Research workbench
X-ray structure of gene product from arabidopsis thaliana AT3G21360
Analyse X-ray structure of gene product from arabidopsis thaliana AT3G21360 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1Y0Z
- Type
- protein
- Length
- 643 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein product of AT3G21360
- UniProt
- Q9LIG0
- Ligands
- FE2, SO4
- Pockets
- 7 · best druggability 0.85
Structure
x-ray diffraction · 2 distinct chains · 28% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Protein product of AT3G21360 | protein | 321 | 28% helix, 29% strand | Q9LIG0 |
| B | Protein product of AT3G21360 | protein | 322 | 28% helix, 27% strand | Q9LIG0 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1195 | 0.85 | 0.86 | 117 | SO4, FE2 |
| 2 | 65 | 0.44 | 0.82 | 14 | empty |
| 3 | 64 | 0.40 | 0.80 | 13 | empty |
| 4 | 120 | 0.40 | 0.75 | 20 | empty |
| 5 | 80 | 0.38 | 0.77 | 16 | empty |
Interfaces
1 interface between chains.
- A–B · 722 Ų buried · 15 hydrogen bonds · protein-protein
Compared structures
- 1Y0Z · X-ray structure of gene product from Arabidopsis thaliana At3g21360 · the same entry in another collection · chain A against A, TM-score 1.00
- Q9LIG0 · AlphaFold monomer V2.0 prediction for clavaminate synthase-like protein AT3G21360 (Q9LIG0) · a predicted model of the same protein · chain B against A, TM-score 0.98
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 Q9LIG0
- Elsewhere: RCSB PDB 1Y0Z · PDBe 1Y0Z · UniProt Q9LIG0
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