5DMZ: PDB entry 5DMZ

Structure of human Bub1 kinase domain phosphorylated at Ser969. Determined by X-ray diffraction at 2.4 Å resolution. Released 16 Dec 2015.

Method
X-ray diffraction
Resolution
2.4 Å
Organism
Homo sapiens
Chains
2
Atoms
5,606
Mol. weight
84.75 kDa
Ligands
MG, ADP
Released
16 Dec 2015

Explore 5DMZ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 17 helices, 18 β-strands

ElementResiduesLengthSheet
β-strand737-73821
α-helix744-7529
α-helix758-7603
β-strand764-76632
α-helix770-7734
β-strand778-78142
β-strand786-795102
β-strand800-80562
β-strand817-82372
α-helix828-84013
α-helix843-8486
β-strand84913
α-helix850-8512
β-strand852-85762
β-strand862-86652
β-strand87313
α-helix874-88310
α-helix891-91020
β-strand913-91424
α-helix920-9223
β-strand923-92423
α-helix927-9304
β-strand943-94423
β-strand951-95224
α-helix9571
β-strand961-96221
α-helix974-9774
β-strand98211
α-helix985-100016
β-strand1006-100945
β-strand1012-101545
α-helix1025-103612
α-helix1044-10463
α-helix1047-106115
α-helix1066-108217
Chain B: 17 helices, 18 β-strands
ElementResiduesLengthSheet
β-strand736-73836
α-helix744-7529
α-helix758-7603
β-strand764-76747
α-helix770-7734
β-strand779-78247
β-strand785-795117
β-strand799-80577
β-strand818-82367
α-helix828-84013
α-helix843-8486
β-strand84918
β-strand852-85877
β-strand862-86657
β-strand87318
α-helix874-88310
α-helix891-91020
β-strand913-91429
α-helix920-9223
β-strand923-92428
α-helix927-9315
β-strand943-94428
β-strand951-95229
α-helix9571
β-strand960-96236
α-helix974-9774
β-strand98216
α-helix985-100016
β-strand1006-1009410
β-strand1012-1015410
α-helix1025-103612
α-helix1041-10433
α-helix1044-10463
α-helix1047-106115
α-helix1066-108116

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Mitotic checkpoint serine/threonine-protein kinase BUB1A, Bprotein365Homo sapiensO43683 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5DMZ_1 Mitotic checkpoint serine/threonine-protein kinase BUB1 (chains A, B)
GPMDPSSLGTVDAPNFIVGNPWDDKLIFKLLSGLSKPVSSYPNTFEWQCKLPAIKPKTEF
QLGSKLVYVHHLLGEGAFAQVYEATQGDLNDAKNKQKFVLKVQKPANPWEFYIGTQLMER
LKPSMQHMFMKFYSAHLFQNGSVLVGELYSYGTLLNAINLYKNTPEKVMPQGLVISFAMR
MLYMIEQVHDCEIIHGDIKPDNFILGNGFLEQDDEDDLSAGLALIDLGQSIDMKLFPKGT
IFTAKCETSGFQCVEMLSNKPWNYQIDYFGVAATVYCMLFGTYMKVKNEGGECKPEGLFR
RLPHLDMWNEFFHVMLNIPDCHHLPSLDLLRQKLKKVFQQHYTNKIRALRNRLIVLLLEC
KRSRK

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg2
ADPAdenosine-5'-diphosphateC10 H15 N5 O10 P22

Primary citation

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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