DNA untwisting enzyme - traducción al ruso
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DNA untwisting enzyme - traducción al ruso

CLASS OF ENZYMES
Dna topoisomerases; DNA topoisomerase; Dna topoisomerases, type ii; Dna topoisomerases, type i; Topoisomerases; DNA topisomerase; EC 5.99.1.2; Type I DNA topoisomerase; Untwisting enzyme; Relaxing enzyme; Nicking-closing enzyme; Swivelase; Omega-protein; Deoxyribonucleate topoisomerase
  • '''Figure 6'''. Structures of antibiotic compounds that target bacterial DNA gyrase and topoisomerase IV.
  • '''Figure 3.'''  Summary of topoisomerase types and catalytic mechanisms.  The topoisomerases are categorized based on whether they catalyze single- (type I) or double-stranded (type II) DNA breaks.  The type I topoisomerases are further subdivided to type IA, IB and IC. Type IA form a transient covalent bond to the 5ʹ DNA phosphate and function via a strand passage mechanism.  Type IB and IC form a transient covalent bond to the 3ʹ DNA phosphate and function via a controlled-rotation mechanism.  Type II topoisomerases are further subdivided into type IIA and IIB. Both form a transient covalent bond to the 5ʹ DNA phosphate of both strands of the duplex and function via a strand-passage mechanism.
  • '''Paused RNA polymerase and limited, short-term topo IIβ-induced DNA double-strand break.'''  The 5' ends of DNA are covalently joined to tyrosine within the topo IIβ dimer-PARP-1 complex.  The [[non-homologous end joining]] DNA repair pathway components DNA-PKcs, Ku70/Ku80 and DNA ligase are also closely associated with the topo IIβ dimer-PARP-1 complex.
  • '''Figure 7.''' Structures of antitumor compounds that target human topoisomerases.
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  • '''Figure 2'''. Topological consequences of DNA metabolism. i) During DNA replication, strand separation leads to positive supercoiling ahead of the advancing protein machinery, and precatenane formation behind. Precatenanes form as the newly-synthesised duplexes wrap around one and other, and, if not removed prior to complete of replication, catenated DNA molecules are formed. ii) During transcription, strand separation leads to positive supercoiling ahead of the advancing protein machinery, and negative supercoil formation behind.<ref name=":1" />
  • '''Figure 5'''. Type II topoisomerase strand-passage mechanism.  (1) G-segment is bound at the DNA-gate and the T-segment is captured.  (2) ATP binding stimulates dimerization of the N-gate, the G-segment is cleaved and the T-segment is passed through the break.  (3) The G-segment is re-ligated and the T-segment exits through the C-gate.  For type IIB topos, there is no C-gate so once the T-segment passes through the G-segment, it is released from the enzyme.  (4) Dissociation of ADP and P<sub>i</sub> allows N-gate opening, a scenario where the enzyme either remains bound to the G-segment, ready to capture a successive T-segment, or (5) dissociates from the G-segment.

DNA untwisting enzyme      

общая лексика

ДНК-раскручивающий фермент

untwisting enzyme         

общая лексика

раскручивающий (ДНК) фермент

синоним

unwinding enzyme

enzymatic         
  • recessive]] fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.
  • The energies of the stages of a [[chemical reaction]]. Uncatalysed (dashed line), substrates need a lot of [[activation energy]] to reach a [[transition state]], which then decays into lower-energy products. When enzyme catalysed (solid line), the enzyme binds the substrates (ES), then stabilizes the transition state (ES<sup>‡</sup>) to reduce the activation energy required to produce products (EP) which are finally released.
  • alt=Lysozyme displayed as an opaque globular surface with a pronounced cleft which the substrate depicted as a stick diagram snuggly fits into.
  • 2E2Q}})
  • 1KW0}})
  • alt=A graph showing that reaction rate increases exponentially with temperature until denaturation causes it to decrease again.
  • 4KXV}})
LARGE BIOLOGICAL MOLECULE THAT ACTS AS A CATALYST
Apoenzyme; Holoenzyme; Enzymes; ENZ; Enzyme action; Mechanisms of enzyme action; Enzymatic; Lock-and-key model (enzyme); Enyzme; Enzymology; Biocatalyst; Biocatalysts; Lock and Key Theory; Enzyme-substrate complex; ENZYME STRUCTURE AND FUNCTION; Holoenzymes; Apoenzymes; Enzymatically; Lock and key model; Encyme; Ensyme; Enyme characteristics; Cofactors and coenzymes; Coenzymes and cofactors; Enzymic; Enzyme preparations; Lock-and-key model; Lock and key theory; Enzime; Haloenzyme; Enzyme type; Regulation mechanism; Enzyme regulation; Carbamidase

[enzai'mætik]

общая лексика

ферментативный

медицина

ферментный

энзиматический

прилагательное

общая лексика

ферментативный

энзимный

Definición

holoenzyme
[?h?l??'?nz??m]
¦ noun Biochemistry a biochemically active compound of an enzyme combined with a coenzyme.

Wikipedia

Topoisomerase

DNA topoisomerases (or topoisomerases) are enzymes that catalyze changes in the topological state of DNA, interconverting relaxed and supercoiled forms, linked (catenated) and unlinked species, and knotted and unknotted DNA. Topological issues in DNA arise due to the intertwined nature of its double-helical structure, which, for example, can lead to overwinding of the DNA duplex during DNA replication and transcription. If left unchanged, this torsion would eventually stop the DNA or RNA polymerases involved in these processes from continuing along the DNA helix. A second topological challenge results from the linking or tangling of DNA during replication. Left unresolved, links between replicated DNA will impede cell division. The DNA topoisomerases prevent and correct these types of topological problems. They do this by binding to DNA and cutting the sugar-phosphate backbone of either one (type I topoisomerases) or both (type II topoisomerases) of the DNA strands. This transient break allows the DNA to be untangled or unwound, and, at the end of these processes, the DNA backbone is resealed. Since the overall chemical composition and connectivity of the DNA do not change, the DNA substrate and product are chemical isomers, differing only in their topology.

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