4YPD: DAPK1 catalytic domain

Crystal Structure of DAPK1 catalytic domain in complex with the hinge binding fragment 4-methylpyridazine. Determined by X-ray diffraction at 1.4 Å resolution. Released 13 May 2015.

Method
X-ray diffraction
Resolution
1.4 Å
Organism
Homo sapiens
Chains
1
Atoms
2,909
Mol. weight
34.02 kDa
Ligands
DKG
Released
13 May 2015

Explore 4YPD in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4YPD contains 16 α-helices and 16 β-strands across 1 chain. 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: 16 helices, 16 β-strands

ElementResiduesLengthSheet
β-strand511
α-helix9-113
β-strand13-2191
β-strand25-3281
β-strand38-4581
β-strand4612
α-helix471
β-strand5612
α-helix58-7013
β-strand7613
α-helix77-782
β-strand79-8461
β-strand88-9471
β-strand10013
α-helix101-1088
α-helix113-13220
β-strand135-13624
α-helix142-1443
β-strand145-14733
β-strand157-15933
β-strand166-16724
β-strand17315
α-helix181-1833
α-helix186-1894
β-strand19415
α-helix197-21216
α-helix222-2309
α-helix238-2414
α-helix246-2538
α-helix260-2623
α-helix264-2652
α-helix266-2716

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Death-associated protein kinase 1Aprotein294Homo sapiensP53355 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4YPD_1 Death-associated protein kinase 1 (chains A)
TVFRQENVDDYYDTGEELGSGQFAVVKKCREKSTGLQYAAKFIKKRRTKSSRRGVSREDI
EREVSILKEIQHPNVITLHEVYENKTDVILILELVAGGELFDFLAEKESLTEEEATEFLK
QILNGVYYLHSLQIAHFDLKPENIMLLDRNVPKPRIKIIDFGLAHKIDFGNEFKNIFGTP
EFVAPEIVNYEPLGLEADMWSIGVITYILLSGASPFLGDTKQETLANVSAVNYEFEDEYF
SNTSALAKDFIRRLLVKDPKKRMTIQDSLQHPWIKPKDTQQALSSAWSHPQFEK

Ligands and cofactors

IDNameFormulaCopies
DKG4-methylpyridazineC5 H6 N21

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

Primary citation

Crystal Structure of DAPK1 catalytic domain in complex with hinge binding fragments. Grum-Tokars, V.L., Minasov, G., Roy, S.M. et al. To be published.

Other PDB entries of the same protein (UniProt P53355 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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