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The low salt (peg) crystal structure of co hemoglobin E (BETAE26K) approaching physiological pH (pH 7.5)

Analyse The low salt (peg) crystal structure of co hemoglobin E (BETAE26K) approaching… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YVQ
Type
protein
Length
574 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin alpha chain; Hemoglobin beta chain
UniProt
P69905, P68871
Ligands
HEM, CMO
Pockets
9 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 77% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin alpha chainprotein14176% helix, 0% strandP69905
B, DHemoglobin beta chainprotein14679% helix, 0% strandP68871

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, D
  • CMO · Carbon monoxide · ion · 4 copies · chains A, B, C, D

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

Pockets

9 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16860.830.8794empty
22070.730.8827HEM, CMO
33050.730.8647empty
42200.710.8628HEM, CMO
51840.700.8725HEM, CMO

Interfaces

6 interfaces between chains.

  • A–B · 903 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 899 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 481 Ų buried · 4 hydrogen bonds · protein-protein
  • A–D · 465 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 430 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 1YVQ · The low salt (PEG) crystal structure of CO Hemoglobin E (betaE26K) approaching… · the same entry in another collection · chain A against A, TM-score 1.00

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