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MolNFT v1 · #28535 · protein

T-to-T(HIGH) quaternary transitions in human hemoglobin: hba oxy (5.0MM ihp, 20% peg) (10 test sets)

1YHE · Hemoglobin alpha chain: “T-to-T(HIGH) quaternary transitions in human hemoglobin: hba oxy (5.0MM ihp, 20% peg) (10 test sets)”. X-ray diffraction, 2 ligands (HEM, OXY), 10 pockets (best druggability 0.81). MolNFT v1 #28535 on…

PDB
1YHE
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, OXY
Pockets
10 · best druggability 0.81

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin alpha chainprotein14179% 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
  • OXY · Oxygen molecule · ion · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111680.810.8291empty
22580.740.8729HEM, OXY
32750.720.8529HEM, OXY
42420.720.8628HEM, OXY
52580.710.8530HEM, OXY

Interfaces

5 interfaces between chains.

  • A–B · 853 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 841 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 708 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 693 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 296 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 1YHE · T-To-T(High) quaternary transitions in human hemoglobin: HbA OXY (5.0MM IHP, 20% PEG) (10… · the same entry in another collection · chain A against A, TM-score 1.00

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