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MolNFT v1 · #150105 · protein

Human NBD1 of cftr in complex with nanobodies D12 and T4

6GJS · Cystic fibrosis transmembrane conductance regulator: “Human NBD1 of cftr in complex with nanobodies D12 and T4”. X-ray diffraction, 2 ligands (ATP, MG), 6 pockets (best druggability 0.67). MolNFT v1 #150105 on GenesisL1: 3D…

PDB
6GJS
Type
protein
Length
458 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cystic fibrosis transmembrane conductance regulator; Nanobody D12; Nanobody T4
EC
3.6.3.49
UniProt
Q20BJ8
Ligands
ATP, MG
Pockets
6 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 17% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACystic fibrosis transmembrane conductance regulator (EC 3.6.3.49)protein21932% helix, 28% strandQ20BJ8
BNanobody D12protein1222% helix, 59% strand—
CNanobody T4protein1175% helix, 61% strand—

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · chains A
  • MG · Magnesium ion · metal · 2 copies · chains A

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

Pockets

6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13340.670.8246MG
22330.530.7636empty
32140.480.7523empty
4860.440.8018empty
5630.350.7813empty

Interfaces

3 interfaces between chains.

  • A–C · 983 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 852 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 27 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6GJS · Human NBD1 of CFTR in complex with nanobodies D12 and T4 · the same entry in another collection · chain A against A, TM-score 1.00

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