GL1X · GenesisL1 explorer

Research workbench

Crystal structure of nitrite and no bound three-domain copper- containing nitrite reductase from hyphomicrobium denitrificans strain 1NES1

Analyse Crystal structure of nitrite and no bound three-domain copper- containing… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6TFD
Type
protein
Length
1,269 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
N0B9M5
Ligands
CU, NO2, NO
Pockets
9 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 9% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CCopper-containing nitrite reductase (EC 1.7.2.1)protein4239% helix, 46% strandN0B9M5

Ligands and binding sites

  • CU · Copper (II) ion · metal · 9 copies · chains A, C, B
  • NO2 · Nitrite ion · ion · 2 copies · chains A, C, B
  • NO · Nitric oxide · ion · chains 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, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16020.860.9189empty
25430.800.8665NO
36130.790.8567empty
43840.770.8756empty
51540.590.8322empty

Interfaces

3 interfaces between chains.

  • A–B · 2468 Ų buried · 40 hydrogen bonds · protein-protein
  • B–C · 2454 Ų buried · 42 hydrogen bonds · protein-protein
  • A–C · 2426 Ų buried · 41 hydrogen bonds · protein-protein

Compared structures

  • 6TFD · Crystal structure of nitrite and NO bound three-domain copper-containing nitrite… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.