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Formate bound to oxidized wild type afnir

Analyse Formate bound to oxidized wild type afnir in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2PP8
Type
protein
Length
1,008 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Copper-containing nitrite reductase
EC
1.7.2.1
UniProt
P38501
Ligands
CU1, CU
Pockets
11 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 11% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CCopper-containing nitrite reductase (EC 1.7.2.1)protein33611% helix, 43% strandP38501

Ligands and binding sites

  • CU1 · Copper (I) ion · metal · 3 copies · chains A, B, C
  • CU · Copper (II) ion · metal · 3 copies · chains A, B, C
  • ACT · Acetate ion · additive · 8 copies · chains A, B, C
  • FMT · Formic acid · additive · 3 copies · chains A, B, C
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12740.840.9631TRS
25310.800.8763ACT
3610.720.9818empty
4600.710.9718empty
51110.490.8037CU, ACT, FMT

Interfaces

3 interfaces between chains.

  • A–B · 2107 Ų buried · 36 hydrogen bonds · protein-protein
  • B–C · 2103 Ų buried · 40 hydrogen bonds · protein-protein
  • A–C · 2091 Ų buried · 37 hydrogen bonds · protein-protein

Compared structures

  • 2PP8 · Formate bound to oxidized wild type AfNiR · the same entry in another collection · chain A against A, TM-score 1.00

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