Research workbench
Crystal structure of human neuron specific enolase at 1.8 ångström
Analyse Crystal structure of human neuron specific enolase at 1.8 ångström in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1TE6
- Type
- protein
- Length
- 867 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Gamma enolase
- EC
- 4.2.1.11
- UniProt
- P09104
- Ligands
- MG, PO4, CL
- Pockets
- 7 · best druggability 0.75
Structure
x-ray diffraction · 2 distinct chains · 45% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Gamma enolase (EC 4.2.1.11) | protein | 434 | 44% helix, 18% strand | P09104 |
| B | Gamma enolase (EC 4.2.1.11) | protein | 433 | 45% helix, 16% strand | P09104 |
Ligands and binding sites
- MG · Magnesium ion · metal · 3 copies · chains A, B
- PO4 · Phosphate ion · ion · chains A
- CL · Chloride ion · ion · chains B
- TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · 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, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1100 | 0.75 | 0.78 | 60 | empty |
| 2 | 347 | 0.61 | 0.78 | 49 | CL |
| 3 | 227 | 0.53 | 0.77 | 35 | empty |
| 4 | 91 | 0.41 | 0.78 | 18 | empty |
| 5 | 79 | 0.35 | 0.76 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 2049 Ų buried · 45 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 P09104
- Elsewhere: RCSB PDB 1TE6 · PDBe 1TE6 · UniProt P09104
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