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Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 12/2010, Volume 107, Issue 52, pp. 22641 - 22646
.... EBV, like other herpesviruses, has three glycoproteins, glycoprotein B (gB), gH, and gL, that form the core membrane fusion machinery mediating viral penetration into the cell... 
Proteins | Epithelial cells | B lymphocytes | Herpesviridae | Human herpesvirus 2 | Viruses | Glycoproteins | Epstein Barr virus infections | Human herpesvirus 4 | Integrins | B-CELLS | EPITHELIAL-CELLS | FORM | GP42 | MULTIDISCIPLINARY SCIENCES | MEMBRANE-FUSION PROTEINS | MUTATIONS | REVEAL | BINDING | Disulfides - metabolism | Herpesvirus 4, Human - genetics | Molecular Chaperones - metabolism | Membrane Glycoproteins - metabolism | Humans | Membrane Glycoproteins - chemistry | Protein Multimerization | Molecular Sequence Data | Molecular Chaperones - chemistry | Viral Proteins - metabolism | Cysteine - genetics | Spodoptera | Multiprotein Complexes - metabolism | Disulfides - chemistry | Viral Envelope Proteins - metabolism | Cysteine - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | Cell Line | Viral Envelope Proteins - genetics | Membrane Fusion | Viral Proteins - chemistry | Crystallization | Molecular Chaperones - genetics | Models, Molecular | Viral Proteins - genetics | Binding Sites - genetics | Cysteine - chemistry | Microscopy, Electron | Membrane Glycoproteins - genetics | Sequence Homology, Amino Acid | Multiprotein Complexes - ultrastructure | Multiprotein Complexes - chemistry | Animals | Viral Envelope Proteins - chemistry | Protein Binding | Herpesvirus 4, Human - metabolism | Virus diseases | Epstein-Barr virus | Research | Chemical properties | Structure | Crystals | Biological Sciences
Journal Article
Nature (London), ISSN 1476-4687, 2016, Volume 535, Issue 7610, pp. 169 - 172
.... There are currently no approved therapeutic drugs or vaccines for the disease. EBOV has a membrane envelope decorated by trimers of a glycoprotein... 
SYSTEM | NIEMANN-PICK C1 | ENTRY | CHOLESTEROL | SMALL-MOLECULE INHIBITORS | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | ANTIBODY | RECEPTOR | INFECTION | HIV-1 VIRION FUSION | Temperature | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Antiviral Agents - metabolism | Endosomes - metabolism | Protein Subunits - metabolism | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Ebolavirus - drug effects | Ibuprofen - chemistry | Antiviral Agents - chemistry | Endosomes - drug effects | Viral Envelope Proteins - metabolism | Conserved Sequence | Marburgvirus - chemistry | Anti-Inflammatory Agents, Non-Steroidal - metabolism | Binding Sites | Membrane Fusion - drug effects | Toremifene - metabolism | Toremifene - pharmacology | Cell Line | Antiviral Agents - pharmacology | Ibuprofen - pharmacology | Models, Molecular | Protein Structure, Quaternary - drug effects | Ibuprofen - metabolism | Virus Attachment - drug effects | Ebolavirus - chemistry | Viral Envelope Proteins - antagonists & inhibitors | Protein Stability - drug effects | Viral Envelope Proteins - chemistry | Hydrophobic and Hydrophilic Interactions | Protein Binding | Ligands | Protein Subunits - chemistry | Toremifene - chemistry | Ebola virus | Glycoproteins | Host-virus relationships | Observations | Health aspects | Drug interactions | Drug therapy | Binding sites | Viral infections | Crystal structure
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2019, Volume 363, Issue 6428, pp. 753 - 756
ABCB1, also known as P-glycoprotein, actively extrudes xenobiotic compounds across the plasma membrane of diverse cells, which contributes to cellular drug resistance and interferes with therapeutic drug delivery... 
MULTIDRUG TRANSPORTER | CONFORMATIONAL-CHANGES | ATPASE ACTIVITY | MECHANISM | MULTIDISCIPLINARY SCIENCES | RESISTANCE | ABC TRANSPORTERS | MOLECULAR-BASIS | BINDING | CANCER | TARIQUIDAR | Mutant Chimeric Proteins - antagonists & inhibitors | Dibenzocycloheptenes - chemistry | Paclitaxel - pharmacology | Humans | Quinolines - chemistry | ATP Binding Cassette Transporter, Subfamily B - chemistry | Phospholipids - chemistry | Substrate Specificity | Antineoplastic Agents, Phytogenic - chemistry | Quinolines - pharmacology | Cholesterol - chemistry | Cryoelectron Microscopy | Hydrolysis | Paclitaxel - chemistry | Protein Domains - drug effects | Animals | ATP Binding Cassette Transporter, Subfamily B - antagonists & inhibitors | Drug Design | Protein Binding | Dibenzocycloheptenes - pharmacology | Mice | Adenosine Triphosphate - chemistry | Antineoplastic Agents, Phytogenic - pharmacology | Binding Sites | Physiological aspects | Glycoproteins | Substrates (Biochemistry) | Structure | Drug delivery systems | Taxol | Substrate inhibition | Phospholipids | Drug delivery | Drug resistance | Electron microscopy | Substrates | Cholesterol | Membrane proteins | Domains | Proteins | Inhibitors | Microscopy | Paclitaxel | Transport | P-Glycoprotein | ATP | Binding sites | Adenosine triphosphate | Cancer
Journal Article
Journal Article
Nature structural & molecular biology, ISSN 1545-9985, 2008, Volume 15, Issue 3, pp. 312 - 317
Journal Article
Chembiochem : a European journal of chemical biology, ISSN 1439-4227, 07/2017, Volume 18, Issue 13, pp. 1317 - 1331
...‐specific markers, we quantitatively assessed cell‐surface‐exposed sialo‐glycoproteins and N‐glycans of hiPSCs, CM progenitors, and CMs... 
cardiomyocytes | glycoproteins | sialic acids | human pluripotent stem cells | proteomics | Staining and Labeling - methods | Fucose - chemistry | Galactose - metabolism | Receptors, G-Protein-Coupled - metabolism | Induced Pluripotent Stem Cells - chemistry | Fucose - metabolism | Humans | Sialic Acids - chemistry | Acetylglucosamine - metabolism | Cell Membrane - chemistry | Receptor, EphA7 - metabolism | Polysaccharides - chemistry | Cell Differentiation | Cell Membrane - metabolism | Gastrins - genetics | Membrane Proteins - metabolism | Receptor, EphA7 - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 2 - genetics | Induced Pluripotent Stem Cells - cytology | Induced Pluripotent Stem Cells - metabolism | Carbohydrate Sequence | Myocytes, Cardiac - cytology | Membrane Proteins - genetics | Glycomics - methods | Ciliary Neurotrophic Factor Receptor alpha Subunit - genetics | Gene Expression Regulation | Sialic Acids - metabolism | Myocytes, Cardiac - chemistry | Gastrins - metabolism | Acetylglucosamine - chemistry | Polysaccharides - metabolism | Laminin - genetics | Galactose - chemistry | Receptor-Like Protein Tyrosine Phosphatases, Class 2 - metabolism | Myocytes, Cardiac - metabolism | Receptors, G-Protein-Coupled - genetics | Laminin - metabolism | Ciliary Neurotrophic Factor Receptor alpha Subunit - metabolism | Polysaccharides | Usage | Analysis | Stem cells | Glycoproteins | Organic acids | Membrane proteins | Gel electrophoresis | Tissue engineering | Capillary electrophoresis | Transplants | Cardiomyocytes | Marking | N-glycans | Patients | Cell surface | Regeneration (physiology) | Proteins | Medicine | Regeneration | Biomarkers | Electrophoresis | Differentiation | Galactose | Pluripotency | Index Medicus
Journal Article