hypoxanthine$37115$ - significado y definición. Qué es hypoxanthine$37115$
Diclib.com
Diccionario ChatGPT
Ingrese una palabra o frase en cualquier idioma 👆
Idioma:

Traducción y análisis de palabras por inteligencia artificial ChatGPT

En esta página puede obtener un análisis detallado de una palabra o frase, producido utilizando la mejor tecnología de inteligencia artificial hasta la fecha:

  • cómo se usa la palabra
  • frecuencia de uso
  • se utiliza con más frecuencia en el habla oral o escrita
  • opciones de traducción
  • ejemplos de uso (varias frases con traducción)
  • etimología

Qué (quién) es hypoxanthine$37115$ - definición

GROUP OF PROTEINS WITH HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE ACTIVITY
HPRT; HGPRT; Hypoxanthine phosphoribosyltransferase; Hypoxanthine/guanine phosphoribosyl transferase; Hypoxanthine phosphoribosyltransferase 1; HPRT1; Hgprt; Hprt; Hypoxanthine-guanine phosphoribosyl transferase; Hypoxanthine guanine phosphoriberyltransform; Hypoxanthine guanine phosphoribory itransferase; High-performace guanine phophoriboost transferase; Hypoxanthine guanine phosphoribosyl transferase; HPRT1 (gene); EC 2.4.2.8; GPRT; IMP:diphosphate phospho-D-ribosyltransferase

Hypoxanthine-guanine phosphoribosyltransferase         
Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) is an enzyme encoded in humans by the HPRT1 gene.
Lesch–Nyhan syndrome         
  • Purine metabolism.
  • Lesch-Nyhan syndrome patient with arm restraints
RARE GENETIC SYNDROME
Lesch-Nyhan Syndrome; Lesch-Nyhan; Lesch-nyhan syndrome; Lesch-nyhans syndrome; Choreoathetosis self-mutilation hyperuricemia syndrome; Complete HPRT deficiency; Complete hypoxanthine-guanine phosphoribosyltransferase deficiency; X-linked primary hyperuricemia; X-linked uric aciduria enzyme defect; HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiency; Hypoxanthine phosphoribosyltransferse (HPRT) deficiency; Juvenile gout, choreoathetosis, mental retardation syndrome; Juvenile hyperuricemia syndrome; Primary hyperuricemia syndrome; Total HPRT deficiency; Total hypoxanthine-guanine phosphoribosyl transferase deficiency; Lesch nyhan; Kelley-Seegmiller syndrome; Kelley-Seegmiller Syndrome; Lesh-Nyhan syndrome; Juvenile gout; Lesch-Nyhan syndrome; Lesch-Nyhan disease; Lesch–Nyhan Syndrome; Kelley-Seegmiller; Kelley–Seegmiller syndrome
Primary hyperuricemia syndrome, Choreoathetosis self-mutilation syndrome, X-linked primary hyperuricemia, HGPRT deficiency
inosine         
CHEMICAL COMPOUND
Inosine nucleotides; ATC code D06BB05; ATCvet code QD06BB05; ATC code G01AX02; ATCvet code QG01AX02; ATC code S01XA10; ATCvet code QS01XA10; C10H12N4O5
['?n?(?)si:n]
¦ noun Biochemistry a compound which is formed in the metabolism of purine and is a nucleoside containing ribose.
Origin
early 20th cent.: from Gk is, in- 'fibre, muscle' + -ose2 + -ine4.

Wikipedia

Hypoxanthine-guanine phosphoribosyltransferase

Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) is an enzyme encoded in humans by the HPRT1 gene.

HGPRT is a transferase that catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate. This reaction transfers the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate (PRPP) to the purine. HGPRT plays a central role in the generation of purine nucleotides through the purine salvage pathway.