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Small laccase from amycolatopsis sp. atcc 39116 complexed with 1-(3,4- dimethoxyphenyl)-2-(2-methoxyphenoxy)-1,3-dihydroxypropane

Analyse Small laccase from amycolatopsis sp. atcc 39116 complexed with 1-(3,4… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TA4
Type
protein
Length
822 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Small laccase, multi-copper oxidase
EC
1.10.3.2
Ligands
TO2, CU
Pockets
7 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
FSmall laccase, multi-copper oxidase (EC 1.10.3.2)protein2825% helix, 41% strand—
DSmall laccase, multi-copper oxidase (EC 1.10.3.2)protein2735% helix, 42% strand—
ESmall laccase, multi-copper oxidase (EC 1.10.3.2)protein2675% helix, 43% strand—

Ligands and binding sites

  • TO2 · (1R,2S)-1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol · ligand · chains F, E
  • CU · Copper (II) ion · metal · 16 copies · chains F, E, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15550.860.9270empty
2680.710.9621empty
3670.690.9620empty
4660.650.9325empty
51460.510.7932empty

Interfaces

3 interfaces between chains.

  • D–E · 1713 Ų buried · 28 hydrogen bonds · protein-protein
  • F–D · 1708 Ų buried · 30 hydrogen bonds · protein-protein
  • F–E · 1682 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 3TA4 · Small laccase from Amycolatopsis sp. ATCC 39116 complexed with… · the same entry in another collection · chain F against F, TM-score 1.00

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