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A novel iron centre in the split-soret cytochrome C from desulfovibrio desulfuricans atcc 27774

Analyse A novel iron centre in the split-soret cytochrome C from desulfovibrio… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1H21
Type
protein
Length
960 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Split-soret cytochrome C
UniProt
P81040
Ligands
HEC
Pockets
12 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 55% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DSplit-soret cytochrome Cprotein24055% helix, 2% strandP81040

Ligands and binding sites

  • HEC · Heme C · ligand · 8 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18380.810.8476HEC
28360.810.8378HEC
31330.620.8635empty
41260.590.8537empty
52570.550.7629empty

Interfaces

3 interfaces between chains.

  • C–D · 4138 Ų buried · 51 hydrogen bonds · protein-protein
  • A–B · 4129 Ų buried · 56 hydrogen bonds · protein-protein
  • B–C · 352 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 16 cofactor (heme c attachment).

Compared structures

  • 1H21 · A novel iron centre in the split-Soret cytochrome c from Desulfovibrio desulfuricans ATCC… · the same entry in another collection · chain D against D, TM-score 1.00
  • P81040 · AlphaFold monomer V2.0 prediction for split-soret cytochrome C (P81040) · a predicted model of the same protein · chain D against A, TM-score 1.00

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