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M76H variant of human ferrochelatase

Analyse M76H variant of human ferrochelatase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4KMM
Type
protein
Length
718 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ferrochelatase, mitochondrial
EC
4.99.1.1
UniProt
P22830
Ligands
CHD, HEM, FES, CL
Pockets
7 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 50% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BFerrochelatase, mitochondrial (EC 4.99.1.1)protein35950% helix, 14% strandP22830

Ligands and binding sites

  • CHD · Cholic acid · ligand · 4 copies · chains A, B
  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • FES · Fe2/s2 (inorganic) cluster · ligand · 2 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · chains A, B

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

Pockets

7 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11180.800.9834empty
27020.790.8371HEM, FES, CHD, CL
36630.770.8277HEM, FES, CHD, CL
42800.600.7926empty
52110.530.7727empty

Interfaces

1 interface between chains.

  • A–B · 1927 Ų buried · 35 hydrogen bonds · protein-protein

Compared structures

  • 4KMM · M76H variant of human ferrochelatase · the same entry in another collection · chain A against A, TM-score 1.00
  • P22830 · AlphaFold monomer V2.0 prediction for ferrochelatase, mitochondrial (P22830) · a predicted model of the same protein · chain A against A, TM-score 0.99

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