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Structure of aquomet hemoglobin bristol-alesha ALPHAWTBETAV67M

Analyse Structure of aquomet hemoglobin bristol-alesha ALPHAWTBETAV67M in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MQI
Type
protein
Length
286 residues
Chains
2
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
6 · best druggability 0.73

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AHemoglobin subunit alphaprotein14077% helix, 0% strandP69905
BHemoglobin subunit betaprotein14680% helix, 0% strandP68871

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12170.730.8829HEM
22210.730.8728HEM
31190.510.8121empty
4880.370.7616empty
5520.330.7817empty

Interfaces

1 interface between chains.

  • A–B · 909 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 4MQI · Structure of Aquomet Hemoglobin Bristol-Alesha alphawtbetaV67M · the same entry in another collection · chain A against A, TM-score 1.00

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