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X-ray crystal structure of TOLUENE/O-xylene monooxygenase hydroxylase T201V mutant

Analyse X-ray crystal structure of TOLUENE/O-xylene monooxygenase hydroxylase T201V… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3N20
Type
protein
Length
896 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Toluene O-xylene monooxygenase component
UniProt
Q6IV66, Q6IV62, Q6IV65
Ligands
FE
Pockets
13 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 63% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AToluene O-xylene monooxygenase componentprotein49165% helix, 2% strandQ6IV66
BToluene O-xylene monooxygenase componentprotein32272% helix, 0% strandQ6IV62
CToluene O-xylene monooxygenase componentprotein8314% helix, 39% strandQ6IV65

Ligands and binding sites

  • FE · Fe (III) ion · metal · 2 copies · chains A
  • GOL · Glycerol · additive · 4 copies · chains A, B
  • P6G · Hexaethylene glycol · additive · 4 copies · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12440.800.9240P6G
21240.730.9221GOL
31280.720.9125P6G
4890.530.8426empty
5670.460.8313empty

Interfaces

2 interfaces between chains.

  • A–B · 4241 Ų buried · 71 hydrogen bonds · protein-protein
  • A–C · 1430 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 3N20 · X-ray Crystal Structure of Toluene/o-Xylene Monooxygenase Hydroxylase T201V Mutant · the same entry in another collection · chain B against B, TM-score 1.00

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