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Compounds identified by virtual docking to a tetrameric EGFR extracellular domain can modulate Grb2 internalization
Ramirez U., Nikonova A., Liu H., Pecherskaya A., Lawrence S., Serebriiskii I., Zhou Y., Robinson M., Einarson M., Golemis E., Jaffe E.
potential target for drug discovery. Methods: Our focus is on the prone EGFR tetramer, which contains a
Comparative Binding Analysis of N-Acetylneuraminic Acid in Bovine Serum Albumin and Human α-1 Acid Glycoprotein
Karthikeyan S., Bharanidharan G., Ragavan S., Kandasamy S., Chinnathambi S., Udayakumar K., Mangaiyarkarasi R., Sundaramoorthy A., Aruna P., Ganesan S.
-acetylneuraminic acid (NANA) drug binding interaction mechanism between bovine serum albumin (BSA) and human α-1 acid
Kinetic regulation of multi-ligand binding proteins
Salakhieva D., Sadreev I., Chen M., Umezawa Y., Evstifeev A., Welsh G., Kotov N.
of multisite binding proteins in a concentration-dependent manner. For example, calcium binding has been shown
Ethanol binding sites on proteins
Khrustalev, V. V., Khrustaleva, T. A., Lelevich, S. V.
This study is on the analysis of ethanol binding sites on 3D structures of nonredundant proteins
Coelenterazine-dependent luciferases as a powerful analytical tool for research and biomedical applications
Krasitskaya V.V.
unclassified drug
Isolation and purification of staphylococcus aureus hibernationpromoting factor inactivating of the ribosome
Ayupov R., Khusainov I., Validov S., Yusupova G., Yusupov M.
aureus hibernation-promoting factor (SaHPF) binds to ribosomes depleting translation and turning
Targeting the Bap1 protein of Vibrio cholerae for screening potent inhibitors and predicting the mutant protein stability: in silico analyses
Kalidas Gowtham, Pranav, R. J.
To target this Bap1 structural protein for screening potent inhibitors of ligands by means
Ancient hybridization and strong adaptation to viruses across African vervet monkey populations
Svardal H.
RAN binding protein 3
NMR assignments of the N-terminal domain of Staphylococcus aureus hibernation promoting factor (SaHPF)
Usachev K., Ayupov R., Validov S., Khusainov I., Yusupov M.
HPF) is a 22.2 kDa stationary-phase protein that binds to the ribosome and turns it to the inactive form
New evidence for dual binding site inhibitors of acetylcholinesterase as improved drugs for treatment of Alzheimer's disease
Zueva I., Dias J., Lushchekina S., Semenov V., Mukhamedyarov M., Pashirova T., Babaev V., Nachon F., Petrova N., Nurullin L., Zakharova L., Ilyin V., Masson P., Petrov K.
in Alzheimer's disease. This study was set up to analyze possible neuroprotective effects of two dual binding

Страница 11 из 1676

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