2FME: Mitotic kinesin eg5

Crystal structure of the mitotic kinesin eg5 (ksp) in complex with mg-adp and (r)-4-(3-hydroxyphenyl)-n,n,7,8-tetramethyl-3,4-dihydroisoquinoline-2(1h)-carboxamide. Determined by X-ray diffraction at 2.1 Å resolution. Released 18 Apr 2006.

Method
X-ray diffraction
Resolution
2.1 Å
Organism
Homo sapiens
Chains
2
Atoms
5,282
Mol. weight
83.66 kDa
Ligands
MG, 3QC, ADP
Released
18 Apr 2006

Explore 2FME in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2FME contains 42 α-helices and 42 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, 21 β-strands

ElementResiduesLengthSheet
β-strand1811
β-strand20-2562
α-helix26-283
α-helix30-323
β-strand3913
β-strand41-4444
β-strand49-5354
β-strand62-6764
β-strand70-7232
α-helix78-814
α-helix82-865
α-helix87-948
β-strand98-10472
α-helix111-1155
β-strand11715
α-helix119-1202
α-helix121-1233
α-helix127-1293
β-strand13315
α-helix135-14612
β-strand154-164112
β-strand167-17042
β-strand181-18222
β-strand183-18646
β-strand194-19746
β-strand202-20322
α-helix207-2093
α-helix210-22718
α-helix231-2344
β-strand236-245102
β-strand258-26582
α-helix266-2683
α-helix269-2713
α-helix290-30415
α-helix311-3133
α-helix315-3195
α-helix321-3233
β-strand329-33682
β-strand33913
α-helix340-3423
α-helix343-35614
β-strand36011
Chain B: 21 helices, 21 β-strands
ElementResiduesLengthSheet
β-strand1817
β-strand20-2568
α-helix26-283
α-helix30-323
β-strand3919
β-strand41-4444
β-strand49-5574
β-strand62-6764
β-strand70-7238
α-helix78-814
α-helix82-865
α-helix87-948
β-strand98-10478
α-helix111-1155
β-strand117110
α-helix119-1202
α-helix121-1233
α-helix127-1293
β-strand133110
α-helix135-14612
β-strand154-164118
β-strand167-17048
β-strand181-18228
β-strand183-186411
β-strand194-197411
β-strand202-20328
α-helix207-2093
α-helix210-22718
α-helix231-2344
β-strand236-248138
β-strand254-265128
α-helix266-2683
α-helix269-2713
α-helix290-30415
α-helix311-3133
α-helix315-3195
α-helix321-3233
β-strand329-33688
β-strand33919
α-helix340-3423
α-helix343-35614
β-strand36017

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Kinesin-like protein KIF11A, Bprotein368Homo sapiensP52732 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>2FME_1 Kinesin-like protein KIF11 (chains A, B)
MASQPNSSAKKKEEKGKNIQVVVRCRPFNLAERKASAHSIVECDPVRKEVSVRTGGLADK
SSRKTYTFDMVFGASTKQIDVYRSVVCPILDEVIMGYNCTIFAYGQTGTGKTFTMEGERS
PNEEYTWEEDPLAGIIPRTLHQIFEKLTDNGTEFSVKVSLLEIYNEELFDLLNPSSDVSE
RLQMFDDPRNKRGVIIKGLEEITVHNKDEVYQILEKGAAKRTTAATLMNAYSSRSHSVFS
VTIHMKETTIDGEELVKIGKLNLVDLAGSENIGRSGAVDKRAREAGNINQSLLTLGRVIT
ALVERTPHVPYRESKLTRILQDSLGGRTRTSIIATISPASLNLEETLSTLEYAHRAKNIL
NKPEVNQK

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg2
3QC(4R)-4-(3-hydroxyphenyl)-N,N,7,8-tetramethyl-3,4-dihydroisoquinoline-2(1H)-carb…C20 H24 N2 O22
ADPAdenosine-5'-diphosphateC10 H15 N5 O10 P22

Primary citation

Inhibitors of human mitotic kinesin Eg5: Characterization of the 4-phenyl-tetrahydroisoquinoline lead series. Tarby, C.M., Kaltenbach III, R.F., Huynh, T. et al. Bioorg Med Chem Lett (2006) 16:2095-2100. DOI 10.1016/j.bmcl.2006.01.056 · 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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