Search Count: 30
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Crystal Structure Of The Ribonuclease Core Of R3B2
Organism: Mucor lusitanicus
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2021-03-31 Classification: RNA BINDING PROTEIN |
Organism: Mucor lusitanicus
Method: X-RAY DIFFRACTION
Release Date: 2021-03-31
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Gsk3011724A Cocrystallised With Mycobacterium Tuberculosis H37Rv Kasa
Organism: Mycobacterium tuberculosis (strain atcc 25618 / h37rv)
Method: X-RAY DIFFRACTION Resolution:2.13 Å Release Date: 2016-09-21 Classification: TRANSFERASE |
Organism: Mycobacterium tuberculosis (strain atcc 25618 / h37rv)
Method: X-RAY DIFFRACTION
Release Date: 2016-09-21
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Structure Of The 1121B Fab Fragment
Organism: Mus musculus, homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-08-24 Classification: IMMUNE SYSTEM Ligands: PO4 |
Organism: Mus musculus, homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: PO4
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Structural Basis For The Function Of Two Anti-Vegf Receptor Antibodies
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-08-24 Classification: IMMUNE SYSTEM/Transferase Ligands: CA, NAG |
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: CA, NAG
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Structural Basis For The Function Of Two Anti-Vegf Receptor Antibodies
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.20 Å Release Date: 2011-08-24 Classification: IMMUNE SYSTEM/Transferase |
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
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Structural Basis For The Function Of Two Anti-Vegf Receptor Antibodies
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2011-08-24 Classification: IMMUNE SYSTEM/Transferase |
Organism: Mus musculus, homo sapiens, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.24 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0C |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0C
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.97 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0D |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0D
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.93 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0E |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0E
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0F |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0F
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.71 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0G
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Fragment-Based Discovery Of The Pyrazol-4-Yl Urea (At9283), A Multi- Targeted Kinase Inhibitor With Potent Aurora Kinase Activity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0F |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0F
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Structure Determination Of Aurora Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2009-01-27 Classification: TRANSFERASE Ligands: L0I |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-01-27
Ligands: L0I
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ1
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ2
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ3
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ4
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ5
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZM
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ7