Synonymer & Anagram | Engelska ordet CYSTINE


CYSTINE

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5

Antal bokstäver

7

Är palindrom

Nej

11
CY
CYS
IN
NE
ST
STI
TI

1

4

10

386
CE
CEI
CEN


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Exempel på hur man kan använda CYSTINE i en mening

  • The thiol is susceptible to oxidation to give the disulfide derivative cystine, which serves an important structural role in many proteins.
  • As a residue in proteins, cystine serves two functions: a site of redox reactions and a mechanical linkage that allows proteins to retain their three-dimensional structure.
  • Cysteine in contrast can react with another cysteine residue to form one cystine and thereby form a cross link stabilizing the whole structure.
  • A variety of syntheses of lanthionine have been published including sulfur extrusion from cystine, ring opening of serine β-lactone, and hetero-conjugate addition of cysteine to dehydroalanine.
  • Cystinuria is an inherited autosomal recessive disease characterized by high concentrations of the amino acid cystine in the urine, leading to the formation of cystine stones in the kidneys, ureters, and bladder.
  • Amino acids (300 mg glutamine; 200 mg arginine; 50 mg each asparagine, cystine, leucine, and isoleucine; 40 mg lysine hydrochloride; 30 mg serine; 20 mg each aspartic acid, glutamic acid, hydroxyproline, proline, threonine, tyrosine, and valine; 15 mg each histidine, methionine, and phenylalanine; 10 mg glycine; 5 mg tryptophan; and 1 mg reduced glutathione).
  • In cystinuria, a hereditary disorder in which high urine cystine levels lead to the formation of cystine stones, penicillamine binds with cysteine to yield a mixed disulfide which is more soluble than cystine.
  • Cystinosis is a lysosomal storage disease characterized by the abnormal accumulation of cystine, the oxidized dimer of the amino acid cysteine.
  • It is caused by mutations in the Norrin cystine knot growth factor gene, also referred to as Norrie Disease Pseudoglioma (NDP) gene.
  • After washing, the hair is treated with a mild solution of hydrogen peroxide, which oxidizes the cysteines back to cystine.
  • As a medication, cysteamine, sold under the brand name Cystagon among others, is indicated to treat cystinosis, a lysosomal storage disease characterized by the abnormal accumulation of cystine, the oxidized dimer of the amino acid cysteine.
  • Although research into mechanically interlocked molecular architectures is primarily focused on artificial compounds, many examples have been found in biological systems including: cystine knots, cyclotides or lasso-peptides such as microcin J25 which are proteins, and a variety of peptides.
  • When glutamine eventually reaches the leaves, it is broken down and used to synthesise protein and non-amide amino acids, such as aspartate, threonine, serine, glutamate, glycine, alanine and cystine.
  • Tiopronin, sold under the brand name Thiola, is a medication used to control the rate of cystine precipitation and excretion in the disease cystinuria.
  • Since the woolen fiber very quickly gets the temperature for breaking up the hydrogen bridges and the steam for hydrolysing the cystine bridges, a relatively quick twist modification is possible which roughly corresponds to the values of an autoclave moderated yarn; however, the steaming quality of the Steamatic steaming process is much better with reference to the evenness of moisture absorption.
  • Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids.
  • Cystinosin is a lysosomal seven-transmembrane protein that functions as an active transporter for the export of cystine molecules out of the lysosome.
  • Tetherin exists as a dimer on the surface of cells, and prevention of dimerisation by mutating the cystine residues, prevents tetherin from inhibiting virus release, although it is still detectable in the cell.
  • The presence of the cyclic cystine knot (CCK) motif was discovered when cyclotides were isolated from various plant families.
  • They demonstrated that cystinosis is a lysosomal storage disease caused by hereditary absence of the transmembrane lysosomal carrier for cystine, and proved that the enzyme gamma-glutamyl transpeptidase was not, contrary to current theory, required for normal transcellular amino acid transport.


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