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Crystal structure of a probable acetyltransferase

Analyse Crystal structure of a probable acetyltransferase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2EUI
Type
protein
Length
603 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Probable acetyltransferase
UniProt
Q9HX01
Pockets
10 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 38% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DProbable acetyltransferaseprotein15337% helix, 31% strandQ9HX01
BProbable acetyltransferaseprotein14638% helix, 34% strandQ9HX01
EProbable acetyltransferaseprotein15138% helix, 32% strandQ9HX01

Pockets

10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14120.770.8755empty
28100.760.8080empty
32330.730.8839empty
41080.490.8018empty
5990.400.7722empty

Interfaces

3 interfaces between chains.

  • D–E · 2909 Ų buried · 61 hydrogen bonds · protein-protein
  • A–B · 2829 Ų buried · 59 hydrogen bonds · protein-protein
  • B–D · 247 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 modified (engineered).

Compared structures

  • 2EUI · Crystal structure of a probable acetyltransferase · the same entry in another collection · chain A against A, TM-score 1.00

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