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Yeast 20S proteasome in complex with vibralactone

Analyse Yeast 20S proteasome in complex with vibralactone in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4LQI
Type
protein
Length
6,368 residues
Chains
28
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proteasome subunit alpha type-2; Proteasome subunit alpha type-3; Proteasome subunit…
EC
3.4.25.1
UniProt
P23639, P23638, P40303, P32379, P40302, P21242, P21243, P25043, P25451, P22141, P30656, P23724, P30657, P38624
Ligands
1Y9
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 14 distinct chains · 35% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, OProteasome subunit alpha type-2 (EC 3.4.25.1)protein25036% helix, 26% strandP23639
B, PProteasome subunit alpha type-3 (EC 3.4.25.1)protein24437% helix, 25% strandP23638
C, QProteasome subunit alpha type-4 (EC 3.4.25.1)protein24137% helix, 23% strandP40303
D, RProteasome subunit alpha type-5 (EC 3.4.25.1)protein24237% helix, 27% strandP32379
E, SProteasome subunit alpha type-6 (EC 3.4.25.1)protein23336% helix, 29% strandP40302
F, TProteasome subunit alpha type-7 (EC 3.4.25.1)protein24438% helix, 25% strandP21242
G, UProteasome subunit alpha type-1 (EC 3.4.25.1)protein24340% helix, 23% strandP21243
H, VProteasome subunit beta type-2 (EC 3.4.25.1)protein22229% helix, 35% strandP25043
I, WProteasome subunit beta type-3 (EC 3.4.25.1)protein20432% helix, 32% strandP25451
J, XProteasome subunit beta type-4 (EC 3.4.25.1)protein19833% helix, 33% strandP22141
K, YProteasome subunit beta type-5 (EC 3.4.25.1)protein21236% helix, 34% strandP30656
L, ZProteasome subunit beta type-6 (EC 3.4.25.1)protein22228% helix, 31% strandP23724
M, aProteasome subunit beta type-7 (EC 3.4.25.1)protein23331% helix, 31% strandP30657
N, bProteasome subunit beta type-1 (EC 3.4.25.1)protein19636% helix, 35% strandP38624

Ligands and binding sites

  • 1Y9 · vibralactone, bound form · ligand · 4 copies · chains K, N, Y, b

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
111130.830.84160empty
29510.820.84113empty
38880.820.84109empty
410910.810.82103empty
510890.790.81102empty

Interfaces

92 interfaces between chains.

  • H–I · 1714 Ų buried · 28 hydrogen bonds · protein-protein
  • V–W · 1711 Ų buried · 24 hydrogen bonds · protein-protein
  • B–C · 1643 Ų buried · 26 hydrogen bonds · protein-protein
  • P–Q · 1604 Ų buried · 24 hydrogen bonds · protein-protein
  • L–V · 1482 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent (covalent ligand).

Compared structures

  • 4LQI · Yeast 20S Proteasome in complex with Vibralactone · the same entry in another collection · chain M against M, TM-score 1.00

Analyse

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