Research workbench
Crystal structure of the protein-kinase a catalytic subunit from criteculus griseus in complex with compounds RKP193 and RKP117
Analyse Crystal structure of the protein-kinase a catalytic subunit from criteculus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6ERT
- Type
- protein
- Length
- 356 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Camp-dependent protein kinase catalytic subunit alpha; Camp-dependent protein kinase…
- EC
- 2.7.11.11
- UniProt
- P25321, A0A061IH64
- Ligands
- BVZ
- Pockets
- 3 · best druggability 0.75
Structure
x-ray diffraction · 2 distinct chains · 38% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Camp-dependent protein kinase catalytic subunit alpha (EC 2.7.11.11) | protein | 338 | 38% helix, 15% strand | P25321 |
| D | Camp-dependent protein kinase inhibitor | protein | 18 | 44% helix, 0% strand | A0A061IH64 |
Ligands and binding sites
- BVZ · [2-[(4-isoquinolin-5-ylsulfonyl-1,4-diazepan-1-yl) methyl]phenyl]-tris(oxidanyl)boranuide · ligand · chains A, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 509 | 0.75 | 0.83 | 45 | BVZ |
| 2 | 78 | 0.41 | 0.78 | 12 | empty |
| 3 | 50 | 0.26 | 0.73 | 11 | empty |
Interfaces
1 interface between chains.
- A–D · 738 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 modified, 1 covalent (phosphorylation, covalent ligand).
Compared structures
- 6ERT · Crystal Structure of the Protein-Kinase A catalytic subunit from Criteculus Griseus in… · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P25321
- Every structure of UniProt A0A061IH64
- Elsewhere: RCSB PDB 6ERT · PDBe 6ERT · UniProt P25321 · UniProt A0A061IH64
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