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Crystal structure analysis of the SER305THR variants of katg from haloarcula marismortui

Analyse Crystal structure analysis of the SER305THR variants of katg from haloarcula… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3UW8
Type
protein
Length
1,428 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catalase-peroxidase 2
EC
1.11.1.21
UniProt
O59651
Ligands
HEM
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 45% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCatalase-peroxidase 2 (EC 1.11.1.21)protein71445% helix, 7% strandO59651

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16970.870.9198empty
23730.860.9443HEM
36570.820.8668HEM
43390.810.9155empty
53910.810.9061empty

Interfaces

1 interface between chains.

  • A–B · 3973 Ų buried · 56 hydrogen bonds · protein-protein

Compared structures

  • 3UW8 · Crystal Structure Analysis of the Ser305Thr Variants of KatG from Haloarcula marismortui · the same entry in another collection · chain A against A, TM-score 1.00
  • O59651 · AlphaFold monomer V2.0 prediction for catalase-peroxidase 2 (O59651) · a predicted model of the same protein · chain A against A, TM-score 1.00

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