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Molecular docking analysis of nitisinone with homogentisate 1,2 dioxygenase
Alkaptonuria is an inherited disease that is caused by homogenticate accumulation. Deficiency or mutation in Homogentisate 1,2 dioxygenase gene (chromosome 3q21-q23) leads to production of incorrectly folded or truncated enzyme. Several studies indicated that competitive inhibitors of Homogentisate...
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| Publicat a: | Bioinformation |
|---|---|
| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Biomedical Informatics
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5498778/ https://ncbi.nlm.nih.gov/pubmed/28690378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630013136 |
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