Search PepX: atp-binding
Results 1 - 50 of 64
Results
| PDB Identifier | Description | Ligand | Receptor | SCOP | pdb.org | |
|---|---|---|---|---|---|---|
  |
1FYN | PHOSPHOTRANSFERASE | B | A | SH3-like barrel |
 |
  |
1H27 | CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 | E | B | Cyclin-like |
|
  |
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) |
|
  |
1Q8U | The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor H-1152P | B | A | Protein kinase-like (PK-like) |
|
  |
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) |
|
  |
1WBP | SRPK1 BOUND TO 9MER DOCKING MOTIF PEPTIDE | B | C |
|
|
  |
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) |
|
  |
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) |
|
  |
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) |
|
  |
2BZK | CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE | A | B |
|
|
  |
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) |
|
  |
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) |
|
  |
2C3I | CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I | A | B |
|
|
  |
2CCH | THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA-LINKED ATP ANALOGUE | E | B | Cyclin-like |
|
  |
2CK3 | AZIDE INHIBITED BOVINE F1-ATPASE | I | HG | Epsilon subunit of F1F0-ATP synthase N-terminal domain |
|
  |
2JAM | CRYSTAL STRUCTURE OF HUMAN CALMODULIN-DEPENDENT PROTEIN KINASE I G | D | A |
|
|
  |
2JDI | GROUND STATE STRUCTURE OF F1-ATPASE FROM BOVINE HEART MITOCHONDRIA (BOVINE F1-ATPASE CRYSTALLISED IN THE ABSENCE OF AZIDE) | I | HG | Epsilon subunit of F1F0-ATP synthase N-terminal domain |
|
  |
2JDO | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE | C | A | Protein kinase-like (PK-like) |
|
  |
2JDR | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH THE INHIBITOR A-443654 | C | A | Protein kinase-like (PK-like) |
|
  |
2JDS | STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A-443654 | I | A | Protein kinase-like (PK-like) |
|
  |
2JDT | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE | I | A |
|
|
  |
2JDV | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH A-443654 | I | A |
|
|
  |
2JLD | EXTREMELY TIGHT BINDING OF RUTHENIUM COMPLEX TO GLYCOGEN SYNTHASE KINASE 3 | E | A |
|
|
  |
2Q0N | Structure of human p21 activating kinase 4 (PAK4) in complex with a consensus peptide | B | A |
|
|
  |
2QME | Crystal structure of human RAC3 in complex with CRIB domain of human p21-activated kinase 1 (PAK1) | I | A |
|
|
  |
2UVY | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH METHYL-(4-(9H-PURIN-6-YL)-BENZYL)-AMINE | I | A |
|
|
  |
2UVZ | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-PHENYL-C-(4-(9H-PURIN-6-YL)-PHENYL)-METHYLAMINE | I | A |
|
|
  |
2UW0 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 6-(4-(4-(4-CHLORO-PHENYL)-PIPERIDIN-4-YL)-PHENYL)-9H-PURINE | I | A |
|
|
  |
2UW3 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE | I | A |
|
|
  |
2UW4 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-(5-METHYL-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
|
|
  |
2UW5 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (R)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
|
|
  |
2UW6 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (S)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE | I | A |
|
|
  |
2UW7 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE | I | A |
|
|
  |
2UW8 | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-CHLORO-PHENYL)-2-PHENYL-ETHYLAMINE | I | A |
|
|
  |
2UW9 | STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE | C | A | Protein kinase-like (PK-like) |
|
  |
2UZV | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS | 2 | A |
|
|
  |
2UZW | PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS | I | E |
|
|
  |
2V3S | STRUCTURAL INSIGHTS INTO THE RECOGNITION OF SUBSTRATES AND ACTIVATORS BY THE OSR1 KINASE | D | A |
|
|
  |
2V51 | STRUCTURE OF MAL-RPEL1 COMPLEXED TO ACTIN | E | A |
|
|
  |
2V52 | STRUCTURE OF MAL-RPEL2 COMPLEXED TO G-ACTIN | M | A |
|
|
  |
2VNW | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE | I | A |
|
|
  |
2VNY | STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)AMINE | I | A |
|
|
  |
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 |
|
|
  |
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 |
|
|
  |
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 |
|
|
  |
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) |
|
  |
2WAX | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE | B | A |
|
|
  |
2WAY | STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE | B | A |
|
|
  |
3BU3 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide | B | A | Protein kinase-like (PK-like) |
|
  |
3BU5 | Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide and ATP | B | C |
|
