Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
"Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A mixed-function oxygenase that catalyzes the hydroxylation of peptidyllysine, usually in protocollagen, to peptidylhydroxylysine. The enzyme utilizes molecular oxygen with concomitant oxidative decarboxylation of the cosubstrate 2-oxoglutarate to succinate. EC 1.14.11.4.
| Descriptor ID |
D008240
|
| MeSH Number(s) |
D08.811.682.690.708.660
|
| Concept/Terms |
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase- Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
- 2-Oxoglutarate 5-Dioxygenase Procollagen-Lysine
- 5-Dioxygenase Procollagen-Lysine, 2-Oxoglutarate
- Procollagen Lysine, 2 Oxoglutarate 5 Dioxygenase
- Lysine 2-Oxoglutarate Dioxygenase
- 2-Oxoglutarate Dioxygenase, Lysine
- Dioxygenase, Lysine 2-Oxoglutarate
- Lysine 2 Oxoglutarate Dioxygenase
- Lysyl Hydroxylase
- Hydroxylase, Lysyl
- Protocollagen Lysyl Hydroxylase
- Hydroxylase, Protocollagen Lysyl
- Collagen Lysyl Hydroxylase
- Hydroxylase, Collagen Lysyl
- Lysine Hydroxylase
- Hydroxylase, Lysine
|
Below are MeSH descriptors whose meaning is more general than "Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase".
Below are MeSH descriptors whose meaning is more specific than "Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase".
This graph shows the total number of publications written about "Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase" by people in this website by year, and whether "Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase" by people in Profiles.
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Vahidnezhad H, Youssefian L, Saeidian AH, Touati A, Pajouhanfar S, Baghdadi T, Shadmehri AA, Giunta C, Kraenzlin M, Syx D, Malfait F, Has C, Lwin SM, Karamzadeh R, Liu L, Guy A, Hamid M, Kariminejad A, Zeinali S, McGrath JA, Uitto J. Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency. Matrix Biol. 2019 08; 81:91-106.
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Watt SA, Dayal JH, Wright S, Riddle M, Pourreyron C, McMillan JR, Kimble RM, Prisco M, Gartner U, Warbrick E, McLean WH, Leigh IM, McGrath JA, Salas-Alanis JC, Tolar J, South AP. Lysyl Hydroxylase 3 Localizes to Epidermal Basement Membrane and Is Reduced in Patients with Recessive Dystrophic Epidermolysis Bullosa. PLoS One. 2015; 10(9):e0137639.