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The NMR structure of protein-glutaminase from chryseobacterium proteolyticum
Analyse The NMR structure of protein-glutaminase from chryseobacterium proteolyticum in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2KSV
- Type
- protein
- Length
- 185 residues
- Chains
- 1
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein-glutaminase
- EC
- 3.5.1.44
- UniProt
- Q9AQQ8
Structure
solution nmr · 1 distinct chain · 23% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Protein-glutaminase (EC 3.5.1.44) | protein | 185 | 23% helix, 24% strand | Q9AQQ8 |
Modifications
Observed in the structure: 4 disulfide (disulfide).
Compared structures
- 2KSV · The NMR structure of protein-glutaminase from Chryseobacterium proteolyticum · 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 Q9AQQ8
- Elsewhere: RCSB PDB 2KSV · PDBe 2KSV · UniProt Q9AQQ8
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