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RESA E80Q

Analyse RESA E80Q in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2H1B
Type
protein
Length
550 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thiol-disulfide oxidoreductase resa
UniProt
P35160
Pockets
5 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BThiol-disulfide oxidoreductase resaprotein13836% helix, 29% strandP35160
C, DThiol-disulfide oxidoreductase resaprotein13736% helix, 28% strandP35160

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 7 copies · chains A, B, C, D
  • ACT · Acetate ion · 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
18200.710.7755empty
21890.450.7428empty
31390.410.7526empty
4850.330.7421empty
5650.320.7515empty

Interfaces

5 interfaces between chains.

  • A–D · 524 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 432 Ų buried · 3 hydrogen bonds · protein-protein
  • B–C · 402 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 260 Ų buried · 2 hydrogen bonds · protein-protein
  • A–B · 42 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 2H1B · ResA E80Q · the same entry in another collection · chain A against A, TM-score 1.00
  • P35160 · AlphaFold monomer V2.0 prediction for thiol-disulfide oxidoreductase resa (P35160) · a predicted model of the same protein · chain A against A, TM-score 0.99

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