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Respiratory complex I from escherichia COLI - conformation 2

Analyse Respiratory complex I from escherichia COLI - conformation 2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7NYU
Type
protein
Length
4,618 residues
Chains
13
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NADH-quinone oxidoreductase subunit a; NADH-quinone oxidoreductase subunit B…
EC
7.1.1.-, 7.1.1.2, 1.6.5.11, 1.6.5.3, 1.6.99.5
UniProt
P0AFC3, P0AFC7, P33599, P0AFD1, P31979, P33602, P0AFD4, P0AFD6, P0AFE0, P0AFE4, A0A1V3W1N5, P0AFE8, P0AFF0
Ligands
SF4, FES, FMN, CA
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 13 distinct chains · 52% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANADH-quinone oxidoreductase subunit a (EC 7.1.1.-)protein9271% helix, 0% strandP0AFC3
BNADH-quinone oxidoreductase subunit B (EC 7.1.1.-)protein15938% helix, 11% strandP0AFC7
DNADH-quinone oxidoreductase subunit C/D (EC 7.1.1.2)protein58839% helix, 15% strandP33599
ENADH-quinone oxidoreductase subunit E (EC 7.1.1.2)protein15651% helix, 12% strandP0AFD1
FNADH-quinone oxidoreductase subunit F (EC 7.1.1.2)protein44142% helix, 13% strandP31979
GNADH-quinone oxidoreductase subunit G (EC 7.1.1.2)protein90731% helix, 19% strandP33602
HNADH-quinone oxidoreductase subunit H (EC 7.1.1.-)protein27064% helix, 0% strandP0AFD4
INADH-quinone oxidoreductase subunit I (EC 7.1.1.2)protein15816% helix, 20% strandP0AFD6
JNADH-quinone oxidoreductase subunit J (EC 7.1.1.-)protein16474% helix, 1% strandP0AFE0
KNADH-quinone oxidoreductase subunit K (EC 7.1.1.-)protein10074% helix, 2% strandP0AFE4
LNADH-quinone oxidoreductase subunit L (EC 1.6.5.11, 1.6.5.3, 1.6.99.5)protein61271% helix, 4% strandA0A1V3W1N5
MNADH-quinone oxidoreductase subunit M (EC 7.1.1.-)protein50470% helix, 2% strandP0AFE8
NNADH-quinone oxidoreductase subunit N (EC 7.1.1.-)protein46773% helix, 1% strandP0AFF0

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 7 copies · chains B, D, F, G, I
  • FES · Fe2/s2 (inorganic) cluster · ligand · 2 copies · chains E, G
  • FMN · Flavin mononucleotide · ligand · chains F
  • CA · Calcium ion · metal · chains G

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
111040.840.8580empty
21730.820.9731empty
36980.810.8477empty
411860.800.82111empty
56760.800.8359empty

Interfaces

30 interfaces between chains.

  • J–K · 3160 Ų buried · 11 hydrogen bonds · protein-protein
  • L–M · 2323 Ų buried · 13 hydrogen bonds · protein-protein
  • B–I · 1984 Ų buried · 28 hydrogen bonds · protein-protein
  • E–F · 1964 Ų buried · 18 hydrogen bonds · protein-protein
  • B–D · 1940 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 11 covalent, 3 modified (covalent ligand, oxidation).

Compared structures

  • 7NYU · Respiratory complex I from Escherichia coli - conformation 2 · the same entry in another collection · chain J against J, TM-score 1.00

Analyse

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