Human PI3KDELTA in complex with LASW1579. Determined by X-ray diffraction at 2.85 Å resolution. Released 1 Feb 2017.
Explore 5M6U in 3D Show helices and sheets RCSB PDB PDBe
5M6U contains 50 α-helices and 45 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 | 19-25 | 7 | 1 |
| β-strand | 31-37 | 7 | 1 |
| β-strand | 41 | 1 | 2 |
| α-helix | 42-53 | 12 | |
| α-helix | 59-61 | 3 | |
| α-helix | 65-67 | 3 | |
| β-strand | 68-73 | 6 | 1 |
| β-strand | 79-81 | 3 | 1 |
| β-strand | 88 | 1 | 2 |
| α-helix | 89-92 | 4 | |
| β-strand | 98-103 | 6 | 1 |
| α-helix | 108-121 | 14 | |
| α-helix | 126-129 | 4 | |
| α-helix | 134-156 | 23 | |
| α-helix | 159-166 | 8 | |
| β-strand | 171 | 1 | 3 |
| β-strand | 192 | 1 | 4 |
| β-strand | 193 | 1 | 5 |
| β-strand | 205 | 1 | 4 |
| α-helix | 213-218 | 6 | |
| β-strand | 239-243 | 5 | 6 |
| β-strand | 246 | 1 | 7 |
| β-strand | 249-250 | 2 | 6 |
| α-helix | 256-258 | 3 | |
| β-strand | 259 | 1 | 3 |
| α-helix | 260-268 | 9 | |
| β-strand | 273 | 1 | 5 |
| β-strand | 274-278 | 5 | 6 |
| α-helix | 279-287 | 9 | |
| β-strand | 322-331 | 10 | 8 |
| β-strand | 340-349 | 10 | 9 |
| β-strand | 352-353 | 2 | 9 |
| β-strand | 358-359 | 2 | 9 |
| β-strand | 363-364 | 2 | 9 |
| β-strand | 370-380 | 11 | 8 |
| α-helix | 381-383 | 3 | |
| β-strand | 389-397 | 9 | 9 |
| β-strand | 416-424 | 9 | 9 |
| β-strand | 426 | 1 | 10 |
| β-strand | 431 | 1 | 11 |
| β-strand | 432 | 1 | 10 |
| α-helix | 433 | 1 | |
| β-strand | 435-440 | 6 | 8 |
| α-helix | 441 | 1 | |
| β-strand | 442-443 | 2 | 9 |
| α-helix | 444-445 | 2 | |
| β-strand | 470-475 | 6 | 8 |
| α-helix | 476-477 | 2 | |
| β-strand | 484 | 1 | 11 |
| α-helix | 485-487 | 3 | |
| α-helix | 488-497 | 10 | |
| α-helix | 505-516 | 12 | |
| α-helix | 525-533 | 9 | |
| α-helix | 535-541 | 7 | |
| α-helix | 543-545 | 3 | |
| α-helix | 546-552 | 7 | |
| α-helix | 558-569 | 12 | |
| α-helix | 571-575 | 5 | |
| α-helix | 576-582 | 7 | |
| α-helix | 590-600 | 11 | |
| α-helix | 605-619 | 15 | |
| α-helix | 628-639 | 12 | |
| α-helix | 641-652 | 12 | |
| α-helix | 658-673 | 16 | |
| α-helix | 676-703 | 28 | |
| α-helix | 708-719 | 12 | |
| α-helix | 722-728 | 7 | |
| β-strand | 731-732 | 2 | 12 |
| β-strand | 739 | 1 | 7 |
| β-strand | 740-741 | 2 | 12 |
| β-strand | 743-744 | 2 | 13 |
| β-strand | 750-751 | 2 | 14 |
| β-strand | 759-762 | 4 | 14 |
| β-strand | 763-764 | 2 | 13 |
| β-strand | 775-780 | 6 | 14 |
| α-helix | 785-803 | 19 | |
| β-strand | 815-819 | 5 | 14 |
| β-strand | 822-826 | 5 | 14 |
| β-strand | 831-833 | 3 | 15 |
| α-helix | 834-838 | 5 | |
| α-helix | 855-861 | 7 | |
| α-helix | 867-889 | 23 | |
| α-helix | 896-898 | 3 | |
| β-strand | 899-902 | 4 | 15 |
| β-strand | 907-909 | 3 | 15 |
| α-helix | 929-932 | 4 | |
| α-helix | 936-942 | 7 | |
| α-helix | 950-969 | 20 | |
| α-helix | 971-980 | 10 | |
| α-helix | 981-984 | 4 | |
| α-helix | 992-1001 | 10 | |
| α-helix | 1008-1026 | 19 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 442-511 | 70 | |
| α-helix | 519-586 | 68 | |
| α-helix | 591-598 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform | A | protein | 1011 | Homo sapiens | O00329 (AlphaFold model) |
| Phosphatidylinositol 3-kinase regulatory subunit alpha | B | protein | 724 | Homo sapiens | P27986 (AlphaFold model) |
>5M6U_1 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform (chains A) NQSVVVDFLLPTGVYLNFPVSRNANLSTIKQLLWHRAQYEPLFHMLSGPEAYVFTCINQT AEQQELEDEQRRLCDVQPFLPVLRLVAREGDRVKKLINSQISLLIGKGLHEFDSLCDPEV NDFRAKMCQFCEEAAARRQQLGWEAWLQYSFPLQLEPSAQTWGPGTLRLPNRALLVNVKF EGSEESFTFQVSTKDVPLALMACALRKKATVFRQPLVEQPEDYTLQVNGRHEYLYGSYPL CQFQYICSCLHSGLTPHLTMVHSSSILAMRDEQSNPAPQVQKPRAKPPPIPAKKPSSVSL WSLEQPFRIELIQGSKVNADERMKLVVQAGLFHGNEMLCKTVSSSEVSVCSEPVWKQRLE FDINICDLPRMARLCFALYAVIEKAKKARSTKKKSKKADCPIAWANLMLFDYKDQLKTGE RCLYMWPSVPDEKGELLNPTGTVRSNPNTDSAAALLICLPEVAPHPVYYPALEKILELGR HSECVHVTEEEQLQLREILERRGSGELYEHEKDLVWKLRHEVQEHFPEALARLLLVTKWN KHEDVAQMLYLLCSWPELPVLSALELLDFSFPDCHVGSFAIKSLRKLTDDELFQYLLQLV QVLKYESYLDCELTKFLLDRALANRKIGHFLFWHLRSEMHVPSVALRFGLILEAYCRGST HHMKVLMKQGEALSKLKALNDFVKLSSQKTPKPQTKELMHLCMRQEAYLEALSHLQSPLD PSTLLAEVCVEQCTFMDSKMKPLWIMYSNEEAGSGGSVGIIFKNGDDLRQDMLTLQMIQL MDVLWKQEGLDLRMTPYGCLPTGDRTGLIEVVLRSDTIANIQLNKSNMAATAAFNKDALL NWLKSKNPGEALDRAIEEFTLSCAGYCVATYVLGIGDRHSDNIMIRESGQLFHIDFGHFL GNFKTKFGINRERVPFILTYDFVHVIQQGKTNNSEKFERFRGYCERAYTILRRHGLLFLH LFALMRAAGLPELSCSKDIQYLKDSLALGKTEEEALKHFRVKFNEALRESW
>5M6U_2 Phosphatidylinositol 3-kinase regulatory subunit alpha (chains B) MSAEGYQYRALYDYKKEREEDIDLHLGDILTVNKGSLVALGFSDGQEARPEEIGWLNGYN ETTGERGDFPGTYVEYIGRKKISPPTPKPRPPRPLPVAPGSSKTEADVEQQALTLPDLAE QFAPPDIAPPLLIKLVEAIEKKGLECSTLYRTQSSSNLAELRQLLDCDTPSVDLEMIDVH VLADAFKRYLLDLPNPVIPAAVYSEMISLAPEVQSSEEYIQLLKKLIRSPSIPHQYWLTL QYLLKHFFKLSQTSSKNLLNARVLSEIFSPMLFRFSAASSDNTENLIKVIEILISTEWNE RQPAPALPPKPPKPTTVANNGMNNNMSLQDAEWYWGDISREEVNEKLRDTADGTFLVRDA STKMHGDYTLTLRKGGNNKLIKIFHRDGKYGFSDPLTFSSVVELINHYRNESLAQYNPKL DVKLLYPVSKYQQDQVVKEDNIEAVGKKLHEYNTQFQEKSREYDRLYEDYTRTSQEIQMK RTAIEAFNETIKIFEEQCQTQERYSKEYIEKFKREGNETEIQRIMHNYEKLKSRISEIVD SRRRLEEDLKKQAAEYREIDKRMNSIKPDLIQLRKTRDQYLMWLTQKGVRQKKLNEWLGN ENTEDQYSLVEDDEDLPHHDEKTWNVGSSNRNKAENLLRGKRDGTFLVRESSKQGCYACS VVVDGEVKHCVINKTATGYGFAEPYNLYSSLKELVLHYQHTSLVQHNDSLNVTLAYPVYA QQRR
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7KA | 4-azanyl-6-[[(1~{S})-1-(4-oxidanylidene-3-phenyl-pyrrolo[2,1-f][1,2,4]triazin-2… | C19 H16 N8 O | 1 |
Discovery of a Potent, Selective, and Orally Available PI3K delta Inhibitor for the Treatment of Inflammatory Diseases. Erra, M., Taltavull, J., Greco, A. et al. ACS Med Chem Lett (2017) 8:118-123. DOI 10.1021/acsmedchemlett.6b00438 · PubMed
Other PDB entries of the same protein (UniProt O00329 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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