Research workbench
The structure of variant D274E of the mo-insertase domain CNX1E from arabidopsis thaliana in complex with AMP
Analyse The structure of variant D274E of the mo-insertase domain CNX1E from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6RMS
- Type
- protein
- Length
- 397 residues
- Chains
- 1
- Method
- x-ray diffraction; solution scattering
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Molybdopterin biosynthesis protein CNX1
- EC
- 2.10.1.1, 2.7.7.75
- UniProt
- Q39054
- Ligands
- AMP, MG, SO4
- Pockets
- 2 · best druggability 0.51
Structure
x-ray diffraction; solution scattering · 1 distinct chain · 22% helix, 34% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Molybdopterin biosynthesis protein CNX1 (EC 2.10.1.1, 2.7.7.75) | protein | 397 | 22% helix, 34% strand | Q39054 |
Ligands and binding sites
- AMP · Adenosine monophosphate · ligand · chains A
- MG · Magnesium ion · metal · chains A
- SO4 · Sulfate ion · ion · chains A
- EDO · 1,2-ethanediol · additive · chains A
- IMD · Imidazole · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 189 | 0.51 | 0.77 | 29 | empty |
| 2 | 51 | 0.43 | 0.83 | 16 | empty |
Modifications
Observed in the structure: 1 modified (oxidation).
Compared structures
- 6RMS · The Structure of variant D274E of the Mo-insertase domain Cnx1E from Arabidopsis thaliana… · the same entry in another collection · chain A against A, TM-score 1.00
- Q39054 · AlphaFold monomer V2.0 prediction for molybdopterin biosynthesis protein CNX1 (Q39054) · a predicted model of the same protein · chain A against A, TM-score 0.99
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 Q39054
- Elsewhere: RCSB PDB 6RMS · PDBe 6RMS · UniProt Q39054
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