7OKW

1.62A X-ray crystal structure of the conserved C-terminal (CCT) of human OSR1

Summary for 7OKW

• Entry DOI: 10.2210/pdb7okw/pdb
• Related: 7o86
• Descriptor: Serine/threonine-protein kinase OSR1, (4S)-2-METHYL-2,4-PENTANEDIOL, CALCIUM ION, ... (6 entities in total)
• Functional Keywords: kinase, transferase, cct, signaling protein
• Biological source: Homo sapiens (Human)
• Total number of polymer chains: 2
• Total formula weight: 22962.32

Authors

Bax, B.D.,Elvers, K.T.,Lipka-Lloyd, M.,Mehellou, Y. (deposition date: 2021-05-18, release date: 2021-09-22, Last modification date: 2024-01-31)

Primary citation

Elvers, K.T.,Lipka-Lloyd, M.,Trueman, R.C.,Bax, B.D.,Mehellou, Y.
Structures of the Human SPAK and OSR1 Conserved C-Terminal (CCT) Domains.
Chembiochem, 23:e202100441-e202100441, 2022

PubMed Abstract: STE20/SPS1-related proline/alanine-rich kinase (SPAK) and oxidative stress responsive 1 (OSR1) kinase are two serine/threonine protein kinases that regulate the function of ion co-transporters through phosphorylation. The highly conserved C-terminal (CCT) domains of SPAK and OSR1 bind to RFx[V/I] peptide sequences from their upstream 'With No Lysine Kinases (WNKs), facilitating their activation via phosphorylation. Thus, the inhibition of SPAK and OSR1 binding, via their CCT domains, to WNK kinases is a plausible strategy for inhibiting SPAK and OSR1 kinases. To facilitate structure-guided drug design of such inhibitors, we expressed and purified human SPAK and OSR1 CCT domains and solved their crystal structures. Interestingly, these crystal structures show a highly conserved primary pocket adjacent to a flexible secondary pocket. We also employed a biophysical strategy and determined the affinity of SPAK and OSR1 CCT domains to short peptides derived from WNK4 and NKCC1. Together, this work provides a platform that facilitates the design of CCT domain specific small molecule binders that inhibit SPAK- and OSR1-activation by WNK kinases, and these could be useful in treating hypertension and ischemic stroke.

PubMed: 34726826
DOI: 10.1002/cbic.202100441

Experimental method

X-RAY DIFFRACTION (1.62 Å)