5XZV: Rad53 1-466

Crystal structure of Rad53 1-466 in complex with AMP-PNP. Determined by X-ray diffraction at 3.1 Å resolution. Released 11 Oct 2017.

Method
X-ray diffraction
Resolution
3.1 Å
Organism
Saccharomyces cerevisiae (strain ATCC 204508 / S288c)
Chains
2
Atoms
5,444
Mol. weight
106.03 kDa
Ligands
ANP
Released
11 Oct 2017

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

Secondary structure: helices and β-sheets

5XZV contains 32 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: 15 helices, 22 β-strands

ElementResiduesLengthSheet
α-helix17-226
β-strand32-3871
β-strand46-4941
α-helix52-576
β-strand64-6852
β-strand88-9362
α-helix95-973
β-strand99-10462
β-strand109-11131
β-strand114-11521
β-strand11812
β-strand122-12432
β-strand129-13351
β-strand140-14781
α-helix149-16315
β-strand197-206103
β-strand210-21783
β-strand223-23083
α-helix231-2344
α-helix238-24811
β-strand25614
β-strand259-26463
β-strand268-27473
β-strand28014
α-helix281-2888
α-helix293-31220
β-strand31615
α-helix322-3243
β-strand325-32954
β-strand334-33744
β-strand34315
α-helix364-3663
α-helix384-40219
α-helix413-42210
α-helix434-4363
α-helix437-4437
α-helix457-4626
Chain B: 17 helices, 20 β-strands
ElementResiduesLengthSheet
β-strand34-3856
α-helix44-452
β-strand46-4836
α-helix52-565
β-strand64-6967
β-strand76-7727
β-strand89-9357
β-strand99-10357
β-strand110-11126
β-strand114-11526
β-strand121-12447
β-strand129-13136
β-strand143-14756
α-helix149-1568
α-helix192-1954
β-strand197-19938
β-strand210-21788
β-strand222-22988
α-helix240-25011
β-strand25619
β-strand259-26468
β-strand269-27468
β-strand28019
α-helix281-2888
α-helix293-31220
α-helix322-3243
β-strand325-32959
β-strand334-33749
α-helix359-3613
α-helix364-3674
α-helix384-40320
α-helix413-4219
α-helix427-4326
α-helix437-44610
α-helix451-4533
α-helix455-4562
α-helix457-4615

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Serine/threonine-protein kinase RAD53A, Bprotein471Saccharomyces cerevisiae (strain ATCC 204508 / S288c)P22216 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5XZV_1 Serine/threonine-protein kinase RAD53 (chains A, B)
MENITQPTQQSTQATQRFLIEKFSQEQIGENIVCRVICTTGQIPIRDLSADISQVLKEKR
SIKKVWTFGRNPACDYHLGNISRLSNKHFQILLGEDGNLLLNDISTNGTWLNGQKVEKNS
NQLLSQGDEITVGVGVESDILSLVIFINDKFKQCLEQNKVDRIRSNLKNTSKIASPGLTS
STASSMVANKTGIFKDFSIIDEVVGQGAFATVKKAIERTTGKTFAVKIISKRKVIGNMDG
VTRELEVLQKLNHPRIVRLKGFYEDTESYYMVMEFVSGGDLMDFVAAHGAVGEDAGREIS
RQILTAIKYIHSMGISHRDLKPDNILIEQDDPVLVKITDFGLAKVQGNGSFMKTFCGTLA
YVAPEVIRGKDTSVSPDEYEERNEYSSLVDMWSMGCLVYVILTGHLPFSGSTQDQLYKQI
GRGSYHEGPLKDFRISEEARDFIDSLLQVDPNNRSTAAKALNHPWIVDSSN

Ligands and cofactors

IDNameFormulaCopies
ANPPhosphoaminophosphonic acid-adenylate esterC10 H17 N6 O12 P32

Primary citation

Phospho-Priming Confers Functionally Relevant Specificities for Rad53 Kinase Autophosphorylation. Chen, E.S., Weng, J.H., Chen, Y.H. et al. Biochemistry (2017) 56:5112-5124. DOI 10.1021/acs.biochem.7b00689 · PubMed

Other PDB entries of the same protein (UniProt P22216 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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