Ananthanarayanan et al., 1981 - Google Patents
Circular dichroism of type 13 β-turn in linear tripeptides containing L-proline and D-alanineAnanthanarayanan et al., 1981
- Document ID
- 17574337380626110620
- Author
- Ananthanarayanan V
- Shyamasundar N
- Publication year
- Publication venue
- Biochemical and Biophysical Research Communications
External Links
Snippet
The linear tripeptides tBoc-L-Prolyl-D-alanyl-L-leucine and tBoc-L-prolyl-D-alanyl-L-valine have been shown, from circular dichroism (CD) and infrared spectral data, to take up the 4→ 1 hydrogen bonded β-turn conformation in organic solvents. The CD spectra of these …
- 238000002983 circular dichroism 0 title abstract description 4
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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- 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
- C07K14/575—Hormones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/06—General 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
- C07K1/061—General 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General 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
- C07K1/113—General 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 without change of the primary structure
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General 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
- C07K1/1072—General 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Barrett et al. | Amino acids and peptides | |
Henderson et al. | Primary structure of human carbonic anhydrase C. | |
Degens et al. | Paleobiochemistry of molluscan shell proteins | |
CN101186940B (en) | Process for obtaining insulin or insulin derivatives with properly bonded cystine bonds | |
Welinder | Amino acid sequence studies of horseradish peroxidase: amino and carboxyl termini, cyanogen bromide and tryptic fragments, the complete sequence, and some structural characteristics of horseradish peroxidase C | |
Kimmerlin et al. | ‘100 years of peptide synthesis’: ligation methods for peptide and protein synthesis with applications to β‐peptide assemblies | |
Tyndall et al. | Macrocycles mimic the extended peptide conformation recognized by aspartic, serine, cysteine and metallo proteases | |
Welinder et al. | Amino‐Acid Sequences of Heme‐Linked, Histidine‐Containing Peptides of Five Peroxidases from Horseradish and Turnip | |
Maeda et al. | Some chemical properties of the venom of the rattlesnake, Crotalus viridis helleri | |
KR100237126B1 (en) | Rapid Synthesis and Search of Peptide Analogs | |
Brady et al. | Approaches to peptidomimetics which serve as surrogates for the cis amide bond: novel disulfide-constrained bicyclic hexapeptide analogs of somatostatic. | |
EP0528854B1 (en) | Fluorogenic peptides and their use in the determination of enzymatic activities | |
Venkatachalapathi et al. | Conformational analysis of small disulfide loops. Spectroscopic and theoretical studies on a synthetic cyclic tetrapeptide containing cystine | |
FI92708B (en) | A method of making a novel polypeptide useful as a medicament | |
Bruschi et al. | Non-heme iron proteins The amino acid sequence of rubredoxin from Desulfovibrio vulgaris | |
KR101155740B1 (en) | Epithelial cell growth promoter | |
Sanger | Some chemical investigations on the structure of insulin | |
Ananthanarayanan et al. | Circular dichroism of type 13 β-turn in linear tripeptides containing L-proline and D-alanine | |
Pallai et al. | Approaches to the synthesis of retro‐inverso peptides | |
Takagi et al. | Aplysia myoglobins with an unusual amino acid sequence | |
Puri et al. | Amino acid sequence of the winged bean (Psophocarpus tetragonolobus) basic lectin. Adenine binding and identification of the active-site tryptophan residue. | |
Kortt et al. | Amino acid sequence of a crystalline seed albumin (winged bean albumin‐1) from Psophocarpus tetragonolobus (L.) DC: Sequence similarity with Kunitz‐type seed inhibitors and 7S storage globulins | |
US5814470A (en) | Melittin-related polypeptides, mixture sets and libraries thereof | |
Avrutina et al. | Fmoc‐assisted synthesis of a 29‐residue cystine‐knot trypsin inhibitor containing a guaninyl amino acid at the P1‐position | |
Pawlak et al. | Synthesis of a novel side‐chain to side‐chain cyclized enkephalin analogue containing a carbonyl bridge |