Search Count: 37
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Pyrococcus Abyssi Rubredoxin @ 0.55 Angstrom Resolution, 50 Kgy Structure
Organism: Pyrococcus abyssi ge5
Method: X-RAY DIFFRACTION Resolution:0.55 Å Release Date: 2026-04-22 Classification: ELECTRON TRANSPORT Ligands: FE |
Organism: Pyrococcus abyssi ge5
Method: X-RAY DIFFRACTION
Release Date: 2026-04-22
Ligands: FE
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Rubredoxin @ 0.57 Angstrom Resolution, 1 Mgy Structure
Organism: Pyrococcus abyssi ge5
Method: X-RAY DIFFRACTION Resolution:0.57 Å Release Date: 2026-04-22 Classification: ELECTRON TRANSPORT Ligands: FE |
Organism: Pyrococcus abyssi ge5
Method: X-RAY DIFFRACTION
Release Date: 2026-04-22
Ligands: FE
 |
Structure Of Ompa-Short In Complex With Nanobody Nb01
Organism: Escherichia coli k-12, Vicugna pacos
Method: X-RAY DIFFRACTION Resolution:2.27 Å Release Date: 2024-07-17 Classification: MEMBRANE PROTEIN Ligands: OCT, CA |
Organism: Escherichia coli k-12, Vicugna pacos
Method: X-RAY DIFFRACTION
Release Date: 2024-07-17
Ligands: OCT, CA
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Structure Of Ompa-Long In Complex With Nanobody Nb39
Organism: Escherichia coli, Vicugna pacos
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2024-07-17 Classification: MEMBRANE PROTEIN |
Organism: Escherichia coli, Vicugna pacos
Method: X-RAY DIFFRACTION
Release Date: 2024-07-17
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Crystal Structure Of Halotag7 Bound To Jf669-Halotag Ligand
Organism: Rhodococcus sp. (in: high g+c gram-positive bacteria)
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2024-06-05 Classification: HYDROLASE Ligands: XSR, CL |
Organism: Rhodococcus sp. (in: high g+c gram-positive bacteria)
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
Ligands: XSR, CL
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Carbonic Anhydrase 2 With Inhibitor (2Z)-2-Benzylidene-3-Oxo-N-(4-Sulfamoylphenyl)Butanamide (11A/D1)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.67 Å Release Date: 2020-08-05 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, GOL, Q64, SO4, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-05
Ligands: ZN, GOL, Q64, SO4, CL
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Carbonic Anhydrase 2 With Inhibitor (2Z)-2-[(4-Methoxyphenyl)Methylidene]-3-Oxo-N-(4-Sulfamoylphenyl)Butanamide (11D/D4)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.33 Å Release Date: 2020-08-05 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, Q6A, GOL, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-05
Ligands: ZN, Q6A, GOL, NA
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Carbonic Anhydrase 2 With Inhibitor (2Z)-3-Oxo-N-(4-Sulfamoylphenyl)-2-[(Thiophen-2-Yl)Methylidene]Butanamide (11G/D7)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2020-08-05 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, GOL, Q6D, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-05
Ligands: ZN, GOL, Q6D, CL
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Crystal Structure Of The Apo Form Of Thioesterase Domain Of Mtb Pks13
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2017-07-05 Classification: TRANSFERASE Ligands: 2Q5 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: 2Q5
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Crystal Structure Of Mtb Pks13 Thioesterase Domain In Complex With Inhibitor Tam1
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2017-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: I28 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: I28
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Crystal Structure Of Mtb Pks13 Thioesterase Domain In Complex With Inhibitor Tam16
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2017-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 5V8, SO4 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: 5V8, SO4
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Crystal Structure Of The D1607N Mutant Form Of Thioesterase Domain Of Mtb Pks13
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2017-07-05 Classification: TRANSFERASE Ligands: 1PE, SO4 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: 1PE, SO4
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Crystal Structure Of Mtb Pks13 Thioesterase Domain In Complex With Inhibitor Tam6
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2017-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: JS1 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: JS1
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Crystal Structure Of Mtb Pks13 Thioesterase Domain In Complex With Inhibitor Tam5
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2017-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: J24 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: J24
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Crystal Structure Of Mtb Pks13 Thioesterase Domain In Complex With Inhibitor Tam3
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2017-07-05 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: I66 |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: I66
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Crystal Structure Of The Bromodomain Of Human Crebbp Bound To The Benzodiazepinone G02773986
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2016-04-20 Classification: PROTEIN BINDING/INHIBITOR Ligands: SCN, 68Y |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-20
Ligands: SCN, 68Y
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Crystal Structure Of The Bromodomain Of Human Crebbp Bound To The Benzodiazepinone G02778174
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.05 Å Release Date: 2016-04-20 Classification: PROTEIN BINDING/INHIBITOR Ligands: EDO, SCN, 69A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-20
Ligands: EDO, SCN, 69A
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Crystal Structure Of The Bromodomain Of Human Crebbp Bound To The Benzodiazepinone G02857790
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.07 Å Release Date: 2016-04-20 Classification: PROTEIN BINDING/INHIBITOR Ligands: ACT, CA, 69B |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-20
Ligands: ACT, CA, 69B
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Cbp In Complex With Cpd23 ((R)-6-(3-(Benzyloxy)Phenyl)-4-Methyl-1,3,4,5-Tetrahydro-2H-Benzo[B][1,4]Diazepin-2-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2016-04-20 Classification: Transcription/Protein Binding Ligands: ZN, 69F, B3P, EDO, NA, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-20
Ligands: ZN, 69F, B3P, EDO, NA, PEG
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Cbp In Complex With Cpd637 ((R)-4-Methyl-6-(1-Methyl-3-(1-Methyl-1H-Pyrazol-4-Yl)-1H-Indazol-5-Yl)-1,3,4,5-Tetrahydro-2H-Benzo[B][1,4]Diazepin-2-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.41 Å Release Date: 2016-04-20 Classification: Transcription/Protein Binding Ligands: ZN, 69E, B3P, EDO, NA, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-20
Ligands: ZN, 69E, B3P, EDO, NA, PEG