Research workbench
X-ray structure of candida antarctica lipase a
Analyse X-ray structure of candida antarctica lipase a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3GUU
- Type
- protein
- Length
- 862 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lipase a
- EC
- 3.1.1.3
- Ligands
- SO4
- Pockets
- 7 · best druggability 0.83
Structure
x-ray diffraction · 1 distinct chain · 42% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Lipase a (EC 3.1.1.3) | protein | 431 | 42% helix, 18% strand | — |
Ligands and binding sites
- SO4 · Sulfate ion · ion · chains B
- 1PE · Pentaethylene glycol · additive · 2 copies · chains A, B
- GOL · Glycerol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 170 | 0.83 | 0.97 | 38 | 1PE |
| 2 | 165 | 0.82 | 0.97 | 34 | 1PE |
| 3 | 178 | 0.44 | 0.74 | 29 | empty |
| 4 | 127 | 0.44 | 0.77 | 20 | empty |
| 5 | 62 | 0.42 | 0.81 | 21 | empty |
Interfaces
1 interface between chains.
- A–B · 568 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
Compared structures
- 3GUU · X-ray structure of Candida Antarctica lipase A · the same entry in another collection · chain B against B, 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
- Elsewhere: RCSB PDB 3GUU · PDBe 3GUU
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