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5MVC

Crystal structure of potent human Dihydroorotate Dehydrogenase inhibitors based on hydroxylated azole scaffolds

Summary for 5MVC
Entry DOI10.2210/pdb5mvc/pdb
DescriptorDihydroorotate dehydrogenase (quinone), mitochondrial, FLAVIN MONONUCLEOTIDE, OROTIC ACID, ... (7 entities in total)
Functional Keywordsdhodh, human dhodh, oxidoreductase
Biological sourceHomo sapiens (Human)
Cellular locationMitochondrion inner membrane ; Single-pass membrane protein : Q02127
Total number of polymer chains1
Total formula weight43913.50
Authors
Goyal, P.,Andersson, M.,Moritzer, A.C.,Sainas, S.,Pippione, A.C.,Boschi, D.,Al-Kadaraghi, S.,Lolli, M.,Friemann, R. (deposition date: 2017-01-16, release date: 2017-03-08, Last modification date: 2024-01-17)
Primary citationSainas, S.,Pippione, A.C.,Giorgis, M.,Lupino, E.,Goyal, P.,Ramondetti, C.,Buccinna, B.,Piccinini, M.,Braga, R.C.,Andrade, C.H.,Andersson, M.,Moritzer, A.C.,Friemann, R.,Mensa, S.,Al-Kadaraghi, S.,Boschi, D.,Lolli, M.L.
Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds.
Eur J Med Chem, 129:287-302, 2017
Cited by
PubMed: 28235702
DOI: 10.1016/j.ejmech.2017.02.017
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.85 Å)
Structure validation

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