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MolNFT v1 · #157812 · protein

Human methemoglobin state 1 determined using single-particle cryo-EM at 200 kev

6NBC · Hemoglobin subunit alpha: “Human methemoglobin state 1 determined using single-particle cryo-EM at 200 kev”. Electron microscopy, 1 ligand (HEM), 7 pockets (best druggability 0.86). MolNFT v1 #157812 on GenesisL1: 3D structure…

PDB
6NBC
Type
protein
Length
566 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin subunit alpha; Hemoglobin subunit beta
UniProt
P69905, P68871
Ligands
HEM
Pockets
7 · best druggability 0.86

Structure

electron microscopy · 2 distinct chains · 79% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin subunit alphaprotein14079% helix, 0% strandP69905
B, DHemoglobin subunit betaprotein14378% 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18880.860.87116empty
22230.740.8827HEM
32290.730.8730HEM
41880.680.8625HEM
51770.680.8625HEM

Interfaces

5 interfaces between chains.

  • C–D · 952 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 939 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 474 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 472 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 383 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 6NBC · human methemoglobin state 1 determined using single-particle cryo-EM at 200 keV · the same entry in another collection · chain A against A, TM-score 1.00

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