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7KDR

Crystal structure of Escherichia coli HPPK in complex with bisubstrate inhibitor HP-75

Summary for 7KDR
Entry DOI10.2210/pdb7kdr/pdb
Related7KDO
Descriptor2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase, 5'-{[(2R,4R)-1-{2-[(2-amino-7,7-dimethyl-4-oxo-3,4,7,8-tetrahydropteridine-6-carbonyl)amino]ethyl}-2-carboxypiperidin-4-yl]sulfonyl}-5'-deoxyadenosine, CHLORIDE ION, ... (5 entities in total)
Functional Keywordsalpha beta, transferase, transferase-inhibitor complex, transferase/inhibitor
Biological sourceEscherichia coli (strain K12)
Total number of polymer chains1
Total formula weight18830.84
Authors
Shaw, G.X.,Shi, G.,Ji, X. (deposition date: 2020-10-09, release date: 2020-12-02, Last modification date: 2023-10-18)
Primary citationShi, G.,Shaw, G.X.,Zhu, F.,Tarasov, S.G.,Ji, X.
Bisubstrate inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: Transition state analogs for high affinity binding.
Bioorg.Med.Chem., 29:115847-115847, 2021
Cited by
PubMed: 33199204
DOI: 10.1016/j.bmc.2020.115847
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.488 Å)
Structure validation

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