Crystal structure of VPS34 in complex with inhibitor SB02024. Determined by X-ray diffraction at 2.06 Å resolution. Released 20 Mar 2024.
Explore 8RXR in 3D Show helices and sheets RCSB PDB PDBe
8RXR contains 66 α-helices and 24 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 | 290-300 | 11 | |
| α-helix | 306-309 | 4 | |
| α-helix | 310-318 | 9 | |
| α-helix | 320-323 | 4 | |
| α-helix | 327-329 | 3 | |
| α-helix | 330-334 | 5 | |
| α-helix | 342-354 | 13 | |
| α-helix | 356-359 | 4 | |
| α-helix | 360-363 | 4 | |
| α-helix | 364-367 | 4 | |
| α-helix | 374-384 | 11 | |
| α-helix | 389-402 | 14 | |
| α-helix | 403-405 | 3 | |
| α-helix | 408-413 | 6 | |
| α-helix | 475-484 | 10 | |
| α-helix | 487-501 | 15 | |
| α-helix | 504-509 | 6 | |
| α-helix | 511-529 | 19 | |
| α-helix | 533-561 | 29 | |
| α-helix | 566-578 | 13 | |
| α-helix | 580-583 | 4 | |
| β-strand | 591-593 | 3 | 1 |
| β-strand | 596-604 | 9 | 1 |
| β-strand | 610-611 | 2 | 1 |
| β-strand | 619-625 | 7 | 1 |
| β-strand | 630-637 | 8 | 1 |
| α-helix | 642-660 | 19 | |
| β-strand | 672-674 | 3 | 1 |
| β-strand | 679-683 | 5 | 1 |
| β-strand | 688-689 | 2 | 2 |
| α-helix | 690-697 | 8 | |
| α-helix | 700-707 | 8 | |
| β-strand | 709 | 1 | 3 |
| α-helix | 714-716 | 3 | |
| β-strand | 717 | 1 | 3 |
| α-helix | 719-739 | 21 | |
| β-strand | 749-751 | 3 | 2 |
| β-strand | 757-759 | 3 | 2 |
| α-helix | 781-786 | 6 | |
| α-helix | 793-811 | 19 | |
| α-helix | 813-821 | 9 | |
| α-helix | 829-832 | 4 | |
| α-helix | 835-837 | 3 | |
| α-helix | 838-846 | 9 | |
| α-helix | 852-870 | 19 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 290-300 | 11 | |
| α-helix | 306-309 | 4 | |
| α-helix | 310-318 | 9 | |
| α-helix | 320-323 | 4 | |
| α-helix | 327-329 | 3 | |
| α-helix | 330-334 | 5 | |
| α-helix | 342-354 | 13 | |
| α-helix | 356-359 | 4 | |
| α-helix | 360-363 | 4 | |
| α-helix | 364-367 | 4 | |
| α-helix | 374-384 | 11 | |
| α-helix | 389-402 | 14 | |
| α-helix | 403-405 | 3 | |
| α-helix | 408-413 | 6 | |
| α-helix | 475-483 | 9 | |
| α-helix | 487-501 | 15 | |
| α-helix | 504-509 | 6 | |
| α-helix | 511-529 | 19 | |
| α-helix | 533-561 | 29 | |
| α-helix | 566-578 | 13 | |
| β-strand | 591-593 | 3 | 4 |
| β-strand | 596-604 | 9 | 4 |
| α-helix | 606-608 | 3 | |
| β-strand | 610-611 | 2 | 4 |
| β-strand | 619-625 | 7 | 4 |
| β-strand | 630-637 | 8 | 4 |
| α-helix | 642-660 | 19 | |
| β-strand | 672-674 | 3 | 4 |
| β-strand | 679-683 | 5 | 4 |
| β-strand | 688-689 | 2 | 5 |
| α-helix | 690-697 | 8 | |
| α-helix | 700-707 | 8 | |
| β-strand | 709 | 1 | 6 |
| α-helix | 714-716 | 3 | |
| β-strand | 717 | 1 | 6 |
| α-helix | 719-739 | 21 | |
| β-strand | 749-751 | 3 | 5 |
| β-strand | 757-759 | 3 | 5 |
| α-helix | 781-786 | 6 | |
| α-helix | 793-811 | 19 | |
| α-helix | 813-821 | 9 | |
| α-helix | 829-832 | 4 | |
| α-helix | 835-837 | 3 | |
| α-helix | 838-845 | 8 | |
| α-helix | 852-870 | 19 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Phosphatidylinositol 3-kinase catalytic subunit type 3 | A, B | protein | 600 | Homo sapiens | Q8NEB9 (AlphaFold model) |
>8RXR_1 Phosphatidylinositol 3-kinase catalytic subunit type 3 (chains A, B) SMSDHDLKPNAATRDQLNIIVSYPPTKQLTYEEQDLVWKFRYYLTNQEKALTKFLKCVNW DLPQEAKQALELLGKWKPMDVEDSLELLSSHYTNPTVRRYAVARLRQADDEDLLMYLLQL VQALKYENFDDIKNGLEPTKKDSQSSVSENVSNSGINSAEIDSSQIITSPLPSVSSPPPA SKTKEVPDGENLEQDLCTFLISRACKNSTLANYLYWYVIVECEDQDTQQRDPKTHEMYLN VMRRFSQALLKGDKSVRVMRSLLAAQQTFVDRLVHLMKAVQRESGNRKKKNERLQALLGD NEKMNLSDVELIPLPLEPQVKIRGIIPETATLFKSALMPAQLFFKTEDGGKYPVIFKHGD DLRQDQLILQIISLMDKLLRKENLDLKLTPYKVLATSTKHGFMQFIQSVPVAEVLDTEGS IQNFFRKYAPSENGPNGISAEVMDTYVKSCAGYCVITYILGVGDRHLDNLLLTKTGKLFH IDFGYILGRDPKPLPPPMKLNKEMVEGMGGTQSEQYQEFRKQCYTAFLHLRRYSNLILNL FSLMVDANIPDIALEPDKTVKKVQDKFRLDLSDEEAVHYMQSLIDESVHALFAAVVEQIH
| ID | Name | Formula | Copies |
|---|---|---|---|
| A1H4E | 4-[(3R)-3-methylmorpholin-4-yl]-2-[(2R)-2-(trifluoromethyl)piperidin-1-yl]-3H-p… | C16 H22 F3 N3 O2 | 2 |
Water and common crystallization additives (GOL, DMS, IMD, PEG) are not listed.
Combining VPS34 inhibitors with STING agonists enhances type I interferon signaling and anti-tumor efficacy. Yu, Y., Bogdan, M., Noman, M.Z. et al. Mol Oncol (2024) 18:1904-1922. DOI 10.1002/1878-0261.13619 · PubMed
Other PDB entries of the same protein (UniProt Q8NEB9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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