Research workbench
Ternary complex of gephe - ADP - molybdenum cluster
Analyse Ternary complex of gephe - ADP - molybdenum cluster in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5ERU
- Type
- protein
- Length
- 414 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Gephyrin
- UniProt
- Q03555
- Ligands
- ADP, MO, CA, MG, PO4, MOO
- Pockets
- 5 · best druggability 0.41
Structure
x-ray diffraction · 1 distinct chain · 21% helix, 33% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Gephyrin | protein | 414 | 21% helix, 33% strand | Q03555 |
Ligands and binding sites
- ADP · Adenosine-5'-diphosphate · ligand · chains A
- MO · Molybdenum atom · metal · 8 copies · chains A
- CA · Calcium ion · metal · chains A
- MG · Magnesium ion · metal · chains A
- PO4 · Phosphate ion · ion · chains A
- MOO · Molybdate ion · ion · chains A
- ACT · Acetate ion · additive · 5 copies · chains A
- MPD · (4S)-2-methyl-2,4-pentanediol · additive · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 124 | 0.41 | 0.75 | 24 | empty |
| 2 | 57 | 0.33 | 0.77 | 18 | empty |
| 3 | 59 | 0.32 | 0.77 | 20 | CA, ADP |
| 4 | 57 | 0.31 | 0.76 | 19 | empty |
| 5 | 62 | 0.31 | 0.74 | 11 | MPD |
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 Q03555
- Elsewhere: RCSB PDB 5ERU · PDBe 5ERU · UniProt Q03555
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