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MolNFT v1 · #125343 · protein

Yeast 20S proteasome with mouse BETA5I (1-138) and mouse BETA6 (97- 111; 118-133) in complex with epoxyketone inhibitor 16

5L69 · Proteasome subunit alpha type-2: “Yeast 20S proteasome with mouse BETA5I (1-138) and mouse BETA6 (97- 111; 118-133) in complex with epoxyketone…”. X-ray diffraction, 3 ligands (79P, MG, CL), 20 pockets (best druggability 0.83).…

PDB
5L69
Type
protein
Length
6,342 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, P28063, P30656, P23724, O09061, P30657, P38624
Ligands
79P, MG, CL
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)protein25035% helix, 25% strandP23639
B, PProteasome subunit alpha type-3 (EC 3.4.25.1)protein24438% helix, 25% strandP23638
C, QProteasome subunit alpha type-4 (EC 3.4.25.1)protein24036% helix, 24% strandP40303
D, RProteasome subunit alpha type-5 (EC 3.4.25.1)protein23538% helix, 27% strandP32379
E, SProteasome subunit alpha type-6 (EC 3.4.25.1)protein23138% helix, 28% strandP40302
F, TProbable proteasome subunit alpha type-7 (EC 3.4.25.1)protein24340% helix, 26% strandP21242
G, UProteasome subunit alpha type-1 (EC 3.4.25.1)protein24140% helix, 23% strandP21243
H, VProteasome subunit beta type-2 (EC 3.4.25.1)protein22629% helix, 34% 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)protein19533% helix, 34% strandP22141
K, YProteasome subunit beta type-8,PROTEASOME subunit beta type-5 (EC 3.4.25.1)protein21136% helix, 34% strandP28063, P30656
L, ZProteasome subunit beta type-6,PROTEASOME subunit beta type-1,PROTEASOME subunit beta type-6,PROTEASOME subunit beta type-1, proteasome subunit beta type-6 (EC 3.4.25.1)protein22228% helix, 33% strandP23724, O09061
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)protein19638% helix, 34% strandP38624

Ligands and binding sites

  • 79P · (2~{S})-3-(1~{H}-indol-3-yl)-~{N}-[(2~{S},3~{S},4~{R})-4-methyl-3,5-bis(oxidanyl)-1-phenyl-pentan-2-yl]-2-[[(2~{R})-2-(2-morpholin-4-ylethanoylamino) propanoyl]amino]propanamide · ligand · 4 copies · chains H, I, K, L, V, W, Y, Z
  • MG · Magnesium ion · metal · 8 copies · chains G, I, Y, J, K, W, L, V, N, a, H, Z
  • CL · Chloride ion · ion · 3 copies · chains G, H, U, V
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains K, 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
110510.830.84150empty
29240.820.8411779P
311280.800.81122empty
48940.790.82101empty
59890.780.80103empty

Interfaces

92 interfaces between chains.

  • V–W · 1730 Ų buried · 29 hydrogen bonds · protein-protein
  • H–I · 1725 Ų buried · 30 hydrogen bonds · protein-protein
  • B–C · 1596 Ų buried · 23 hydrogen bonds · protein-protein
  • P–Q · 1590 Ų buried · 24 hydrogen bonds · protein-protein
  • H–Z · 1542 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 5L69 · Yeast 20S proteasome with mouse beta5i (1-138) and mouse beta6 (97-111; 118-133) in… · the same entry in another collection · chain K against K, TM-score 1.00

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