Search PepX: zinc-finger
47 results
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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2J6F | N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) BOUND TO CBL-B PEPTIDE | C | A |
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2J7X | STRUCTURE OF ESTRADIOL-BOUND ESTROGEN RECEPTOR BETA LBD IN COMPLEX WITH LXXLL MOTIF FROM NCOA5 | B | A | Nuclear receptor ligand-binding domain |
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2J7Y | STRUCTURE OF 17-EPIESTRIOL-BOUND ESTROGEN RECEPTOR BETA LBD IN COMPLEX WITH LXXLL MOTIF FROM NCOA5 | B | A | Nuclear receptor ligand-binding domain |
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2JF9 | ESTROGEN RECEPTOR ALPHA LBD IN COMPLEX WITH A TAMOXIFEN-SPECIFIC PEPTIDE ANTAGONIST | P | AC |
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2QPY | AR LBD with small molecule | B | A | Nuclear receptor ligand-binding domain |
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2QR9 | Crystal Structure of the Estrogen Receptor Alpha Ligand Binding Domain Complexed with an Oxabicyclic Derivative Compound | C | A |
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2QSE | Crystal Structure of the Estrogen Receptor Alpha Ligand Binding Domain complexed with Burned Meat Compound 4-OH-PhIP | C | A |
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2QXM | Crystal Structure of the Estrogen Receptor Alpha Ligand Binding Domain Complexed to Burned Meat Compound PhIP | C | A |
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2QZO | Crystal Structure of the Estrogen Receptor Alpha Ligand Binding Domain Complexed with WAY-169916 | C | A |
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2VP7 | DECODING OF METHYLATED HISTONE H3 TAIL BY THE PYGO-BCL9 WNT SIGNALING COMPLEX | B | A |
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2VPB | DECODING OF METHYLATED HISTONE H3 TAIL BY THE PYGO-BCL9 WNT SIGNALING COMPLEX | B | A |
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2VPE | DECODING OF METHYLATED HISTONE H3 TAIL BY THE PYGO-BCL9 WNT SIGNALING COMPLEX | D | C |
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2VPG | DECODING OF METHYLATED HISTONE H3 TAIL BY THE PYGO-BCL9 WNT SIGNALING COMPLEX | B | A |
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2ZFX | Crystal structure of the rat vitamin D receptor ligand binding domain complexed with YR301 and a synthetic peptide containing the NR2 box of DRIP 205 | C | A |
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2ZJD | Crystal Structure of LC3-p62 complex | D | C | beta-Grasp (ubiquitin-like) |
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2ZL9 | 2-Substituted-16-ene-22-thia-1alpha,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs: Synthesis, biological evaluation and crystal structure | C | A | Nuclear receptor ligand-binding domain |
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2ZLA | 2-Substituted-16-ene-22-thia-1alpha,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs: Synthesis, biological evaluation and crystal structure | C | A | Nuclear receptor ligand-binding domain |
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2ZLC | 2-Substituted-16-ene-22-thia-1alpha,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs: Synthesis, biological evaluation and crystal structure | C | A | Nuclear receptor ligand-binding domain |
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2ZMH | Crystal Structure of Rat Vitamin D Receptor Bound to Adamantyl Vitamin D Analogs: Structural Basis for Vitamin D Receptor Antagonism and/or Partial Agonism | C | A | Nuclear receptor ligand-binding domain |
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2ZMI | Crystal Structure of Rat Vitamin D Receptor Bound to Adamantyl Vitamin D Analogs: Structural Basis for Vitamin D Receptor Antagonism and/or Partial Agonism | C | A | Nuclear receptor ligand-binding domain |
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2ZMJ | Crystal Structure of Rat Vitamin D Receptor Bound to Adamantyl Vitamin D Analogs: Structural Basis for Vitamin D Receptor Antagonism and/or Partial Agonism | C | A | Nuclear receptor ligand-binding domain |
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2ZXN | A New Class of Vitamin D Receptor Ligands that Induce Structural Rearrangement of the Ligand-binding Pocket | C | A |
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3BEJ | Structure of human FXR in complex with MFA-1 and co-activator peptide | E | A | Nuclear receptor ligand-binding domain |
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3BQD | Doubling the Size of the Glucocorticoid Receptor Ligand Binding Pocket by Deacylcortivazol | B | A | Nuclear receptor ligand-binding domain |
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3CS8 | Structural and Biochemical Basis for the Binding Selectivity of PPARg to PGC-1a | B | A | Nuclear receptor ligand-binding domain |
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3CWD | Molecular recognition of nitro-fatty acids by PPAR gamma | C | A | Nuclear receptor ligand-binding domain |
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3D24 | Crystal structure of ligand-binding domain of estrogen-related receptor alpha (ERRalpha) in complex with the peroxisome proliferators-activated receptor coactivator-1alpha box3 peptide (PGC-1alpha) | B | A | Nuclear receptor ligand-binding domain |
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3D9T | CIAP1-BIR3 in complex with N-terminal peptide from Caspase-9 (ATPFQE) | C | A | Inhibitor of apoptosis (IAP) repeat |
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3D9U | The BIR3 domain of cIAP1 in complex with the N terminal peptide from SMAC/DIABLO (AVPIAQ). | B | A | Inhibitor of apoptosis (IAP) repeat |
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3DCT | FXR with SRC1 and GW4064 | B | A | Nuclear receptor ligand-binding domain |
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3E7C | Glucocorticoid Receptor LBD bound to GSK866 | D | B |
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3E94 | Crystal structure of RXRalpha ligand binding domain in complex with tributyltin and a coactivator fragment | B | A |
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3EMH | Structural basis of WDR5-MLL interaction | B | A |
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3EQS | Crystal structure of human MDM2 in complex with a 12-mer peptide inhibitor | B | A |
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3EQY | Crystal structure of human MDMX in complex with a 12-mer peptide inhibitor | C | A |
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3ET1 | Structure of PPARalpha with 3-[5-Methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-propionic acid | P | A |
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3ET3 | Structure of PPARgamma with 3-[5-Methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-propionic acid | P | A |
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3F7D | SF-1 LBD bound by phosphatidylcholine | B | A |
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3FUG | Crystal Structure of the Retinoid X Receptor Ligand Binding Domain Bound to the Synthetic Agonist 3-[4-Hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-phenyl]acrylic Acid | B | A |
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3FUR | Crystal Structure of PPARg in complex with INT131 | H | A |
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3FXV | Identification of an N-oxide pyridine GW4064 analogue as a potent FXR agonist | B | A |
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3G03 | Structure of human MDM2 in complex with high affinity peptide | B | ACD |
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3G8I | Aleglitazar, a new, potent, and balanced PPAR alpha/gamma agonist for the treatment of type II diabetes | Z | A |
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3G9E | Aleglitaar. a new. potent, and balanced dual ppara/g agonist for the treatment of type II diabetes | B | A |
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3GYU | Nuclear receptor DAF-12 from parasitic nematode Strongyloides stercoralis in complex with its physiological ligand dafachronic acid delta 7 | B | A |
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3H0A | Crystal Structure of Peroxisome Proliferator-Activated Receptor Gamma (PPARg) and Retinoic Acid Receptor Alpha (RXRa) in Complex with 9-cis Retinoic Acid, Co-activator Peptide, and a Partial Agonist | B | A |
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3GYT | Nuclear receptor DAF-12 from parasitic nematode Strongyloides stercoralis in complex with its physiological ligand dafachronic acid delta 4 | B | A |
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