Structure of human Bub1 kinase domain phosphorylated at Ser969. Determined by X-ray diffraction at 2.4 Å resolution. Released 16 Dec 2015.
Explore 5DMZ in 3D Show helices and sheets RCSB PDB PDBe
5DMZ contains 34 α-helices and 36 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 |
|---|---|---|---|
| β-strand | 737-738 | 2 | 1 |
| α-helix | 744-752 | 9 | |
| α-helix | 758-760 | 3 | |
| β-strand | 764-766 | 3 | 2 |
| α-helix | 770-773 | 4 | |
| β-strand | 778-781 | 4 | 2 |
| β-strand | 786-795 | 10 | 2 |
| β-strand | 800-805 | 6 | 2 |
| β-strand | 817-823 | 7 | 2 |
| α-helix | 828-840 | 13 | |
| α-helix | 843-848 | 6 | |
| β-strand | 849 | 1 | 3 |
| α-helix | 850-851 | 2 | |
| β-strand | 852-857 | 6 | 2 |
| β-strand | 862-866 | 5 | 2 |
| β-strand | 873 | 1 | 3 |
| α-helix | 874-883 | 10 | |
| α-helix | 891-910 | 20 | |
| β-strand | 913-914 | 2 | 4 |
| α-helix | 920-922 | 3 | |
| β-strand | 923-924 | 2 | 3 |
| α-helix | 927-930 | 4 | |
| β-strand | 943-944 | 2 | 3 |
| β-strand | 951-952 | 2 | 4 |
| α-helix | 957 | 1 | |
| β-strand | 961-962 | 2 | 1 |
| α-helix | 974-977 | 4 | |
| β-strand | 982 | 1 | 1 |
| α-helix | 985-1000 | 16 | |
| β-strand | 1006-1009 | 4 | 5 |
| β-strand | 1012-1015 | 4 | 5 |
| α-helix | 1025-1036 | 12 | |
| α-helix | 1044-1046 | 3 | |
| α-helix | 1047-1061 | 15 | |
| α-helix | 1066-1082 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 736-738 | 3 | 6 |
| α-helix | 744-752 | 9 | |
| α-helix | 758-760 | 3 | |
| β-strand | 764-767 | 4 | 7 |
| α-helix | 770-773 | 4 | |
| β-strand | 779-782 | 4 | 7 |
| β-strand | 785-795 | 11 | 7 |
| β-strand | 799-805 | 7 | 7 |
| β-strand | 818-823 | 6 | 7 |
| α-helix | 828-840 | 13 | |
| α-helix | 843-848 | 6 | |
| β-strand | 849 | 1 | 8 |
| β-strand | 852-858 | 7 | 7 |
| β-strand | 862-866 | 5 | 7 |
| β-strand | 873 | 1 | 8 |
| α-helix | 874-883 | 10 | |
| α-helix | 891-910 | 20 | |
| β-strand | 913-914 | 2 | 9 |
| α-helix | 920-922 | 3 | |
| β-strand | 923-924 | 2 | 8 |
| α-helix | 927-931 | 5 | |
| β-strand | 943-944 | 2 | 8 |
| β-strand | 951-952 | 2 | 9 |
| α-helix | 957 | 1 | |
| β-strand | 960-962 | 3 | 6 |
| α-helix | 974-977 | 4 | |
| β-strand | 982 | 1 | 6 |
| α-helix | 985-1000 | 16 | |
| β-strand | 1006-1009 | 4 | 10 |
| β-strand | 1012-1015 | 4 | 10 |
| α-helix | 1025-1036 | 12 | |
| α-helix | 1041-1043 | 3 | |
| α-helix | 1044-1046 | 3 | |
| α-helix | 1047-1061 | 15 | |
| α-helix | 1066-1081 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Mitotic checkpoint serine/threonine-protein kinase BUB1 | A, B | protein | 365 | Homo sapiens | O43683 (AlphaFold model) |
>5DMZ_1 Mitotic checkpoint serine/threonine-protein kinase BUB1 (chains A, B) GPMDPSSLGTVDAPNFIVGNPWDDKLIFKLLSGLSKPVSSYPNTFEWQCKLPAIKPKTEF QLGSKLVYVHHLLGEGAFAQVYEATQGDLNDAKNKQKFVLKVQKPANPWEFYIGTQLMER LKPSMQHMFMKFYSAHLFQNGSVLVGELYSYGTLLNAINLYKNTPEKVMPQGLVISFAMR MLYMIEQVHDCEIIHGDIKPDNFILGNGFLEQDDEDDLSAGLALIDLGQSIDMKLFPKGT IFTAKCETSGFQCVEMLSNKPWNYQIDYFGVAATVYCMLFGTYMKVKNEGGECKPEGLFR RLPHLDMWNEFFHVMLNIPDCHHLPSLDLLRQKLKKVFQQHYTNKIRALRNRLIVLLLEC KRSRK
Role of Intrinsic and Extrinsic Factors in the Regulation of the Mitotic Checkpoint Kinase Bub1. Breit, C., Bange, T., Petrovic, A. et al. PLoS One (2015) 10:e0144673-e0144673. DOI 10.1371/journal.pone.0144673 · PubMed
Other PDB entries of the same protein (UniProt O43683 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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