Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

1SQI

Structural basis for inhibitor selectivity revealed by crystal structures of plant and mammalian 4-hydroxyphenylpyruvate dioxygenases

Summary for 1SQI
Entry DOI10.2210/pdb1sqi/pdb
Related1SQD
Descriptor4-hydroxyphenylpyruvic acid dioxygenase, FE (III) ION, (1-TERT-BUTYL-5-HYDROXY-1H-PYRAZOL-4-YL)[6-(METHYLSULFONYL)-4'-METHOXY-2-METHYL-1,1'-BIPHENYL-3-YL]METHANONE, ... (4 entities in total)
Functional Keywordsrat 4-hydroxyphenylpyruvate dioxygenase, biosynthetic protein
Biological sourceRattus norvegicus (Norway rat)
Cellular locationCytoplasm: P32755
Total number of polymer chains2
Total formula weight91458.90
Authors
Yang, C.,Pflugrath, J.W.,Camper, D.L.,Foster, M.L.,Pernich, D.J.,Walsh, T.A. (deposition date: 2004-03-18, release date: 2004-08-17, Last modification date: 2024-02-14)
Primary citationYang, C.,Pflugrath, J.W.,Camper, D.L.,Foster, M.L.,Pernich, D.J.,Walsh, T.A.
Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and Mammalian 4-hydroxyphenylpyruvate dioxygenases
Biochemistry, 43:10414-10423, 2004
Cited by
PubMed Abstract: A high degree of selectivity toward the target site of the pest organism is a desirable attribute for new safer agrochemicals. To assist in the design of novel herbicides, we determined the crystal structures of the herbicidal target enzyme 4-hydroxyphenylpyruvate dioxygenase (HPPD; EC 1.13.11.27) from the plant Arabidopsis thaliana with and without an herbicidal benzoylpyrazole inhibitor that potently inhibits both plant and mammalian HPPDs. We also determined the structure of a mammalian (rat) HPPD in complex with the same nonselective inhibitor. From a screening campaign of over 1000 HPPD inhibitors, six highly plant-selective inhibitors were found. One of these had remarkable (>1600-fold) selectivity toward the plant enzyme and was cocrystallized with Arabidopsis HPPD. Detailed comparisons of the plant and mammalian HPPD-ligand structures suggest a structural basis for the high degree of plant selectivity of certain HPPD inhibitors and point to design strategies to obtain potent and selective inhibitors of plant HPPD as agrochemical leads.
PubMed: 15301540
DOI: 10.1021/bi049323o
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.15 Å)
Structure validation

248335

PDB entries from 2026-01-28

PDB statisticsPDBj update infoContact PDBjnumon