Biochemistry, Genetics and Molecular Biology
Small Molecule
100%
Amino Acids
71%
Conformation
71%
Wild Type
62%
Protein Structure
61%
C-Terminus
58%
N-Terminus
57%
Missense
47%
Potassium Channel
47%
Binding Site
46%
Molecular Model
44%
Neratinib
42%
Epidermal Growth Factor Receptor
42%
Protein Complexes
42%
Protein Modeling
42%
Centrin
42%
ROMK
42%
Structure Prediction
42%
Computer Simulation
39%
Kinase
38%
Phosphotransferase
38%
Conformational Change
38%
Crystal Structure
36%
IC50
31%
Protein Design
31%
EF Hand
30%
Genetic Divergence
28%
Afatinib
28%
Evolution
28%
Solution and Solubility
26%
Protein Function
26%
Binding Protein
25%
Glycosylation
25%
Gain of Function Mutation
23%
Mutagenesis
22%
Rare Variant
22%
Exome Sequencing
22%
Cytotoxic T Cell
21%
Protein Interaction
21%
Fibroblast Growth Factor
21%
Protein-Protein Interaction
21%
Peptidomimetic
21%
Lipophilicity
21%
KCNC2
21%
Nucleic Acid
21%
Cytochrome C Oxidase
21%
Signal Recognition Particle Receptor
21%
Melanocortin
21%
Aptamer
21%
Targeting Protein
21%
Keyphrases
Rosetta
84%
Pathogenic Variants
64%
Kir1.1
52%
Kir Channels
44%
Phosphoinositide 3-kinase (PI3K)
42%
HIV-1 Capsid
42%
Kir7.1
42%
Oncogene
42%
C2 Domain
42%
Domain Deletion
42%
Centrin
42%
PIK3CA
42%
Ca2+
42%
Lung Cancer
42%
Potassium Channel
42%
Small Molecule Inhibitors
35%
Protein Modeling
35%
Gain-of-function mutation
34%
Missense Variants
33%
Human Epidermal Growth Factor Receptor 2 (HER2)
32%
Molecular Modeling
32%
Molecular Dynamics Simulation
30%
Human Immunodeficiency Virus Type 1 (HIV-1)
29%
Capsid
29%
Binding Site
29%
EF-hand Protein
28%
Ligand Docking
28%
Afatinib
28%
Conformational Change
27%
HER2-mutant
27%
Neratinib
27%
Molecular Mechanism
26%
Protein Function
26%
Protein Complex
26%
Virion
26%
Calcium-binding Proteins
26%
N-terminal Domain
26%
Variants of Uncertain Significance
25%
Breast Cancer
25%
Gating Properties
24%
Helix
24%
Thrombin
24%
Specific Genes
23%
Genetic Variants
23%
HER2 Inhibitors
23%
Likely Pathogenic Variant
23%
Thermodynamic Stability
23%
Disease Association
22%
Pathogenicity
22%
Rare Variants
22%
