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Crystal structure of schistosoma mansoni arginase in complex with inhibitor bec

Analyse Crystal structure of schistosoma mansoni arginase in complex with inhibitor bec in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Q3V
Type
protein
Length
1,343 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Arginase
EC
3.5.3.1
UniProt
Q6WVP6
Ligands
S2C, MN
Pockets
9 · best druggability 0.73

Structure

x-ray diffraction · 4 distinct chains · 40% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AArginase (EC 3.5.3.1)protein33740% helix, 16% strandQ6WVP6
BArginase (EC 3.5.3.1)protein33841% helix, 16% strandQ6WVP6
CArginase (EC 3.5.3.1)protein33941% helix, 16% strandQ6WVP6
DArginase (EC 3.5.3.1)protein32938% helix, 16% strandQ6WVP6

Ligands and binding sites

  • S2C · S-2-(boronoethyl)-L-cysteine · ligand · 3 copies · chains A, B, C
  • MN · Manganese (II) ion · metal · 8 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 6 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15630.730.8157empty
21060.440.7924S2C
3870.420.7919S2C
4780.400.7920S2C
5840.400.7824empty

Interfaces

3 interfaces between chains.

  • A–B · 288 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 265 Ų buried · 5 hydrogen bonds · protein-protein
  • A–D · 44 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4Q3V · Crystal structure of Schistosoma mansoni arginase in complex with inhibitor BEC · the same entry in another collection · chain C against C, TM-score 1.00

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