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MolNFT v1 · #147502 · protein

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

6EF1 · Proteasome subunit alpha type-1: “Yeast 26S proteasome bound to ubiquitinated substrate (5D motor state)”. Electron microscopy, 2 ligands (ATP, ADP), 20 pockets (best druggability 0.90). MolNFT v1 #147502 on GenesisL1: 3D structure…

PDB
6EF1
Type
protein
Length
3,294 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 0.90

Structure

electron microscopy · 14 distinct chains · 36% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProteasome subunit alpha type-1 (EC 3.4.25.1)protein23937% helix, 17% strandP21243
BProteasome subunit alpha type-2 (EC 3.4.25.1)protein25034% helix, 19% strandP23639
CProteasome subunit alpha type-3 (EC 3.4.25.1)protein23833% helix, 19% strandP23638
DProteasome subunit alpha type-4 (EC 3.4.25.1)protein23434% helix, 17% strandP40303
EProteasome subunit alpha type-5 (EC 3.4.25.1)protein24233% helix, 18% strandP32379
FProteasome subunit alpha type-6 (EC 3.4.25.1)protein23333% helix, 22% strandP40302
GProbable proteasome subunit alpha type-7 (EC 3.4.25.1)protein24335% helix, 21% strandP21242
H26S proteasome regulatory subunit 7 homologprotein25441% helix, 4% strandP33299
I26S proteasome regulatory subunit 4 homologprotein27136% helix, 3% strandP40327
J26S proteasome regulatory subunit 8 homologprotein27339% helix, 5% strandQ01939
K26S proteasome regulatory subunit 6B homologprotein27634% helix, 1% strandP33298
L26S proteasome subunit RPT4protein26446% helix, 4% strandP53549
M26S proteasome regulatory subunit 6Aprotein26240% helix, 6% strandP33297
sModel substrate polypeptideprotein150% helix, 0% strand—

Ligands and binding sites

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

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
111280.900.92178empty
29870.870.88128empty
39650.850.87115ATP
411710.850.86158ADP
56930.840.88106empty

Interfaces

36 interfaces between chains.

  • J–K · 1542 Ų buried · 10 hydrogen bonds · protein-protein
  • F–G · 1346 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1345 Ų buried · 8 hydrogen bonds · protein-protein
  • A–G · 1344 Ų buried · 15 hydrogen bonds · protein-protein
  • I–J · 1331 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 6EF1 · Yeast 26S proteasome bound to ubiquitinated substrate (5D motor state) · the same entry in another collection · chain s against s, TM-score 1.00

Analyse

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