[go: up one dir, main page]

Walker, 1952 - Google Patents

Arginosuccinic acid from Chlorella

Walker, 1952

View PDF
Document ID
6599713669510544990
Author
Walker J
Publication year
Publication venue
Proceedings of the National Academy of Sciences

External Links

Snippet

BIOCHEMISTRY: JB WALKER but when sufficient malate or fumarate was also added, arginosuccinic acid was formed instead of citrulline. In arginosuccinate production arginine could notbe replaced by citrul-line, ornithine, creatine, or guanidine, while the role of …
Continue reading at www.pnas.org (PDF) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates

Similar Documents

Publication Publication Date Title
Walker Arginosuccinic acid from Chlorella
Delpierre et al. Inactivation of pepsin by diphenyldiazomethane.
US4640893A (en) Novel rhodamine derivatives as fluorogenic substrates for proteinases
US4557862A (en) Rhodamine derivatives as fluorogenic substrates for proteinases
Gale et al. The assimilation of amino acids by bacteria. 20. The incorporation of labelled amino acids by disrupted staphylococcal cells
Borsook et al. Incorporation in vitro of labeled amino acids into proteins of rabbit reticulocytes
US5393669A (en) Compositions and methods for protein structural determinations
Ha et al. ATPase kinetics of recombinant bovine 70 kDa heat shock cognate protein and its amino-terminal ATPase domain
Barton-Wright The microbiological assay of amino acids. I. The assay of tryptophan, leucine, iso leucine, valine, cystine, methionine, lysine, phenylalanine, histidine, arginine and threonine
Gapski et al. Synthesis of a fluorescent derivative of amethopterin
Narita Reaction of Anhydrous Formic Acid with Proteins1
US4782139A (en) Selective chemical removal of a protein amino-terminal residue
Wolfrom et al. The relation between the structure of heparin and its anticoagulant activity
EP0689541B1 (en) Pterin derivatives and their use for the preparation of immunoassays
EP0003786A1 (en) Stereoselective separation of phenylglycine derivatives and 4-hydroxyphenylglycine derivatives with enzyme-containing polymers
Denoël et al. Stereoselective synthesis of lanthionine derivatives in aqueous solution and their incorporation into the peptidoglycan of Escherichia coli
Hishizawa et al. Studies on the formation of transfer ribonucleic acid-ribosome complexes: XVII. The effect of tRNA on aminoacyl-oligonucleotide binding to ribosomes
Troll The reaction of naphthoquinone-4-sulfonate with imino acids
Walker Biosynthesis of canavaninosuccinic acid from canavanine and fumarate in kidney
FREIST et al. Threonyl‐tRNA, Lysyl‐tRNA and Arginyl‐tRNA Synthetases from Baker's Yeast: Substrate Specificity with Regard to ATP Analogues
US3560483A (en) 1,4-dialkyl-3,6-diphenylepi(thio,dithia or tetrathia)-2,5-piperazinediones
Heymann et al. The preparation and some biological properties of the asparagine analog L-2-amino-2-carboxyethanesulfonamide
ES2243251T3 (en) PROTEINS AND AMINATED ACIDS, ISOTOPICALLY MARKING AND SITE SPECIFICS, AND BIOCHEMICAL PRECURSORS INTENDED FOR THESE PROTEINS AND AMINATED ACIDS.
US3755081A (en) Process for preparing l-serine
CA1133471A (en) Cephapirin salts with amino acids