MolNFT v1 · #179339 · protein
Kelch domain of human KEAP1 bound to NRF2 cyclic peptide, C[BAL- npetge]
7K2L · Kelch-like ech-associated protein 1: “Kelch domain of human KEAP1 bound to NRF2 cyclic peptide, C[BAL- npetge]”. X-ray diffraction, 5 pockets (best druggability 0.72). MolNFT v1 #179339 on GenesisL1: 3D structure, binding sites and…
- PDB
- 7K2L
- Type
- protein
- Length
- 580 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Kelch-like ech-associated protein 1; NRF2 cyclic PEPTIDE,C[BAL-npetge]
- UniProt
- Q14145
- Pockets
- 5 · best druggability 0.72
Structure
x-ray diffraction · 3 distinct chains · 0% helix, 50% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | Kelch-like ech-associated protein 1 | protein | 289 | 0% helix, 49% strand | Q14145 |
| A | Kelch-like ech-associated protein 1 | protein | 284 | 0% helix, 52% strand | Q14145 |
| P | NRF2 cyclic PEPTIDE,C[BAL-npetge] | protein | 7 | 0% helix, 0% strand | — |
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 487 | 0.72 | 0.82 | 54 | empty |
| 2 | 556 | 0.72 | 0.81 | 58 | empty |
| 3 | 52 | 0.56 | 0.90 | 17 | empty |
| 4 | 110 | 0.48 | 0.80 | 29 | empty |
| 5 | 95 | 0.34 | 0.74 | 25 | empty |
Interfaces
2 interfaces between chains.
- B–A · 505 Ų buried · 7 hydrogen bonds · protein-protein
- A–P · 445 Ų buried · 13 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 modified (nonstandard).
Compared structures
- 7K2L · Kelch domain of human KEAP1 bound to Nrf2 cyclic peptide, c[BAL-NPETGE] · the same entry in another collection · chain B against B, 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 Q14145
- Elsewhere: RCSB PDB 7K2L · PDBe 7K2L · UniProt Q14145
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