Search PepX: zinc
Results 1 - 50 of 62
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1SDX | Crystal structure of the zinc saturated C-terminal half of bovine lactoferrin at 2.0 A resolution reveals two additional zinc binding sites | E | A | Periplasmic binding protein-like II |
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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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2R28 | The complex Structure of Calmodulin Bound to a Calcineurin Peptide | C | AB | EF Hand-like |
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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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2VZD | CRYSTAL STRUCTURE OF THE C-TERMINAL CALPONIN HOMOLOGY DOMAIN OF ALPHA PARVIN IN COMPLEX WITH PAXILLIN LD1 MOTIF | C | A |
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2VZG | CRYSTAL STRUCTURE OF THE C-TERMINAL CALPONIN HOMOLOGY DOMAIN OF ALPHA-PARVIN IN COMPLEX WITH PAXILLIN LD2 MOTIF | A | B |
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2VZI | CRYSTAL STRUCTURE OF THE C-TERMINAL CALPONIN HOMOLOGY DOMAIN OF ALPHA-PARVIN IN COMPLEX WITH PAXILLIN LD4 MOTIF | A | B |
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2W0P | CRYSTAL STRUCTURE OF THE FILAMIN A REPEAT 21 COMPLEXED WITH THE MIGFILIN PEPTIDE | C | AB | Immunoglobulin-like beta-sandwich |
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2W73 | HIGH-RESOLUTION STRUCTURE OF THE COMPLEX BETWEEN CALMODULIN AND A PEPTIDE FROM CALCINEURIN A | K | ABF |
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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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3DDA | Crystal structure of the catalytic domain of Botulinum neurotoxin serotype a with a snap-25 peptide | B | A |
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3DDB | Crystal structure of the catalytic domain of Botulinum neurotoxin serotype a with a substrate analog peptide | B | A |
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3DOW | Complex structure of GABA type A receptor associated protein and its binding epitope on calreticulin | B | A |
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3DXC | Crystal structure of the intracellular domain of human APP in complex with Fe65-PTB2 | D | C |
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3DXD | Crystal structure of the intracellular domain of human APP (T668E mutant) in complex with Fe65-PTB2 | D | C |
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3DXE | Crystal structure of the intracellular domain of human APP (T668A mutant) in complex with Fe65-PTB2 | B | A |
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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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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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