Research workbench
Structure of the CUL1-RBX1-SKP1-F BOXSKP2 scf ubiquitin ligase complex
Analyse Structure of the CUL1-RBX1-SKP1-F BOXSKP2 scf ubiquitin ligase complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1LDK
- Type
- protein
- Length
- 971 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cullin homolog; Ring-box protein 1; Cyclin A/CDK2-associated protein P19; SKP2-like…
- UniProt
- Q13616, P62877, P63208, Q13309
- Ligands
- ZN
- Pockets
- 12 · best druggability 0.77
Structure
x-ray diffraction · 5 distinct chains · 50% helix, 4% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cullin homolog | protein | 358 | 70% helix, 0% strand | Q13616 |
| B | Cullin homolog | protein | 366 | 41% helix, 6% strand | Q13616 |
| C | Ring-box protein 1 | protein | 88 | 5% helix, 15% strand | P62877 |
| D | Cyclin A/CDK2-associated protein P19 | protein | 118 | 52% helix, 3% strand | P63208 |
| E | SKP2-like protein type gamma | protein | 41 | 51% helix, 0% strand | Q13309 |
Ligands and binding sites
- ZN · Zinc ion · metal · 3 copies · chains C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 518 | 0.77 | 0.84 | 63 | empty |
| 2 | 467 | 0.75 | 0.84 | 45 | empty |
| 3 | 381 | 0.69 | 0.81 | 59 | empty |
| 4 | 228 | 0.68 | 0.85 | 31 | empty |
| 5 | 78 | 0.56 | 0.86 | 27 | empty |
Interfaces
5 interfaces between chains.
- B–C · 2433 Ų buried · 25 hydrogen bonds · protein-protein
- A–B · 966 Ų buried · 14 hydrogen bonds · protein-protein
- D–E · 767 Ų buried · 4 hydrogen bonds · protein-protein
- A–D · 724 Ų buried · 8 hydrogen bonds · protein-protein
- A–E · 302 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 disulfide (disulfide).
Compared structures
- 1LDK · Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF Ubiquitin Ligase Complex · the same entry in another collection · chain E against E, TM-score 1.00
- Q13616 · AlphaFold monomer V2.0 prediction for cullin-1 (Q13616) · a predicted model of the same protein · chain A against A, TM-score 0.97
- P63208 · AlphaFold monomer V2.0 prediction for S-phase kinase-associated protein 1 (P63208) · a predicted model of the same protein · chain D against A, TM-score 0.94
- Q13309 · AlphaFold monomer V2.0 prediction for S-phase kinase-associated protein 2 (Q13309) · a predicted model of the same protein · chain E against A, TM-score 0.82
- P62877 · AlphaFold monomer V2.0 prediction for E3 ubiquitin-protein ligase RBX1 (P62877) · a predicted model of the same protein · chain C against A, TM-score 0.57
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 Q13616
- Every structure of UniProt P62877
- Every structure of UniProt P63208
- Every structure of UniProt Q13309
- Elsewhere: RCSB PDB 1LDK · PDBe 1LDK · UniProt Q13616 · UniProt P62877 · UniProt P63208 · UniProt Q13309
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