Search PepX: cytoplasm
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Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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2JK9 | THE STRUCTURE OF SPLA-RYANODINE RECEPTOR DOMAIN AND SOCS BOX CONTAINING 1 IN COMPLEX WITH A PAR-4 PEPTIDE | B | A |
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2QL5 | Crystal Structure of caspase-7 with inhibitor AC-DMQD-CHO | G | ABCD |
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2QL7 | Crystal Structure of Caspase-7 with inhibitor AC-IEPD-CHO | G | ABCD |
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2QL9 | Crystal Structure of Caspase-7 with inhibitor AC-DQMD-CHO | G | ABCD |
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2QLB | Crystal Structure of caspase-7 with inhibitor AC-ESMD-CHO | G | ABCD |
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2QME | Crystal structure of human RAC3 in complex with CRIB domain of human p21-activated kinase 1 (PAK1) | I | A |
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2V51 | STRUCTURE OF MAL-RPEL1 COMPLEXED TO ACTIN | E | A |
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2V52 | STRUCTURE OF MAL-RPEL2 COMPLEXED TO G-ACTIN | M | A |
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2V8C | MOUSE PROFILIN IIA IN COMPLEX WITH THE PROLINE-RICH DOMAIN OF VASP | C | A |
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2VJ0 | CRYSTAL STRUCTURE OF THE ALPHA-ADAPTIN APPENDAGE DOMAIN, FROM THE AP2 ADAPTOR COMPLEX, IN COMPLEX WITH AN FXDNF PEPTIDE FROM AMPHIPHYSIN1 AND A WVXF PEPTIDE FROM SYNAPTOJANIN P170 | Q | A | Subdomain of clathrin and coatomer appendage domain |
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2VM6 | HUMAN BCL2-A1 IN COMPLEX WITH BIM-BH3 PEPTIDE | B | A |
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2VNW | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE | I | A |
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2VNY | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)AMINE | I | A |
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2VO0 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE | I | A |
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2VO3 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE | I | A |
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2VO6 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE | I | A |
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2VO7 | STRUCTURE OF PKA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE | I | A | Protein kinase-like (PK-like) |
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2VOF | STRUCTURE OF MOUSE A1 BOUND TO THE PUMA BH3-DOMAIN | D | BA |
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2VOG | STRUCTURE OF MOUSE A1 BOUND TO THE BMF BH3-DOMAIN | B | A |
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2VOH | STRUCTURE OF MOUSE A1 BOUND TO THE BAK BH3-DOMAIN | B | A |
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2VOI | STRUCTURE OF MOUSE A1 BOUND TO THE BID BH3-DOMAIN | 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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2W10 | MONA SH3C IN COMPLEX | C | B |
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2W9R | STRUCTURAL BASIS OF N-END RULE SUBSTRATE RECOGNITION IN ESCHERICHIA COLI BY THE CLPAP ADAPTOR PROTEIN CLPS | B | A |
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2WAX | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE | B | A |
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2WAY | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE | B | A |
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2Z32 | Crystal structure of Keap1 complexed with Prothymosin alpha | B | A | 6-bladed beta-propeller |
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2Z34 | Crystal structure of SpCia1/Asf1 complex with Hip1 | C | DA | Immunoglobulin-like beta-sandwich |
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2Z5S | Molecular basis for the inhibition of p53 by Mdmx | R | O |
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2Z5T | Molecular basis for the inhibition of p53 by Mdmx | P | MO |
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2ZJD | Crystal Structure of LC3-p62 complex | D | C | beta-Grasp (ubiquitin-like) |
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2ZNE | Crystal structure of Zn2+-bound form of des3-23ALG-2 complexed with Alix ABS peptide | D | B |
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2ZPY | Crystal structure of the mouse radxin FERM domain complexed with the mouse CD44 cytoplasmic peptide | B | A | beta-Grasp (ubiquitin-like) |
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3BIN | Structure of the DAL-1 and TSLC1 (372-383) complex | B | A |
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3BL2 | Crystal Structure of M11, the BCL-2 Homolog of Murine Gamma-herpesvirus 68, Complexed with Mouse Beclin1 (residues 106-124) | C | A |
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3BO8 | The High Resolution Crystal Structure of HLA-A1 Complexed with the MAGE-A1 Peptide | C | A |
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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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3BRH | Protein Tyrosine Phosphatase PTPN-22 (Lyp) bound to the mono-Phosphorylated Lck active site peptide | C | A |
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3BRL | Crystal Structure of LC8 S88E / Swa | C | A |
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3C3O | ALIX Bro1-domain:CHMIP4A co-crystal structure | B | A |
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3C3Q | ALIX Bro1-domain:CHMIP4B co-crystal structure | B | A |
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3C3R | ALIX BRO1 CHMP4C complex | B | A |
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3CHW | Complex of Dictyostelium discoideum Actin with Profilin and the Last Poly-Pro of Human VASP | V | P | Profilin-like |
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3CQU | Crystal Structure of Akt-1 complexed with substrate peptide and inhibitor | C | A |
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3CQW | Crystal Structure of Akt-1 complexed with substrate peptide and inhibitor | C | A |
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3CXW | Crystal structure of human proto-oncogene serine threonine kinase (PIM1) in complex with a consensus peptide and a beta carboline ligand I | B | A |
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3CY2 | Crystal structure of human proto-oncogene serine threonine kinase (PIM1) in complex with a consensus peptide and a beta carboline ligand II | B | A |
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