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MolNFT v2 · #151698 · protein

Crystal Structure of Arg184Gln mutant of Human Prolidase with Mn ions and Cacodylate ligand

6H2P · Xaa-Pro dipeptidase: “Crystal Structure of Arg184Gln mutant of Human Prolidase with Mn ions and Cacodylate ligand”. X-ray diffraction at 1.479, 1 ligand (MN), 9 pockets (best druggability 0.83). MolNFT v2 #151698 on GenesisL1: 3D…

PDB
6H2P
Type
protein
Length
959 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.479
Source
Homo sapiens
Molecule
Xaa-Pro dipeptidase
EC
3.4.13.9
UniProt
P12955
Ligands
MN
Pockets
9 · best druggability 0.83

Structure

x-ray diffraction · resolution 1.479 · 2 distinct chains · 38% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AXaa-Pro dipeptidase (EC 3.4.13.9)protein47739% helix, 17% strandP12955
BXaa-Pro dipeptidase (EC 3.4.13.9)protein48238% helix, 17% strandP12955

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B
  • GOL · Glycerol · additive · 5 copies · chains A, B
  • CAC · Cacodylate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18690.830.8568GOL
211020.810.82101CAC, GOL
35660.750.8270GOL
43860.730.8444CAC
5700.490.8424empty

Interfaces

1 interface between chains.

  • A–B · 3019 Ų buried · 42 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6H2P · Crystal structure of ARG184GLN mutant of human prolidase with mn ions and cacodylate… · 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 1.00

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