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Crystal structure of a periplasmic heme binding protein from shigella dysenteriae

Analyse Crystal structure of a periplasmic heme binding protein from shigella… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2R7A
Type
protein
Length
1,021 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bacterial heme binding protein
UniProt
O70018
Ligands
HEM
Pockets
9 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 45% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DBacterial heme binding proteinprotein25545% helix, 17% strandO70018
BBacterial heme binding proteinprotein25645% helix, 18% strandO70018

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110840.810.82142empty
24610.710.8156empty
32680.700.8557HEM
43210.690.8347empty
5810.470.8224empty

Interfaces

5 interfaces between chains.

  • B–D · 1138 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 1125 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 672 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 152 Ų buried · 0 hydrogen bonds · protein-protein
  • A–B · 17 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 2R7A · Crystal Structure of a Periplasmic Heme Binding Protein from Shigella dysenteriae · the same entry in another collection · chain A against A, TM-score 1.00

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