GL1X · GenesisL1 explorer

MolNFT v1 · #157825 · protein

T.ELONGATUS ndh (data-set 1)

6NBQ · NAD(P)H-quinone oxidoreductase subunit H: “T.ELONGATUS ndh (data-set 1)”. Electron microscopy, 1 ligand (SF4), 20 pockets (best druggability 0.86). MolNFT v1 #157825 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6NBQ
Type
protein
Length
3,755 residues
Chains
17
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NAD(P)H-quinone oxidoreductase subunit H; NAD(P)H-quinone oxidoreductase subunit J…
EC
1.6.5.-, 7.1.1.-, 1.6.5.11
UniProt
Q8DJD9, Q8DJ01, Q8DKZ4, Q8DL31, Q8DJU2, Q8DKZ3, Q8DLN5, Q8DMU4, Q8DL61, Q8DJ02, Q8DL29, V5V507, Q8DKX9, Q8DKY0, Q8DMR6, Q8DL30
Ligands
SF4
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 17 distinct chains · 50% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HNAD(P)H-quinone oxidoreductase subunit H (EC 1.6.5.-)protein39242% helix, 13% strandQ8DJD9
JNAD(P)H-quinone oxidoreductase subunit J (EC 1.6.5.-)protein16119% helix, 25% strandQ8DJ01
KNAD(P)H-quinone oxidoreductase subunit K (EC 1.6.5.-)protein21229% helix, 10% strandQ8DKZ4
INAD(P)H-quinone oxidoreductase subunit I (EC 1.6.5.-)protein18421% helix, 10% strandQ8DL31
NNAD(P)H-quinone oxidoreductase subunit N (EC 1.6.5.-)protein14828% helix, 20% strandQ8DJU2
LNAD(P)H-quinone oxidoreductase subunit L (EC 1.6.5.-)protein6652% helix, 0% strandQ8DKZ3
MNAD(P)H-quinone oxidoreductase subunit M (EC 1.6.5.-)protein11133% helix, 26% strandQ8DLN5
ONAD(P)H-quinone oxidoreductase subunit O (EC 1.6.5.-)protein6916% helix, 33% strandQ8DMU4
STLR0636 proteinprotein570% helix, 37% strandQ8DL61
ANdhaprotein35954% helix, 0% strand—
CNAD(P)H-quinone oxidoreductase subunit 3 (EC 7.1.1.-)protein9371% helix, 0% strandQ8DJ02
ENAD(P)H-quinone oxidoreductase subunit 4L (EC 1.6.5.-)protein10176% helix, 2% strandQ8DL29
PProton-translocating NADH-quinone dehydrogenase subunit P ndhpprotein4243% helix, 0% strandV5V507
FNADH dehydrogenase subunit 5protein58259% helix, 3% strandQ8DKX9
DNAD(P)H-quinone oxidoreductase chain 4 1 (EC 1.6.5.-)protein50467% helix, 1% strandQ8DKY0
BNAD(P)H-quinone oxidoreductase subunit 2 (EC 7.1.1.-)protein48367% helix, 2% strandQ8DMR6
GNADH-quinone oxidoreductase subunit J (EC 1.6.5.11)protein19153% helix, 0% strandQ8DL30

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 3 copies · chains H, K, I

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
17320.860.8973empty
211230.850.8691empty
35760.850.9079empty
410660.820.8393empty
510230.810.82116empty

Interfaces

49 interfaces between chains.

  • E–G · 3302 Ų buried · 18 hydrogen bonds · protein-protein
  • B–G · 2560 Ų buried · 13 hydrogen bonds · protein-protein
  • F–D · 2491 Ų buried · 14 hydrogen bonds · protein-protein
  • K–M · 2433 Ų buried · 38 hydrogen bonds · protein-protein
  • C–G · 2087 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 6NBQ · T.elongatus NDH (data-set 1) · the same entry in another collection · chain O against O, TM-score 1.00

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