Research workbench
Hexadecameric hub domain of camkii beta
Analyse Hexadecameric hub domain of camkii beta in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7URZ
- Type
- protein
- Length
- 508 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- CALCIUM/CALMODULIN-dependent protein kinase type II subunit beta
- EC
- 2.7.11.17
- UniProt
- Q13554
- Pockets
- 8 · best druggability 0.75
Structure
x-ray diffraction · 4 distinct chains · 27% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| G | CALCIUM/CALMODULIN-dependent protein kinase type II subunit beta (EC 2.7.11.17) | protein | 125 | 28% helix, 43% strand | Q13554 |
| A | CALCIUM/CALMODULIN-dependent protein kinase type II subunit beta (EC 2.7.11.17) | protein | 119 | 29% helix, 45% strand | Q13554 |
| B | CALCIUM/CALMODULIN-dependent protein kinase type II subunit beta (EC 2.7.11.17) | protein | 132 | 27% helix, 42% strand | Q13554 |
| C | CALCIUM/CALMODULIN-dependent protein kinase type II subunit beta (EC 2.7.11.17) | protein | 132 | 24% helix, 41% strand | Q13554 |
Pockets
8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 92 | 0.75 | 0.97 | 22 | empty |
| 2 | 175 | 0.67 | 0.86 | 31 | empty |
| 3 | 220 | 0.65 | 0.83 | 31 | empty |
| 4 | 268 | 0.60 | 0.79 | 22 | empty |
| 5 | 141 | 0.47 | 0.77 | 26 | empty |
Interfaces
3 interfaces between chains.
- G–A · 598 Ų buried · 5 hydrogen bonds · protein-protein
- A–B · 597 Ų buried · 6 hydrogen bonds · protein-protein
- G–C · 590 Ų buried · 7 hydrogen bonds · protein-protein
Compared structures
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 Q13554
- Elsewhere: RCSB PDB 7URZ · PDBe 7URZ · UniProt Q13554
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