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MolNFT v1 · #119296 · protein

Structure of the fesii (shethna) protein of azotobacter vinelandii

5FRT · Dimeric (2FE-2S) protein: “Structure of the fesii (shethna) protein of azotobacter vinelandii”. X-ray diffraction, 1 ligand (FES), 4 pockets (best druggability 0.71). MolNFT v1 #119296 on GenesisL1: 3D structure, binding sites and…

PDB
5FRT
Type
protein
Length
581 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dimeric (2FE-2S) protein
UniProt
Q44501
Ligands
FES
Pockets
4 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 20% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DDimeric (2FE-2S) proteinprotein11922% helix, 24% strandQ44501
EDimeric (2FE-2S) proteinprotein10518% helix, 28% strandQ44501

Ligands and binding sites

  • FES · Fe2/s2 (inorganic) cluster · ligand · 5 copies · chains A, B, C, D, E

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16230.710.7979empty
22640.680.8432empty
32320.660.8433empty
4640.370.7815empty

Interfaces

7 interfaces between chains.

  • A–B · 1259 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 1059 Ų buried · 12 hydrogen bonds · protein-protein
  • B–E · 366 Ų buried · 3 hydrogen bonds · protein-protein
  • D–E · 276 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 136 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 5FRT · Structure of the FeSII (shethna) protein of Azotobacter vinelandii · the same entry in another collection · chain E against E, TM-score 1.00
  • Q44501 · AlphaFold monomer V2.0 prediction for protein fesii (Q44501) · a predicted model of the same protein · chain E against A, TM-score 0.89

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