释义 |
peptide
pep·tide P0180000 (pĕp′tīd′)n. Any of various natural or synthetic compounds containing two or more amino acids joined by peptide bonds that link the carboxyl group of one amino acid to the amino group of another. [pept(one) + -ide.] pep·tid′ic (-tĭd′ĭk) adj.pep·tid′i·cal·ly adv.peptide (ˈpɛptaɪd) n (Elements & Compounds) any of a group of compounds consisting of two or more amino acids linked by chemical bonding between their respective carboxyl and amino groups. See also peptide bond, polypeptidepep•tide (ˈpɛp taɪd) n. a compound containing two or more amino acids in which the carboxyl group of one acid is linked to the amino group of the other. [1905–10; pept (ic) + -ide] pep·tide (pĕp′tīd′) A chemical compound that is composed of a chain of two or more amino acids and is usually smaller than a protein. Some hormones and antibiotics are peptides.ThesaurusNoun | 1. | peptide - amide combining the amino group of one amino acid with the carboxyl group of another; usually obtained by partial hydrolysis of proteinamide - any organic compound containing the group -CONH2fibrinopeptide - peptide released from the amino end of fibrinogen by the action of thrombin to form fibrin during clotting of the bloodpolypeptide - a peptide containing 10 to more than 100 amino acidsendorphin - a neurochemical occurring naturally in the brain and having analgesic properties | Translations
peptide
peptide, organic compound composed of amino acidsamino acid , any one of a class of simple organic compounds containing carbon, hydrogen, oxygen, nitrogen, and in certain cases sulfur. These compounds are the building blocks of proteins. ..... Click the link for more information. linked together chemically by peptide bonds. The peptide bond always involves a single covalent link between the α-carboxyl (oxygen-bearing carbon) of one amino acid and the amino nitrogen of a second amino acid. In the formation of a peptide bond from two amino acids, a molecule of water is eliminated. Small peptides with fewer than about ten constituent amino acids are called oligopeptides, and peptides with more than ten amino acids are termed polypeptides. Compounds with molecular weights of more than 10,000 (50–100 amino acids) are usually termed proteins. Organisms commonly contain appreciable quantities of low-molecular-weight peptides some arising from proteins while others are synthesized directly. Certain of these molecules are unusual in that they incorporate amino acids not found in proteins such as amino acids of the d-configuration. Among the biological peptides are many with physiological or antibacterial activity, such as the peptide hormones oxytocinoxytocin , hormone released from the posterior lobe of the pituitary gland that facilitates uterine contractions and the milk-ejection reflex. The structure of oxytocin, a cyclic peptide consisting of nine amino acids, was determined in 1953 and in the same year it was ..... Click the link for more information. and vasopressin; adrenocorticotropic hormoneadrenocorticotropic hormone , polypeptide hormone secreted by the anterior pituitary gland. Its chief function is to stimulate the cortex of the adrenal gland to secrete adrenocortical steroids, chief among them cortisone. ..... Click the link for more information. (ACTH), secreted by the pituitary gland; and several cyclic peptides, in which the amino-acid sequence forms a ring structure rather than a straight chain, such as the antibiotics tyrocidin and gramicidingramicidin , antibiotic obtained from the bacterial species Bacillus brevis, which is found in soil. Gramicidin is particularly effective against gram-positive bacteria (see Gram's stain). ..... Click the link for more information. . Laboratory synthesis of peptides has risen to the level of a well-defined art in recent years. Synthetic peptides, composed of as many as a hundred amino acids in specified sequence, have been prepared in the laboratory with good purity and high yields.Peptide A compound that is made up of two or more amino acids joined by covalent bonds which are formed by the elimination of a molecule of H2O from the amino group of one amino acid and the carboxyl group of the next amino acid. Peptides larger than about 50 amino acid residues are usually classified as proteins. Glutathione is the most abundant peptide in mammalian tissue. Hormones such as oxytocin (8), vasopressin (8), glucagon (29), and adrenocorticotropic hormone (39) are peptides whose structures have been deduced; in parentheses are the numbers of amino acid residues for each peptide. For each step in the biological synthesis of a peptide or protein there is a specific enzyme or enzyme complex that catalyzes each reaction in an ordered fashion along the biosynthetic route. However, it is noteworthy that, although the biological synthesis of proteins is directed by messenger RNA on cellular structures called ribosomes, the biological synthesis of peptides does not require either messenger RNA or ribosomes. See Amino acids, Protein, Ribonucleic acid (RNA), Ribosomes Peptide an organic substance consisting of identical or different amino-acid residues joined by peptide bonds. Peptides are classified according to the number of component amino-acid residues as dipeptides, tripeptides, tetrapeptides, and so on, and as polypeptides. Small quantities of low-molecular-weight peptides occur in nearly all living cells. For example, the tripeptide glutathione is widely distributed in plant and animal tissues, and the dipeptides anserine and carnosine are present in the muscle tissue of vertebrates. Many natural biologically active substances are classified as peptides, including certain hormones (insulin, adrenocortico-trophic hormone, glucagon, vasopressin, oxytocin), antibiotics (gramicidin, bacillin), and angiotensins and kinins, which are present in blood plasma. The peptide molecule is a linear or branched chain. If the molecule is linear, it has two termini with one terminal amino group (—NH2) and one terminal carboxyl group (—COOH). Peptides with a closed-chain structure are called cyclopeptides, which include many bacterial toxins, hormones, and antibiotics. Many natural peptides contain amino acids that are not present in proteins, for example, D-amino acids. Peptides exhibit amphoteric properties, give biuret (beginning with tripeptides) and ninhydrin reactions, and dissolve readily in water, acids, and alkalies but are practically insoluble in organic solvents. They decompose upon heating to 200°-300°C. In living cells, peptides are synthesized from amino acids or formed during the enzymatic breakdown of proteins. Chemical synthesis is used to obtain many biologically active natural peptides and their numerous analogues. Advancements in peptide chemistry have resolved many complex problems in modern biochemistry and molecular biology, such as the deciphering of the genetic code. REFERENCEKhimiia biologicheski aktivnykh prirodnykh soedinenii. Moscow, 1970.N. N. CHERNOV peptide[′pep‚tīd] (biochemistry) A compound of two or more amino acids joined by peptide bonds. peptide any of a group of compounds consisting of two or more amino acids linked by chemical bonding between their respective carboxyl and amino groups peptide
peptide [pep´tīd] any member of a class of compounds of low molecular weight that yield two or more amino acids" >amino acids on hydrolysis. They are the constituent parts of proteins and are formed by loss of water from the NH2 and COOH groups of adjacent amino acids. Peptides are known as dipeptides, tripeptides, tetrapeptides, and so on depending on the number of amino acids in the molecule. See also polypeptide.vasoactive intestinal peptide vasoactive intestinal polypeptide.pep·tide (pep'tīd), A compound of two or more amino acids in which a carboxyl group of one is united with an amino group of another, with the elimination of a molecule of water, thus forming a peptide bond, -CO-NH-; that is, a substituted amide. See also: polypeptide. Compare: eupeptide bond, isopeptide bond. peptide (pĕp′tīd′)n. Any of various natural or synthetic compounds containing two or more amino acids joined by peptide bonds that link the carboxyl group of one amino acid to the amino group of another. pep·tid′ic (-tĭd′ĭk) adj.pep·tid′i·cal·ly adv.peptide A biomolecule consisting of two or more amino acids joined by a peptide bond, which combine to make proteins.pep·tide (pep'tīd) A compound of two or more amino acids in which a carboxyl group of one is united with an amino group of another, with the elimination of a molecule of water, thus forming a peptide bond, -CO-NH-; i.e., a substituted amide. Compare: bioregulatorpeptide A chain of two or more AMINO ACIDS linked by peptide bonds between the amino and carboxyl groups of adjacent acids. Large peptides, containing many amino acids, are called polypeptides. Chains of linked polypeptides, are called PROTEINS. Peptides occur widely in the body. Many HORMONES are peptides.peptide any of a group of compounds consisting of two or more amino acids linked by chemical bonding. See PEPTIDE BOND, DIPEPTIDE.pep·tide (pep'tīd) Compound of two or more amino acids in which a carboxyl group of one is united with an amino group of another, with the elimination of a molecule of water, thus forming a peptide bond. peptide Related to peptide: peptide bondWords related to peptidenoun amide combining the amino group of one amino acid with the carboxyl group of anotherRelated Words- amide
- fibrinopeptide
- polypeptide
- endorphin
|