MolNFT v1 · #155370 · protein
Crystal structure of human rootletin 1108-1317
6L5J: “Crystal structure of human rootletin 1108-1317”. X-ray diffraction, 5 pockets (best druggability 0.59). MolNFT v1 #155370 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6L5J
- Type
- protein
- Length
- 825 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Rootletin
- UniProt
- Q5TZA2
- Pockets
- 5 · best druggability 0.59
Structure
x-ray diffraction · 3 distinct chains · 98% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Rootletin | protein | 208 | 98% helix, 0% strand | Q5TZA2 |
| B, C | Rootletin | protein | 208 | 99% helix, 0% strand | Q5TZA2 |
| D | Rootletin | protein | 201 | 98% helix, 0% strand | Q5TZA2 |
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 | 446 | 0.59 | 0.75 | 51 | empty |
| 2 | 288 | 0.58 | 0.77 | 31 | empty |
| 3 | 259 | 0.50 | 0.74 | 25 | empty |
| 4 | 99 | 0.36 | 0.75 | 18 | empty |
| 5 | 66 | 0.33 | 0.76 | 16 | empty |
Interfaces
6 interfaces between chains.
- C–D · 5065 Ų buried · 14 hydrogen bonds · protein-protein
- A–B · 4955 Ų buried · 14 hydrogen bonds · protein-protein
- A–C · 773 Ų buried · 9 hydrogen bonds · protein-protein
- A–D · 360 Ų buried · 2 hydrogen bonds · protein-protein
- B–C · 314 Ų buried · 1 hydrogen bond · protein-protein
Modifications
Observed in the structure: 17 modified, 1 disulfide (engineered, disulfide).
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 Q5TZA2
- Elsewhere: RCSB PDB 6L5J · PDBe 6L5J · UniProt Q5TZA2
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