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T-to-T(HIGH) quaternary transitions in human hemoglobin: BETAW37H deoxy low-salt (10 test sets)

Analyse T-to-T(HIGH) quaternary transitions in human hemoglobin: BETAW37H deoxy… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1Y4B
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
Pockets
9 · best druggability 0.80

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin alpha chainprotein14177% helix, 0% strandP69905
B, DHemoglobin beta chainprotein14677% 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111800.800.8293empty
22750.740.8628HEM
32610.730.8632HEM
42820.730.8529HEM
52410.720.8629HEM

Interfaces

5 interfaces between chains.

  • C–D · 864 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 852 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 696 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 673 Ų buried · 9 hydrogen bonds · protein-protein
  • A–C · 302 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 1Y4B · T-To-T(High) quaternary transitions in human hemoglobin: betaW37H deoxy low-salt (10 test… · the same entry in another collection · chain A against A, TM-score 1.00

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