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Cryo-EM structure of nucleotide-free ABCA3

Analyse Cryo-EM structure of nucleotide-free ABCA3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7W01
Type
protein
Length
1,598 residues
Chains
1
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phospholipid-transporting ATPase ABCA3
EC
7.6.2.1, 7.6.2.2
UniProt
Q99758
Ligands
POV, PX4, NAG
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 1 distinct chain · 41% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhospholipid-transporting ATPase ABCA3 (EC 7.6.2.1, 7.6.2.2)protein159841% helix, 10% strandQ99758

Ligands and binding sites

  • POV · (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate · ligand · 3 copies · chains A
  • PX4 · 1,2-dimyristoyl-sn-glycero-3-phosphocholine · ligand · 2 copies · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19360.840.8692empty
26740.750.8167empty
38590.720.7759empty
42350.690.8539empty
51850.690.8729empty

Modifications

Observed in the structure: 2 glycan, 1 disulfide (N-glycosylation, disulfide).

Compared structures

  • 7W01 · Cryo-EM structure of nucleotide-free ABCA3 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q99758 · AlphaFold monomer V2.0 prediction for phospholipid-transporting ATPase ABCA3 (Q99758) · a predicted model of the same protein · chain A against A, TM-score 0.81

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