MolNFT v1 · #50886 · protein
Staphylococcal nuclease. proposed mechanism of action based on structure of enzyme-thymidine 3(PRIME),5(PRIME)-biphosphate-calcium ion complex at 1.5-ångströms resolution
2SNS · Thermonuclease precursor: “Staphylococcal nuclease. proposed mechanism of action based on structure of enzyme-thymidine…”. X-ray diffraction, 2 ligands (THP, CA), 1 pocket (best druggability 0.38). MolNFT v1 #50886 on GenesisL1: 3D…
- PDB
- 2SNS
- Type
- protein
- Length
- 141 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Thermonuclease precursor
- EC
- 3.1.31.1
- UniProt
- P00644
- Ligands
- THP, CA
- Pockets
- 1 · best druggability 0.38
Structure
x-ray diffraction · 1 distinct chain · 21% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Thermonuclease precursor (EC 3.1.31.1) | protein | 141 | 21% helix, 23% strand | P00644 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 70 | 0.38 | 0.79 | 15 | THP |
Compared structures
- 2SNS · Staphylococcal nuclease. proposed mechanism of action based on structure of… · 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 P00644
- Elsewhere: RCSB PDB 2SNS · PDBe 2SNS · UniProt P00644
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