[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Niebler et al., 1969 - Google Patents

The amino acid sequence of the L-glutamic acid containing mureins of Micrococcus luteus and M. freudenreichii

Niebler et al., 1969

Document ID
14610661334747846872
Author
Niebler E
Schleifer K
Kandler O
Publication year
Publication venue
Biochemical and Biophysical Research Communications

External Links

Snippet

The mureins (peptidoglycans) known so far, contain 1 mole of D-glutamic acid per mole of murein subunit (1, 2, 3). Studying the mureins of micrococci, we found two strains, which contain 2 moles of glutamic acid per subunit, one of the D-and one of the L-configuration …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
    • C07K5/101Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/12General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups

Similar Documents

Publication Publication Date Title
Payne et al. The primary structure of alamethicin
Kimmel et al. The properties of papain
Brew et al. The complete amino acid sequence of bovine α-lactalbumin
Kauffman et al. The basic proline-rich proteins in human parotid saliva from a single subject
Ambler et al. The use of thermolysin in amino acid sequence determination.
Ryle et al. Parapepsins: two proteolytic enzymes associated with porcine pepsin
NOMOTO et al. A proteolytic enzyme of Streptomyces griseus VII. Substrate specificity of Streptomyces griseus protease
Spencer Structural studies and organic ligand-binding properties of bovine plasma albumin
Ong et al. The amino-terminal sequence of porcine pepsinogen
FUJIMAKI et al. Applying proteolytic enzymes on soybean. 3. Diffusable bitter peptides and free amino acids in peptic hydrolyzate of soybean protein
Harboe et al. The Activation of Bovine Pepsinogen: SEQUENCE OF THE PEPTIDES RELEASED, IDENTIFICATION OF A PEPSIN INHIBITOR
KR850001288A (en) Method for preparing aprotinin homologue
JPS6339237B2 (en)
Maita et al. Amino‐acid sequence of the L‐1 light chain of chicken cardiac‐muscle myosin
Brew et al. The isolation and characterization of the tryptic, chymotryptic, peptic, and cyanogen bromide peptides from bovine α-lactalbumin
Frøyshov et al. On the biosynthesis of bacitracin by a soluble enzyme complex from Bacillus licheniformis
Niebler et al. The amino acid sequence of the L-glutamic acid containing mureins of Micrococcus luteus and M. freudenreichii
Doonan et al. The primary structure of aspartate aminotransferase from pig heart muscle determined in part using a protease with specificity for lysine
König et al. The amino acid sequence of the peptide moiety of the pseudomurein from Methanobacterium thermoautotrophicum
Sengupta et al. Comparative studies on calotropins DI and DII from the latex of Calotropis gigantea
Ishii et al. Amino acid sequence studies of the light subunit of methylamine dehydrogenase from Pseudomonas AM1: existence of two residues binding the prosthetic group
Kress et al. The Basic Trypsin Inhibitor of Bovine Pancreas: IX. LOCATION OF THE REACTIVE SITE IN THE CARBOXAMIDOMETHYL DERIVATIVE
Scawen et al. The Amino‐Acid Sequence of Plastocyanin from Sambucus nigra L.(Elder)
Puigserver et al. A method for improving the nutritional value of food proteins: covalent attachment of amino acids
Ozols et al. The amino acid sequence of the tryptic peptides from cytochrome b5