Research workbench
Klebsiella pneumoniae Seryl-tRNA Synthetase in Complex with 5'-O-(N-(L-seryl)-Sulfamoyl)uridine
Analyse Klebsiella pneumoniae Seryl-tRNA Synthetase in Complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6HI0
- Type
- protein
- Length
- 428 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.25
- Source
- Klebsiella pneumoniae
- Molecule
- Serine--tRNA ligase
- EC
- 6.1.1.11
- UniProt
- W9BNU9
- Ligands
- FZK, CA
- Pockets
- 3 · best druggability 0.74
Structure
x-ray diffraction · resolution 2.25 · 1 distinct chain · 43% helix, 20% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Serine--tRNA ligase (EC 6.1.1.11) | protein | 428 | 43% helix, 20% strand | W9BNU9 |
Ligands and binding sites
- FZK · 5'-O-(N-(L-seryl)-Sulfamoyl)uridine · ligand · chains A
- CA · Calcium ion · metal · 3 copies · chains A
- EDO · 1,2-ethanediol · additive · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 684 | 0.74 | 0.80 | 61 | EDO, FZK, CA |
| 2 | 151 | 0.53 | 0.80 | 22 | empty |
| 3 | 70 | 0.36 | 0.77 | 14 | empty |
Compared structures
- 6HI0 · Klebsiella pneumoniae seryl-tRNA synthetase in complex with 5'-O-(N… · the same entry in another collection · chain A against A, TM-score 1.00
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 W9BNU9
- Elsewhere: RCSB PDB 6HI0 · PDBe 6HI0 · UniProt W9BNU9
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