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Structure of leishmania major peroxidase D211N mutant

Analyse Structure of leishmania major peroxidase D211N mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5AMM
Type
protein
Length
534 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ascorbate peroxidase
EC
1.11.1.11, 1.11.1.5
UniProt
Q4Q3K2
Ligands
HEM, K, CA
Pockets
4 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 51% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAscorbate peroxidase (EC 1.11.1.11, 1.11.1.5)protein26751% helix, 7% strandQ4Q3K2

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • K · Potassium ion · metal · 2 copies · chains A, B
  • CA · Calcium ion · metal · 2 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, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14520.800.8750HEM
24520.790.8747HEM
31920.510.7730empty
4660.330.7612empty

Interfaces

1 interface between chains.

  • A–B · 267 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 5AMM · Structure of Leishmania major peroxidase D211N mutant · the same entry in another collection · chain A against A, TM-score 1.00

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