Search Count: 10
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Structure Of Line-1 Orf2P With Template:Primer Hybrid
Organism: Homo sapiens, Synthetic construct
Method: ELECTRON MICROSCOPY Release Date: 2024-01-10 Classification: RNA BINDING PROTEIN/RNA/DNA Ligands: TTP, MG |
Organism: Homo sapiens, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2024-01-10
Ligands: TTP, MG
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Structure Of Line-1 Orf2P With An Oligo(A) Template
Organism: Homo sapiens, Synthetic construct
Method: ELECTRON MICROSCOPY Release Date: 2024-01-10 Classification: RNA BINDING PROTEIN/RNA |
Organism: Homo sapiens, Synthetic construct
Method: ELECTRON MICROSCOPY
Release Date: 2024-01-10
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Long Interspersed Nuclear Element 1 (Line-1) Reverse Transcriptase Ternary Complex With Hybrid Duplex And Dttp
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2023-12-20 Classification: REPLICATION Ligands: CIT, TTP, EDO, DMS, DIO, MG, CL |
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2023-12-20
Ligands: CIT, TTP, EDO, DMS, DIO, MG, CL
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Factor Xia In Complex With The Inhibitor 4-{2-[(1S)-1-({[Trans-4-(Aminomethyl)Cyclohexyl]Carbonyl}Amino)-2-Phenylethyl]-1H-Imidazol-4-Yl}Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2014-12-03 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 39D, SO4, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-12-03
Ligands: 39D, SO4, EDO
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Factor Xia In Complex With The Inhibitor (2S)-6-Amino-N-{(1S)-1-[4-(3-Amino-2H-Indazol-6-Yl)-5-Chloro-1H-Imidazol-2-Yl]-2-Phenylethyl}-2-Ethylhexanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2014-12-03 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 39F, SO4, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-12-03
Ligands: 39F, SO4, EDO
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(4-Carbamimidoylphenyl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NJ, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NJ, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(1-Aminoisoquinolin-6-Yl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NK, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NK, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(3-Carbamoylphenyl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NL, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NL, CA, SO4, GOL
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Crystal Structure Of The Complex Formed Between Trypsin And A Designed Synthetic Highly Potent Inhibitor In The Presence Of Benzamidine At 0.97 A Resolution
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:0.97 Å Release Date: 2006-01-17 Classification: HYDROLASE Ligands: CA, 1NJ, BEN, MES, GOL |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2006-01-17
Ligands: CA, 1NJ, BEN, MES, GOL
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Structure Of Trypsin (Orthorhombic) With 1-(4-Tert-Butylcarbamoyl- Piperazine-1-Carbonyl)-3-(3-Guanidino-Propyl)-4-Oxo-Azetidine-2-Carboxylic Acid
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2004-06-08 Classification: HYDROLASE Ligands: CA, SO4, 169 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2004-06-08
Ligands: CA, SO4, 169