GL1X · GenesisL1 explorer

Research workbench

Crystal structure of yeast 20S proteasome in complex with ligand 2A

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

PDB
3NZJ
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)protein24138% helix, 23% strandP40303
D, RProteasome component PUP2 (EC 3.4.25.1)protein24236% helix, 27% strandP32379
E, SProteasome component PRE5 (EC 3.4.25.1)protein23336% helix, 28% strandP40302
F, TProteasome component C1 (EC 3.4.25.1)protein24439% helix, 26% strandP21242
G, UProteasome component C7-alpha (EC 3.4.25.1)protein24340% 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)protein19832% helix, 34% strandP22141
K, YProteasome component PRE2 (EC 3.4.25.1)protein21235% helix, 34% 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)protein19636% helix, 35% strandP38624
3, 4Tmc-95A mimic ligand 2Aprotein30% 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
110020.830.84150empty
29710.820.83114empty
311170.800.82106empty
47500.800.84108empty
511440.800.81105empty

Interfaces

96 interfaces between chains.

  • V–W · 1726 Ų buried · 26 hydrogen bonds · protein-protein
  • H–I · 1723 Ų buried · 28 hydrogen bonds · protein-protein
  • B–C · 1648 Ų buried · 23 hydrogen bonds · protein-protein
  • P–Q · 1615 Ų buried · 20 hydrogen bonds · protein-protein
  • H–Z · 1478 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

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

Compared structures

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

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.