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Exploring cystine dense peptide space to open a unique molecular toolbox

Analyse Exploring cystine dense peptide space to open a unique molecular toolbox in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ATU
Type
protein
Length
879 residues
Chains
18
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Elafin
UniProt
P19957
Pockets
13 · best druggability 0.78

Structure

x-ray diffraction · 4 distinct chains · 6% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, G, H, RElafinprotein496% helix, 20% strandP19957
C, DElafinprotein476% helix, 30% strandP19957
E, F, I, M, N, OElafinprotein506% helix, 24% strandP19957
J, K, L, P, QElafinprotein486% helix, 21% strandP19957

Pockets

13 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18310.780.8178empty
25440.730.8178empty
32810.500.7434empty
41070.430.7821empty
51720.420.7326empty

Interfaces

32 interfaces between chains.

  • D–R · 571 Ų buried · 4 hydrogen bonds · protein-protein
  • M–N · 366 Ų buried · 4 hydrogen bonds · protein-protein
  • A–D · 329 Ų buried · 4 hydrogen bonds · protein-protein
  • G–N · 318 Ų buried · 3 hydrogen bonds · protein-protein
  • B–C · 316 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 72 disulfide (disulfide).

Compared structures

  • 6ATU · Exploring Cystine Dense Peptide Space to Open a Unique Molecular Toolbox · the same entry in another collection · chain K against K, TM-score 1.00

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