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MolNFT v1 · #147503 · protein

Yeast 26S proteasome bound to ubiquitinated substrate (5T motor state)

6EF2 · Proteasome subunit alpha type-1: “Yeast 26S proteasome bound to ubiquitinated substrate (5T motor state)”. Electron microscopy, 2 ligands (ATP, ADP), 20 pockets (best druggability 0.83). MolNFT v1 #147503 on GenesisL1: 3D structure…

PDB
6EF2
Type
protein
Length
3,290 residues
Chains
14
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proteasome subunit alpha type-1; Proteasome subunit alpha type-2; Proteasome subunit…
EC
3.4.25.1
UniProt
P21243, P23639, P23638, P40303, P32379, P40302, P21242, P33299, P40327, Q01939, P33298, P53549, P33297
Ligands
ATP, ADP
Pockets
20 · best druggability 0.83

Structure

electron microscopy · 14 distinct chains · 35% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProteasome subunit alpha type-1 (EC 3.4.25.1)protein23832% helix, 18% strandP21243
BProteasome subunit alpha type-2 (EC 3.4.25.1)protein24928% helix, 18% strandP23639
CProteasome subunit alpha type-3 (EC 3.4.25.1)protein24131% helix, 15% strandP23638
DProteasome subunit alpha type-4 (EC 3.4.25.1)protein24132% helix, 17% strandP40303
EProteasome subunit alpha type-5 (EC 3.4.25.1)protein24732% helix, 15% strandP32379
FProteasome subunit alpha type-6 (EC 3.4.25.1)protein23229% helix, 22% strandP40302
GProbable proteasome subunit alpha type-7 (EC 3.4.25.1)protein24634% helix, 20% strandP21242
H26S proteasome regulatory subunit 7 homologprotein26540% helix, 9% strandP33299
I26S proteasome regulatory subunit 4 homologprotein26037% helix, 6% strandP40327
J26S proteasome regulatory subunit 8 homologprotein26238% helix, 10% strandQ01939
K26S proteasome regulatory subunit 6B homologprotein25938% helix, 5% strandP33298
L26S proteasome subunit RPT4protein26444% helix, 5% strandP53549
M26S proteasome regulatory subunit 6Aprotein27040% helix, 9% strandP33297
sModel substrate polypeptideprotein160% helix, 0% strand—

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 4 copies · chains H, I, J, K, M
  • ADP · Adenosine-5'-diphosphate · ligand · 2 copies · chains K, L

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
111060.830.84117ATP
24780.810.8872empty
33620.800.8953empty
47140.800.8484ATP
511270.780.8097empty

Interfaces

35 interfaces between chains.

  • J–K · 1835 Ų buried · 12 hydrogen bonds · protein-protein
  • H–I · 1768 Ų buried · 17 hydrogen bonds · protein-protein
  • I–J · 1709 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 1389 Ų buried · 17 hydrogen bonds · protein-protein
  • D–E · 1344 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 6EF2 · Yeast 26S proteasome bound to ubiquitinated substrate (5T motor state) · the same entry in another collection · chain s against s, TM-score 1.00

Analyse

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