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MolNFT v1 · #27906 · protein

The T-to-T high transitions in human hemoglobin: wild-type deoxy hb a (low salt, one test set)

1XXT · Hemoglobin alpha chain: “The T-to-T high transitions in human hemoglobin: wild-type deoxy hb a (low salt, one test set)”. X-ray diffraction, 1 ligand (HEM), 8 pockets (best druggability 0.80). MolNFT v1 #27906 on GenesisL1: 3D…

PDB
1XXT
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
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 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

8 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110530.800.8276empty
22760.730.8629HEM
32290.730.8730HEM
42660.710.8531HEM
52230.710.8628HEM

Interfaces

5 interfaces between chains.

  • A–B · 863 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 848 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 712 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 703 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 300 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 1XXT · The T-to-T High Transitions in Human Hemoglobin: wild-type deoxy Hb A (low salt, one test… · the same entry in another collection · chain A against A, TM-score 1.00

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