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・ Peptide amphiphiles
・ Peptide bond
・ Peptide computing
・ Peptide deformylase
・ Peptide hormone
・ Peptide library
・ Peptide mass fingerprinting
・ Peptide methionine sulfoxide reductase
・ Peptide microarray
・ Peptide nucleic acid
・ Peptide PHI
・ Peptide plane flipping
・ Peptide sequence
・ Peptide sequence tag
・ Peptide spectral library
Peptide synthesis
・ Peptide T
・ Peptide transporter 1
・ Peptide vaccine
・ Peptide YY
・ Peptide-aspartate beta-dioxygenase
・ Peptide-mass fingerprint
・ Peptide-methionine (R)-S-oxide reductase
・ Peptide-methionine (S)-S-oxide reductase
・ Peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase
・ Peptide-O-fucosyltransferase
・ Peptide-transporting ATPase
・ Peptide-tryptophan 2,3-dioxygenase
・ Peptidergic
・ Peptides (journal)


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Peptide synthesis : ウィキペディア英語版
Peptide synthesis

In organic chemistry, peptide synthesis is the production of peptides, which are organic compounds in which multiple amino acids are linked via amide bonds, also known as peptide bonds. The biological process of producing long peptides (proteins) is known as protein biosynthesis.
== Chemistry ==
Peptides are synthesized by coupling the carboxyl group or C-terminus of one amino acid to the amino group or N-terminus of another. Due to the possibility of unintended reactions, protecting groups are usually necessary. Chemical peptide synthesis starts at the C-terminal end of the peptide and ends at the N-terminus. This is the opposite of protein biosynthesis, which starts at the N-terminal end.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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