GL1X · GenesisL1 explorer

Research workbench

Crystal structure of mn superoxide dismutase mutant M27V from trichoderma reesei

Analyse Crystal structure of mn superoxide dismutase mutant M27V from trichoderma reesei in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TIR
Type
protein
Length
829 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Superoxide dismutase
EC
1.15.1.1
UniProt
G0RQS7
Ligands
MN
Pockets
11 · best druggability 0.58

Structure

x-ray diffraction · 2 distinct chains · 58% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASuperoxide dismutase (EC 1.15.1.1)protein20859% helix, 12% strandG0RQS7
B, C, DSuperoxide dismutase (EC 1.15.1.1)protein20757% helix, 12% strandG0RQS7

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11430.580.8326empty
21510.570.8225empty
31590.560.8126empty
41350.530.8123empty
51970.450.7424empty

Interfaces

6 interfaces between chains.

  • B–D · 1110 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 1107 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 953 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 948 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 106 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 5TIR · Crystal Structure of Mn Superoxide Dismutase mutant M27V from Trichoderma reesei · 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.