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Crystal structure of wild-type human prolidase with mn ions

Analyse Crystal structure of wild-type human prolidase with mn ions in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5M4G
Type
protein
Length
964 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Xaa-pro dipeptidase
EC
3.4.13.9
UniProt
P12955
Ligands
MN, OH
Pockets
8 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AXaa-pro dipeptidase (EC 3.4.13.9)protein48138% helix, 16% strandP12955
BXaa-pro dipeptidase (EC 3.4.13.9)protein48338% helix, 17% strandP12955

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B
  • OH · Hydroxide ion · ion · 2 copies · chains A, B
  • GOL · Glycerol · additive · 7 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17680.830.8654GOL
29700.820.83104GOL, MN, OH
310810.810.82104OH, GOL
4630.460.8324empty
5620.440.8220empty

Interfaces

1 interface between chains.

  • A–B · 2996 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 5M4G · Crystal Structure of Wild-Type Human Prolidase with Mn ions · the same entry in another collection · chain A against A, TM-score 1.00
  • P12955 · AlphaFold monomer V2.0 prediction for xaa-pro dipeptidase (P12955) · a predicted model of the same protein · chain A against A, TM-score 0.99

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