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2PRL

The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site

Summary for 2PRL
Entry DOI10.2210/pdb2prl/pdb
Related1D3G 2PRH 2PRM
DescriptorDihydroorotate dehydrogenase, mitochondrial, SULFATE ION, ACETATE ION, ... (8 entities in total)
Functional Keywordsprotein inhibitor complex, oxidoreductase
Biological sourceHomo sapiens (human)
Cellular locationMitochondrion inner membrane ; Single-pass membrane protein : Q02127
Total number of polymer chains1
Total formula weight41219.83
Authors
Walse, B.,Dufe, V.T.,Al-Karadaghi, S. (deposition date: 2007-05-04, release date: 2008-05-20, Last modification date: 2023-08-30)
Primary citationWalse, B.,Dufe, V.T.,Svensson, B.,Fritzson, I.,Dahlberg, L.,Khairoullina, A.,Wellmar, U.,Al-Karadaghi, S.
The structures of human dihydroorotate dehydrogenase with and without inhibitor reveal conformational flexibility in the inhibitor and substrate binding sites
Biochemistry, 47:8929-8936, 2008
Cited by
PubMed: 18672895
DOI: 10.1021/bi8003318
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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