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Thermolysin (E.C.3.4.24.27) complexed with (2-sulphanylheptanoyl)-phe- ala. parameters for zn-bidentation of mercaptoacyldipeptides in metalloendopeptidase
Analyse Thermolysin (E.C.3.4.24.27) complexed with (2-sulphanylheptanoyl)-phe- ala.… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1QF1
- Type
- protein
- Length
- 316 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein (thermolysin)
- EC
- 3.4.24.27
- UniProt
- P00800
- Ligands
- TI1, CA, ZN
- Pockets
- 1 · best druggability 0.49
Structure
x-ray diffraction · 1 distinct chain · 42% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Protein (thermolysin) (EC 3.4.24.27) | protein | 316 | 42% helix, 17% strand | P00800 |
Ligands and binding sites
- TI1 · [2(R,S)-2-sulfanylheptanoyl]-phe-ala · ligand · chains A
- CA · Calcium ion · metal · 4 copies · chains A
- ZN · Zinc ion · metal · chains A
- DMS · Dimethyl sulfoxide · additive · 2 copies · chains A
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 | 135 | 0.49 | 0.79 | 31 | ZN, TI1, DMS |
Compared structures
- 1QF1 · Thermolysin (E.C.3.4.24.27) complexed with (2-sulphanylheptanoyl)-phe-ala. parameters for… · 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 P00800
- Elsewhere: RCSB PDB 1QF1 · PDBe 1QF1 · UniProt P00800
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