Human MST3 (STK24) kinase in complex with inhibitor MR24. Determined by X-ray diffraction at 1.85 Å resolution. Released 8 Nov 2023.
Explore 8QLR in 3D Show helices and sheets RCSB PDB PDBe
8QLR contains 37 α-helices and 20 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 |
|---|---|---|---|
| β-strand | 27 | 1 | 3 |
| α-helix | 32-35 | 4 | |
| β-strand | 36-44 | 9 | 3 |
| β-strand | 49-55 | 7 | 3 |
| β-strand | 61-68 | 8 | 3 |
| α-helix | 76-88 | 13 | |
| β-strand | 94 | 1 | 4 |
| α-helix | 95-96 | 2 | |
| β-strand | 97-103 | 7 | 3 |
| β-strand | 106-112 | 7 | 3 |
| β-strand | 118 | 1 | 4 |
| α-helix | 119-122 | 4 | |
| α-helix | 127-129 | 3 | |
| α-helix | 130-149 | 20 | |
| α-helix | 159-161 | 3 | |
| β-strand | 162-164 | 3 | 4 |
| β-strand | 170-172 | 3 | 4 |
| α-helix | 175-177 | 3 | |
| α-helix | 200-203 | 4 | |
| α-helix | 211-226 | 16 | |
| α-helix | 236-245 | 10 | |
| α-helix | 247-249 | 3 | |
| α-helix | 257-266 | 10 | |
| α-helix | 271-273 | 3 | |
| α-helix | 275-276 | 2 | |
| α-helix | 277-280 | 4 | |
| α-helix | 284-289 | 6 | |
| α-helix | 293-295 | 3 | |
| α-helix | 296-301 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 27 | 1 | 1 |
| α-helix | 32-35 | 4 | |
| β-strand | 36-44 | 9 | 1 |
| β-strand | 48-55 | 8 | 1 |
| β-strand | 60-68 | 9 | 1 |
| α-helix | 76-87 | 12 | |
| β-strand | 94 | 1 | 2 |
| α-helix | 95-96 | 2 | |
| β-strand | 97-103 | 7 | 1 |
| β-strand | 106-111 | 6 | 1 |
| β-strand | 117-118 | 2 | 2 |
| α-helix | 119-122 | 4 | |
| α-helix | 127-129 | 3 | |
| α-helix | 130-149 | 20 | |
| α-helix | 159-161 | 3 | |
| β-strand | 162-164 | 3 | 2 |
| β-strand | 170-172 | 3 | 2 |
| α-helix | 200-204 | 5 | |
| α-helix | 211-226 | 16 | |
| α-helix | 236-245 | 10 | |
| α-helix | 247-249 | 3 | |
| α-helix | 257-266 | 10 | |
| α-helix | 271-273 | 3 | |
| α-helix | 275-276 | 2 | |
| α-helix | 277-280 | 4 | |
| α-helix | 284-289 | 6 | |
| α-helix | 293-296 | 4 | |
| α-helix | 297-303 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Serine/threonine-protein kinase 24 | A, B | protein | 306 | Homo sapiens | Q9Y6E0 (AlphaFold model) |
>8QLR_1 Serine/threonine-protein kinase 24 (chains A, B) MRAQLWGLALNKRRATLPHPGGSTNLKADPEELFTKLEKIGKGSFGEVFKGIDNRTQKVV AIKIIDLEEAEDEIEDIQQEITVLSQCDSPYVTKYYGSYLKDTKLWIIMEYLGGGSALDL LEPGPLDETQIATILREILKGLDYLHSEKKIHRDIKAANVLLSEHGEVKLADFGVAGQLT DTQIKRNTFVGTPFWMAPEVIKQSAYDSKADIWSLGITAIELARGEPPHSELHPMKVLFL IPKNNPPTLEGNYSKPLKEFVEACLNKEPSFRPTAKELLKHKFILRNAKKTSYLTELIDA HHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| VYN | 8-(4-azanylbutyl)-2-[1,3-bis(oxidanyl)propan-2-ylamino]-6-[2-chloranyl-4-(6-met… | C26 H29 Cl N6 O3 | 2 |
Water and common crystallization additives (EDO) are not listed.
Development of Selective Pyrido[2,3- d ]pyrimidin-7(8 H )-one-Based Mammalian STE20-Like (MST3/4) Kinase Inhibitors. Rak, M., Menge, A., Tesch, R. et al. J Med Chem (2024) 67:3813-3842. DOI 10.1021/acs.jmedchem.3c02217 · PubMed
Other PDB entries of the same protein (UniProt Q9Y6E0 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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