Search Count: 22
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.57 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNO, CL, TAU |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.74 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNV, CL |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.53 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNN, CL, TAU |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.81 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNR, CL |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNW, SO3, CL |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNU, CL, TAU |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNQ, CL, TAU |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.51 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNP, CL, TAU |
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Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.57 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: A1JNT, SO3, CL, TAU |
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Penicillin-Binding Protein 1B (Pbp-1B) In Complex With A Monobactam (Aztreonam)
Organism: Streptococcus pneumoniae
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2026-02-18 Classification: TRANSFERASE Ligands: AZR, CL, TAU |
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Crystal Structure Of The Receptor Tyrosine Kinase Human Her2 (Erbb2) Yvma Mutant Kinase Domain In Complex With Inhibitor Compound 27
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2024-06-12 Classification: SIGNALING PROTEIN,TRANSFERASE/INHIBITOR Ligands: W9N, PEG, CL |
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Structure Of Carbamoylated Human Butyrylcholinesterase Upon Reaction With 3-(((2-Cycloheptylethyl)(Methyl)Amino)Methyl)-1H-Indol-7-Yl N,N-Dimethylcarbamate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.13 Å Release Date: 2023-02-01 Classification: HYDROLASE Ligands: SO4, CL, NA, M8X, NAG, GOL |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2021-12-22 Classification: Hydrolase/Hydrolase Inhibitor Ligands: GDP, 6IC, MG |
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Crystal Structure Of Kras G12D With Compound 15 (4-(4-[(1R,5S)-3,8-Diazabicyclo[3.2.1]Octan-3-Yl]-8-Fluoro-2-{[(2S)-1-Methylpyrrolidin-2-Yl]Methoxy}Pyrido[4,3-D]Pyrimidin-7-Yl)Naphthalen-2-Ol) Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.27 Å Release Date: 2021-12-22 Classification: HYDROLASE/INHIBITOR Ligands: GDP, MG, 7L8 |
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Crystal Structure Of Kras G12D With Compound 25 (4-(4-[(1R,5S)-3,8-Diazabicyclo[3.2.1]Octan-3-Yl]-8-Fluoro-2-{[(2R,4R,7As)-2-Fluorotetrahydro-1H-Pyrrolizin-7A(5H)-Yl]Methoxy}Pyrido[4,3-D]Pyrimidin-7-Yl)Naphthalen-2-Ol) Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.59 Å Release Date: 2021-12-22 Classification: HYDROLASE/INHIBITOR Ligands: GDP, MG, 7NL, GOL, EDO |
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Crystal Structure Of Kras G12D With Compound 24 (4-(4-[(1R,5S)-3,8-Diazabicyclo[3.2.1]Octan-3-Yl]-8-Fluoro-2-{[(2S,4S,7Ar)-2-Fluorotetrahydro-1H-Pyrrolizin-7A(5H)-Yl]Methoxy}Pyrido[4,3-D]Pyrimidin-7-Yl)Naphthalen-2-Ol) Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.56 Å Release Date: 2021-12-22 Classification: HYDROLASE/INHIBITOR Ligands: GDP, 7NZ, MG |
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Kras G12D In Complex With Compound 5B (7-(8-Chloronaphthalen-1-Yl)-8-Fluoro-2-{[(2S)-1-Methylpyrrolidin-2-Yl]Methoxy}-4-(Piperazin-1-Yl)Pyrido[4,3-D]Pyrimidine)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2021-12-22 Classification: HYDROLASE/INHIBITOR Ligands: GDP, MG, 7IZ, GOL |
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Crystal Structure Of Kras G12D With Compound 36 (4-[(1R,5S)-3,8-Diazabicyclo[3.2.1]Octan-3-Yl]-7-(8-Ethynyl-7-Fluoronaphthalen-1-Yl)-8-Fluoro-2-{[(4S,7As)-Tetrahydro-1H-Pyrrolizin-7A(5H)-Yl]Methoxy}Pyrido[4,3-D]Pyrimidine) Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.29 Å Release Date: 2021-12-22 Classification: HYDROLASE/INHIBITOR Ligands: GDP, 7OE, MG |
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Structure Of Recombinant Human Butyrylcholinesterase In Complex With A Coumarin-Based Fluorescent Probe Linked To Sulfonamide Type Inhibitor.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2020-01-22 Classification: HYDROLASE Ligands: NAG, EDO, CL, PEG, KJT, PGE |
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Structure Of Recombinant Human Butyrylcholinesterase In Complex With A Fluorescent Coumarin-Based Probe
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2020-01-15 Classification: HYDROLASE Ligands: NAG, JU5, SO4 |