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Structure of a crystal form of human methemoglobin indicative of fiber formation

Analyse Structure of a crystal form of human methemoglobin indicative of fiber formation in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ODQ
Type
protein
Length
574 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin subunit alpha; Hemoglobin subunit beta
UniProt
P69905, P68871
Ligands
HEM
Pockets
9 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 75% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CHemoglobin subunit alphaprotein14175% helix, 0% strandP69905
B, DHemoglobin subunit betaprotein14675% 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, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110780.840.8592HEM
27870.820.8569empty
31300.800.9725empty
4710.750.9825empty
52220.720.8729HEM

Interfaces

6 interfaces between chains.

  • C–D · 944 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 916 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 529 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 524 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 169 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3ODQ · Structure of a Crystal Form of Human Methemoglobin Indicative of Fiber Formation · the same entry in another collection · chain A against A, TM-score 1.00

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