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Deoxy hemoglobin (a-gly-C:V1M,L29W,H58Q; B,D:V1M)

Analyse Deoxy hemoglobin (a-gly-C:V1M,L29W,H58Q; B,D:V1M) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1O1L
Type
protein
Length
575 residues
Chains
3
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
7 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 76% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemoglobin alpha chainprotein28376% 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, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111340.790.8193empty
22460.730.8729HEM
32330.730.8728HEM
42420.730.8731HEM
52410.690.8530HEM

Interfaces

2 interfaces between chains.

  • A–D · 1516 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 1515 Ų buried · 18 hydrogen bonds · protein-protein

Compared structures

  • 1O1L · Deoxy hemoglobin (A-GLY-C:V1M,L29W,H58Q; B,D:V1M) · the same entry in another collection · chain A against A, TM-score 1.00

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