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Structure of dps from microbacterium arborescens in the low iron form

Analyse Structure of dps from microbacterium arborescens in the low iron form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2YJJ
Type
protein
Length
1,796 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Afp
UniProt
Q1X6M4
Ligands
OFE, FE
Pockets
20 · best druggability 0.60

Structure

x-ray diffraction · 6 distinct chains · 78% helix, 3% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, KAfpprotein14979% helix, 3% strandQ1X6M4
BAfpprotein15177% helix, 3% strandQ1X6M4
D, I, JAfpprotein14878% helix, 3% strandQ1X6M4
E, F, LAfpprotein15078% helix, 3% strandQ1X6M4
GAfpprotein15775% helix, 3% strandQ1X6M4
HAfpprotein14779% helix, 3% strandQ1X6M4

Ligands and binding sites

  • OFE · Iron(II) oxide · ligand · 10 copies · chains A, B, C, E, I, D, J, F, G, H, K, L
  • FE · Fe (III) ion · metal · 2 copies · chains A, B, K, L

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
11000.600.8717empty
22880.590.7842empty
33460.580.7651empty
4940.580.8716empty
51040.580.8617empty

Interfaces

30 interfaces between chains.

  • G–H · 1390 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 1385 Ų buried · 23 hydrogen bonds · protein-protein
  • C–I · 1372 Ų buried · 24 hydrogen bonds · protein-protein
  • K–L · 1360 Ų buried · 22 hydrogen bonds · protein-protein
  • D–J · 1358 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 2YJJ · Structure of Dps from MICROBACTERIUM ARBORESCENS in the low iron form · the same entry in another collection · chain A against A, TM-score 1.00

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