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MolNFT v1 · #183662 · protein

Respiratory complex I from escherichia COLI - conformation 1

7NYR · NADH-quinone oxidoreductase subunit B: “Respiratory complex I from escherichia COLI - conformation 1”. Electron microscopy, 4 ligands (SF4, FES, FMN), 20 pockets (best druggability 0.84). MolNFT v1 #183662 on GenesisL1: 3D…

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

Structure

electron microscopy · 13 distinct chains · 52% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BNADH-quinone oxidoreductase subunit B (EC 7.1.1.-)protein15938% helix, 13% strandP0AFC7
DNADH-quinone oxidoreductase subunit C/D (EC 7.1.1.2)protein58838% helix, 15% strandP33599
ENADH-quinone oxidoreductase subunit E (EC 7.1.1.2)protein15652% 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
INADH-quinone oxidoreductase subunit I (EC 7.1.1.2)protein15817% helix, 20% strandP0AFD6
KNADH-quinone oxidoreductase subunit K (EC 7.1.1.-)protein10074% helix, 3% strandP0AFE4
JNADH-quinone oxidoreductase subunit J (EC 7.1.1.-)protein16474% helix, 2% strandP0AFE0
ANADH-quinone oxidoreductase subunit a (EC 7.1.1.-)protein9271% helix, 0% strandP0AFC3
HNADH-quinone oxidoreductase subunit H (EC 7.1.1.-)protein27063% helix, 0% strandP0AFD4
MNADH-quinone oxidoreductase subunit M (EC 7.1.1.-)protein50470% helix, 2% strandP0AFE8
LNADH-quinone oxidoreductase subunit L (EC 1.6.5.11, 1.6.5.3, 1.6.99.5)protein61271% helix, 4% strandA0A1V3W1N5
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
111330.840.8579empty
210440.810.8295empty
34130.800.8855empty
45190.790.8664empty
51340.790.9732empty

Interfaces

30 interfaces between chains.

  • K–J · 3288 Ų buried · 13 hydrogen bonds · protein-protein
  • M–L · 2523 Ų buried · 12 hydrogen bonds · protein-protein
  • B–I · 1995 Ų buried · 27 hydrogen bonds · protein-protein
  • E–F · 1994 Ų buried · 24 hydrogen bonds · protein-protein
  • B–D · 1941 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 7NYR · Respiratory complex I from Escherichia coli - conformation 1 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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