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Arginase-descarboxy-nor-noha complex

Analyse Arginase-descarboxy-nor-noha complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1T4R
Type
protein
Length
942 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Arginase 1
EC
3.5.3.1
UniProt
P07824
Ligands
AHI, MN
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CArginase 1 (EC 3.5.3.1)protein31440% helix, 17% strandP07824

Ligands and binding sites

  • AHI · 3-{[(E)-amino(hydroxyimino)methyl]amino}propan-1-aminium · ligand · 3 copies · chains A, B, C
  • MN · Manganese (II) ion · metal · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111970.800.81104empty
22560.570.7830empty
31220.470.7822empty
4840.450.8119AHI
5970.450.8018AHI

Interfaces

3 interfaces between chains.

  • B–C · 977 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 949 Ų buried · 12 hydrogen bonds · protein-protein
  • A–C · 945 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 1T4R · arginase-descarboxy-nor-NOHA complex · the same entry in another collection · chain A against A, TM-score 1.00
  • P07824 · AlphaFold monomer V2.0 prediction for arginase-1 (P07824) · a predicted model of the same protein · chain C against A, TM-score 1.00

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