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MolNFT v1 · #5917 · protein

Anabaena PCC7119 FERREDOXIN:FERREDOXIN-NADP+-reductase complex

1EWY · Ferredoxin-NADP reductase: “Anabaena PCC7119 FERREDOXIN:FERREDOXIN-NADP+-reductase complex”. X-ray diffraction, 2 ligands (FAD, FES), 13 pockets (best druggability 0.75). MolNFT v1 #5917 on GenesisL1: 3D structure, binding sites and…

PDB
1EWY
Type
protein
Length
704 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ferredoxin-NADP reductase; Ferredoxin I
EC
1.18.1.2
UniProt
P21890, P0A3C8
Ligands
FAD, FES
Pockets
13 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 23% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BFerredoxin-NADP reductase (EC 1.18.1.2)protein30326% helix, 27% strandP21890
CFerredoxin Iprotein9813% helix, 30% strandP0A3C8

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, C, B
  • FES · Fe2/s2 (inorganic) cluster · ligand · chains C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14160.750.8459FAD
21110.750.9527empty
33050.690.8434empty
42950.680.8334FAD
51010.660.9027empty

Interfaces

3 interfaces between chains.

  • A–C · 823 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 767 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 586 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1EWY · Anabaena PCC7119 FERREDOXIN:FERREDOXIN-NADP+-reductase complex · the same entry in another collection · chain A against A, TM-score 1.00
  • P21890 · AlphaFold monomer V2.0 prediction for ferredoxin--NADP reductase (P21890) · a predicted model of the same protein · chain A against A, TM-score 0.97
  • P0A3C8 · AlphaFold monomer V2.0 prediction for ferredoxin-1 (P0A3C8) · a predicted model of the same protein · chain C against A, TM-score 0.96

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