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MolNFT v1 · #103957 · protein

Crystal structure of the C-type cytochrome soru from sinorhizobium meliloti

4PWA · Putative cytochrome C: “Crystal structure of the C-type cytochrome soru from sinorhizobium meliloti”. X-ray diffraction, 1 ligand (HEC), 7 pockets (best druggability 0.73). MolNFT v1 #103957 on GenesisL1: 3D structure, binding sites…

PDB
4PWA
Type
protein
Length
344 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative cytochrome C
UniProt
Q92M25
Ligands
HEC
Pockets
7 · best druggability 0.73

Structure

x-ray diffraction · 3 distinct chains · 57% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPutative cytochrome Cprotein8656% helix, 7% strandQ92M25
CPutative cytochrome Cprotein8558% helix, 7% strandQ92M25
DPutative cytochrome Cprotein8756% helix, 7% strandQ92M25

Ligands and binding sites

  • HEC · Heme C · ligand · 4 copies · chains A, C, B, D

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
12430.730.8738HEC
22440.720.8737HEC
32000.660.8429HEC
42110.660.8430HEC
55480.640.7648empty

Interfaces

4 interfaces between chains.

  • B–D · 519 Ų buried · 2 hydrogen bonds · protein-protein
  • C–D · 511 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 429 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 413 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 cofactor (heme c attachment).

Compared structures

  • 4PWA · Crystal structure of the c-type cytochrome SorU from Sinorhizobium meliloti · the same entry in another collection · chain A against A, TM-score 1.00

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