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The crystal structure of human deoxyhaemoglobin at 1.74 ångströms resolution

Analyse The crystal structure of human deoxyhaemoglobin at 1.74 ångströms resolution in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3HHB
Type
protein
Length
574 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin (deoxy) (alpha chain); Hemoglobin (deoxy) (beta chain)
UniProt
P01922, P02023
Ligands
HEM, PO4
Pockets
8 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 79% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin (deoxy) (alpha chain)protein14178% helix, 0% strandP01922
B, DHemoglobin (deoxy) (beta chain)protein14681% helix, 0% strandP02023

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, D
  • PO4 · Phosphate ion · ion · 2 copies · chains B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19710.820.8389empty
22550.750.8829HEM
32110.740.8930HEM
42300.730.8730HEM
52670.730.8631HEM

Interfaces

5 interfaces between chains.

  • A–B · 847 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 847 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 716 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 716 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 303 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 3HHB · The crystal structure of human deoxyhaemoglobin at 1.74 ångströms resolution · the same entry in another collection · chain D against D, TM-score 1.00

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