Medicine & Life Sciences
Proteins
100%
Neoplasms
87%
src Homology Domains
78%
Histones
72%
Daptomycin
71%
DNA
68%
Dimerization
68%
Phosphorylation
66%
human ISG15 protein
61%
Phosphopyruvate Hydratase
60%
Synthetic Lethal Mutations
56%
X Ray Crystallography
54%
human CDK2 protein
53%
Binding Sites
52%
Poly(ADP-ribose) Polymerase Inhibitors
51%
protein phosphatase inhibitor-2
47%
Chromones
44%
Pharmacokinetics
42%
Crystallization
41%
Receptor Protein-Tyrosine Kinases
41%
linrodostat
41%
Apoenzymes
41%
osimertinib
41%
Mutation
40%
Phosphogluconate Dehydrogenase
40%
Ligands
39%
Enterococcus
37%
Glutaminase
37%
Orphan Nuclear Receptors
36%
Platelet-Derived Growth Factor alpha Receptor
36%
Salmonella typhimurium
35%
Operon
35%
Influenza B virus
34%
Indoleamine-Pyrrole 2,3,-Dioxygenase
34%
Enterobacteriaceae
34%
Enterococcus faecium
33%
Staphylococcus aureus
33%
Peptides
32%
Focal Adhesion Protein-Tyrosine Kinases
32%
Phospholipases
31%
Escherichia coli Proteins
31%
Deoxyribonuclease I
30%
Cyclin-Dependent Kinase 2
30%
Focal Adhesions
30%
Carbohydrate Metabolism
29%
Oxidative Phosphorylation
29%
Influenza A virus
28%
Disulfides
27%
Salts
27%
Cell Wall
26%
Chemistry
Protein
76%
Bromodomain-Containing Protein 4 Inhibitor
53%
Binding Site
45%
Pharmacokinetics
41%
Hemolysin
39%
Aminopyrimidine
38%
Metabolic
38%
Glutamine
37%
Poly(ADPribose)
35%
Chromone
35%
Oligomerization
33%
Growth Inhibition
30%
Inorganic Salt
28%
Antiinflammatory
28%
Histone
27%
Tyrosine
26%
Mutation
24%
Drug Target
23%
Coenzyme A
23%
Once Daily
21%
Permeability
20%
Molecule
20%
Polarization
19%
Kynurenine
18%
NMR Spectroscopy
17%
Binding Agent
17%
Co Crystallization
15%
Pharmacological Metabolism
14%
Histidine Residue
14%
% Inhibition
14%
Crystallography
13%
Crystal Structure
12%
Hexane
11%
Reduction
11%
Carboxylation
10%
Pantothenate
10%
Lethal
10%
Plastic Property
9%
Dose
9%
Oligomer
8%