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MolNFT v1 · #67979 · protein

Cryo-EM structure of 9-fold symmetric ratcpn-beta in ATP-binding state

3J1F · Chaperonin beta subunit: “Cryo-EM structure of 9-fold symmetric ratcpn-beta in ATP-binding state”. Electron microscopy, 2 ligands (ATP, MG), 20 pockets (best druggability 0.81). MolNFT v1 #67979 on GenesisL1: 3D structure, binding…

PDB
3J1F
Type
protein
Length
9,090 residues
Chains
18
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chaperonin beta subunit
UniProt
Q877H2
Ligands
ATP, MG
Pockets
20 · best druggability 0.81

Structure

electron microscopy · 1 distinct chain · 50% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, K, L, M, N, O, P, Q, R, SChaperonin beta subunitprotein50550% helix, 18% strandQ877H2

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 18 copies · chains A, B, C, D, E, F, G, H, I, K, L, M, N, O, P, Q, R, S
  • MG · Magnesium ion · metal · 18 copies · chains A, B, C, D, E, F, G, H, I, K, L, M, N, O, P, Q, R, S

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19760.810.8295ATP, MG
29980.800.8198ATP, MG
38170.800.8386ATP, MG
49920.800.8193ATP, MG
511510.800.81111ATP, MG

Interfaces

30 interfaces between chains.

  • M–N · 821 Ų buried · 18 hydrogen bonds · protein-protein
  • N–O · 819 Ų buried · 15 hydrogen bonds · protein-protein
  • B–C · 814 Ų buried · 13 hydrogen bonds · protein-protein
  • L–M · 808 Ų buried · 11 hydrogen bonds · protein-protein
  • K–L · 807 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 3J1F · Cryo-EM structure of 9-fold symmetric rATcpn-beta in ATP-binding state · the same entry in another collection · chain N against N, TM-score 1.00

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