7VDQ: Cyclin-dependent kinase 5

The structure of cyclin-dependent kinase 5 (CDK5) in complex with p25 and Compound 7. Determined by X-ray diffraction at 2.91 Å resolution. Released 9 Mar 2022.

Method
X-ray diffraction
Resolution
2.91 Å
Organism
Homo sapiens
Chains
4
Atoms
6,944
Mol. weight
114.29 kDa
Ligands
64V
Released
9 Mar 2022

Explore 7VDQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7VDQ contains 42 α-helices and 22 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: 15 helices, 11 β-strands

ElementResiduesLengthSheet
β-strand4-13101
β-strand16-2381
β-strand29-3681
α-helix44-5512
β-strand6312
β-strand66-7271
β-strand75-8171
β-strand85-8622
α-helix87-937
α-helix100-11920
β-strand122-12323
α-helix129-1313
β-strand132-13432
β-strand140-14232
β-strand149-15023
α-helix165-1673
α-helix170-1734
α-helix182-19514
α-helix208-21912
α-helix221-2233
α-helix228-2325
α-helix257-26610
α-helix271-2733
α-helix275-2762
α-helix277-2815
α-helix284-2863
Chain B: 13 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand4-634
β-strand19-2354
β-strand29-3684
α-helix44-5512
β-strand6315
β-strand66-7274
β-strand75-8174
β-strand85-8625
α-helix87-937
α-helix100-11920
β-strand122-12326
α-helix129-1313
β-strand132-13435
β-strand140-14235
β-strand149-15026
α-helix165-1673
α-helix170-1734
α-helix182-19514
α-helix208-21912
α-helix228-2325
α-helix257-26610
α-helix271-2733
α-helix277-2815
α-helix284-2863
Chain C: 7 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix148-16215
α-helix172-18716
α-helix198-21114
α-helix219-23719
α-helix246-2483
α-helix254-27724
α-helix279-29012
Chain D: 7 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix148-1547
α-helix174-18714
α-helix198-20811
α-helix219-23719
α-helix246-2483
α-helix254-27724
α-helix279-29012

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Cyclin-dependent-like kinase 5A, Bprotein292Homo sapiensQ00535 (AlphaFold model)
Cyclin-dependent kinase 5 activator 1, p25C, Dprotein209Homo sapiensQ15078 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>7VDQ_1 Cyclin-dependent-like kinase 5 (chains A, B)
SQKYEKLEKIGEGTYGTVFKAKNRETHEIVALKRVRLDDDDEGVPSSALREICLLKELKH
KNIVRLHDVLHSDKKLTLVFEFCDQDLKKYFDSCNGDLDPEIVKSFLFQLLKGLGFCHSR
NVLHRDLKPQNLLINRNGELKLADFGLARAFGIPVRCYSAEVVTLWYRPPDVLFGAKLYS
TSIDMWSAGCIFAELANAGRPLFPGNDVDDQLKRIFRLLGTPTEEQWPSMTKLPDYKPYP
MYPATTSLVNVVPKLNATGRDLLQNLLKCNPVQRISAEEALQHPYFSDFCPP
Sequence of entity 2 (C, D), FASTA
>7VDQ_2 Cyclin-dependent kinase 5 activator 1, p25 (chains C, D)
MQPPPAQPPAPPASQLSGSQTGGSSSVKKAPHPAVTSAGTPKRVIVQASTSELLRCLGEF
LCRRCYRLKHLSPTDPVLWLRSVDRSLLLQGWQDQGFITPANVVFLYMLCRDVISSEVGS
DHELQAVLLTCLYLSYSYMGNEISYPLKPFLVESCKEAFWDRCLSVINLMSSKMLQINAD
PHYFTQVFSDLKNESGQEDKKRLLLGLDR

Ligands and cofactors

IDNameFormulaCopies
64V2-[[7-[[2-fluoranyl-4-[3-(hydroxymethyl)pyrazol-1-yl]phenyl]amino]-1,6-naphthyr…C26 H28 F N7 O32

Primary citation

Discovery and Optimization of Highly Selective Inhibitors of CDK5. Daniels, M.H., Malojcic, G., Clugston, S.L. et al. J Med Chem (2022) 65:3575-3596. DOI 10.1021/acs.jmedchem.1c02069 · PubMed

Other PDB entries of the same protein (UniProt Q00535 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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