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Cryo-EM structure of the human ABCB6 (coproporphyrin III-bound)

Analyse Cryo-EM structure of the human ABCB6 (coproporphyrin III-bound) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DNY
Type
protein
Length
1,146 residues
Chains
2
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ATP-binding cassette sub-family B member 6, mitochondrial
UniProt
Q9NP58
Ligands
Y01, HT9
Pockets
16 · best druggability 0.81

Structure

electron microscopy · 2 distinct chains · 65% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AATP-binding cassette sub-family B member 6, mitochondrialprotein57165% helix, 9% strandQ9NP58
BATP-binding cassette sub-family B member 6, mitochondrialprotein57565% helix, 5% strandQ9NP58

Ligands and binding sites

  • Y01 · Cholesterol hemisuccinate · ligand · 5 copies · chains A, B
  • HT9 · coproporphyrin III · ligand · chains A, B

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

Pockets

16 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18200.810.8386empty
21580.750.9233empty
35210.710.8054empty
4640.700.9621empty
51560.630.8532empty

Interfaces

1 interface between chains.

  • A–B · 5402 Ų buried · 27 hydrogen bonds · protein-protein

Compared structures

  • 7DNY · Cryo-EM structure of the human ABCB6 (coproporphyrin III-bound) · the same entry in another collection · chain B against B, TM-score 1.00
  • Q9NP58 · AlphaFold monomer V2.0 prediction for ATP-binding cassette sub-family B member 6… · a predicted model of the same protein · chain B against A, TM-score 0.90

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