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Crystal structure of the yeast 20S proteasome in complex with 2B

Analyse Crystal structure of the yeast 20S proteasome in complex with 2B in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3NZW
Type
protein
Length
6,374 residues
Chains
30
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Proteasome component Y7; Proteasome component Y13; Proteasome component PRE6; Proteasome…
EC
3.4.25.1
UniProt
P23639, P23638, P40303, P32379, P40302, P21242, P21243, P25043, P25451, P22141, P30656, P23724, P30657, P38624
Ligands
BOC, ABN
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 15 distinct chains · 35% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, OProteasome component Y7 (EC 3.4.25.1)protein25036% helix, 26% strandP23639
B, PProteasome component Y13 (EC 3.4.25.1)protein24437% helix, 25% strandP23638
C, QProteasome component PRE6 (EC 3.4.25.1)protein24137% helix, 23% strandP40303
D, RProteasome component PUP2 (EC 3.4.25.1)protein24237% helix, 27% strandP32379
E, SProteasome component PRE5 (EC 3.4.25.1)protein23337% helix, 28% strandP40302
F, TProteasome component C1 (EC 3.4.25.1)protein24438% helix, 25% strandP21242
G, UProteasome component C7-alpha (EC 3.4.25.1)protein24338% helix, 23% strandP21243
H, VProteasome component PUP1 (EC 3.4.25.1)protein22229% helix, 35% strandP25043
I, WProteasome component PUP3 (EC 3.4.25.1)protein20432% helix, 33% strandP25451
J, XProteasome component C11 (EC 3.4.25.1)protein19834% helix, 34% strandP22141
K, YProteasome component PRE2 (EC 3.4.25.1)protein21235% helix, 32% strandP30656
L, ZProteasome component C5 (EC 3.4.25.1)protein22228% helix, 31% strandP23724
M, 1Proteasome component PRE4 (EC 3.4.25.1)protein23331% helix, 31% strandP30657
N, 2Proteasome component PRE3 (EC 3.4.25.1)protein19638% helix, 35% strandP38624
3, 4Tmc-95A mimic ligand 2Bprotein30% helix, 0% strand—

Ligands and binding sites

  • BOC · Tert-butyl hydrogen carbonate · ligand · 2 copies · chains K, L, 3, Y, Z, 4
  • ABN · Benzylamine · ligand · 2 copies · chains K, 3, Y, 4
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains K, 3, Y, 4

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
19570.830.84144empty
29740.830.84106empty
39470.810.83113empty
48760.810.84120empty
511570.810.82116empty

Interfaces

96 interfaces between chains.

  • H–I · 1699 Ų buried · 27 hydrogen bonds · protein-protein
  • V–W · 1693 Ų buried · 28 hydrogen bonds · protein-protein
  • B–C · 1637 Ų buried · 24 hydrogen bonds · protein-protein
  • P–Q · 1584 Ų buried · 23 hydrogen bonds · protein-protein
  • H–Z · 1464 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent, 4 modified (covalent ligand, nonstandard).

Compared structures

  • 3NZW · Crystal structure of the yeast 20S proteasome in complex with 2b · the same entry in another collection · chain B against B, TM-score 1.00

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