thioester bond covalent


This process is experimental and the keywords may be updated as the learning algorithm improves. They also participate in the synthesis of a number of other cellular components, including peptides, fatty acids, sterols, terpenes, porphyrins, and others. Proc Natl Acad Sci USA 75: 5165–5169, Parker CJ, Soldata CM, Ross WF (1984) Abnormality of glycophorin-α on paroxysmal nocturnal hemoglobinemia erythrocytes.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) KC622314. domain on Cpa, the N-terminal domain of Cpa (CpaN). Remove maintenance message Structural model for covalent adhesion of the Streptococcus pyogenes pilus through a thioester bond. Academic, New York, p 239, Nonaka M, Nakayama K, Yeul YD, Takahashi M (1985) Complete nueleotide and derived amino acid sequence of the fourth component of mouse complement (C4). EMBO J 5: 2873–2881, Zhao B, Musci G, Susawara Y, Berliner LJ (1988) Spin label and fluorescence studies of the thioester bonds in human α, James S. McDonnell Department of Genetics, MRC Immunochemistry Unit, Department of Biochemistry, https://doi.org/10.1007/978-3-642-74977-3_4, Current Topics in Microbiology and Immunology. Thioesters are common intermediates in many biosynthetic reactions, including the formation and degradation of fatty acids and mevalonate, precursor to steroids. Thus, thioesters are common intermediates in the conversion of alkyl halides to alkyl thiols. 167.86.90.180. Dev Comp Immunol 11:279–286, Law SKA (1983) Non-enzymic activation of the covalent binding reaction of the complement protein C3. Mol Immunol 25: 821–828, Yu CY, Belt KT, Cortes CM, Campbell RD, Porter RR (1986) Structural basis of the polymorphism of human complement components C4A and C4B: gene size reactivity and antigenicity. Biochemistry 20: 4458–4467, Janatova J, Tack BF (1981) Fourth component of human complement: studies of an amine-sensitive site comprised of a thiol component. Here, we have characterized a second active thioester-containing Eventually, [these] thioesters could have served to usher in ATP through its ability to support the formation of bonds between phosphate groups. J Biol Chem 260: 10936–10943, O’Neill GJ, Yang SY, Dupont B (1978) Two HLA-linked loci controlling the fourth component of human complement. Unable to display preview.

Biochem J 211: 381–389, Law SK, Levine RP (1977) Interaction between the third complement protein and cell surface macromolecules.
Download preview PDF. Immunogenetics 21: 299–311, Sepich DS, Noonan DJ, Ogata RT (1985) Complement cDNA sequence of the fourth component of murine complement.

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