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A carboxypeptidase is a protease enzyme that hydrolyzes a peptide bond at the carboxy-terminal end of a protein or peptide. 3D cartoon model, secondary structure color scheme, PDB 2v77, white background.

Intestinal microbiome,Probiotics health benefits,Gut bacteria,lactococcus, propionibacterium, bifidobacterium.

Botulinum toxin neurotoxic protein, 3D rendering. Produced by Clostridium botulinum. Cosmetically used to treat wrinkles.

A molecular model of Human Insulin. Isolated on black.

Avibactam is a diazobicyclooctane inhibitor of gram-negative and gram-positive bacteria. Avibactam (red) inhibits the bacterial enzyme beta-lactamase (blue) of Clostridioides difficile.

Cytochrome P450 molecule. CYP 3A4 is the most promiscuous of the human CYP enzymes. Molecular model. 3D rendering. Illustration

Evolution of nanotechnology and self-proliferation of therapeutic agents

3D cartoon and Gaussian surface models. PDB 3kqg, chain id color scheme, white background.

$Organic objects form a triangle. Artificial space incorporating organic materials.\nThis work was policy within one month. It is also an original work for this brief and cannot be used elsewhere.$

3D CG rendered image of scientifically accurate Enterobacteria Bacteriophage phiX174 Capsid Structure based on PDB : 1CD3 (capsomere)

PKM2 plays key roles in reprogramming cancer cells from energy production to growth (Warburg Effect). The dimeric form of the enzyme is not only less active in glycolysis but can also move into the nucleus to promote the transcription of other cancer-causing genes. A substrate analogon (red) is bound to the active site. PKM2 is a target for anti-cancer therapies. PDB entry: 6WP3.

Indoleamine 2,3 dioxygenase 1 (IDO1) protein. Tryptophan catabolic enzyme of the kynurenine pathway. 3D illustration.

Drug in capsule that begins to dissolve in the body

3D cartoon model, secondary structure color scheme, PDB 4krf, white background

$In recent years, the presence of bacteria in the body has been reported as the cause of various biological phenomena, and the subject of bacteria is often a hot topic. This image shows bacteria under a microscope. These images of bacteria can be used universally for both good and bad bacteria.\nThis image was not created by AI.$

Collagen protein molecule. Molecular model. 3D rendering. Illustration

The amyloid beta peptide (light blue) is a component of the amyloid precursor protein, which is bound to a cell membrane. The gamma secretase enzyme cuts the free form, that aggregates to amyloid plaques. Source: PDB entries 2beg, 1mwp

Molecular Model of Human Insulin with disulfide bonds shown.

Glucose-6-phosphate dehydrogenase (G6PD) protein. Enzyme of the pentose phosphate pathway that generates co-enzyme NADPH. 3D illustration.

Covid-19 Coronavirus Variants Omicron Delta Gamma Beta Alpha Pandemic Virus Disease Mutation

3D cartoon and Gaussian surface models, chain id color scheme, PDB 4ci9, white background

Squash preparation of onion root tip cells stained to reveal chromosomes, Bright field illumination, light microscopy. This image was taken with the X40 objective lens. Depth of focus is extremely low at this magnification. Smaller apertures give greater depth of focus, but image quality deteriorates and resolution is greatly reduced. The aperture in this image was optimised for contrast and resolution. Chromatic abberation is inevitable in light microscopy, but has been kept to a minimum in this image.

Cholera toxin, molecular model. Cholera toxin (choleragen) is a protein complex secreted by the bacterium Vibrio cholerae, that causes the disease cholera. It is made up of a wedge-shaped A subunit (right part of illustration) and five B subunits (left part of illustration) that form a ring which binds to the intestinal lining. In its most severe forms, cholera is one of the most rapidly fatal illnesses known.

A space-filling molecular model of collagen, a fibrous protein that provides structural support in animals. It has a distinctive triple helix structure. Isolated on black.

PETase (left) degrades polyethylene terephtalate (PET) into monohydroxyethyl terephthalate (MHET) and MHETase degrades MHET ethylene glycol (EG) and terephthalic acid (TPA). The substrates in the binding sites are depicted in red.

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