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Chemical compound
Glycylglycine is the dipeptide of glycine, making it the simplest peptide. The compound was first synthesized by Emil Fischer and Ernest Fourneau in 1901
Glycylglycine
Amino acid
beginning with the formation of glycylglycine: 2 H 3N+ CH 2COO− → H 3N+ CH 2CONHCH 2COO− + H2O Pyrolysis of glycine or glycylglycine gives 2,5-diketopiperazine
Glycine
Class of enzymes
the hydrolysis of 2,5-diketopiperazine to glycylglycine: 2,5-diketopiperazine H2O glycylglycine This enzyme is a hydrolase, one acting on carbon-nitrogen
2,5-dioxopiperazine_hydrolase
Index of chemical compounds with the same molecular formula
naturally occurring α-amino acids that is used to biosynthesize proteins. Glycylglycine: a dipeptide synthesized from glycine residues that functions as a gamma-glutamyl
C4H8N2O3
Buffering agents for biochemical and biological research
HEPPS 8.10 7.6–8.6 1972 Tricine 8.15 7.4–8.8 1966 Glycinamide 8.20 1966 Glycylglycine 8.20 7.5–8.9 1966 Bicine 8.35 7.6–9.0 1966 TAPS 8.55 7.7–9.1 1972
Good's_buffers
Chemical process of joining two molecular entities by bonds of any kind
acids can also form dimers, which are called dipeptides. An example is glycylglycine, consisting of two glycine molecules joined by a peptide bond. Other
Dimerization
(antimicrobial) against Staphylococcus aureus. Lysostaphin is a 27 kDa glycylglycine endopeptidase, an antibacterial enzyme which is capable of cleaving
Lysostaphin
Chemical compound
P305+P351+P338 Related compounds Related compounds Acetylcysteine Glycylglycine Iminodiacetic acid Nitrilotriacetic acid N-Oxalylglycine Tiopronin Bucillamine
N-Acetylglycinamide
Shortest peptide molecule, containing two amino acids joined by a single peptide bond
Glycylglycine is the simplest dipeptide.
Dipeptide
Chemical compound
(oral, rat) Related compounds Related alkanoic acids Acetylcysteine Glycylglycine Iminodiacetic acid Nitrilotriacetic acid N-Oxalylglycine Bucillamine
Tiopronin
Index of chemical compounds with the same name
Diglycine may refer to: Glycylglycine, dipeptide of glycine Iminodiacetic acid, an acid This set index article lists chemical compounds articles associated
Diglycine
Chemical compound
(352 °F; 451 K) Related compounds Related alkanoic acids Acetylcysteine Glycylglycine Nitrilotriacetic acid N-Oxalylglycine Tiopronin Bucillamine Oxalyldiaminopropionic
Iminodiacetic_acid
Chemical compound
M01CC02 (WHO) Related compounds Related Alkanoic acids Acetylcysteine Glycylglycine Iminodiacetic acid Nitrilotriacetic acid N-Oxalylglycine Tiopronin
Bucillamine
Chemical compound
Related compounds Related alkanoic acids N-Acetylaspartylglutamic acid Glycylglycine α-Aminobutyric acid Except where otherwise noted, data are given for
Ophthalmic_acid
Scientific method
Cameleons consist of two different fluorescent proteins, CaM, M13, and a glycylglycine linker. In the absence of Ca2+, only the donor blue-shifted fluorescent
Calcium_imaging
Chemical compound
(pKb) 11.170 Related compounds Related compounds N-Acetylglycinamide Glycylglycine Oxalyldiaminopropionic acid Except where otherwise noted, data are given
N-Oxalylglycine
in collaboration with Ernest Fourneau, synthesizes the dipeptide, glycylglycine, and also publishes his work on the hydrolysis of casein. Edith Humphrey
1901_in_science
MeSH D12.644.456.345.360.300 – enalaprilat MeSH D12.644.456.345.575 – glycylglycine MeSH D12.644.456.345.600 – lisinopril MeSH D12.644.456.400 – n-formylmethionine
List_of_MeSH_codes_(D12.644)
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