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Crystal structure of metal-citrate-binding protein (mcta) of ABC transporter endogenously bound to MG2+-citrate complex (form II)

Analyse Crystal structure of metal-citrate-binding protein (mcta) of ABC transporter… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7F6F
Type
protein
Length
673 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Iron ABC transporter, periplasmic iron-binding protein
UniProt
Q53VZ2
Ligands
MG, CO2
Pockets
8 · best druggability 0.46

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AIron ABC transporter, periplasmic iron-binding proteinprotein33747% helix, 18% strandQ53VZ2
BIron ABC transporter, periplasmic iron-binding proteinprotein33647% helix, 18% strandQ53VZ2

Ligands and binding sites

  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • CO2 · Carbon dioxide · ion · chains B
  • EDO · 1,2-ethanediol · additive · 4 copies · chains A, B
  • CIT · Citric acid · additive · 2 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains B
  • PGO · S-1,2-propanediol · additive · chains A

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

Pockets

8 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11240.460.7819empty
21170.440.7721empty
3560.390.8116MG, CIT
4990.390.7618empty
51000.390.7618empty

Interfaces

1 interface between chains.

  • A–B · 709 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 7F6F · Crystal structure of metal-citrate-binding protein (MctA) of ABC transporter endogenously… · the same entry in another collection · chain A against A, TM-score 1.00

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