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Cryo-EM structure of the plectasin fibril (single strand)

Analyse Cryo-EM structure of the plectasin fibril (single strand) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7OAG
Type
protein
Length
1,000 residues
Chains
25
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fungal defensin plectasin
UniProt
Q53I06
Pockets
19 · best druggability 0.81

Structure

electron microscopy · 1 distinct chain · 35% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, YFungal defensin plectasinprotein4035% helix, 18% strandQ53I06

Pockets

19 pockets found on a 1 Å grid, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17860.810.84138empty
25910.790.8490empty
35400.780.8495empty
42630.700.8548empty
53090.700.8450empty

Interfaces

89 interfaces between chains.

  • P–T · 421 Ų buried · 3 hydrogen bonds · protein-protein
  • I–M · 417 Ų buried · 3 hydrogen bonds · protein-protein
  • F–J · 415 Ų buried · 3 hydrogen bonds · protein-protein
  • B–F · 414 Ų buried · 3 hydrogen bonds · protein-protein
  • Q–U · 410 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 75 disulfide (disulfide).

Compared structures

  • 7OAG · Cryo-EM structure of the plectasin fibril (single strand) · the same entry in another collection · chain J against J, TM-score 1.00

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