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Structure of 4-hydroxyphenylacetate 3-monooxygenase (hpab), oxygenase component from escherichia COLI

Analyse Structure of 4-hydroxyphenylacetate 3-monooxygenase (hpab), oxygenase component… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6EB0
Type
protein
Length
2,072 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.37
Source
Escherichia coli (strain B / BL21-DE3)
Molecule
4-hydroxyphenylacetate 3-monooxygenase, oxygenase subunit
UniProt
A0A140NG21
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · resolution 2.37 · 1 distinct chain · 54% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D4-hydroxyphenylacetate 3-monooxygenase, oxygenase subunitprotein51854% helix, 14% strandA0A140NG21

Ligands and binding sites

  • ACT · Acetate ion · additive · 3 copies · chains A, C, B, D

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

Pockets

20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19480.850.8688ACT
2920.780.9924empty
3830.760.9821empty
43730.740.8548empty
54890.740.8254empty

Interfaces

6 interfaces between chains.

  • B–C · 4714 Ų buried · 63 hydrogen bonds · protein-protein
  • A–D · 4714 Ų buried · 61 hydrogen bonds · protein-protein
  • B–D · 3634 Ų buried · 48 hydrogen bonds · protein-protein
  • A–C · 3609 Ų buried · 39 hydrogen bonds · protein-protein
  • A–B · 499 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6EB0 · Structure of 4-hydroxyphenylacetate 3-monooxygenase (hpab), oxygenase component from… · the same entry in another collection · chain A against A, TM-score 1.00

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