7dpi

From Proteopedia
Jump to navigation Jump to search

Plasmodium falciparum cytoplasmic Phenylalanyl-tRNA synthetase in complex with BRD7929Plasmodium falciparum cytoplasmic Phenylalanyl-tRNA synthetase in complex with BRD7929

Structural highlights

7dpi is a 4 chain structure with sequence from Plasmodium falciparum. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 3.597Å
Ligands:,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

Q8I246_PLAF7

Publication Abstract from PubMed

Bicyclic azetidine compounds possess antimalarial activity via targeting of the cytoplasmic Plasmodium falciparum (Pf) protein translation enzyme phenylalanine-tRNA synthetase (cFRS). These drugs kill parasites both in vitro and in vivo, including the blood, liver, and transmission developmental stages. Here we present the co-crystal structure of PfcFRS with a potent inhibitor, the bicyclic azetidine BRD7929. Our studies reveal high-affinity binding of BRD7929 with PfcFRS along with exquisite specificity compared with the human enzyme, leading in turn to potent and selective inhibition of the parasite enzyme. Our co-crystal structure shows that BRD7929 binds in the active site in the alpha subunit of PfcFRS, where it occupies the amino acid site, an auxiliary site, and partially the ATP site. This structural snapshot of inhibitor-bound PfcFRS thus provides a platform for the structure-guided optimization of novel antimalarial compounds.

Inhibition of Plasmodium falciparum phenylalanine tRNA synthetase provides opportunity for antimalarial drug development.,Sharma M, Mutharasappan N, Manickam Y, Harlos K, Melillo B, Comer E, Tabassum H, Parvez S, Schreiber SL, Sharma A Structure. 2022 Jul 7;30(7):962-972.e3. doi: 10.1016/j.str.2022.03.017. Epub 2022 , Apr 22. PMID:35460612[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Sharma M, Mutharasappan N, Manickam Y, Harlos K, Melillo B, Comer E, Tabassum H, Parvez S, Schreiber SL, Sharma A. Inhibition of Plasmodium falciparum phenylalanine tRNA synthetase provides opportunity for antimalarial drug development. Structure. 2022 Jul 7;30(7):962-972.e3. PMID:35460612 doi:10.1016/j.str.2022.03.017

7dpi, resolution 3.60Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA