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Role of hydrogen bonding in the active site of human manganese superoxide dismutase

Analyse Role of hydrogen bonding in the active site of human manganese superoxide… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1SZX
Type
protein
Length
396 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Superoxide dismutase [mn], mitochondrial
EC
1.15.1.1
UniProt
P04179
Ligands
MN
Pockets
2 · best druggability 0.54

Structure

x-ray diffraction · 1 distinct chain · 56% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BSuperoxide dismutase [mn], mitochondrial (EC 1.15.1.1)protein19856% helix, 13% strandP04179

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11870.540.7922empty
21920.540.7923empty

Interfaces

1 interface between chains.

  • A–B · 919 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 1SZX · Role Of Hydrogen Bonding In The Active Site Of Human Manganese Superoxide Dismutase · the same entry in another collection · chain A against A, TM-score 1.00
  • P04179 · AlphaFold monomer V2.0 prediction for superoxide dismutase [mn], mitochondrial (P04179) · a predicted model of the same protein · chain A against A, TM-score 1.00

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