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Crystal structure of legionella pneumophila aminopeptidase a in complex with aspartic acid

Analyse Crystal structure of legionella pneumophila aminopeptidase a in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ZIE
Type
protein
Length
1,700 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aminopeptidase N
EC
3.4.11.2
UniProt
Q5ZVE3
Ligands
ASP
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BAminopeptidase N (EC 3.4.11.2)protein85043% helix, 23% strandQ5ZVE3

Ligands and binding sites

  • ASP · Aspartic acid · 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, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110130.830.84110ASP
24590.770.8551empty
32010.700.8844ASP
41190.690.9122empty
51480.690.8925empty

Interfaces

1 interface between chains.

  • A–B · 770 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 5ZIE · Crystal structure of Legionella pneumophila aminopeptidase A in complex with aspartic acid · the same entry in another collection · chain A against A, TM-score 1.00

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