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High-resolution X-ray study of deoxyhemoglobin rothschild 37BETA TRP-> arg: a mutation that creates an intersubunit chloride-binding site

Analyse High-resolution X-ray study of deoxyhemoglobin rothschild 37BETA TRP-> arg: a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1HBB
Type
protein
Length
574 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hemoglobin a (deoxy) (alpha chain); Hemoglobin a (deoxy) (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 a (deoxy) (alpha chain)protein14176% helix, 0% strandP69905
B, DHemoglobin a (deoxy) (beta chain)protein14679% 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
110460.800.8178empty
22260.740.8831HEM
32520.730.8630HEM
42000.720.8827HEM
52590.710.8529HEM

Interfaces

5 interfaces between chains.

  • A–B · 867 Ų buried · 11 hydrogen bonds · protein-protein
  • C–D · 856 Ų buried · 9 hydrogen bonds · protein-protein
  • A–D · 713 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 704 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 298 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 1HBB · High-resolution X-ray study of deoxyhemoglobin rothschild 37BETA TRP-> arg: a mutation… · the same entry in another collection · chain C against C, TM-score 1.00

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