Literature DB >> 999637

Alternative products in the reaction of 2-nitro-5-thiocyanatobenzoic acid with thiol groups.

N C Price.   

Abstract

2-Nitro-5-thiocyanatobenzoic acid has been proposed as a reagent for converting thiol groups in proteins into their S-cyano derivatives. Evidence was obtained for formation of both the S-cyano derivative and the mixed disulphide derivative. Formation of the S-cyano derivative can be promoted by addition of excess of CN-to the reaction mixture.

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Year:  1976        PMID： 999637      PMCID： PMC1164054          DOI： 10.1042/bj1590177

Source DB:  PubMed          Journal:  Biochem J        ISSN： 0264-6021            Impact factor:   3.857


  8 in total

1.  Tissue sulfhydryl groups.

Authors:  G L ELLMAN
Journal:  Arch Biochem Biophys       Date:  1959-05       Impact factor: 4.013

2.  Simple alkanethiol groups for temporary blocking of sulfhydryl groups of enzymes.

Authors:  D J Smith; E T Maggio; G L Kenyon
Journal:  Biochemistry       Date:  1975-02-25       Impact factor: 3.162

3.  The crystallization and properties of glyceraldehyde-3-phosphate dehydrogenase isolated from rabbit muscle by a simplified procedure.

Authors:  R E Amelunxen; D O Carr
Journal:  Biochim Biophys Acta       Date:  1967-03-15

4.  A study of the sulfhydryl groups of the catalytic subunit of Escherichia coli aspartate transcarbamylase. The use of enzyme--5-thio-2-nitrobenzoate mixed disulfides as intermediates in modifying enzyme sulfhydryl groups.

Authors:  T C Vanaman; G R Stark
Journal:  J Biol Chem       Date:  1970-07-25       Impact factor: 5.157

5.  Cytoplasmic aspartate aminotransferase: syncatalytic sulfhydryl group modification.

Authors:  W Birchmeier; K J Wilson; P Christen
Journal:  J Biol Chem       Date:  1973-03-10       Impact factor: 5.157

6.  Amino acid effector binding to rabbit muscle pyruvate kinase.

Authors:  F J Kayne; N C Price
Journal:  Arch Biochem Biophys       Date:  1973-11       Impact factor: 4.013

Review 7.  Chemical approaches to the properties of active sites of enzymes.

Authors:  B L Vallee; J F Riordan
Journal:  Annu Rev Biochem       Date:  1969       Impact factor: 23.643

8.  The reaction of papain with Ellman's reagent (5,5'-dithiobis- (2-nitrobenzoate) dianion).

Authors:  K Brocklehurst; M Kierstan; G Little
Journal:  Biochem J       Date:  1972-07       Impact factor: 3.857
  8 in total
  5 in total

1.  Optimization and applications of CDAP labeling for the assignment of cysteines.

Authors:  Gary D Pipes; Andrew A Kosky; Jeffrey Abel; Yu Zhang; Michael J Treuheit; Gerd R Kleemann
Journal:  Pharm Res       Date:  2005-07-22       Impact factor: 4.200

2.  Reply to Giamogante et al.: The effect of low cyanide on O2 consumption is best observed in physiological, rather than reductionist, systems.

Authors:  Karim Zuhra; Csaba Szabo
Journal:  Proc Natl Acad Sci U S A       Date:  2021-09-28       Impact factor: 11.205

3.  13C-n.m.r. of the cyanylated apoflavodoxin and flavodoxin from Clostridium pasteurianum.

Authors:  G M Doherty; S G Mayhew; J P Malthouse
Journal:  Biochem J       Date:  1993-08-15       Impact factor: 3.857

4.  Rat liver guanidinoacetate methyltransferase. Proximity of cysteine residues at positions 15, 90 and 219 as revealed by site-directed mutagenesis and chemical modification.

Authors:  Y Takata; T Date; M Fujioka
Journal:  Biochem J       Date:  1991-07-15       Impact factor: 3.857

Review 5.  The two faces of cyanide: an environmental toxin and a potential novel mammalian gasotransmitter.

Authors:  Karim Zuhra; Csaba Szabo
Journal:  FEBS J       Date:  2021-08-05       Impact factor: 5.622
  5 in total

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