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MolNFT v1 · #4764 · protein

High-resolution X-ray study of deoxy recombinant human hemoglobins synthesized from beta-globins having mutated amino termini

1DXV · Hemoglobin (deoxy) (alpha chain): “High-resolution X-ray study of deoxy recombinant human hemoglobins synthesized from beta-globins having…”. X-ray diffraction, 2 ligands (HEM, SO4), 7 pockets (best druggability 0.80). MolNFT v1…

PDB
1DXV
Type
protein
Length
574 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin (deoxy) (alpha chain); Hemoglobin (deoxy) (beta chain)
UniProt
P69905, P68871
Ligands
HEM, SO4
Pockets
7 · best druggability 0.80

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin (deoxy) (alpha chain)protein14177% helix, 0% strandP69905
B, DHemoglobin (deoxy) (beta chain)protein14681% helix, 0% strandP68871

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains A, B, C, D
  • SO4 · Sulfate ion · ion · 2 copies · chains 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
18190.800.8381empty
22650.740.8730HEM
32220.740.8827HEM
42060.730.8827HEM
52720.720.8630HEM

Interfaces

5 interfaces between chains.

  • A–B · 852 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 849 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 724 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 718 Ų buried · 9 hydrogen bonds · protein-protein
  • A–C · 298 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 1DXV · High-resolution X-ray study of deoxy recombinant human hemoglobins synthesized from… · the same entry in another collection · chain C against C, TM-score 1.00

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