Search PepX: Phosphorylase Kinase. domain 1
Results 1 - 50 of 54
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
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1APM | 2.0 ANGSTROM REFINED CRYSTAL STRUCTURE OF THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A PEPTIDE INHIBITOR AND DETERGENT | I | E | Protein kinase-like (PK-like) |
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1CDK | CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT (E.C.2.7.1.37) (PROTEIN KINASE A) COMPLEXED WITH PROTEIN KINASE INHIBITOR PEPTIDE FRAGMENT 5-24 (PKI(5-24) ISOELECTRIC VARIANT CA) AND MN2+ ADENYLYL IMIDODIPHOSPHATE (MNAMP-PNP) AT PH 5.6 AND 7C AND 4C | I | A | Protein kinase-like (PK-like) |
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1FMO | CRYSTAL STRUCTURE OF A POLYHISTIDINE-TAGGED RECOMBINANT CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH THE PEPTIDE INHIBITOR PKI(5-24) AND ADENOSINE | I | E | Protein kinase-like (PK-like) |
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1IR3 | PHOSPHORYLATED INSULIN RECEPTOR TYROSINE KINASE IN COMPLEX WITH PEPTIDE SUBSTRATE AND ATP ANALOG | B | A | Protein kinase-like (PK-like) |
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1K3A | Structure of the Insulin-like Growth Factor 1 Receptor Kinase | B | A | Protein kinase-like (PK-like) |
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1LEW | CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS NUCLEAR SUBSTRATE MEF2A | B | A | Protein kinase-like (PK-like) |
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1LEZ | CRYSTAL STRUCTURE OF MAP KINASE P38 COMPLEXED TO THE DOCKING SITE ON ITS ACTIVATOR MKK3B | B | A | Protein kinase-like (PK-like) |
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1NVQ | The Complex Structure Of Checkpoint Kinase Chk1/UCN-01 | B | A | Protein kinase-like (PK-like) |
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1NVR | The Complex Structure Of Checkpoint Kinase Chk1/Staurosporine | B | A | Protein kinase-like (PK-like) |
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1NVS | The Complex Structure Of Checkpoint Kinase Chk1/SB218078 | B | A | Protein kinase-like (PK-like) |
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1O6K | STRUCTURE OF ACTIVATED FORM OF PKB KINASE DOMAIN S474D WITH GSK3 PEPTIDE AND AMP-PNP | C | A | Protein kinase-like (PK-like) |
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1O6L | CRYSTAL STRUCTURE OF AN ACTIVATED AKT/PROTEIN KINASE B (PKB-PIF CHIMERA) TERNARY COMPLEX WITH AMP-PNP AND GSK3 PEPTIDE | C | A | Protein kinase-like (PK-like) |
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1O9U | GLYCOGEN SYNTHASE KINASE 3 BETA COMPLEXED WITH AXIN PEPTIDE | B | A | Protein kinase-like (PK-like) |
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1Q61 | PKA triple mutant model of PKB | I | A | Protein kinase-like (PK-like) |
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1Q62 | PKA double mutant model of PKB | I | A | Protein kinase-like (PK-like) |
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1Q8T | The Catalytic Subunit of cAMP-dependent Protein Kinase (PKA) in Complex with Rho-kinase Inhibitor Y-27632 | B | A | Protein kinase-like (PK-like) |
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1Q8U | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor H-1152P | B | A | Protein kinase-like (PK-like) |
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1Q8W | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor Fasudil (HA-1077) | B | A | Protein kinase-like (PK-like) |
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1QMZ | PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX | E | C | Protein kinase-like (PK-like) |
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1SMH | Protein kinase A variant complex with completely ordered N-terminal helix | B | A | Protein kinase-like (PK-like) |
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1STC | CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH STAUROSPORINE | I | E | Protein kinase-like (PK-like) |
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1SVE | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 1 | B | A | Protein kinase-like (PK-like) |
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1SVG | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 4 | B | A | Protein kinase-like (PK-like) |
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1SVH | Crystal Structure of Protein Kinase A in Complex with Azepane Derivative 8 | B | A | Protein kinase-like (PK-like) |
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1UKH | Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125 | B | A | Protein kinase-like (PK-like) |
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1XH4 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH5 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH6 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH7 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH8 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1XH9 | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A |
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1XHA | Crystal Structures of Protein Kinase B Selective Inhibitors in Complex with Protein Kinase A and Mutants | B | A | Protein kinase-like (PK-like) |
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1YDR | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H7 PROTEIN KINASE INHIBITOR 1-(5-ISOQUINOLINESULFONYL)-2-METHYLPIPERAZINE | I | E | Protein kinase-like (PK-like) |
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1YDS | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H8 PROTEIN KINASE INHIBITOR [N-(2-METHYLAMINO)ETHYL]-5-ISOQUINOLINESULFONAMIDE | I | E | Protein kinase-like (PK-like) |
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1YDT | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H89 PROTEIN KINASE INHIBITOR N-[2-(4-BROMOCINNAMYLAMINO)ETHYL]-5-ISOQUINOLINE | I | E | Protein kinase-like (PK-like) |
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1ZYS | Co-crystal structure of Checkpoint Kinase Chk1 with a pyrrolo-pyridine inhibitor | B | A |
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2BFY | COMPLEX OF AURORA-B WITH INCENP AND HESPERIDIN. | D | A |
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2BZK | CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE | A | B |
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2C1A | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL)AMIDE | I | A | Protein kinase-like (PK-like) |
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2C1B | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH (4R,2S)-5\'-(4-(4-CHLOROBENZYLOXY)PYRROLIDIN-2-YLMETHANESULFONYL)ISOQUINOLINE | I | A | Protein kinase-like (PK-like) |
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2C3I | CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I | A | B |
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2ERZ | Crystal Structure of c-AMP Dependent Kinase (PKA) bound to hydroxyfasudil | I | E | Protein kinase-like (PK-like) |
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2F7E | PKA complexed with (S)-2-(1H-Indol-3-yl)-1-(5-isoquinolin-6-yl-pyridin-3-yloxymethyl-etylamine | I | E | Protein kinase-like (PK-like) |
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2F7X | Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine | I | E | Protein kinase-like (PK-like) |
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2FYS | Crystal structure of Erk2 complex with KIM peptide derived from MKP3 | D | BA | Protein kinase-like (PK-like) |
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2GFC | cAMP-dependent protein kinase PKA catalytic subunit with PKI-5-24 | I | A | Protein kinase-like (PK-like) |
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2GNF | Protein kinase A fivefold mutant model of Rho-kinase with Y-27632 | I | A |
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2GNG | Protein kinase A fivefold mutant model of Rho-kinase | I | A |
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2GNH | PKA five fold mutant model of Rho-kinase with H1152P | I | A |
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2GNI | PKA fivefold mutant model of Rho-kinase with inhibitor Fasudil (HA1077) | I | A |
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