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MolNFT v1 · #157241 · protein

Structure of the 6TH type III domain from human fibronectin

6MSV: “Structure of the 6TH type III domain from human fibronectin”. X-ray diffraction, 11 pockets (best druggability 0.85). MolNFT v1 #157241 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6MSV
Type
protein
Length
1,015 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fibronectin
UniProt
P02751
Pockets
11 · best druggability 0.85

Structure

x-ray diffraction · 7 distinct chains · 0% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFibronectinprotein860% helix, 52% strandP02751
B, G, J, LFibronectinprotein830% helix, 53% strandP02751
CFibronectinprotein850% helix, 51% strandP02751
DFibronectinprotein900% helix, 49% strandP02751
E, F, KFibronectinprotein840% helix, 52% strandP02751
HFibronectinprotein890% helix, 48% strandP02751
IFibronectinprotein810% helix, 56% strandP02751

Ligands and binding sites

  • GOL · Glycerol · additive · 2 copies · chains B, L, F

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

Pockets

11 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111630.850.86116empty
22700.690.8544empty
3860.680.9329empty
46760.660.7558GOL
51340.660.8924empty

Interfaces

26 interfaces between chains.

  • E–K · 792 Ų buried · 11 hydrogen bonds · protein-protein
  • A–J · 754 Ų buried · 15 hydrogen bonds · protein-protein
  • G–H · 752 Ų buried · 12 hydrogen bonds · protein-protein
  • C–I · 743 Ų buried · 12 hydrogen bonds · protein-protein
  • B–L · 733 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 6MSV · Structure of the 6th type III domain from human fibronectin · the same entry in another collection · chain L against L, TM-score 1.00

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