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Acinetobacter sp. tol 5 ataa ydd-DALL3 domains in C-terminal stalk fused to GCN4 adaptors (CSTALKC1II)

Analyse Acinetobacter sp. tol 5 ataa ydd-DALL3 domains in C-terminal stalk fused to… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WQA
Type
protein
Length
603 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Trimeric autotransporter adhesin
UniProt
K7ZP88
Ligands
NI, PO4, CL
Pockets
2 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 50% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CTrimeric autotransporter adhesinprotein20150% helix, 14% strandK7ZP88

Ligands and binding sites

  • NI · Nickel (II) ion · metal · chains A, B, C
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B
  • CL · Chloride ion · ion · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11450.790.9621empty
2870.790.9822empty

Interfaces

3 interfaces between chains.

  • A–C · 4907 Ų buried · 78 hydrogen bonds · protein-protein
  • A–B · 4803 Ų buried · 70 hydrogen bonds · protein-protein
  • B–C · 4780 Ų buried · 70 hydrogen bonds · protein-protein

Compared structures

  • 3WQA · Acinetobacter sp. Tol 5 AtaA YDD-DALL3 domains in C-terminal stalk fused to GCN4 adaptors… · the same entry in another collection · chain A against A, TM-score 1.00

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