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MolNFT v1 · #171873 · protein

Respiratory complex I from thermus thermophilus, NAD+ dataset, major state

6ZJL · NADH-quinone oxidoreductase subunit 1: “Respiratory complex I from thermus thermophilus, NAD+ dataset, major state”. Electron microscopy, 3 ligands (SF4, FES, FMN), 20 pockets (best druggability 0.87). MolNFT v1 #171873 on…

PDB
6ZJL
Type
protein
Length
4,646 residues
Chains
15
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NADH-quinone oxidoreductase subunit 1; NADH-quinone oxidoreductase subunit 2…
EC
7.1.1.-
UniProt
Q56222, Q56221, Q56223, Q56220, Q56219, Q56218, Q56224, Q5SKZ7, Q56217, Q56225, Q56226, Q56227, Q56228, Q56229, Q60019
Ligands
SF4, FES, FMN
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 15 distinct chains · 51% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
1NADH-quinone oxidoreductase subunit 1 (EC 7.1.1.-)protein43743% helix, 12% strandQ56222
2NADH-quinone oxidoreductase subunit 2 (EC 7.1.1.-)protein17843% helix, 12% strandQ56221
3NADH-quinone oxidoreductase subunit 3 (EC 7.1.1.-)protein75425% helix, 19% strandQ56223
4NADH-quinone oxidoreductase subunit 4 (EC 7.1.1.-)protein38447% helix, 11% strandQ56220
5NADH-quinone oxidoreductase subunit 5 (EC 7.1.1.-)protein19619% helix, 18% strandQ56219
6NADH-quinone oxidoreductase subunit 6 (EC 7.1.1.-)protein16633% helix, 13% strandQ56218
9NADH-quinone oxidoreductase subunit 9 (EC 7.1.1.-)protein18022% helix, 19% strandQ56224
7NADH-quinone oxidoreductase subunit 15 (EC 7.1.1.-)protein12733% helix, 31% strandQ5SKZ7
ANADH-quinone oxidoreductase subunit 7 (EC 7.1.1.-)protein11764% helix, 0% strandQ56217
JNADH-quinone oxidoreductase subunit 10 (EC 7.1.1.-)protein16074% helix, 0% strandQ56225
KNADH-quinone oxidoreductase subunit 11 (EC 7.1.1.-)protein9580% helix, 2% strandQ56226
LNADH-quinone oxidoreductase subunit 12 (EC 7.1.1.-)protein60570% helix, 2% strandQ56227
MNADH-quinone oxidoreductase subunit 13 (EC 7.1.1.-)protein46771% helix, 4% strandQ56228
NNADH-quinone oxidoreductase subunit 14 (EC 7.1.1.-)protein42773% helix, 1% strandQ56229
HNADH-quinone oxidoreductase subunit 8 (EC 7.1.1.-)protein35363% helix, 0% strandQ60019

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 7 copies · chains 1, 3, 4, 6, 9
  • FES · Fe2/s2 (inorganic) cluster · ligand · 2 copies · chains 2, 3
  • FMN · Flavin mononucleotide · ligand · chains 1

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19150.870.8991empty
211660.830.8598empty
36290.780.8360empty
49090.780.8064empty
51070.760.9721empty

Interfaces

35 interfaces between chains.

  • J–K · 3509 Ų buried · 16 hydrogen bonds · protein-protein
  • A–H · 3310 Ų buried · 16 hydrogen bonds · protein-protein
  • 4–5 · 2955 Ų buried · 42 hydrogen bonds · protein-protein
  • 1–2 · 2938 Ų buried · 32 hydrogen bonds · protein-protein
  • L–M · 2450 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 6ZJL · Respiratory complex I from Thermus thermophilus, NAD+ dataset, major state · the same entry in another collection · chain 9 against 9, TM-score 1.00

Analyse

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