9DEK: USP7

USP7 in complex with macrocycle inhibitor MC02. Determined by X-ray diffraction at 2.0 Å resolution. Released 5 Mar 2025.

Method
X-ray diffraction
Resolution
2.0 Å
Organisms
Homo sapiens, synthetic construct
Chains
4
Atoms
6,155
Mol. weight
88.87 kDa
Released
5 Mar 2025

Explore 9DEK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

9DEK contains 42 α-helices and 43 β-strands across 4 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, 22 β-strands

ElementResiduesLengthSheet
β-strand21611
α-helix225-2339
α-helix236-2449
α-helix252-2543
α-helix256-26914
α-helix2731
β-strand27411
α-helix2751
α-helix277-2837
α-helix288-2925
α-helix296-31015
α-helix319-3246
β-strand326-33492
β-strand34012
β-strand343-34752
β-strand350-35233
β-strand35914
α-helix360-3689
α-helix369-3702
β-strand371-37332
β-strand379-38025
α-helix382-3843
β-strand386-38725
β-strand389-39572
β-strand401-40663
β-strand409-41246
β-strand417-42046
β-strand42614
β-strand430-43233
α-helix434-4363
β-strand43712
β-strand447-459133
β-strand462-46983
β-strand478-48143
β-strand484-48743
α-helix490-4934
α-helix495-4973
β-strand511-520103
α-helix524-5274
α-helix533-5353
α-helix538-55215
Chain B: 21 helices, 21 β-strands
ElementResiduesLengthSheet
β-strand21617
α-helix225-2339
α-helix236-2449
α-helix252-2543
α-helix256-26914
α-helix2731
β-strand27417
α-helix2751
α-helix277-2837
α-helix288-2925
α-helix296-31116
α-helix319-3246
β-strand326-33498
β-strand340-34788
β-strand350-35239
β-strand359110
α-helix360-3689
α-helix3701
β-strand371-37338
β-strand379-380211
α-helix382-3843
β-strand386-387211
β-strand389-39578
β-strand401-40669
β-strand409-412412
α-helix413-4153
β-strand417-420412
β-strand426110
β-strand430-43239
α-helix434-4363
β-strand43718
β-strand447-459139
β-strand462-46989
β-strand478-48149
β-strand484-48749
α-helix490-4934
α-helix495-4973
β-strand511-520109
α-helix521-5233
α-helix524-5274
α-helix533-5353
α-helix538-54710
Chains C and D: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix11-133

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ubiquitin carboxyl-terminal hydrolase 7A, Bprotein368Homo sapiensQ93009 (AlphaFold model)
Macrocycle peptide MC02C, Dprotein16synthetic construct
Sequence of entity 1 (A, B), FASTA
>9DEK_1 Ubiquitin carboxyl-terminal hydrolase 7 (chains A, B)
MGSSHHHHHHSSGLVPRGSHMKKHTGYVGLKNQGATCYMNSLLQTLFFTNQLRKAVYMMP
TEGDDSSKSVPLALQRVFYELQHSDKPVGTKKLTKSFGWETLDSFMQHDVQELCRVLLDN
VENKMKGTCVEGTIPKLFRGKMVSYIQCKEVDYRSDRREDYYDIQLSIKGKKNIFESFVD
YVAVEQLDGDNKYDAGEHGLQEAEKGVKFLTLPPVLHLQLMRFMYDPQTDQNIKINDRFE
FPEQLPLDEFLQKTDPKDPANYILHAVLVHSGDNHGGHYVVYLNPKGDGKWCKFDDDVVS
RCTKEEAIEHNYGGHDDDLSVRHCTNAYMLVYIRESKLSEVLQAVTDHDIPQQLVERLQE
EKRIEAQK
Sequence of entity 2 (C, D), FASTA
>9DEK_2 Macrocycle peptide  MC02 (chains C, D)
XFVTXGYLXVSXRRCG

Primary citation

Discovery and characterization of potent macrocycle inhibitors of ubiquitin-specific protease-7. Miranda, R., Anson, F., Smith, S.T. et al. Structure (2025) 33:705-717.e4. DOI 10.1016/j.str.2025.01.021 · PubMed

Other PDB entries of the same protein (UniProt Q93009 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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