GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the yeast 20S proteasome in complex with homobelactosin C

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

PDB
3E47
Type
protein
Length
6,368 residues
Chains
28
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
ESY
Pockets
20 · best druggability 0.82

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
A, OProteasome component Y7 (EC 3.4.25.1)protein25035% helix, 25% strandP23639
B, PProteasome component Y13 (EC 3.4.25.1)protein24438% 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)protein23336% helix, 30% 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)protein19833% helix, 33% strandP22141
K, YProteasome component PRE2 (EC 3.4.25.1)protein21236% helix, 33% strandP30656
L, ZProteasome component C5 (EC 3.4.25.1)protein22229% helix, 32% strandP23724
M, 1Proteasome component PRE4 (EC 3.4.25.1)protein23331% helix, 32% strandP30657
N, 2Proteasome component PRE3 (EC 3.4.25.1)protein19638% helix, 34% strandP38624

Ligands and binding sites

  • ESY · benzyl N-[(benzyloxy)carbonyl]-L-alanyl-N~6~-[(2R,3S,4S)-3-formyl-2-hydroxy-4-methylhexanoyl]-L-lysinate · ligand · 2 copies · chains J, K, W, X, I, Y

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
19240.820.84123empty
210700.820.83125empty
38770.810.84108empty
410750.800.82100empty
511600.800.82115empty

Interfaces

92 interfaces between chains.

  • V–W · 1711 Ų buried · 28 hydrogen bonds · protein-protein
  • H–I · 1707 Ų buried · 27 hydrogen bonds · protein-protein
  • B–C · 1636 Ų buried · 28 hydrogen bonds · protein-protein
  • P–Q · 1587 Ų buried · 23 hydrogen bonds · protein-protein
  • H–Z · 1464 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 3E47 · Crystal Structure of the Yeast 20S Proteasome in Complex with Homobelactosin C · 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.