6IIM: USP14 catalytic domain with IU1-206

USP14 catalytic domain with IU1-206. Determined by X-ray diffraction at 2.21 Å resolution. Released 12 Dec 2018.

Method
X-ray diffraction
Resolution
2.21 Å
Organism
Homo sapiens
Chains
2
Atoms
5,712
Mol. weight
91.9 kDa
Ligands
A8L
Released
12 Dec 2018

Explore 6IIM in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 19 helices, 23 β-strands

ElementResiduesLengthSheet
α-helix103-1053
β-strand106-10721
α-helix114-12411
α-helix127-1359
α-helix147-16519
β-strand169-17021
α-helix173-18210
α-helix184-1874
β-strand18912
α-helix1941
β-strand19512
α-helix196-1972
α-helix200-21415
α-helix216-2183
α-helix242-2476
β-strand249-25793
α-helix264-2652
β-strand266-27273
β-strand275-27844
β-strand28515
α-helix286-2938
β-strand295-30283
β-strand307-319133
β-strand32116
β-strand324-32964
β-strand33117
α-helix3411
β-strand34217
α-helix3431
β-strand34815
β-strand352-35434
α-helix356-3583
β-strand35913
α-helix361-37515
β-strand41216
β-strand417-427114
β-strand435-44394
β-strand446-45164
β-strand454-45854
α-helix460-4645
α-helix465-4673
β-strand474-48294
Chain B: 13 helices, 23 β-strands
ElementResiduesLengthSheet
β-strand106-10728
α-helix114-12411
α-helix127-1359
α-helix147-16620
β-strand169-17028
α-helix173-18210
α-helix184-1874
β-strand18919
β-strand19519
α-helix200-21415
α-helix216-2183
α-helix242-2476
β-strand249-256810
β-strand266-272710
β-strand275-278411
β-strand285112
α-helix286-2938
β-strand295-297310
β-strand312-319810
β-strand321113
β-strand324-329611
β-strand348112
β-strand352-354311
α-helix356-3583
β-strand359110
α-helix361-37212
β-strand406114
β-strand409114
β-strand412113
β-strand417-4271111
β-strand435-443911
β-strand446-451611
β-strand454-458511
α-helix460-4645
α-helix465-4673
β-strand474-482911

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ubiquitin carboxyl-terminal hydrolase 14A, Bprotein399Homo sapiensP54578 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6IIM_1 Ubiquitin carboxyl-terminal hydrolase 14 (chains A, B)
QLASAMELPCGLTNLGNTCYMNATVQCIRSVPELKDALKRYAGALRASGEMASAQYITAA
LRDLFDSMDKTSSSIPPIILLQFLHMAFPQFAEKGEQGQYLQQDANECWIQMMRVLQQKL
EAIEDDSVKETDSSSASAATPSKKKSLIDQFFGVEFETTMKCTESEEEEVTKGKENQLQL
SCFINQEVKYLFTGLKLRLQEEITKQSPTLQRNALYIKSSKISRLPAYLTIQMVRFFYKE
KESVNAKVLKDVKFPLMLDMYELCTPELQEKMVSFRSKFKDLEDKKVNQQPNTSDKKSSP
QKEVKYEPFSFADDIGSNNCGYYDLQAVLTHQGRSSSSGHYVSWVKRKQDEWIKFDDDKV
SIVTPEDILRLSGGGDWHIAYVLLYGPRRVEIMEEESEQ

Ligands and cofactors

IDNameFormulaCopies
A8L1-[1-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-2-(4-hydroxypiperidin-1-yl)e…C19 H23 Cl N2 O22

Primary citation

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:

Browse structure collections

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