Target type: molecularfunction
Binding to a carbohydrate derivative. [GOC:pr]
Carbohydrate derivative binding is a molecular function that encompasses the ability of proteins and other molecules to interact with modified carbohydrate structures. These modifications can include the addition of functional groups, such as phosphates, sulfates, or acetyl groups, or the attachment of other molecules, such as lipids or proteins. Carbohydrate derivatives play diverse roles in cellular processes, including cell signaling, adhesion, and recognition.
The binding of carbohydrate derivatives by proteins can be highly specific, with individual proteins recognizing and binding to specific modifications on specific carbohydrates. This specificity is essential for regulating a wide range of biological processes.
Examples of carbohydrate derivatives that are commonly bound by proteins include:
* **Glycoproteins:** Proteins with attached carbohydrate chains.
* **Glycolipids:** Lipids with attached carbohydrate chains.
* **Proteoglycans:** Proteins with attached glycosaminoglycan chains.
* **Phosphorylated carbohydrates:** Carbohydrates with attached phosphate groups.
* **Sulfated carbohydrates:** Carbohydrates with attached sulfate groups.
* **Acetylated carbohydrates:** Carbohydrates with attached acetyl groups.
The binding of carbohydrate derivatives by proteins can occur through a variety of mechanisms, including:
* **Hydrogen bonding:** The formation of hydrogen bonds between the protein and the carbohydrate derivative.
* **Van der Waals interactions:** Weak, short-range interactions between the protein and the carbohydrate derivative.
* **Hydrophobic interactions:** Interactions between non-polar regions of the protein and the carbohydrate derivative.
* **Electrostatic interactions:** Interactions between charged groups on the protein and the carbohydrate derivative.
The specific mechanism of binding can vary depending on the structure of the protein and the carbohydrate derivative.
Carbohydrate derivative binding plays a critical role in a wide range of cellular processes, including:
* **Cell signaling:** Carbohydrate derivatives can act as ligands for cell surface receptors, triggering intracellular signaling pathways.
* **Cell adhesion:** Carbohydrate derivatives can mediate cell-cell interactions, playing a role in tissue formation and development.
* **Immune recognition:** Carbohydrate derivatives on the surface of pathogens can be recognized by the immune system, triggering an immune response.
* **Protein folding:** Carbohydrate derivatives can play a role in the folding and stability of proteins.
* **Enzyme activity:** Carbohydrate derivatives can act as substrates, cofactors, or inhibitors of enzymatic reactions.
The study of carbohydrate derivative binding is an active area of research, with ongoing efforts to understand the complex interactions between proteins and these modified carbohydrates. This knowledge has the potential to lead to the development of new therapies for a variety of diseases, including cancer, infections, and autoimmune disorders.'
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Protein | Definition | Taxonomy |
---|---|---|
Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 | A glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q06210] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
aaptamine | aaptamine: natural product from sea sponge Aaptos aaptos; structure given in first source; RN from CA Index Guide 1984 | ||
n(3)-(4-methoxyfumaroyl)-2,3-diaminopropionic acid | N(3)-(4-methoxyfumaroyl)-2,3-diaminopropionic acid : A monocarboxylic acid amide obtained by the formal condensation of the terminal amino group of 3-amino-L-alanine with the carboxy group of (2E)-4-methoxy-4-oxobut-2-enoic acid. N(3)-(4-methoxyfumaroyl)-2,3-diaminopropionic acid: inhibits glucosamine synthetase in E coli; structure given in first source; RN given refers to (S-(E)-isomer) | enoate ester; methyl ester; monocarboxylic acid amide | metabolite |