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Mm-cpn deltalid with ATP

Analyse Mm-cpn deltalid with ATP in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3IZN
Type
protein
Length
7,856 residues
Chains
16
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chaperonin
UniProt
Q877G8
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 1 distinct chain · 52% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, PChaperoninprotein49152% helix, 18% strandQ877G8

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110240.840.85105empty
29480.820.8494empty
37030.810.8574empty
48930.800.8270empty
511410.800.81105empty

Interfaces

24 interfaces between chains.

  • L–M · 1862 Ų buried · 24 hydrogen bonds · protein-protein
  • G–H · 1860 Ų buried · 24 hydrogen bonds · protein-protein
  • D–E · 1858 Ų buried · 24 hydrogen bonds · protein-protein
  • C–D · 1858 Ų buried · 24 hydrogen bonds · protein-protein
  • A–H · 1858 Ų buried · 24 hydrogen bonds · protein-protein

Compared structures

  • 3IZN · Mm-cpn deltalid with ATP · the same entry in another collection · chain A against A, TM-score 1.00

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