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Histidine peptides

Effect of Various Histidine Peptides on the Rate of Hydrolysis of p-Nitrophenyl Acetate at pH 7.73 ... [Pg.208]

Hart BR, Shea KJ. Molecular imprinting for the recognition of N-terminal histidine peptides in aqueous solution. Macromolecules 2002 35 6192-6201. [Pg.423]

This is indeed the case. Table XVIII summarizes preliminary results (Shaltiel and Patchornik, 1961) on the reaction of some histidine peptide... [Pg.271]

Another possible aspect of histidine peptide cleavage is introduced by the great lability of 4(5H)-imidazolones (CXXXIII) (Freter el al., 19.57 Brown and Kies, 1959). In their lability and eagerness to open up to forma-raidino acids (CXXXIV) they almost resemble anhydrides (Kny and Witkop, 1959). It is not unlikely that such 4(5H)-imidazolones can be produced nonenzymatically. Such selective oxidation of a histidine peptide to a 4(5H)-imidazolone derivative introduces the possibility of translacta-... [Pg.272]

At the present exploratory level the cleavage of histidine peptides has to await further refinement in order to be applicable to proteins and to qualify as a selective cleavage. [Pg.273]

In a histidine peptide containing no tryptophan and no tyrosine NBS may be used to advantage for the cleavage of the peptide bond next to... [Pg.297]

Ljungquist C., Breitholtz A., Brink-Nilsson H., Moks T., Uhlen M. and Nilsson B. 1989. Immobilization and affinity purification of recombinant proteins using histidine peptide fusions, Eur. J. Biochem., 186, 563. [Pg.100]

The polymerizable methacrylamide-NTA-Ni mixed-complex was prepared by combining aqueous solutions of NTA monomer with NiS04. The prepolymerization complex was then formed by addition of the N-terminal histidine peptide his-ala. The octahedral geometry of 46 was confirmed by comparing the electronic spectra for 46 with known absorbance bands of octahedral complexes of Ni(II) [32]. In addition, negative-ion electrospray mass spectroscopy of 46 showed peaks corresponding to the lithium salt of 46 (m/z = 546). [Pg.161]

The characteristic P-alanyl histidine peptides, camosine, anserine and balenine, of muscle are described in section 1.3.4.2. Their contribution to taste is discussed in 12.9.1. [Pg.584]


See other pages where Histidine peptides is mentioned: [Pg.51]    [Pg.490]    [Pg.276]    [Pg.403]    [Pg.64]    [Pg.221]    [Pg.270]    [Pg.271]    [Pg.271]    [Pg.271]    [Pg.208]    [Pg.161]    [Pg.307]    [Pg.28]    [Pg.328]    [Pg.322]    [Pg.22]    [Pg.254]    [Pg.107]    [Pg.260]    [Pg.266]    [Pg.322]    [Pg.114]    [Pg.270]   
See also in sourсe #XX -- [ Pg.22 , Pg.29 , Pg.394 ]

See also in sourсe #XX -- [ Pg.22 , Pg.29 , Pg.394 ]




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Cationic peptides histidine-rich

Histidine containing peptides

Histidine peptides, hydrolysis

Histidines histidine-containing peptides

Peptide histidine isoleucine

Peptide histidine methionine

Peptide histidine methionine (PHM

Peptide, amino acid sequence histidine-containing

Peptides histidine-/methionine-containing

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