5ZO8: Eg5 motor domain

Eg5 motor domain in complex with STLC-type inhibitor PVEI0021 (P21 type). Determined by X-ray diffraction at 2.2 Å resolution. Released 10 Oct 2018.

Method
X-ray diffraction
Resolution
2.2 Å
Organism
Homo sapiens
Chains
2
Atoms
5,467
Mol. weight
84.72 kDa
Ligands
4C5, MG, ADP
Released
10 Oct 2018

Explore 5ZO8 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5ZO8 contains 41 α-helices and 43 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: 21 helices, 22 β-strands

ElementResiduesLengthSheet
β-strand17-1821
α-helix191
β-strand20-2562
α-helix26-283
β-strand41-4443
β-strand49-5353
β-strand63-6753
β-strand70-7232
α-helix78-814
α-helix82-865
α-helix87-948
β-strand9714
β-strand98-10582
α-helix111-1155
β-strand11715
α-helix119-1202
α-helix121-1233
β-strand13315
α-helix135-14814
β-strand153-164122
β-strand167-17042
β-strand18212
β-strand183-18646
β-strand194-19746
β-strand202-20432
α-helix207-2093
α-helix210-22718
α-helix231-2344
β-strand236-248132
β-strand254-265122
α-helix266-2683
α-helix290-30314
α-helix311-3133
α-helix315-3195
α-helix321-3233
β-strand328-33692
α-helix340-3423
α-helix343-35513
α-helix356-3583
α-helix3591
β-strand360-36121
β-strand36514
β-strand36612
Chain B: 20 helices, 21 β-strands
ElementResiduesLengthSheet
β-strand17-1827
α-helix191
β-strand20-2568
α-helix26-283
β-strand41-4449
β-strand49-5359
β-strand63-6759
β-strand70-7238
α-helix78-814
α-helix82-865
α-helix87-948
β-strand97110
β-strand98-10588
α-helix111-1155
β-strand117111
α-helix119-1202
α-helix121-1233
β-strand133111
α-helix135-14814
β-strand153-164128
β-strand167-17048
β-strand18218
β-strand183-187512
β-strand190-197812
β-strand202-20438
α-helix207-2093
α-helix210-22718
α-helix231-2344
β-strand236-248138
β-strand254-265128
α-helix266-2683
α-helix290-30314
α-helix311-3133
α-helix315-3195
α-helix321-3233
β-strand329-33688
α-helix340-3423
α-helix343-35614
α-helix3591
β-strand360-36127
β-strand365110

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Kinesin-like protein KIF11A, Bprotein367Homo sapiensP52732 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5ZO8_1 Kinesin-like protein KIF11 (chains A, B)
MNHKVHMKNIQVVVRCRPFNLAERKASAHSIVECDPVRKEVSVRTGGLADKSSRKTYTFD
MVFGASTKQIDVYRSVVCPILDEVIMGYNCTIFAYGQTGTGKTFTMEGERSPNEEYTWEE
DPLAGIIPRTLHQIFEKLTDNGTEFSVKVSLLEIYNEELFDLLNPSSDVSERLQMFDDPR
NKRGVIIKGLEEITVHNKDEVYQILEKGAAKRTTAATLMNAYSSRSHSVFSVTIHMKETT
IDGEELVKIGKLNLVDLAGSENIGRSGAVDKRAREAGNINQSLLTLGRVITALVERTPHV
PYRESKLTRILQDSLGGRTRTSIIATISPASLNLEETLSTLEYAHRAKNILNKPEVNQKL
QHHHHHH

Ligands and cofactors

IDNameFormulaCopies
4C5(2R)-2-azanyl-3-[(4-methoxyphenyl)-diphenyl-methyl]sulfanyl-propanoic acidC23 H23 N O3 S2
MGMagnesium ionMg2
ADPAdenosine-5'-diphosphateC10 H15 N5 O10 P22

Water and common crystallization additives (NA, SO4) are not listed.

Primary citation

Structural and Thermodynamic Basis of the Enhanced Interaction between Kinesin Spindle Protein Eg5 and STLC-type Inhibitors. Yokoyama, H., Sawada, J.I., Sato, K. et al. ACS Omega (2018) 3:12284-12294. DOI 10.1021/acsomega.8b00778 · PubMed

Other PDB entries of the same protein (UniProt P52732 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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