Research workbench
UBA1 in complex with ub-MLN7243 covalent adduct
Analyse UBA1 in complex with ub-MLN7243 covalent adduct in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5L6J
- Type
- protein
- Length
- 2,161 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P22515, P05759
- Ligands
- 61T, CL, SO4
Structure
x-ray diffraction · 3 distinct chains.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | — | protein | 1006 | — | P22515 |
| B, D | — | protein | 76 | — | P05759 |
| C | — | protein | 1003 | — | P22515 |
Ligands and binding sites
- 61T · [(1~{R},2~{R},3~{S},4~{R})-2,3-bis(oxidanyl)-4-[[2-[3-(trifluoromethylsulfanyl)phenyl]pyrazolo[1,5-a]pyrimidin-7-yl]amino]cyclopentyl]methyl sulfamate · ligand · 2 copies · chains A, B, C, D
- CL · Chloride ion · ion · 4 copies · chains A, C
- SO4 · Sulfate ion · ion · 3 copies · chains A, C
- GOL · Glycerol · additive · 16 copies · chains A, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
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 P22515
- Every structure of UniProt P05759
- Elsewhere: RCSB PDB 5L6J · PDBe 5L6J · UniProt P22515 · UniProt P05759
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