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Crystal structure of hasap capturing iron tetraphenylporphyrin

Analyse Crystal structure of hasap capturing iron tetraphenylporphyrin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7EMO
Type
protein
Length
552 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Heme acquisition protein hasap
UniProt
G3XD33
Ligands
MQP, PO4
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 29% helix, 35% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHeme acquisition protein hasapprotein18630% helix, 34% strandG3XD33
B, CHeme acquisition protein hasapprotein18328% helix, 37% strandG3XD33

Ligands and binding sites

  • MQP · [5,10,15,20-tetraphenylporphyrinato(2-)-kappa~4~n~21~, n~22~,n~23~,n~24~]iron · ligand · 3 copies · chains A, B, C
  • PO4 · Phosphate ion · ion · 2 copies · chains C, B
  • CXS · 3-cyclohexyl-1-propylsulfonic acid · additive · 3 copies · chains A, B, C
  • NHE · 2-[N-cyclohexylamino]ethane sulfonic acid · additive · 3 copies · chains B, C
  • GOL · Glycerol · additive · chains C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18890.780.8176MQP, CXS
22110.590.8027CXS
31480.550.8122MQP
41810.520.7822PO4

Interfaces

2 interfaces between chains.

  • A–B · 506 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 278 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7EMO · Crystal Structure of HasAp Capturing Iron Tetraphenylporphyrin · the same entry in another collection · chain A against A, TM-score 1.00

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