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Search Count: 33

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9R2C image
Cpkrs In Complex With Inhibitor Ddd01038762

9R32 image
Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01887015

9R3F image
Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01932549

9R3G image
Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum / Plasmodium Falciparum Chimera Complexed With L-Lysine And Inhibitor Ddd02174286

9R3R image
Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01827593

9CLL image
Plasmodium Falciparum Tyrosyl-Trna Synthetase In Complex With Ml471-Tyr

8E25 image
Crystal Structure Of Sars-Cov-2 Main Protease M49I Mutant In Complex With Nirmatrelvir

8E26 image
Crystal Structure Of Sars-Cov-2 Main Protease N142S Mutant In Complex With Nirmatrelvir

8DZ0 image
Crystal Structure Of Sars-Cov-2 Main Protease In Complex With Ensitrelvir

8DZ1 image
Crystal Structure Of Sars-Cov-2 Main Protease Mutant M49I In Complex With Ensitrelvir

8DZ2 image
Crystal Structure Of Sars-Cov-2 Main Protease In Complex With Nirmatrelvir

8DZ6 image
Crystal Structure Of Sars-Cov-2 Main Protease Mutant Q189K In Complex With Nirmatrelvir

8DZA image
Crystal Structure Of Sars-Cov-2 Main Protease A193T Mutant In Complex With Nirmatrelvir

8DZ9 image
Crystal Structure Of Sars-Cov-2 Main Protease G143S Mutant In Complex With Nirmatrelvir

8E1Y image
Crystal Structure Of Sars-Cov-2 Main Protease A193S Mutant In Complex With Nirmatrelvir

7MLK image
Crystal Structure Of Human Pi3Ka (P110A Subunit) With Mmv085400 Bound To The Active Site Determined At 2.9 Angstroms Resolution

7LXT image
Structure Of Plasmodium Falciparum 20S Proteasome With Bound Bortezomib

7LXU image
Structure Of Plasmodium Falciparum 20S Proteasome With Bound Mpi-5

7LXV image
Structure Of Human 20S Proteasome With Bound Mpi-5

7KYK image
Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm589 (Ethyl 3-Methyl-4-((4-(Trifluoromethyl)Benzo[D]Oxazol-7-Yl)Methyl)-1H-Pyrrole-2-Carboxylate)
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