USP14 catalytic domain with IU1-206. Determined by X-ray diffraction at 2.21 Å resolution. Released 12 Dec 2018.
Explore 6IIM in 3D Show helices and sheets RCSB PDB PDBe
6IIM contains 32 α-helices and 46 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 103-105 | 3 | |
| β-strand | 106-107 | 2 | 1 |
| α-helix | 114-124 | 11 | |
| α-helix | 127-135 | 9 | |
| α-helix | 147-165 | 19 | |
| β-strand | 169-170 | 2 | 1 |
| α-helix | 173-182 | 10 | |
| α-helix | 184-187 | 4 | |
| β-strand | 189 | 1 | 2 |
| α-helix | 194 | 1 | |
| β-strand | 195 | 1 | 2 |
| α-helix | 196-197 | 2 | |
| α-helix | 200-214 | 15 | |
| α-helix | 216-218 | 3 | |
| α-helix | 242-247 | 6 | |
| β-strand | 249-257 | 9 | 3 |
| α-helix | 264-265 | 2 | |
| β-strand | 266-272 | 7 | 3 |
| β-strand | 275-278 | 4 | 4 |
| β-strand | 285 | 1 | 5 |
| α-helix | 286-293 | 8 | |
| β-strand | 295-302 | 8 | 3 |
| β-strand | 307-319 | 13 | 3 |
| β-strand | 321 | 1 | 6 |
| β-strand | 324-329 | 6 | 4 |
| β-strand | 331 | 1 | 7 |
| α-helix | 341 | 1 | |
| β-strand | 342 | 1 | 7 |
| α-helix | 343 | 1 | |
| β-strand | 348 | 1 | 5 |
| β-strand | 352-354 | 3 | 4 |
| α-helix | 356-358 | 3 | |
| β-strand | 359 | 1 | 3 |
| α-helix | 361-375 | 15 | |
| β-strand | 412 | 1 | 6 |
| β-strand | 417-427 | 11 | 4 |
| β-strand | 435-443 | 9 | 4 |
| β-strand | 446-451 | 6 | 4 |
| β-strand | 454-458 | 5 | 4 |
| α-helix | 460-464 | 5 | |
| α-helix | 465-467 | 3 | |
| β-strand | 474-482 | 9 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 106-107 | 2 | 8 |
| α-helix | 114-124 | 11 | |
| α-helix | 127-135 | 9 | |
| α-helix | 147-166 | 20 | |
| β-strand | 169-170 | 2 | 8 |
| α-helix | 173-182 | 10 | |
| α-helix | 184-187 | 4 | |
| β-strand | 189 | 1 | 9 |
| β-strand | 195 | 1 | 9 |
| α-helix | 200-214 | 15 | |
| α-helix | 216-218 | 3 | |
| α-helix | 242-247 | 6 | |
| β-strand | 249-256 | 8 | 10 |
| β-strand | 266-272 | 7 | 10 |
| β-strand | 275-278 | 4 | 11 |
| β-strand | 285 | 1 | 12 |
| α-helix | 286-293 | 8 | |
| β-strand | 295-297 | 3 | 10 |
| β-strand | 312-319 | 8 | 10 |
| β-strand | 321 | 1 | 13 |
| β-strand | 324-329 | 6 | 11 |
| β-strand | 348 | 1 | 12 |
| β-strand | 352-354 | 3 | 11 |
| α-helix | 356-358 | 3 | |
| β-strand | 359 | 1 | 10 |
| α-helix | 361-372 | 12 | |
| β-strand | 406 | 1 | 14 |
| β-strand | 409 | 1 | 14 |
| β-strand | 412 | 1 | 13 |
| β-strand | 417-427 | 11 | 11 |
| β-strand | 435-443 | 9 | 11 |
| β-strand | 446-451 | 6 | 11 |
| β-strand | 454-458 | 5 | 11 |
| α-helix | 460-464 | 5 | |
| α-helix | 465-467 | 3 | |
| β-strand | 474-482 | 9 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ubiquitin carboxyl-terminal hydrolase 14 | A, B | protein | 399 | Homo sapiens | P54578 (AlphaFold model) |
>6IIM_1 Ubiquitin carboxyl-terminal hydrolase 14 (chains A, B) QLASAMELPCGLTNLGNTCYMNATVQCIRSVPELKDALKRYAGALRASGEMASAQYITAA LRDLFDSMDKTSSSIPPIILLQFLHMAFPQFAEKGEQGQYLQQDANECWIQMMRVLQQKL EAIEDDSVKETDSSSASAATPSKKKSLIDQFFGVEFETTMKCTESEEEEVTKGKENQLQL SCFINQEVKYLFTGLKLRLQEEITKQSPTLQRNALYIKSSKISRLPAYLTIQMVRFFYKE KESVNAKVLKDVKFPLMLDMYELCTPELQEKMVSFRSKFKDLEDKKVNQQPNTSDKKSSP QKEVKYEPFSFADDIGSNNCGYYDLQAVLTHQGRSSSSGHYVSWVKRKQDEWIKFDDDKV SIVTPEDILRLSGGGDWHIAYVLLYGPRRVEIMEEESEQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| A8L | 1-[1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-2-(4-hydroxypiperidin-1-yl)e… | C19 H23 Cl N2 O2 | 2 |
Small molecule inhibitors reveal allosteric regulation of USP14 via steric blockade. Wang, Y., Jiang, Y., Ding, S. et al. Cell Res (2018) 28:1186-1194. DOI 10.1038/s41422-018-0091-x · PubMed
Other PDB entries of the same protein (UniProt P54578 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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