Medicine & Life Sciences
Penicillin-Binding Proteins
100%
Histidine Kinase
89%
Biological Products
49%
Lactams
42%
Proteins
38%
Bacteria
37%
Adenosine Triphosphate
36%
Streptococcus pneumoniae
32%
Anti-Bacterial Agents
29%
Sulfhydryl Compounds
26%
Peptidoglycan
26%
thiophosphoric acid
25%
UDP-galactopyranose mutase
25%
Cell Division
24%
Streptomyces coelicolor
23%
Mass Spectrometry
23%
Metabolomics
20%
Streptomyces
19%
Phosphotransferases
19%
Phosphoproteins
18%
Intramolecular Transferases
17%
Cell Wall
17%
Hydroxyl Radical
16%
Virulence
16%
Lactones
16%
Metabolome
14%
Siderophores
14%
ferrioxamine B
14%
Bacillus subtilis
14%
Uridine Diphosphate
13%
Iron
13%
Microbial Drug Resistance
12%
streptorubin B
12%
Carboxylic Acids
12%
cephalosporin C
12%
Escherichia coli
11%
Galactose
11%
Enzymes
11%
Fluorescence Polarization
10%
Phosphorylation
10%
borrelidin
10%
Microbiota
10%
Growth
10%
Ligands
9%
adenosine 5'-O-(3-thiotriphosphate)
9%
Ion Mobility Spectrometry
9%
Histidine
9%
actinorhodin
9%
Carbapenems
9%
Pharmaceutical Preparations
8%
Chemical Compounds
Histidine
57%
Occurrence in Nature
56%
Probe
53%
Protein
42%
Chemoselectivity
30%
Antimicrobial Agent
29%
Metabolite
21%
Molecule
16%
Resistance
16%
Metal Oxide
13%
Collisionally Activated Dissociation (CAD)
12%
Nanomaterial
12%
Siderophore
11%
Phosphotransferase Inhibitor
11%
Benzoisochromanequinone
11%
Mass Spectrometry
11%
Borrelidin
9%
Ferrioxamine B
9%
Fluorescence
9%
Cephalosporin C
8%
Non Prescription Drug
8%
Hydroxyl
8%
Drug Target
8%
Metabolic
8%
Superbase
7%
Polymyxin
7%
Tyrosine Kinase Inhibitor
7%
Biosynthesis
7%
Molecular Modeling
7%
Nucleoside Triphosphate
7%
Desilylation
7%
Silyl Ether
6%
Fragmentation
6%
Threonine
6%
Neutralization Reaction
6%
Modification
6%
Environment
6%
Molecular Cluster
6%
Tyrosine
6%
Ligand
6%
Phenol
6%
Carboxylic Acid
6%
Peptide
6%
Block Like Crystal
5%
Uridine
5%
Serine
5%
Reaction Yield
5%
Lectin
5%