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.
Explore 5XZV in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 17-22 | 6 | |
| β-strand | 32-38 | 7 | 1 |
| β-strand | 46-49 | 4 | 1 |
| α-helix | 52-57 | 6 | |
| β-strand | 64-68 | 5 | 2 |
| β-strand | 88-93 | 6 | 2 |
| α-helix | 95-97 | 3 | |
| β-strand | 99-104 | 6 | 2 |
| β-strand | 109-111 | 3 | 1 |
| β-strand | 114-115 | 2 | 1 |
| β-strand | 118 | 1 | 2 |
| β-strand | 122-124 | 3 | 2 |
| β-strand | 129-133 | 5 | 1 |
| β-strand | 140-147 | 8 | 1 |
| α-helix | 149-163 | 15 | |
| β-strand | 197-206 | 10 | 3 |
| β-strand | 210-217 | 8 | 3 |
| β-strand | 223-230 | 8 | 3 |
| α-helix | 231-234 | 4 | |
| α-helix | 238-248 | 11 | |
| β-strand | 256 | 1 | 4 |
| β-strand | 259-264 | 6 | 3 |
| β-strand | 268-274 | 7 | 3 |
| β-strand | 280 | 1 | 4 |
| α-helix | 281-288 | 8 | |
| α-helix | 293-312 | 20 | |
| β-strand | 316 | 1 | 5 |
| α-helix | 322-324 | 3 | |
| β-strand | 325-329 | 5 | 4 |
| β-strand | 334-337 | 4 | 4 |
| β-strand | 343 | 1 | 5 |
| α-helix | 364-366 | 3 | |
| α-helix | 384-402 | 19 | |
| α-helix | 413-422 | 10 | |
| α-helix | 434-436 | 3 | |
| α-helix | 437-443 | 7 | |
| α-helix | 457-462 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 34-38 | 5 | 6 |
| α-helix | 44-45 | 2 | |
| β-strand | 46-48 | 3 | 6 |
| α-helix | 52-56 | 5 | |
| β-strand | 64-69 | 6 | 7 |
| β-strand | 76-77 | 2 | 7 |
| β-strand | 89-93 | 5 | 7 |
| β-strand | 99-103 | 5 | 7 |
| β-strand | 110-111 | 2 | 6 |
| β-strand | 114-115 | 2 | 6 |
| β-strand | 121-124 | 4 | 7 |
| β-strand | 129-131 | 3 | 6 |
| β-strand | 143-147 | 5 | 6 |
| α-helix | 149-156 | 8 | |
| α-helix | 192-195 | 4 | |
| β-strand | 197-199 | 3 | 8 |
| β-strand | 210-217 | 8 | 8 |
| β-strand | 222-229 | 8 | 8 |
| α-helix | 240-250 | 11 | |
| β-strand | 256 | 1 | 9 |
| β-strand | 259-264 | 6 | 8 |
| β-strand | 269-274 | 6 | 8 |
| β-strand | 280 | 1 | 9 |
| α-helix | 281-288 | 8 | |
| α-helix | 293-312 | 20 | |
| α-helix | 322-324 | 3 | |
| β-strand | 325-329 | 5 | 9 |
| β-strand | 334-337 | 4 | 9 |
| α-helix | 359-361 | 3 | |
| α-helix | 364-367 | 4 | |
| α-helix | 384-403 | 20 | |
| α-helix | 413-421 | 9 | |
| α-helix | 427-432 | 6 | |
| α-helix | 437-446 | 10 | |
| α-helix | 451-453 | 3 | |
| α-helix | 455-456 | 2 | |
| α-helix | 457-461 | 5 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Serine/threonine-protein kinase RAD53 | A, B | protein | 471 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | P22216 (AlphaFold model) |
>5XZV_1 Serine/threonine-protein kinase RAD53 (chains A, B) MENITQPTQQSTQATQRFLIEKFSQEQIGENIVCRVICTTGQIPIRDLSADISQVLKEKR SIKKVWTFGRNPACDYHLGNISRLSNKHFQILLGEDGNLLLNDISTNGTWLNGQKVEKNS NQLLSQGDEITVGVGVESDILSLVIFINDKFKQCLEQNKVDRIRSNLKNTSKIASPGLTS STASSMVANKTGIFKDFSIIDEVVGQGAFATVKKAIERTTGKTFAVKIISKRKVIGNMDG VTRELEVLQKLNHPRIVRLKGFYEDTESYYMVMEFVSGGDLMDFVAAHGAVGEDAGREIS RQILTAIKYIHSMGISHRDLKPDNILIEQDDPVLVKITDFGLAKVQGNGSFMKTFCGTLA YVAPEVIRGKDTSVSPDEYEERNEYSSLVDMWSMGCLVYVILTGHLPFSGSTQDQLYKQI GRGSYHEGPLKDFRISEEARDFIDSLLQVDPNNRSTAAKALNHPWIVDSSN
| ID | Name | Formula | Copies |
|---|---|---|---|
| ANP | Phosphoaminophosphonic acid-adenylate ester | C10 H17 N6 O12 P3 | 2 |
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:
MolViewer shows 5XZV directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.