 × 240; 2.31 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s016.ogv 40 s, 426 × 240; 2.24 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s017.ogv 40 s, 426 × 240; 2.16 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s018.ogv 40 s, 426 × 240; 2.43 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s019.ogv 40 s, 426 × 240; 2.36 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s020.ogv 40 s, 426 × 240; 2.34 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s021.ogv 40 s, 426 × 240; 2.34 MB
-Hairpin-Mediated-Formation-of-Structurally-Distinct-Multimers-of-Neurotoxic-Prion-Peptides-pone.0087354.s022.ogv 2 min 0 s, 426 × 240; 10.41 MB
A-Compact-Multifunctional-Fusion-Module-Directs-Cholesterol-Dependent-Homomultimerization-and-ppat.1004023.s003.ogv 12 s, 1,392 × 1,040; 1.13 MB
A-Real-Time-All-Atom-Structural-Search-Engine-for-Proteins-pcbi.1003750.s008.ogv 37 s, 876 × 534; 10.81 MB
A-Refined-Model-of-the-Prototypical-Salmonella-SPI-1-T3SS-Basal-Body-Reveals-the-Molecular-Basis-ppat.1003307.s015.ogv 15 s, 908 × 594; 10.57 MB
A-Steered-Molecular-Dynamics-Study-of-Binding-and-Translocation-Processes-in-the-GABA-Transporter-pone.0039360.s011.ogv 18 s, 928 × 1,008; 37.05 MB
A-Steered-Molecular-Dynamics-Study-of-Binding-and-Translocation-Processes-in-the-GABA-Transporter-pone.0039360.s012.ogv 17 s, 848 × 1,008; 34.47 MB
A-Steered-Molecular-Dynamics-Study-of-Binding-and-Translocation-Processes-in-the-GABA-Transporter-pone.0039360.s013.ogv 17 s, 768 × 1,008; 33.15 MB
A-Structural-Model-for-Binding-of-the-Serine-Rich-Repeat-Adhesin-GspB-to-Host-Carbohydrate-Receptors-ppat.1002112.s005.ogv 13 s, 2,000 × 1,250; 4.64 MB
A-Structural-Model-of-the-Genome-Packaging-Process-in-a-Membrane-Containing-Double-Stranded-DNA-pbio.1002024.s021.ogv 57 s, 768 × 576; 20.79 MB
A-Structural-Model-of-the-Genome-Packaging-Process-in-a-Membrane-Containing-Double-Stranded-DNA-pbio.1002024.s022.ogv 33 s, 768 × 576; 7.58 MB
A-Structural-Model-of-the-Genome-Packaging-Process-in-a-Membrane-Containing-Double-Stranded-DNA-pbio.1002024.s023.ogv 49 s, 768 × 576; 15.48 MB
A-Topological-Framework-for-the-Computation-of-the-HOMFLY-Polynomial-and-Its-Application-to-Proteins-pone.0018693.s005.ogv 21 s, 960 × 540; 818 KB
Activation-of-Alpha-Chymotrypsin-by-Three-Phase-Partitioning-Is-Accompanied-by-Aggregation-pone.0049241.s002.ogv 30 s, 640 × 480; 5.06 MB
Activation-of-Alpha-Chymotrypsin-by-Three-Phase-Partitioning-Is-Accompanied-by-Aggregation-pone.0049241.s003.ogv 30 s, 640 × 480; 1.6 MB
Activation-of-Alpha-Chymotrypsin-by-Three-Phase-Partitioning-Is-Accompanied-by-Aggregation-pone.0049241.s004.ogv 30 s, 640 × 480; 2.12 MB
Activation-of-Alpha-Chymotrypsin-by-Three-Phase-Partitioning-Is-Accompanied-by-Aggregation-pone.0049241.s005.ogv 30 s, 640 × 480; 2.5 MB
Adding-Diverse-Noncanonical-Backbones-to-Rosetta-Enabling-Peptidomimetic-Design-pone.0067051.s003.ogv 35 s, 720 × 576; 76 KB
Allosteric-Regulation-of-Serine-Protease-HtrA2-through-Novel-Non-Canonical-Substrate-Binding-Pocket-pone.0055416.s006.ogv 35 s, 640 × 480; 10.26 MB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s008.ogv 57 s, 1,920 × 1,080; 570 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s009.ogv 54 s, 1,920 × 1,080; 540 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s010.ogv 54 s, 1,920 × 1,080; 530 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s011.ogv 54 s, 1,920 × 1,080; 522 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s012.ogv 36 s, 1,920 × 1,080; 364 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s013.ogv 54 s, 1,920 × 1,080; 545 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s014.ogv 21 s, 1,920 × 1,080; 256 KB
An-Automatic-Refolding-Apparatus-for-Preparative-Scale-Protein-Production-pone.0045891.s015.ogv 39 s, 1,920 × 1,080; 400 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s017.ogv 11 s, 750 × 500; 417 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s018.ogv 16 s, 500 × 500; 293 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s019.ogv 10 s, 1,050 × 350; 177 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s020.ogv 17 s, 300 × 300; 88 KB
An-Essential-Nonredundant-Role-for-Mycobacterial-DnaK-in-Native-Protein-Folding-pgen.1004516.s021.ogv 16 s, 300 × 300; 63 KB
An-Intrinsically-Disordered-Region-of-the-Adenovirus-Capsid-Is-Implicated-in-Neutralization-by-pone.0061571.s004.ogv 37 s, 640 × 480; 10.39 MB
An-Intrinsically-Disordered-Region-of-the-Adenovirus-Capsid-Is-Implicated-in-Neutralization-by-pone.0061571.s005.ogv 22 s, 640 × 480; 9.14 MB
Analysis-of-Trafficking-Stability-and-Function-of-Human-Connexin-26-Gap-Junction-Channels-with-pone.0070916.s001.ogv 56 s, 600 × 500; 36.54 MB
Are-Coiled-Coils-of-Dimeric-Kinesins-Unwound-during-Their-Walking-on-Microtubule?-pone.0036071.s008.ogv 17 s, 504 × 478; 7.72 MB
Are-Coiled-Coils-of-Dimeric-Kinesins-Unwound-during-Their-Walking-on-Microtubule?-pone.0036071.s009.ogv 17 s, 504 × 478; 7.81 MB
Are-Coiled-Coils-of-Dimeric-Kinesins-Unwound-during-Their-Walking-on-Microtubule?-pone.0036071.s010.ogv 17 s, 504 × 478; 7.89 MB
Are-Coiled-Coils-of-Dimeric-Kinesins-Unwound-during-Their-Walking-on-Microtubule?-pone.0036071.s011.ogv 17 s, 504 × 478; 8.01 MB
ATP-Dependent-Rotational-Motion-of-Group-II-Chaperonin-Observed-by-X-ray-Single-Molecule-Tracking-pone.0064176.s011.ogv 7.5 s, 640 × 480; 327 KB
ATTRACT-EM-A-New-Method-for-the-Computational-Assembly-of-Large-Molecular-Machines-Using-Cryo-EM-pone.0049733.s002.ogv 23 s, 800 × 800; 3.16 MB
ATTRACT-EM-A-New-Method-for-the-Computational-Assembly-of-Large-Molecular-Machines-Using-Cryo-EM-pone.0049733.s003.ogv 14 s, 1,000 × 498; 964 KB
ATTRACT-EM-A-New-Method-for-the-Computational-Assembly-of-Large-Molecular-Machines-Using-Cryo-EM-pone.0049733.s004.ogv 29 s, 1,000 × 498; 1.19 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s010.ogv 59 s, 720 × 480; 10.61 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s011.ogv 1 min 2 s, 720 × 480; 5.63 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s012.ogv 2 min 22 s, 720 × 480; 5.1 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s013.ogv 6 min 12 s, 720 × 480; 8.99 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s014.ogv 5 min 43 s, 720 × 480; 6.77 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s015.ogv 1 min 17 s, 720 × 480; 7.63 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s016.ogv 38 s, 720 × 480; 2.16 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s017.ogv 2 min 51 s, 720 × 480; 5.91 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s018.ogv 6 min 22 s, 720 × 480; 8.99 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s019.ogv 4 min 50 s, 720 × 480; 5.61 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s020.ogv 8.5 s, 720 × 480; 863 KB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s021.ogv 39 s, 720 × 480; 2.83 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s022.ogv 2 min 52 s, 720 × 480; 4.65 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s023.ogv 8 min 13 s, 720 × 480; 9.05 MB
BCLFold---De-Novo-Prediction-of-Complex-and-Large-Protein-Topologies-by-Assembly-of-Secondary-pone.0049240.s024.ogv 5 min 5 s, 720 × 480; 4.79 MB
Bin2-Is-a-Membrane-Sculpting-N-BAR-Protein-That-Influences-Leucocyte-Podosomes-Motility-and-pone.0052401.s010.ogv 31 s, 640 × 614; 2.79 MB
Bin2-Is-a-Membrane-Sculpting-N-BAR-Protein-That-Influences-Leucocyte-Podosomes-Motility-and-pone.0052401.s011.ogv 37 s, 576 × 550; 2.59 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s005.ogv 17 s, 768 × 576; 3.57 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s006.ogv 19 s, 768 × 576; 5.02 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s007.ogv 19 s, 768 × 576; 7.29 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s008.ogv 19 s, 768 × 576; 7.07 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s009.ogv 27 s, 768 × 576; 10.86 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s010.ogv 9.6 s, 768 × 576; 3.7 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s011.ogv 9.6 s, 768 × 576; 3.59 MB
Changes-in-Dynamics-upon-Oligomerization-Regulate-Substrate-Binding-and-Allostery-in-Amino-Acid-pcbi.1002201.s012.ogv 19 s, 768 × 576; 6.31 MB
ComEA-Is-Essential-for-the-Transfer-of-External-DNA-into-the-Periplasm-in-Naturally-Transformable-pgen.1004066.s011.ogv 0.0 s, 1,056 × 1,056; 14.44 MB
ComEA-Is-Essential-for-the-Transfer-of-External-DNA-into-the-Periplasm-in-Naturally-Transformable-pgen.1004066.s012.ogv 2.0 s, 53 × 53; 5 KB
ComEA-Is-Essential-for-the-Transfer-of-External-DNA-into-the-Periplasm-in-Naturally-Transformable-pgen.1004066.s013.ogv 4.0 s, 70 × 70; 8 KB
ComEA-Is-Essential-for-the-Transfer-of-External-DNA-into-the-Periplasm-in-Naturally-Transformable-pgen.1004066.s014.ogv 6.3 s, 70 × 70; 10 KB
Compact-Conformations-of-Human-Protein-Disulfide-Isomerase-pone.0103472.s006.ogv 9.6 s, 688 × 544; 14.92 MB
Computational-and-Experimental-Characterization-of-dVHL-Establish-a-Drosophila-Model-of-VHL-Syndrome-pone.0109864.s005.ogv 8.7 s, 960 × 720; 1.7 MB
Computational-Simulation-of-the-Activation-Cycle-of-Gα-Subunit-in-the-G-Protein-Cycle-Using-an-pone.0159528.s011.ogv 17 s, 1,920 × 1,080; 7.84 MB
Computational-Study-of-Synthetic-Agonist-Ligands-of-Ionotropic-Glutamate-Receptors-pone.0058774.s003.ogv 3.3 s, 1,920 × 1,168; 6.4 MB
Computational-Study-of-Synthetic-Agonist-Ligands-of-Ionotropic-Glutamate-Receptors-pone.0058774.s004.ogv 3.3 s, 1,920 × 1,168; 6.51 MB
Computational-Study-of-Synthetic-Agonist-Ligands-of-Ionotropic-Glutamate-Receptors-pone.0058774.s005.ogv 3.3 s, 1,920 × 1,168; 6.68 MB
Conformational-Change-Induced-Repeat-Domain-Expansion-Regulates-Rap-Phosphatase-Quorum-Sensing-pbio.1001512.s007.ogv 20 s, 800 × 768; 2.02 MB
Conformational-Sampling-and-Nucleotide-Dependent-Transitions-of-the-GroEL-Subunit-Probed-by-pcbi.1002004.s005.ogv 1 min 40 s, 480 × 480; 3.8 MB
Conformational-Transition-Pathway-in-the-Activation-Process-of-Allosteric-Glucokinase-pone.0055857.s005.ogv 12 s, 640 × 688; 1.83 MB
Conformational-Transition-Pathway-in-the-Activation-Process-of-Allosteric-Glucokinase-pone.0055857.s006.ogv 12 s, 784 × 704; 3.65 MB
Contribution-of-the-CR-Domain-to-P-Selectin-Lectin-Domain-Allostery-by-Regulating-the-Orientation-pone.0118083.s012.ogv 15 s, 1,280 × 1,248; 7.47 MB
Controlled-In-Meso-Phase-Crystallization-–-A-Method-for-the-Structural-Investigation-of-Membrane-pone.0035458.s006.ogv 2 min 6 s, 480 × 320; 4.35 MB
Coupled-Protein-Diffusion-and-Folding-in-the-Cell-pone.0113040.s002.ogv 4.0 s, 103 × 124; 18 KB
Cryo-Electron-Tomography-of-Marburg-Virus-Particles-and-Their-Morphogenesis-within-Infected-Cells-pbio.1001196.s010.ogv 26 s, 1,590 × 1,063; 8.04 MB
Cryo-Electron-Tomography-of-Marburg-Virus-Particles-and-Their-Morphogenesis-within-Infected-Cells-pbio.1001196.s011.ogv 6.7 s, 768 × 768; 9.03 MB
Cryo-Electron-Tomography-of-Marburg-Virus-Particles-and-Their-Morphogenesis-within-Infected-Cells-pbio.1001196.s012.ogv 6.6 s, 652 × 652; 5.74 MB
Cryo-Electron-Tomography-of-Marburg-Virus-Particles-and-Their-Morphogenesis-within-Infected-Cells-pbio.1001196.s013.ogv 14 s, 816 × 752; 7.25 MB
Cryo-EM-Structure-of-Isomeric-Molluscan-Hemocyanin-Triggered-by-Viral-Infection-pone.0098766.s008.ogv 29 s, 300 × 300; 11.35 MB
Cryo-EM-Structure-of-Isomeric-Molluscan-Hemocyanin-Triggered-by-Viral-Infection-pone.0098766.s009.ogv 4.1 s, 600 × 600; 678 KB
Crystal-Structures-of-the-Novel-Cytosolic-5-Nucleotidase-IIIB-Explain-Its-Preference-for-m7GMP-pone.0090915.s005.ogv 19 s, 942 × 631; 3.49 MB
Design-Rules-for-Selective-Binding-of-Nuclear-Localization-Signals-to-Minor-Site-of-Importin-pone.0091025.s015.ogv 13 s, 1,328 × 1,664; 43.39 MB
Dimer-Formation-Enhances-Structural-Differences-between-Amyloid-β-Protein-(1–40)-and-(1–42)-An-pone.0034345.s012.ogv 33 s, 610 × 626; 10.45 MB
Dimer-Formation-Enhances-Structural-Differences-between-Amyloid-β-Protein-(1–40)-and-(1–42)-An-pone.0034345.s013.ogv 33 s, 610 × 626; 8.64 MB
Distinctive-Effects-of-Cytochalasin-B-in-Chick-Primary-Myoblasts-and-Fibroblasts-pone.0154109.s001.ogv 17 s, 580 × 346; 1.06 MB
Distinctive-Effects-of-Cytochalasin-B-in-Chick-Primary-Myoblasts-and-Fibroblasts-pone.0154109.s002.ogv 5.8 s, 768 × 768; 4.8 MB
Distinctive-Effects-of-Cytochalasin-B-in-Chick-Primary-Myoblasts-and-Fibroblasts-pone.0154109.s004.ogv 5.8 s, 768 × 768; 1.43 MB
Distinctive-Effects-of-Cytochalasin-B-in-Chick-Primary-Myoblasts-and-Fibroblasts-pone.0154109.s006.ogv 5.8 s, 618 × 618; 1.13 MB
Distinctive-Effects-of-Cytochalasin-B-in-Chick-Primary-Myoblasts-and-Fibroblasts-pone.0154109.s007.ogv 20 s, 452 × 330; 1.3 MB
Dual-Chaperone-Role-of-the-C-Terminal-Propeptide-in-Folding-and-Oligomerization-of-the-Pore-Forming-ppat.1002135.s004.ogv 30 s, 640 × 480; 10.07 MB
Dual-Chaperone-Role-of-the-C-Terminal-Propeptide-in-Folding-and-Oligomerization-of-the-Pore-Forming-ppat.1002135.s005.ogv 42 s, 640 × 480; 13.16 MB
DyneinDynactin-Mediated-Transport-of-Kinetochore-Components-off-Kinetochores-and-onto-Spindle-Poles-pone.0016494.s008.ogv 2.7 s, 606 × 603; 852 KB
Force-Induced-Unfolding-Simulations-of-the-Human-Notch1-Negative-Regulatory-Region-Possible-Roles-pone.0022837.s003.ogv 0.0 s, 928 × 832; 22.1 MB
Formation-of-Cystine-Slipknots-in-Dimeric-Proteins-pone.0057443.s001.ogv 28 s, 1,024 × 768; 2.51 MB
Formation-of-Cystine-Slipknots-in-Dimeric-Proteins-pone.0057443.s002.ogv 28 s, 1,024 × 768; 22.44 MB
FRET-Assisted-Determination-of-CLN3-Membrane-Topology-pone.0102593.s001.ogv 25 s, 1,536 × 512; 5.26 MB
GFPs-Mechanical-Intermediate-States-pone.0046962.s003.ogv 1 min 9 s, 852 × 480; 23.95 MB
High-Affinity-Antigen-Recognition-of-the-Dual-Specific-Variants-of-Herceptin-Is-Entropy-Driven-in-pone.0017887.s001.ogv 7.4 s, 640 × 480; 424 KB
Identification-of-a-Novel-Drug-Lead-That-Inhibits-HCV-Infection-and-Cell-to-Cell-Transmission-by-pone.0111333.s002.ogv 15 s, 352 × 288; 1.85 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s011.ogv 32 s, 496 × 476; 16.49 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s012.ogv 48 s, 572 × 532; 24.53 MB
Identification-of-SerThr-kinase-and-Forkhead-Associated-Domains-in-Mycobacterium-ulcerans-pntd.0003315.s013.ogv 48 s, 572 × 532; 18.65 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s006.ogv 16 s, 1,920 × 1,080; 5.19 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s007.ogv 16 s, 1,920 × 1,080; 5.05 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s008.ogv 16 s, 1,920 × 1,080; 4.53 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s009.ogv 16 s, 1,920 × 1,080; 5.58 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s010.ogv 16 s, 1,920 × 1,080; 5.36 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s011.ogv 16 s, 1,920 × 1,080; 5.84 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s012.ogv 16 s, 1,920 × 1,080; 6.45 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s013.ogv 16 s, 1,920 × 1,080; 5.31 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s014.ogv 16 s, 1,920 × 1,080; 4.63 MB
In-silico-Analysis-of-Conformational-Changes-Induced-by-Mutation-of-Aromatic-Binding-Residues-pone.0028778.s015.ogv 16 s, 1,920 × 1,080; 5.06 MB
Insights-into-the-Mechanism-of-Bovine-CD38NAD+Glycohydrolase-from-the-X-Ray-Structures-of-Its-pone.0034918.s009.ogv 2.0 s, 1,673 × 870; 283 KB
Integrated-Analysis-of-Residue-Coevolution-and-Protein-Structure-in-ABC-Transporters-pone.0036546.s016.ogv 22 s, 400 × 673; 12.82 MB
Integrated-Analysis-of-Residue-Coevolution-and-Protein-Structure-in-ABC-Transporters-pone.0036546.s017.ogv 14 s, 450 × 750; 12.03 MB
Integrated-Analysis-of-Residue-Coevolution-and-Protein-Structure-in-ABC-Transporters-pone.0036546.s018.ogv 14 s, 450 × 750; 11.25 MB
LRRK2-Transport-Is-Regulated-by-Its-Novel-Interacting-Partner-Rab32-pone.0111632.s008.ogv 2.0 s, 2,136 × 1,024; 3.55 MB
LRRK2-Transport-Is-Regulated-by-Its-Novel-Interacting-Partner-Rab32-pone.0111632.s009.ogv 2.7 s, 864 × 434; 265 KB
Mapping-the-Conformational-Dynamics-and-Pathways-of-Spontaneous-Steric-Zipper-Peptide-pone.0019129.s010.ogv 20 s, 670 × 834; 5.03 MB
Mechanisms-of-the-Scaffold-Subunit-in-Facilitating-Protein-Phosphatase-2A-Methylation-pone.0086955.s003.ogv 12 s, 800 × 800; 9.36 MB
Membrane-Sensitive-Conformational-States-of-Helix-8-in-the-Metabotropic-Glu2-Receptor-a-Class-C-GPCR-pone.0042023.s020.ogv 53 s, 480 × 368; 4.98 MB
Microsecond-Molecular-Dynamics-Simulations-of-Intrinsically-Disordered-Proteins-Involved-in-the-pone.0027371.s001.ogv 0.0 s, 464 × 416; 17.8 MB
Microsecond-Molecular-Dynamics-Simulations-of-Intrinsically-Disordered-Proteins-Involved-in-the-pone.0027371.s002.ogv 0.0 s, 480 × 416; 6.67 MB
Monitoring-and-Scoring-Counter-Diffusion-Protein-Crystallization-Experiments-in-Capillaries-by-in-pone.0033545.s003.ogv 22 s, 640 × 480; 701 KB
Monitoring-and-Scoring-Counter-Diffusion-Protein-Crystallization-Experiments-in-Capillaries-by-in-pone.0033545.s004.ogv 14 s, 310 × 134; 35 KB
New-Insights-into-the-In-Silico-Prediction-of-HIV-Protease-Resistance-to-Nelfinavir-pone.0087520.s025.ogv 21 s, 1,920 × 1,080; 27.7 MB
New-Insights-into-the-In-Silico-Prediction-of-HIV-Protease-Resistance-to-Nelfinavir-pone.0087520.s026.ogv 17 s, 1,920 × 1,080; 20.93 MB
New-Insights-into-the-In-Silico-Prediction-of-HIV-Protease-Resistance-to-Nelfinavir-pone.0087520.s027.ogv 21 s, 1,920 × 1,080; 26.21 MB
New-Insights-into-the-In-Silico-Prediction-of-HIV-Protease-Resistance-to-Nelfinavir-pone.0087520.s028.ogv 16 s, 1,920 × 1,080; 20.46 MB
Novel-Allosteric-Sites-on-Ras-for-Lead-Generation-pone.0025711.s006.ogv 9.7 s, 640 × 328; 3.02 MB
Nucleosome Complex model.ogv 8.4 s, 1,280 × 624; 2.31 MB
Ontogeny-of-Recognition-Specificity-and-Functionality-for-the-Broadly-Neutralizing-Anti-HIV-ppat.1004403.s001.ogv 15 s, 1,406 × 830; 10.66 MB
Ontogeny-of-Recognition-Specificity-and-Functionality-for-the-Broadly-Neutralizing-Anti-HIV-ppat.1004403.s002.ogv 15 s, 1,444 × 818; 9.92 MB
Operating-Mechanism-and-Molecular-Dynamics-of-Pheromone-Binding-Protein-ASP1-as-Influenced-by-pH-pone.0110565.s001.ogv 2 min 13 s, 660 × 568; 64.74 MB
Operating-Mechanism-and-Molecular-Dynamics-of-Pheromone-Binding-Protein-ASP1-as-Influenced-by-pH-pone.0110565.s002.ogv 2 min 13 s, 712 × 584; 83.46 MB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v001.ogv 20 s, 512 × 512; 3.2 MB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v002.ogv 12 s, 330 × 330; 147 KB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v003.ogv 20 s, 194 × 194; 1.29 MB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v004.ogv 12 s, 530 × 512; 571 KB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v005.ogv 21 s, 1,387 × 1,109; 5.03 MB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v006.ogv 30 s, 295 × 295; 412 KB
Phosphoinositide-mediated-oligomerization-of-a-defensin-induces-cell-lysis-elife01808v007.ogv 40 s, 267 × 267; 880 KB
RNA-Mimicry-by-the-Fap7-Adenylate-Kinase-in-Ribosome-Biogenesis-pbio.1001860.s006.ogv 8.7 s, 1,052 × 768; 3.89 MB
Role-of-Decorin-Core-Protein-in-Collagen-Organisation-in-Congenital-Stromal-Corneal-Dystrophy-(CSCD)-pone.0147948.s001.ogv 13 s, 410 × 364; 3.34 MB
Role-of-Decorin-Core-Protein-in-Collagen-Organisation-in-Congenital-Stromal-Corneal-Dystrophy-(CSCD)-pone.0147948.s002.ogv 26 s, 958 × 679; 3.61 MB
Role-of-Decorin-Core-Protein-in-Collagen-Organisation-in-Congenital-Stromal-Corneal-Dystrophy-(CSCD)-pone.0147948.s003.ogv 12 s, 958 × 679; 1.4 MB
Role-of-Decorin-Core-Protein-in-Collagen-Organisation-in-Congenital-Stromal-Corneal-Dystrophy-(CSCD)-pone.0147948.s004.ogv 6.6 s, 958 × 679; 1.21 MB
Spastins-Microtubule-Binding-Properties-and-Comparison-to-Katanin-pone.0050161.s006.ogv 10 min 49 s, 594 × 232; 48.12 MB
Spastins-Microtubule-Binding-Properties-and-Comparison-to-Katanin-pone.0050161.s007.ogv 2 min 3 s, 232 × 310; 6.92 MB
Spastins-Microtubule-Binding-Properties-and-Comparison-to-Katanin-pone.0050161.s008.ogv 44 s, 500 × 500; 12.4 MB
Spastins-Microtubule-Binding-Properties-and-Comparison-to-Katanin-pone.0050161.s009.ogv 1.0 s, 500 × 500; 1.88 MB
Spatial-Temporal-Study-of-Rab1b-Dynamics-and-Function-at-the-ER-Golgi-Interface-pone.0160838.s002.ogv 37 s, 1,920 × 1,080; 7.13 MB
Spatial-Temporal-Study-of-Rab1b-Dynamics-and-Function-at-the-ER-Golgi-Interface-pone.0160838.s003.ogv 50 s, 640 × 360; 776 KB
Spatial-Temporal-Study-of-Rab1b-Dynamics-and-Function-at-the-ER-Golgi-Interface-pone.0160838.s004.ogv 50 s, 1,280 × 720; 4.59 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s019.ogv 7.1 s, 1,440 × 1,080; 4.02 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s020.ogv 7.0 s, 1,440 × 1,080; 4.06 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s021.ogv 6.0 s, 1,440 × 1,080; 4.63 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s022.ogv 6.0 s, 1,440 × 1,080; 3.67 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s023.ogv 1.2 s, 1,440 × 1,080; 680 KB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s024.ogv 7.0 s, 1,440 × 1,080; 3.95 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s025.ogv 7.1 s, 1,440 × 1,080; 3.82 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s026.ogv 7.0 s, 1,440 × 1,080; 4.14 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s027.ogv 9.1 s, 640 × 480; 3.97 MB
Stapled-BH3-Peptides-against-MCL-1-Mechanism-and-Design-Using-Atomistic-Simulations-pone.0043985.s028.ogv 9.8 s, 640 × 480; 3.27 MB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s006.ogv 11 s, 384 × 288; 416 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s007.ogv 11 s, 384 × 288; 416 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s008.ogv 12 s, 384 × 288; 333 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s009.ogv 13 s, 352 × 240; 1.34 MB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s010.ogv 3.3 s, 334 × 897; 675 KB
Stretching-Actin-Filaments-within-Cells-Enhances-their-Affinity-for-the-Myosin-II-Motor-Domain-pone.0026200.s011.ogv 6.3 s, 231 × 264; 440 KB

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