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Ferric R-state human aquomethemoglobin

Analyse Ferric R-state human aquomethemoglobin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3P5Q
Type
protein
Length
285 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin subunit alpha; Hemoglobin subunit beta
UniProt
P69905, P68871
Ligands
MBN, HEM
Pockets
5 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 78% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemoglobin subunit alphaprotein13978% helix, 0% strandP69905
BHemoglobin subunit betaprotein14677% helix, 0% strandP68871

Ligands and binding sites

  • MBN · Toluene · ligand · 3 copies · chains A
  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11290.790.9623MBN
22010.730.8825HEM
31760.680.8624HEM
41090.490.8120empty
5710.380.7819empty

Interfaces

1 interface between chains.

  • A–B · 928 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 3P5Q · Ferric R-state human aquomethemoglobin · the same entry in another collection · chain A against A, TM-score 1.00

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