MolNFT v1 · #176011 · protein
Mitf bhlhlz apo structure
7D8S · Microphthalmia-associated transcription FACTOR,METHIONYL…: “Mitf bhlhlz apo structure”. X-ray diffraction, 1 ligand (SO4), 10 pockets (best druggability 0.65). MolNFT v1 #176011 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 7D8S
- Type
- protein
- Length
- 724 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Microphthalmia-associated transcription FACTOR,METHIONYL- tRNA synthetase beta subunit
- UniProt
- O75030, O66738
- Ligands
- SO4
- Pockets
- 10 · best druggability 0.65
Structure
x-ray diffraction · 4 distinct chains · 33% helix, 27% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Microphthalmia-associated transcription FACTOR,METHIONYL- tRNA synthetase beta subunit | protein | 185 | 32% helix, 26% strand | O75030, O66738 |
| B | Microphthalmia-associated transcription FACTOR,METHIONYL- tRNA synthetase beta subunit | protein | 180 | 33% helix, 27% strand | O75030, O66738 |
| C | Microphthalmia-associated transcription FACTOR,METHIONYL- tRNA synthetase beta subunit | protein | 184 | 33% helix, 27% strand | O75030, O66738 |
| D | Microphthalmia-associated transcription FACTOR,METHIONYL- tRNA synthetase beta subunit | protein | 175 | 35% helix, 27% strand | O75030, O66738 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 3 copies · chains B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 316 | 0.65 | 0.81 | 46 | SO4 |
| 2 | 291 | 0.61 | 0.79 | 41 | SO4 |
| 3 | 109 | 0.46 | 0.79 | 20 | empty |
| 4 | 126 | 0.43 | 0.76 | 19 | empty |
| 5 | 59 | 0.39 | 0.80 | 19 | empty |
Interfaces
6 interfaces between chains.
- B–C · 2750 Ų buried · 42 hydrogen bonds · protein-protein
- A–D · 2732 Ų buried · 43 hydrogen bonds · protein-protein
- C–D · 1504 Ų buried · 13 hydrogen bonds · protein-protein
- A–B · 1449 Ų buried · 10 hydrogen bonds · protein-protein
- B–D · 517 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 disulfide (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 O75030
- Every structure of UniProt O66738
- Elsewhere: RCSB PDB 7D8S · PDBe 7D8S · UniProt O75030 · UniProt O66738
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