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MolNFT v1 · #134903 · protein

Crystal structure of mn superoxide dismutase mutant M27V from trichoderma reesei

5TIR: “Crystal structure of mn superoxide dismutase mutant M27V from trichoderma reesei”. X-ray diffraction, 1 ligand (MN), 11 pockets (best druggability 0.58). MolNFT v1 #134903 on GenesisL1: 3D structure, binding sites and pockets in…

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

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