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Search Count: 24

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3N00 image
Crystal Structure Of A Deletion Mutant Of Human Reverba Ligand Binding Domain Bound With An Ncor Id1 Peptide Determined To 2.60A

2P54 image
A Crystal Structure Of Ppar Alpha Bound With Src1 Peptide And Gw735

1YOK image
Crystal Structure Of Human Lrh-1 Bound With Tif-2 Peptide And Phosphatidylglycerol

1YOW image
Human Steroidogenic Factor 1 Lbd With Bound Co-Factor Peptide

1Y0S image
Crystal Structure Of Ppar Delta Complexed With Gw2331

1YMT image
Mouse Sf-1 Lbd

1RDT image
Crystal Structure Of A New Rexinoid Bound To The Rxralpha Ligand Binding Doamin In The Rxralpha/Ppargamma Heterodimer

1M2Z image
Crystal Structure Of A Dimer Complex Of The Human Glucocorticoid Receptor Ligand-Binding Domain Bound To Dexamethasone And A Tif2 Coactivator Motif

1KE5 image
Cdk2 Complexed With N-Methyl-4-{[(2-Oxo-1,2-Dihydro-3H-Indol-3-Ylidene)Methyl]Amino}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2002-05-14
Classification: TRANSFERASE
Ligands: LS1

1KE6 image
Cyclin-Dependent Kinase 2 (Cdk2) Complexed With N-Methyl-{4-[2-(7-Oxo-6,7-Dihydro-8H-[1,3]Thiazolo[5,4-E]Indol-8-Ylidene)Hydrazino]Phenyl}Methanesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2002-05-14
Classification: TRANSFERASE
Ligands: LS2

1KE7 image
Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 3-{[(2,2-Dioxido-1,3-Dihydro-2-Benzothien-5-Yl)Amino]Methylene}-5-(1,3-Oxazol-5-Yl)-1,3-Dihydro-2H-Indol-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2002-05-14
Classification: TRANSFERASE
Ligands: LS3

1KE8 image
Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 4-{[(2-Oxo-1,2-Dihydro-3H-Indol-3-Ylidene)Methyl]Amino}-N-(1,3-Thiazol-2-Yl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2002-05-14
Classification: TRANSFERASE
Ligands: LS4

1KE9 image
Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 3-{[4-({[Amino(Imino)Methyl]Aminosulfonyl)Anilino]Methylene}-2-Oxo-2,3-Dihydro-1H-Indole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2002-05-14
Classification: TRANSFERASE
Ligands: LS5

1KKQ image
Crystal Structure Of The Human Ppar-Alpha Ligand-Binding Domain In Complex With An Antagonist Gw6471 And A Smrt Corepressor Motif

1K74 image
The 2.3 Angstrom Resolution Crystal Structure Of The Heterodimer Of The Human Ppargamma And Rxralpha Ligand Binding Domains Respectively Bound With Gw409544 And 9-Cis Retinoic Acid And Co-Activator Peptides.

1K7L image
The 2.5 Angstrom Resolution Crystal Structure Of The Human Pparalpha Ligand Binding Domain Bound With Gw409544 And A Co-Activator Peptide.

1G5Y image
The 2.0 Angstrom Resolution Crystal Structure Of The Rxralpha Ligand Binding Domain Tetramer In The Presence Of A Non-Activating Retinoic Acid Isomer.

1G1U image
The 2.5 Angstrom Resolution Crystal Structure Of The Rxralpha Ligand Binding Domain In Tetramer In The Absence Of Ligand

1FM6 image
The 2.1 Angstrom Resolution Crystal Structure Of The Heterodimer Of The Human Rxralpha And Ppargamma Ligand Binding Domains Respectively Bound With 9-Cis Retinoic Acid And Rosiglitazone And Co-Activator Peptides.

1FM9 image
The 2.1 Angstrom Resolution Crystal Structure Of The Heterodimer Of The Human Rxralpha And Ppargamma Ligand Binding Domains Respectively Bound With 9-Cis Retinoic Acid And Gi262570 And Co-Activator Peptides.
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