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Hexameric structure of copper-containing nitrite reductase of an anammox organism ksu-1

Analyse Hexameric structure of copper-containing nitrite reductase of an anammox… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ZL1
Type
protein
Length
1,224 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative copper-type nitrite reductase
UniProt
I3IR93
Ligands
CU, CA, SO4
Pockets
9 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 6% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DPutative copper-type nitrite reductaseprotein3066% helix, 46% strandI3IR93

Ligands and binding sites

  • CU · Copper (II) ion · metal · 9 copies · chains A, B, C, D
  • CA · Calcium ion · metal · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14920.830.8949empty
23190.830.9340CU
38240.700.7695empty
4800.340.7515empty
5620.330.7614empty

Interfaces

4 interfaces between chains.

  • B–C · 1484 Ų buried · 27 hydrogen bonds · protein-protein
  • C–D · 1476 Ų buried · 26 hydrogen bonds · protein-protein
  • B–D · 1475 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 556 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 5ZL1 · Hexameric structure of copper-containing nitrite reductase of an anammox organism KSU-1 · the same entry in another collection · chain A against A, TM-score 1.00

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