GL1X · GenesisL1 explorer

Research workbench

Atomic resolution crystal structure of human superoxide dismutase

Analyse Atomic resolution crystal structure of human superoxide dismutase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2V0A
Type
protein
Length
306 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Superoxide dismutase
EC
1.15.1.1
UniProt
P00441
Ligands
CU, ZN, SO4
Pockets
2 · best druggability 0.59

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, FSuperoxide dismutase (EC 1.15.1.1)protein1537% helix, 40% strandP00441

Ligands and binding sites

  • CU · Copper (II) ion · metal · 2 copies · chains A, F
  • ZN · Zinc ion · metal · 2 copies · chains A, F
  • SO4 · Sulfate ion · ion · 3 copies · chains A, F
  • ACT · Acetate ion · additive · chains F

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11810.590.8226empty
21050.360.7420empty

Interfaces

1 interface between chains.

  • A–F · 703 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 2V0A · Atomic resolution crystal structure of Human Superoxide Dismutase · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.