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Yeast 20S proteasome in complex with pr-VI modulator

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

PDB
4X6Z
Type
protein
Length
6,359 residues
Chains
30
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proteasome subunit beta type-6; Proteasome subunit beta type-7; Proteasome subunit alpha…
EC
3.4.25.1
UniProt
P23724, P30657, P21243, P23639, P23638, P40303, P32379, P40302, P21242, P38624, P25043, P25451, P22141, P30656
Ligands
MG
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 18 distinct chains · 35% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
1, MProteasome subunit beta type-6 (EC 3.4.25.1)protein22229% helix, 32% strandP23724
2, NProteasome subunit beta type-7 (EC 3.4.25.1)protein23331% helix, 30% strandP30657
AProteasome subunit alpha type-1 (EC 3.4.25.1)protein24240% helix, 23% strandP21243
BProteasome subunit alpha type-2 (EC 3.4.25.1)protein24835% helix, 26% strandP23639
C, QProteasome subunit alpha type-3 (EC 3.4.25.1)protein24435% helix, 25% strandP23638
D, RProteasome subunit alpha type-4 (EC 3.4.25.1)protein24136% helix, 24% strandP40303
E, SProteasome subunit alpha type-5 (EC 3.4.25.1)protein24236% helix, 26% strandP32379
F, TProteasome subunit alpha type-6 (EC 3.4.25.1)protein23234% helix, 28% strandP40302
G, UProbable proteasome subunit alpha type-7 (EC 3.4.25.1)protein24439% helix, 26% strandP21242
H, VProteasome subunit beta type-1 (EC 3.4.25.1)protein19638% helix, 35% strandP38624
IProteasome subunit beta type-2 (EC 3.4.25.1)protein22129% helix, 34% strandP25043
J, XProteasome subunit beta type-3 (EC 3.4.25.1)protein20432% helix, 33% strandP25451
K, YProteasome subunit beta type-4 (EC 3.4.25.1)protein19634% helix, 34% strandP22141
L, ZProteasome subunit beta type-5 (EC 3.4.25.1)protein21236% helix, 34% strandP30656
OProteasome subunit alpha type-1 (EC 3.4.25.1)protein24139% helix, 23% strandP21243
PProteasome subunit alpha type-2 (EC 3.4.25.1)protein24935% helix, 26% strandP23639
WProteasome subunit beta type-2 (EC 3.4.25.1)protein22030% helix, 35% strandP25043
a, eSynthetic peptide (polymer)protein30% helix, 0% strand—

Ligands and binding sites

  • MG · Magnesium ion · metal · 56 copies · chains 1, 2, T, I, B, C, D, F, H, J, K, L, E, M, N, G, O, P, Q, R, S, V, W, U, X, Y, Z
  • GOL · Glycerol · additive · 38 copies · chains 1, Z, 2, V, A, H, I, G, D, E, F, N, B, J, K, L, Y, M, O, W, U, S, T, X
  • MPD · (4S)-2-methyl-2,4-pentanediol · additive · 9 copies · chains 1, 2, K, L, M, N, T, V, P, W, X, Z

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
19700.830.84151MPD
29790.800.81109empty
310120.790.81112MG
49810.790.8197MG
510250.790.81102MG

Interfaces

95 interfaces between chains.

  • I–J · 1760 Ų buried · 27 hydrogen bonds · protein-protein
  • W–X · 1687 Ų buried · 28 hydrogen bonds · protein-protein
  • C–D · 1651 Ų buried · 26 hydrogen bonds · protein-protein
  • Q–R · 1641 Ų buried · 26 hydrogen bonds · protein-protein
  • 1–I · 1513 Ų buried · 23 hydrogen bonds · protein-protein

Compared structures

  • 4X6Z · Yeast 20S proteasome in complex with PR-VI modulator · the same entry in another collection · chain 2 against 2, TM-score 1.00

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