GL1X · GenesisL1 explorer

MolNFT v2 · #118004 · protein

The crystal structure of SeMet-CT

5EGF · TqaA: “The crystal structure of SeMet-CT”. X-ray diffraction at 2.29, 20 pockets (best druggability 0.85). MolNFT v2 #118004 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5EGF
Type
protein
Length
1,771 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.29
Source
Penicillium aethiopicum
Molecule
TqaA
UniProt
F1CWE4
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · resolution 2.29 · 3 distinct chains · 33% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DTqaAprotein44233% helix, 24% strandF1CWE4
BTqaAprotein44333% helix, 24% strandF1CWE4
CTqaAprotein44434% helix, 23% strandF1CWE4

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 35 copies · chains A, B, C, D
  • C8E · (hydroxyethyloxy)tri(ethyloxy)octane · additive · 4 copies · chains A, D, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17670.850.8757EDO, C8E
27080.840.8759C8E, EDO
34430.740.8344EDO
46360.730.8060EDO
53720.720.8345EDO

Interfaces

4 interfaces between chains.

  • B–C · 1160 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 1040 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 940 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 924 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 modified (engineered).

Compared structures

  • 5EGF · The crystal structure of semet-ct · the same entry in another collection · chain A against A, TM-score 1.00

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