Research workbench
Yeast 20S proteasome with human BETA2C (S171G) in complex with onx 0914
Analyse Yeast 20S proteasome with human BETA2C (S171G) in complex with onx 0914 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6HTC
- Type
- protein
- Length
- 6,292 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, Q99436, P25451, P22141, P30656, P23724, P30657, P38624
- Ligands
- GQK, MG, CL, SO4
- Pockets
- 20 · best druggability 0.79
Structure
x-ray diffraction · 14 distinct chains · 36% helix, 29% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, O | Proteasome subunit alpha type-2 (EC 3.4.25.1) | protein | 240 | 36% helix, 26% strand | P23639 |
| B, P | Proteasome subunit alpha type-3 (EC 3.4.25.1) | protein | 244 | 39% helix, 25% strand | P23638 |
| C, Q | Proteasome subunit alpha type-4 (EC 3.4.25.1) | protein | 240 | 39% helix, 23% strand | P40303 |
| D, R | Proteasome subunit alpha type-5 (EC 3.4.25.1) | protein | 235 | 39% helix, 28% strand | P32379 |
| E, S | Proteasome subunit alpha type-6 (EC 3.4.25.1) | protein | 231 | 38% helix, 29% strand | P40302 |
| F, T | Probable proteasome subunit alpha type-7 (EC 3.4.25.1) | protein | 243 | 40% helix, 25% strand | P21242 |
| G, U | Proteasome subunit alpha type-1 (EC 3.4.25.1) | protein | 241 | 40% helix, 23% strand | P21243 |
| H, V | Proteasome subunit beta type-7 (EC 3.4.25.1) | protein | 219 | 30% helix, 35% strand | Q99436 |
| I, W | Proteasome subunit beta type-3 (EC 3.4.25.1) | protein | 204 | 32% helix, 33% strand | P25451 |
| J, X | Proteasome subunit beta type-4 (EC 3.4.25.1) | protein | 195 | 33% helix, 34% strand | P22141 |
| K, Y | Proteasome subunit beta type-5 (EC 3.4.25.1) | protein | 212 | 35% helix, 34% strand | P30656 |
| L, Z | Proteasome subunit beta type-6 (EC 3.4.25.1) | protein | 222 | 28% helix, 32% strand | P23724 |
| M, a | Proteasome subunit beta type-7 (EC 3.4.25.1) | protein | 224 | 32% helix, 33% strand | P30657 |
| N, b | Proteasome subunit beta type-1 (EC 3.4.25.1) | protein | 196 | 36% helix, 34% strand | P38624 |
Ligands and binding sites
- GQK · (2~{S})-3-(4-methoxyphenyl)-~{N}-[(2~{S},3~{R})-4-methyl-3,4-bis(oxidanyl)-1-phenyl-pentan-2-yl]-2-[[(2~{S})-2-(2-morpholin-4-ylethanoylamino) propanoyl]amino]propanamide · ligand · 6 copies · chains H, I, K, L, N, V, W, Y, Z, b
- MG · Magnesium ion · metal · 10 copies · chains G, I, H, K, W, N, a, L, V, Y, Z
- CL · Chloride ion · ion · 2 copies · chains G, U
- SO4 · Sulfate ion · ion · 2 copies · chains N, b
- MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 4 copies · chains H, Z, J, K, L, V, X, 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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 717 | 0.79 | 0.83 | 86 | empty |
| 2 | 949 | 0.79 | 0.81 | 90 | empty |
| 3 | 1130 | 0.78 | 0.80 | 129 | GQK, MG |
| 4 | 969 | 0.78 | 0.80 | 101 | empty |
| 5 | 1046 | 0.78 | 0.79 | 112 | empty |
Interfaces
88 interfaces between chains.
- V–W · 1703 Ų buried · 28 hydrogen bonds · protein-protein
- H–I · 1691 Ų buried · 27 hydrogen bonds · protein-protein
- B–C · 1613 Ų buried · 24 hydrogen bonds · protein-protein
- P–Q · 1575 Ų buried · 24 hydrogen bonds · protein-protein
- O–P · 1471 Ų buried · 16 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 covalent (covalent ligand).
Compared structures
- 6HTC · Yeast 20S proteasome with human beta2c (S171G) in complex with ONX 0914 · the same entry in another collection · chain B against B, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P23639
- Every structure of UniProt P23638
- Every structure of UniProt P40303
- Every structure of UniProt P32379
- Every structure of UniProt P40302
- Every structure of UniProt P21242
- Every structure of UniProt P21243
- Every structure of UniProt Q99436
- Every structure of UniProt P25451
- Every structure of UniProt P22141
- Every structure of UniProt P30656
- Every structure of UniProt P23724
- Every structure of UniProt P30657
- Every structure of UniProt P38624
- Elsewhere: RCSB PDB 6HTC · PDBe 6HTC · UniProt P23639 · UniProt P23638 · UniProt P40303 · UniProt P32379 · UniProt P40302 · UniProt P21242 · UniProt P21243 · UniProt Q99436 · UniProt P25451 · UniProt P22141 · UniProt P30656 · UniProt P23724 · UniProt P30657 · UniProt P38624
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