8FEC: J-PKAc chimera

Structure of J-PKAc chimera complexed with Aplithianine derivative. Determined by X-ray diffraction at 2.7 Å resolution. Released 18 Oct 2023.

Method
X-ray diffraction
Resolution
2.7 Å
Organism
Homo sapiens
Chains
4
Atoms
7,064
Mol. weight
100.31 kDa
Ligands
XU0
Released
18 Oct 2023

Explore 8FEC in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

8FEC contains 45 α-helices and 30 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: 19 helices, 14 β-strands

ElementResiduesLengthSheet
α-helix4-74
α-helix16-2914
α-helix41-5515
α-helix57-8630
α-helix95-973
β-strand98-10691
β-strand111-11771
β-strand123-13081
α-helix131-1366
α-helix140-15213
β-strand15812
β-strand161-16661
β-strand170-17671
β-strand18212
α-helix183-1897
α-helix195-21420
β-strand217-21823
α-helix224-2263
β-strand227-22932
β-strand235-23732
β-strand244-24523
β-strand25014
β-strand25515
α-helix257-2593
α-helix262-2654
β-strand27014
α-helix273-28816
α-helix298-30710
α-helix318-32710
α-helix344-3474
α-helix350-3523
α-helix357-3615
α-helix386-3894
Chain B: 23 helices, 14 β-strands
ElementResiduesLengthSheet
α-helix4-74
α-helix16-2813
α-helix32-343
α-helix40-5516
α-helix57-8630
α-helix95-973
β-strand98-10586
β-strand111-11776
β-strand123-13086
α-helix131-1366
α-helix140-15011
β-strand15817
α-helix159-1602
β-strand161-16666
β-strand170-17676
α-helix1771
β-strand18217
α-helix183-1908
α-helix195-21420
β-strand217-21828
α-helix224-2263
β-strand227-22937
β-strand235-23737
β-strand244-24528
β-strand25019
β-strand255110
α-helix257-2593
α-helix262-2654
β-strand27019
α-helix273-28816
α-helix298-30710
α-helix318-32710
α-helix332-3343
α-helix343-3475
α-helix350-3523
α-helix357-3626
α-helix366-3672
Chain I: 2 helices, 1 β-strand
ElementResiduesLengthSheet
α-helix6-127
α-helix18-214
β-strand2215
Chain J: 1 helix, 1 β-strand
ElementResiduesLengthSheet
α-helix6-127
β-strand22110

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alphaAprotein405Homo sapiensP17612 (AlphaFold model), P25685 (AlphaFold model)
cAMP-dependent protein kinase inhibitor alphaI, Jprotein20Homo sapiensP61925 (AlphaFold model)
DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alphaBprotein405Homo sapiensP17612 (AlphaFold model), P25685 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>8FEC_1 DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alpha (chains A)
GKDYYQTLGLARGASDEEIKRAYRRQALRYHPDKNKEPGAEEKFKEIAEAYDVLSDPRKR
EIFDRYGEEVKEFLAKAKEDFLKKWESPAQNTAHLDQFERIKTLGTGSFGRVMLVKHKET
GNHYAMKILDKQKVVKLKQIEHTLNEKRILQAVNFPFLVKLEFSFKDNSNLYMVMEYVPG
GEMFSHLRRIGRFSEPHARFYAAQIVLTFEYLHSLDLIYRDLKPENLLIDQQGYIQVTDF
GFAKRVKGRTWTLCGTPEYLAPEIILSKGYNKAVDWWALGVLIYEMAAGYPPFFADQPIQ
IYEKIVSGKVRFPSHFSSDLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATTDWIAI
YQRKVEAPFIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF
Sequence of entity 2 (I, J), FASTA
>8FEC_2 cAMP-dependent protein kinase inhibitor alpha (chains I, J)
TTYADFIASGRTGRRNAIHD
Sequence of entity 3 (B), FASTA
>8FEC_3 DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alpha (chains B)
GKDYYQTLGLARGASDEEIKRAYRRQALRYHPDKNKEPGAEEKFKEIAEAYDVLSDPRKR
EIFDRYGEEVKEFLAKAKEDFLKKWESPAQNTAHLDQFERIKTLGTGSFGRVMLVKHKET
GNHYAMKILDKQKVVKLKQIEHTLNEKRILQAVNFPFLVKLEFSFKDNSNLYMVMEYVPG
GEMFSHLRRIGRFSEPHARFYAAQIVLTFEYLHSLDLIYRDLKPENLLIDQQGYIQVTDF
GFAKRVKGRTWTLCGTPEYLAPEIILSKGYNKAVDWWALGVLIYEMAAGYPPFFADQPIQ
IYEKIVSGKVRFPSHFSSDLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATTDWIAI
YQRKVEAPFIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF

Ligands and cofactors

IDNameFormulaCopies
XU06-[(6P)-6-(4-bromo-1-methyl-1H-imidazol-5-yl)-2,3-dihydro-4H-1,4-thiazin-4-yl]-…C13 H12 Br N7 S2

Primary citation

Discovery and Synthesis of a Naturally Derived Protein Kinase Inhibitor that Selectively Inhibits Distinct Classes of Serine/Threonine Kinases. Du, L., Wilson, B.A.P., Li, N. et al. J Nat Prod (2023) 86:2283-2293. DOI 10.1021/acs.jnatprod.3c00394 · PubMed

Other PDB entries of the same protein (UniProt P17612 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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