The latter is converted to orotate by dihydroorotate oxidase. The net reaction is: (S)-Dihydroorotate + O2 → Orotate + H2O2 ...
... (EC 1.3.98.1, dihydroorotate oxidase, pyr4 (gene)) is an enzyme with systematic name (S ... dihydroorotate:fumarate oxidoreductase. This enzyme catalyses the following chemical reaction (S)-dihydroorotate + fumarate ... Dihydroorotate+dehydrogenase+(fumarate) at the US National Library of Medicine Medical Subject Headings (MeSH) Biology portal v ... Björnberg O, Rowland P, Larsen S, Jensen KF (December 1997). "Active site of dihydroorotate dehydrogenase A from Lactococcus ...
H2O2-forming NADH oxidase was purified from O2-sensitive Bifidobacterium bifidum and was identified as a b-type dihydroorotate ...
... dihydroorotate oxidase MeSH D08.811.682.660.325 - dihydrouracil dehydrogenase (nad+) MeSH D08.811.682.660.350 - dihydrouracil ... sarcosine oxidase MeSH D08.811.682.662.640 - proline oxidase MeSH D08.811.682.662.680 - pyridoxamine-phosphate oxidase MeSH ... d-amino-acid oxidase MeSH D08.811.682.664.500.261 - d-aspartate oxidase MeSH D08.811.682.664.500.398 - glutamate dehydrogenase ... proline oxidase MeSH D08.811.682.664.500.848 - protein-lysine 6-oxidase MeSH D08.811.682.664.500.924 - valine dehydrogenase ( ...
... flavoprotein Succinate dehydrogenase Alternative oxidase Cytochrome bc1 complex Cytochrome c Cytochrome c oxidase F-ATPase ATP- ... Cytochrome P450 Translocase of the inner membrane Glutamate aspartate transporter Pyrimidine metabolism Dihydroorotate ... HtrA serine peptidase 2 Adrenodoxin reductase Heme biosynthesis Protoporphyrinogen oxidase Ferrochelatase Uncoupling protein ...
Complex IV/Cytochrome c oxidase. *Coenzyme Q10 synthesis: COQ2. *COQ3. *COQ4. *COQ5 ...
Proline oxidase. *Pyrroline-5-carboxylate reductase. *1-Pyrroline-5-carboxylate dehydrogenase/ALDH4A1 ...
"Cytochrome c oxidase deficiency". Genetics Home Reference.. This article incorporates text from this source, which is in the ... also known as the cytochrome c oxidase deficiency. Cytochrome c oxidase deficiency is a rare genetic condition that can affect ... "Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA ...
... and cytochrome c oxidase (complex IV).[1] Complex I is the largest and most complicated enzyme of the electron transport chain. ... electron-transferring flavoprotein or dihydroorotate dehydrogenase in mammalian mitochondria) pass through complex I to reduce ...
Proline oxidase. *Pyrroline-5-carboxylate reductase. *1-Pyrroline-5-carboxylate dehydrogenase/ALDH4A1 ...
The ribosome has three binding sites for tRNA molecules that span the space between the two ribosomal subunits: the A (aminoacyl),[19] P (peptidyl), and E (exit) sites. In addition, the ribosome has two other sites for tRNA binding that are used during mRNA decoding or during the initiation of protein synthesis. These are the T site (named elongation factor Tu) and I site (initiation).[20][21] By convention, the tRNA binding sites are denoted with the site on the small ribosomal subunit listed first and the site on the large ribosomal subunit listed second. For example, the A site is often written A/A, the P site, P/P, and the E site, E/E.[20] The binding proteins like L27, L2, L14, L15, L16 at the A- and P- sites have been determined by affinity labeling by A.P. Czernilofsky et al. (Proc. Natl. Acad. Sci, USA, pp. 230-34, 1974). Once translation initiation is complete, the first aminoacyl tRNA is located in the P/P site, ready for the elongation cycle described below. During translation ...
"Pfam entry: Cholesterol oxidase". Archived from the original on 2007-09-29. Retrieved 2007-01-25. "Pfam entry: Retinal pigment ... "Pfam entry:Dihydroorotate dehydrogenase". Archived from the original on 2007-09-26. Retrieved 2007-01-25. "Pfam entry: FMN- ... phospholipases and cholesterol oxidases), cell wall oligosaccharides (glycosyltransferase and transglycosidases), or proteins ( ...
acyl-CoA oxidase Ja 1.3.5.1 succinaat-dehydrogenase (ubichinon) Ja 1.3.5.2 dihydroorotate dehydrogenase Ja ... cytochroom-c-oxidase Ja Externe links[bewerken , brontekst bewerken]. *Integrated Enzyme Database (European Bioinformatics ...
Dihydroorotate dehydrogenase. *Coproporphyrinogen III oxidase. *Protoporphyrinogen oxidase. *Bilirubin oxidase. *Acyl-CoA ...
Dihydroorotate dehydrogenase. *Coproporphyrinogen III oxidase. *Protoporphyrinogen oxidase. *Bilirubin oxidase. *Acyl-CoA ...
Dihydroorotate dehydrogenase. *Coproporphyrinogen III oxidase. *Protoporphyrinogen oxidase. *Bilirubin oxidase. *Acyl-CoA ...
Dihydrobenzophenanthridine oxidase. *Sarcosine oxidase. *Proline oxidase. 1.5.5: quinone acceptor. *Electron-transferring- ...
Uridine phosphorylase or pyrimidine-nucleoside phosphorylase adds ribose 1-phosphate to the free base uracil, forming uridine. Uridine kinase (aka uridine-cytidine kinase) can then phosphorylate this nucleoside into uridine monophosphate (UMP). UMP/CMP kinase (EC 2.7.4.14) can phosphorylate UMP into uridine diphosphate, which nucleoside diphosphate kinase can phosphorylate into uridine triphosphate. Thymidine phosphorylase or pyrimidine-nucleoside phosphorylase adds 2-deoxy-alpha-D-ribose 1-phosphate to thymine, forming thymidine. Thymidine kinase can then phosphorylate this compound into thymidine monophosphate (TMP). Thymidylate kinase can phosphorylate TMP into thymidine diphosphate, which nucleoside diphosphate kinase can phosphorylate into thymidine triphosphate. The nucleosides cytidine and deoxycytidine can be salvaged along the uracil pathway by cytidine deaminase, which converts them to uridine and deoxyuridine, respectively. Alternatively, uridine-cytidine kinase can phosphorylate them ...
Hypoxanthine is then oxidized to form xanthine and then uric acid through the action of xanthine oxidase. The other purine ...
Dihydroorotate dehydrogenase. *Coproporphyrinogen III oxidase. *Protoporphyrinogen oxidase. *Bilirubin oxidase. *Acyl-CoA ...