Search Count: 24
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 1)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.41 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, A1I1D |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, A1I1D
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 2)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.86 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, KZ0 |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, KZ0
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 3)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.84 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, KZ0 |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, KZ0
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 4)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.35 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, A1I1E |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, A1I1E
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 5)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.67 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, R06 |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, R06
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Cryo-Em Structure Of Shigella Flexneri Lptde In Complex With A Bicyclic Peptide Binder (Compound 12)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.48 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, A1I1D |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, A1I1D
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 13)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.86 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, R06 |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, R06
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Cryo-Em Structure Of Shigella Flexneri Lptde Bound By A Bicyclic Peptide Molecule (Compound 16)
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY Resolution:2.54 Å Release Date: 2025-10-15 Classification: MEMBRANE PROTEIN Ligands: LMT, PLM, Z41, A1I4O |
Organism: Shigella flexneri, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-15
Ligands: LMT, PLM, Z41, A1I4O
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Discovery Of An Orally Bioavailable Reversible Covalent Sars-Cov-2 Mpro Inhibitor With Pan-Coronavirus Activity
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.37 Å Release Date: 2025-08-20 Classification: HYDROLASE/INHIBOTOR Ligands: A1L7M |
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: A1L7M
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Discovery Of An Orally Bioavailable Reversible Covalent Sars-Cov-2 Mpro Inhibitor With Pan-Coronavirus Activity
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2025-08-20 Classification: HYDROLASE/INHIBITOR |
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
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Discovery Of An Orally Bioavailable Reversible Covalent Sars-Cov-2 Mpro Inhibitor With Pan-Coronavirus Activity
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2025-08-20 Classification: HYDROLASE/INHIBITOR |
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
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Discovery Of An Orally Bioavailable Reversible Covalent Sars-Cov-2 Mpro Inhibitor With Pan-Coronavirus Activity
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.47 Å Release Date: 2025-08-20 Classification: HYDROLASE/INHIBITOR Ligands: A1L7M |
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: A1L7M
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Discovery Of An Orally Bioavailable Reversible Covalent Sars-Cov-2 Mpro Inhibitor With Pan-Coronavirus Activity
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2025-08-20 Classification: HYDROLASE/INHIBITOR Ligands: A1L7M |
Organism: Severe acute respiratory syndrome coronavirus 2, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: A1L7M
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The Structure Of E. Coli Penicillin Binding Protein 3 (Pbp3) In Complex With A Bicyclic Peptide Inhibitor
Organism: Escherichia coli, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2024-04-03 Classification: HYDROLASE Ligands: 29N |
Organism: Escherichia coli, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2024-04-03
Ligands: 29N
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Mettl3-Mettl14 Heterodimer Bound To The Sam Competitive Small Molecule Inhibitor Stm3006
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.21 Å Release Date: 2023-09-20 Classification: RNA BINDING PROTEIN Ligands: QWR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-09-20
Ligands: QWR
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Crystal Structure Of Kat6A In Complex With Inhibitor Ctx-648 (Pf-9363)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.58 Å Release Date: 2023-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: R7L, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-07-05
Ligands: R7L, ZN
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N-Terminal Bromodomain Of Human Brd4 With Ibet-Bd1 (Gsk778)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.28 Å Release Date: 2020-04-01 Classification: TRANSCRIPTION Ligands: GLU, LWB, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-04-01
Ligands: GLU, LWB, EDO
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C-Terminal Bromodomain Of Human Brd2 With Ibet-Bd1 (Gsk778)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2020-04-01 Classification: TRANSCRIPTION Ligands: LWB, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-04-01
Ligands: LWB, EDO
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C-Terminal Bromodomain Of Human Brd2 With Ibet-Bd2 (Gsk046)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2020-04-01 Classification: TRANSCRIPTION Ligands: EDO, LW5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-04-01
Ligands: EDO, LW5
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N-Terminal Bromodomain Of Human Brd4 With Ibet-Bd2 (Gsk046)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2020-04-01 Classification: TRANSCRIPTION Ligands: EDO, LW5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-04-01
Ligands: EDO, LW5