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MolNFT v1 · #126937 · protein

The study of the X-ray induced enzymatic reduction of molecular oxygen to water for laccase from steccherinum MURASHKINSKYI.THE fifth structure of the series with total exposition time 123 min.

5MHW · Laccase 2: “The study of the X-ray induced enzymatic reduction of molecular oxygen to water for laccase from steccherinum…”. X-ray diffraction, 5 ligands (NAG, BMA, CU), 5 pockets (best druggability 0.52). MolNFT v1 #126937 on…

PDB
5MHW
Type
protein
Length
499 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Laccase 2
EC
1.10.3.2
UniProt
I1VE66
Ligands
NAG, BMA, CU, NA, OXY
Pockets
5 · best druggability 0.52

Structure

x-ray diffraction · 1 distinct chain · 12% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALaccase 2 (EC 1.10.3.2)protein49912% helix, 37% strandI1VE66

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • CU · Copper (II) ion · metal · 4 copies · chains A
  • NA · Sodium ion · metal · chains A
  • OXY · Oxygen molecule · ion · 2 copies · chains A
  • CIT · Citric acid · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11010.520.8217empty
21640.460.7632empty
31050.440.7819empty
4820.360.7617empty
5520.310.7718empty

Modifications

Observed in the structure: 2 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 5MHW · The study of the X-ray induced enzymatic reduction of molecular oxygen to water for… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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