Research workbench
Structure of recombinant mouse collagenase-3 (mmp-13)
Analyse Structure of recombinant mouse collagenase-3 (mmp-13) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1CXV
- Type
- protein
- Length
- 320 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein (collagenase-3)
- EC
- 3.4.24.-
- UniProt
- P33435
- Ligands
- CBP, ZN, CA
- Pockets
- 3 · best druggability 0.63
Structure
x-ray diffraction · 1 distinct chain · 25% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Protein (collagenase-3) (EC 3.4.24.-) | protein | 160 | 25% helix, 19% strand | P33435 |
Ligands and binding sites
- CBP · 2-{4-[4-(4-chloro-phenoxy)-benzenesulfonyl]-tetrahydro-pyran-4-yl}-N-hydroxy-acetamide · ligand · 2 copies · chains A, B
- ZN · Zinc ion · metal · 4 copies · chains A, B
- CA · Calcium ion · metal · 4 copies · chains A, B
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 | 325 | 0.63 | 0.79 | 41 | ZN, CBP |
| 2 | 338 | 0.61 | 0.78 | 47 | ZN, CBP |
| 3 | 112 | 0.39 | 0.75 | 17 | empty |
Interfaces
1 interface between chains.
- A–B · 760 Ų buried · 7 hydrogen bonds · protein-protein
Compared structures
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 P33435
- Elsewhere: RCSB PDB 1CXV · PDBe 1CXV · UniProt P33435
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