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Heterodimeric ABC exporter tmrab in inward-facing wide conformation

Analyse Heterodimeric ABC exporter tmrab in inward-facing wide conformation in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6RAN
Type
protein
Length
1,287 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Multidrug resistance ABC transporter ATP-binding and permease protein; Nanobody NB9F10
UniProt
Q72J05, Q72J04
Pockets
16 · best druggability 0.83

Structure

electron microscopy · 3 distinct chains · 59% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMultidrug resistance ABC transporter ATP-binding and permease proteinprotein59265% helix, 9% strandQ72J05
BMultidrug resistance ABC transporter ATP-binding and permease proteinprotein57466% helix, 10% strandQ72J04
CNanobody NB9F10protein1212% helix, 50% strand—

Pockets

16 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111620.830.84102empty
24050.620.7745empty
32540.610.7932empty
41900.510.7729empty
51210.490.7914empty

Interfaces

2 interfaces between chains.

  • A–B · 6158 Ų buried · 21 hydrogen bonds · protein-protein
  • B–C · 685 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6RAN · Heterodimeric ABC exporter TmrAB in inward-facing wide conformation · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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