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Crystal structure of gkap mutant G209D/R230H from geobacillus kaustophilus HTA426

Analyse Crystal structure of gkap mutant G209D/R230H from geobacillus kaustophilus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TNB
Type
protein
Length
648 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphotriesterase
EC
3.5.-.-
UniProt
Q5KZU5
Ligands
CO
Pockets
4 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPhosphotriesterase (EC 3.5.-.-)protein32447% helix, 15% strandQ5KZU5

Ligands and binding sites

  • CO · Cobalt (II) ion · metal · 4 copies · chains A, B

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110280.760.7899empty
25920.730.8064empty
3960.410.7718empty
4780.390.7819empty

Interfaces

1 interface between chains.

  • A–B · 1643 Ų buried · 35 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (carboxylation).

Compared structures

  • 3TNB · Crystal structure of GkaP mutant G209D/R230H from Geobacillus kaustophilus HTA426 · the same entry in another collection · chain A against A, TM-score 1.00

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