MolNFT v1 · #38125 · protein
PKA five fold mutant model of rho-kinase with H1152P
2GNH · Camp-dependent protein kinase, alpha-catalytic subunit: “PKA five fold mutant model of rho-kinase with H1152P”. X-ray diffraction, 1 ligand (H52), 5 pockets (best druggability 0.82). MolNFT v1 #38125 on GenesisL1: 3D structure…
- PDB
- 2GNH
- Type
- protein
- Length
- 361 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Camp-dependent protein kinase, alpha-catalytic subunit; Camp-dependent protein kinase…
- EC
- 2.7.11.11
- UniProt
- P00517, P61926
- Ligands
- H52
- Pockets
- 5 · best druggability 0.82
Structure
x-ray diffraction · 2 distinct chains · 37% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Camp-dependent protein kinase, alpha-catalytic subunit (EC 2.7.11.11) | protein | 341 | 38% helix, 15% strand | P00517 |
| I | Camp-dependent protein kinase inhibitor alpha | protein | 20 | 30% helix, 0% strand | P61926 |
Ligands and binding sites
- H52 · (S)-2-methyl-1-[(4-methyl-5-isoquinoline)sulfonyl]-homopiperazine · ligand · 2 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 355 | 0.82 | 0.91 | 42 | H52 |
| 2 | 192 | 0.56 | 0.79 | 29 | empty |
| 3 | 95 | 0.40 | 0.77 | 16 | empty |
| 4 | 76 | 0.32 | 0.74 | 14 | empty |
| 5 | 52 | 0.31 | 0.77 | 16 | empty |
Interfaces
1 interface between chains.
- A–I · 1155 Ų buried · 18 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 modified (phosphorylation).
Compared structures
- 2GNH · PKA five fold mutant model of Rho-kinase with H1152P · the same entry in another collection · chain A against A, TM-score 1.00
- P61926 · AlphaFold monomer V2.0 prediction for camp-dependent protein kinase inhibitor alpha… · a predicted model of the same protein · chain I against A, TM-score 0.38
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 P00517
- Every structure of UniProt P61926
- Elsewhere: RCSB PDB 2GNH · PDBe 2GNH · UniProt P00517 · UniProt P61926
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