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T-to-T(HIGH) quaternary transitions in human hemoglobin: DESHIS146BETA deoxy low-salt

Analyse T-to-T(HIGH) quaternary transitions in human hemoglobin: DESHIS146BETA deoxy… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1Y85
Type
protein
Length
572 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
Pockets
8 · best druggability 0.80

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin alpha chainprotein14176% helix, 0% strandP69905
B, DHemoglobin beta chainprotein14577% helix, 0% strandP68871

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, 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, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110140.800.8275empty
22370.730.8729HEM
32720.720.8530HEM
43050.720.8437HEM
52310.710.8627HEM

Interfaces

5 interfaces between chains.

  • A–B · 863 Ų buried · 8 hydrogen bonds · protein-protein
  • C–D · 849 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 672 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 665 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 292 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 1Y85 · T-To-T(High) quaternary transitions in human hemoglobin: desHIS146beta deoxy low-salt · the same entry in another collection · chain A against A, TM-score 1.00

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