9TW3: Human VPS34-CI
Cryo-EM structure of human VPS34-CI in complex with GABARAP - alternative conformation. Determined by electron microscopy at 3.6 Å resolution. Released 5 Aug 2026.
- Method
- Electron microscopy
- Resolution
- 3.6 Å
- Organism
- Homo sapiens
- Chains
- 7
- Atoms
- 23,420
- Mol. weight
- 440.49 kDa
- Ligands
- MG, GDP, MYR, ZN
- Released
- 5 Aug 2026
Explore 9TW3 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
9TW3 contains 142 α-helices and 104 β-strands across 7 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.
Chain A: 41 helices, 29 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 7-11 | 5 | 1 |
| β-strand | 18-27 | 10 | 2 |
| α-helix | 29-31 | 3 | |
| α-helix | 35-40 | 6 | |
| α-helix | 42-46 | 5 | |
| β-strand | 58-65 | 8 | 3 |
| β-strand | 68-69 | 2 | 3 |
| β-strand | 74-75 | 2 | 3 |
| α-helix | 76-78 | 3 | |
| β-strand | 85-96 | 12 | 2 |
| α-helix | 97-99 | 3 | |
| β-strand | 104-113 | 10 | 3 |
| β-strand | 119-128 | 10 | 3 |
| β-strand | 130 | 1 | 4 |
| β-strand | 135 | 1 | 1 |
| β-strand | 136 | 1 | 4 |
| α-helix | 137 | 1 | |
| β-strand | 140-145 | 6 | 2 |
| β-strand | 146 | 1 | 3 |
| α-helix | 157 | 1 | |
| α-helix | 171-183 | 13 | |
| α-helix | 191-194 | 4 | |
| α-helix | 197-204 | 8 | |
| α-helix | 209-211 | 3 | |
| β-strand | 215-221 | 7 | 2 |
| β-strand | 223-226 | 4 | 5 |
| β-strand | 229-231 | 3 | 5 |
| β-strand | 232-234 | 3 | 1 |
| α-helix | 269-272 | 4 | |
| α-helix | 281-285 | 5 | |
| α-helix | 290-299 | 10 | |
| α-helix | 310-318 | 9 | |
| α-helix | 322-325 | 4 | |
| α-helix | 331-333 | 3 | |
| α-helix | 347-350 | 4 | |
| α-helix | 356-359 | 4 | |
| α-helix | 365-367 | 3 | |
| α-helix | 374-384 | 11 | |
| α-helix | 387-388 | 2 | |
| α-helix | 396-401 | 6 | |
| α-helix | 402-405 | 4 | |
| α-helix | 475-483 | 9 | |
| α-helix | 487-501 | 15 | |
| α-helix | 504-509 | 6 | |
| α-helix | 511-529 | 19 | |
| α-helix | 533-559 | 27 | |
| α-helix | 566-578 | 13 | |
| β-strand | 591-592 | 2 | 6 |
| β-strand | 600-604 | 5 | 6 |
| β-strand | 610-611 | 2 | 6 |
| β-strand | 619-625 | 7 | 6 |
| β-strand | 630-637 | 8 | 6 |
| α-helix | 642-659 | 18 | |
| β-strand | 672-674 | 3 | 6 |
| β-strand | 679-683 | 5 | 6 |
| β-strand | 688-689 | 2 | 7 |
| α-helix | 690-696 | 7 | |
| α-helix | 700-707 | 8 | |
| β-strand | 709 | 1 | 8 |
| α-helix | 714-716 | 3 | |
| β-strand | 717 | 1 | 8 |
| α-helix | 719-739 | 21 | |
| β-strand | 749-751 | 3 | 7 |
| β-strand | 757-759 | 3 | 7 |
| α-helix | 781-787 | 7 | |
| α-helix | 793-810 | 18 | |
| α-helix | 813-820 | 8 | |
| α-helix | 829-832 | 4 | |
| α-helix | 838-846 | 9 | |
| α-helix | 852-867 | 16 | |
Chain B: 69 helices, 49 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-21 | 6 | |
| β-strand | 27-34 | 8 | 9 |
| β-strand | 39-44 | 6 | 9 |
| β-strand | 49-56 | 8 | 9 |
| α-helix | 65-77 | 13 | |
| β-strand | 84 | 1 | 10 |
| β-strand | 89-90 | 2 | 9 |
| β-strand | 98-104 | 7 | 9 |
| β-strand | 108-109 | 2 | 10 |
| α-helix | 110-113 | 4 | |
| α-helix | 119-120 | 2 | |
| α-helix | 122-140 | 19 | |
| β-strand | 154-156 | 3 | 10 |
| β-strand | 162-164 | 3 | 10 |
| β-strand | 175-176 | 2 | 11 |
| α-helix | 181-186 | 6 | |
| β-strand | 194 | 1 | 12 |
| α-helix | 199-201 | 3 | |
| β-strand | 202-203 | 2 | 11 |
| α-helix | 204 | 1 | |
| α-helix | 239-253 | 15 | |
| β-strand | 260 | 1 | 12 |
| α-helix | 261-268 | 8 | |
| α-helix | 275-278 | 4 | |
| α-helix | 284-293 | 10 | |
| α-helix | 304-310 | 7 | |
| β-strand | 312 | 1 | 13 |
| β-strand | 316 | 1 | 13 |
| α-helix | 318-319 | 2 | |
| α-helix | 320-324 | 5 | |
| α-helix | 325-328 | 4 | |
| α-helix | 339-348 | 10 | |
| α-helix | 350-357 | 8 | |
| α-helix | 375-382 | 8 | |
| α-helix | 383-385 | 3 | |
| α-helix | 392-405 | 14 | |
| α-helix | 411-413 | 3 | |
| α-helix | 414-418 | 5 | |
| α-helix | 419-425 | 7 | |
| α-helix | 431-445 | 15 | |
| α-helix | 453-455 | 3 | |
| α-helix | 458 | 1 | |
| α-helix | 459-463 | 5 | |
| α-helix | 468-472 | 5 | |
| α-helix | 476-484 | 9 | |
| α-helix | 486-505 | 20 | |
| α-helix | 526-529 | 4 | |
| α-helix | 531-545 | 15 | |
| α-helix | 550-559 | 10 | |
| α-helix | 561-568 | 8 | |
| α-helix | 570-572 | 3 | |
| α-helix | 573-577 | 5 | |
| α-helix | 578-581 | 4 | |
| α-helix | 582-586 | 5 | |
| α-helix | 591-599 | 9 | |
| α-helix | 601-605 | 5 | |
| α-helix | 610-612 | 3 | |
| α-helix | 613-623 | 11 | |
| α-helix | 631-635 | 5 | |
| α-helix | 638-645 | 8 | |
| α-helix | 650-656 | 7 | |
| α-helix | 661-665 | 5 | |
| α-helix | 670-685 | 16 | |
| α-helix | 688-690 | 3 | |
| α-helix | 691-695 | 5 | |
| α-helix | 696-698 | 3 | |
| β-strand | 703 | 1 | 14 |
| α-helix | 713-717 | 5 | |
| β-strand | 720 | 1 | 14 |
| α-helix | 721-725 | 5 | |
| α-helix | 726-733 | 8 | |
| α-helix | 738-752 | 15 | |
| α-helix | 760-762 | 3 | |
| α-helix | 765-776 | 12 | |
| α-helix | 782-789 | 8 | |
| α-helix | 791-802 | 12 | |
| β-strand | 818-820 | 3 | 5 |
| α-helix | 821-824 | 4 | |
| β-strand | 829-831 | 3 | 1 |
| α-helix | 939-965 | 27 | |
| α-helix | 973-976 | 4 | |
| β-strand | 984-989 | 6 | 15 |
| β-strand | 996-1001 | 6 | 16 |
| β-strand | 1007-1012 | 6 | 16 |
| β-strand | 1017-1021 | 5 | 16 |
| α-helix | 1024-1026 | 3 | |
| β-strand | 1037-1038 | 2 | 16 |
| β-strand | 1045-1049 | 5 | 17 |
| β-strand | 1056-1061 | 6 | 17 |
| β-strand | 1065-1071 | 7 | 17 |
| β-strand | 1082-1089 | 8 | 17 |
| β-strand | 1098-1106 | 9 | 18 |
| β-strand | 1108-1116 | 9 | 18 |
| β-strand | 1120-1125 | 6 | 18 |
| β-strand | 1130-1136 | 7 | 18 |
| α-helix | 1139-1141 | 3 | |
| β-strand | 1144-1149 | 6 | 19 |
| β-strand | 1155-1160 | 6 | 19 |
| β-strand | 1164-1169 | 6 | 19 |
| β-strand | 1174-1180 | 7 | 19 |
| β-strand | 1187-1192 | 6 | 20 |
| β-strand | 1199-1204 | 6 | 20 |
| β-strand | 1209-1214 | 6 | 20 |
| β-strand | 1220-1225 | 6 | 20 |
| α-helix | 1230 | 1 | |
| α-helix | 1236-1238 | 3 | |
| β-strand | 1242-1248 | 7 | 21 |
| α-helix | 1250-1252 | 3 | |
| β-strand | 1255-1260 | 6 | 21 |
| β-strand | 1265-1269 | 5 | 21 |
| α-helix | 1273-1275 | 3 | |
| β-strand | 1277-1278 | 2 | 21 |
| β-strand | 1288-1295 | 8 | 20 |
| β-strand | 1298-1305 | 8 | 20 |
| α-helix | 1322-1324 | 3 | |
| β-strand | 1332-1339 | 8 | 15 |
| β-strand | 1343-1349 | 7 | 15 |
| β-strand | 1354-1358 | 5 | 15 |
Chain C: 7 helices, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 97-99 | 3 | 22 |
| α-helix | 111-126 | 16 | |
| β-strand | 136 | 1 | 23 |
| α-helix | 138-169 | 32 | |
| α-helix | 176-266 | 91 | |
| α-helix | 269-273 | 5 | |
| β-strand | 277-279 | 3 | 24 |
| β-strand | 282-285 | 4 | 24 |
| β-strand | 288-289 | 2 | 24 |
| α-helix | 300-321 | 22 | |
| β-strand | 328-331 | 4 | 25 |
| β-strand | 338-341 | 4 | 25 |
| β-strand | 349-350 | 2 | 25 |
| α-helix | 363-383 | 21 | |
| β-strand | 395-397 | 3 | 26 |
| β-strand | 402-404 | 3 | 26 |
| β-strand | 412-414 | 3 | 26 |
| α-helix | 422-446 | 25 | |
Chain D: 14 helices, 6 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 54 | 1 | 23 |
| α-helix | 56-60 | 5 | |
| α-helix | 75-99 | 25 | |
| α-helix | 101-127 | 27 | |
| α-helix | 130-152 | 23 | |
| α-helix | 154-204 | 51 | |
| β-strand | 209-211 | 3 | 27 |
| β-strand | 260-262 | 3 | 27 |
| β-strand | 269-271 | 3 | 27 |
| β-strand | 275 | 1 | 28 |
| α-helix | 276-278 | 3 | |
| α-helix | 279-286 | 8 | |
| α-helix | 298-302 | 5 | |
| α-helix | 303-321 | 19 | |
| α-helix | 331-333 | 3 | |
| α-helix | 341-361 | 21 | |
| α-helix | 366-368 | 3 | |
| β-strand | 373 | 1 | 28 |
| α-helix | 374-382 | 9 | |
| α-helix | 399-401 | 3 | |
Chain E: 5 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 3-5 | 3 | |
| α-helix | 8-23 | 16 | |
| α-helix | 27-43 | 17 | |
| α-helix | 44-46 | 3 | |
| α-helix | 51-77 | 27 | |
Chain F: 6 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 1-2 | 2 | |
| α-helix | 4-6 | 3 | |
| α-helix | 11-17 | 7 | |
| α-helix | 20-24 | 5 | |
| β-strand | 28-32 | 5 | 22 |
| β-strand | 48-52 | 5 | 22 |
| β-strand | 56 | 1 | 29 |
| α-helix | 57-60 | 4 | |
| β-strand | 80 | 1 | 30 |
| β-strand | 83 | 1 | 30 |
| β-strand | 90 | 1 | 29 |
| α-helix | 91-97 | 7 | |
| β-strand | 105-106 | 2 | 22 |
Chain G: 0 helices, 2 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 17 | 1 | 31 |
| β-strand | 24 | 1 | 31 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Phosphatidylinositol 3-kinase catalytic subunit type 3 | A | protein | 887 | Homo sapiens | Q8NEB9 (AlphaFold model) |
| Phosphoinositide 3-kinase regulatory subunit 4 | B | protein | 1371 | Homo sapiens | Q99570 (AlphaFold model) |
| Beclin-1 | C, G | protein | 450 | Homo sapiens | Q14457 (AlphaFold model) |
| Beclin 1-associated autophagy-related key regulator | D | protein | 493 | Homo sapiens | Q6ZNE5 (AlphaFold model) |
| Nuclear receptor-binding factor 2 | E | protein | 84 | Homo sapiens | Q96F24 |
| Gamma-aminobutyric acid receptor-associated protein | F | protein | 119 | Homo sapiens | O95166 |
Sequence of entity 1 (A), FASTA
>9TW3_1 Phosphatidylinositol 3-kinase catalytic subunit type 3 (chains A)
MGEAEKFHYIYSCDLDINVQLKIGSLEGKREQKSYKAVLEDPMLKFSGLYQETCSDLYVT
CQVFAEGKPLALPVRTSYKAFSTRWNWNEWLKLPVKYPDLPRNAQVALTIWDVYGPGKAV
PVGGTTVSLFGKYGMFRQGMHDLKVWPNVEADGSEPTKTPGRTSSTLSEDQMSRLAKLTK
AHRQGHMVKVDWLDRLTFREIEMINESEKRSSNFMYLMVEFRCVKCDDKEYGIVYYEKDG
DESSPILTSFELVKVPDPQMSMENLVESKHHKLARSLRSGPSDHDLKPNAATRDQLNIIV
SYPPTKQLTYEEQDLVWKFRYYLTNQEKALTKFLKCVNWDLPQEAKQALELLGKWKPMDV
EDSLELLSSHYTNPTVRRYAVARLRQADDEDLLMYLLQLVQALKYENFDDIKNGLEPTKK
DSQSSVSENVSNSGINSAEIDSSQIITSPLPSVSSPPPASKTKEVPDGENLEQDLCTFLI
SRACKNSTLANYLYWYVIVECEDQDTQQRDPKTHEMYLNVMRRFSQALLKGDKSVRVMRS
LLAAQQTFVDRLVHLMKAVQRESGNRKKKNERLQALLGDNEKMNLSDVELIPLPLEPQVK
IRGIIPETATLFKSALMPAQLFFKTEDGGKYPVIFKHGDDLRQDQLILQIISLMDKLLRK
ENLDLKLTPYKVLATSTKHGFMQFIQSVPVAEVLDTEGSIQNFFRKYAPSENGPNGISAE
VMDTYVKSCAGYCVITYILGVGDRHLDNLLLTKTGKLFHIDFGYILGRDPKPLPPPMKLN
KEMVEGMGGTQSEQYQEFRKQCYTAFLHLRRYSNLILNLFSLMVDANIPDIALEPDKTVK
KVQDKFRLDLSDEEAVHYMQSLIDESVHALFAAVVEQIHKFAQYWRK
Sequence of entity 2 (B), FASTA
>9TW3_2 Phosphoinositide 3-kinase regulatory subunit 4 (chains B)
MGNQLAGIAPSQILSVESYFSDIHDFEYDKSLGSTRFFKVARAKHREGLVVVKVFAIQDP
TLPLTSYKQELEELKIRLNSAQNCLPFQKASEKASEKAAMLFRQYVRDNLYDRISTRPFL
NNIEKRWIAFQILTAVDQAHKSGVRHGDIKTENVMVTSWNWVLLTDFASFKPTYLPEDNP
ADFNYFFDTSRRRTCYIAPERFVDGGMFATELEYMRDPSTPLVDLNSNQRTRGELKRAMD
IFSAGCVIAELFTEGVPLFDLSQLLAYRNGHFFPEQVLNKIEDHSIRELVTQMIHREPDK
RLEAEDYLKQQRGNAFPEIFYTFLQPYMAQFAKETFLSADERILVIRKDLGNIIHNLCGH
DLPEKAEGEPKENGLVILVSVITSCLQTLKYCDSKLAALELILHLAPRLSVEILLDRITP
YLLHFSNDSVPRVRAEALRTLTKVLALVKEVPRNDINIYPEYILPGIAHLAQDDATIVRL
AYAENIALLAETALRFLELVQLKNLNMENDPNNEEIDEVTHPNGNYDTELQALHEMVQQK
VVTLLSDPENIVKQTLMENGITRLCVFFGRQKANDVLLSHMITFLNDKNDWHLRGAFFDS
IVGVAAYVGWQSSSILKPLLQQGLSDAEEFVIVKALYALTCMCQLGLLQKPHVYEFASDI
APFLCHPNLWIRYGAVGFITVVARQISTADVYCKLMPYLDPYITQPIIQIERKLVLLSVL
KEPVSRSIFDYALRSKDITSLFRHLHMRQKKRNGSLPDCPPPEDPAIAQLLKKLLSQGMT
EEEEDKLLALKDFMMKSNKAKANIVDQSHLHDSSQKGVIDLAALGITGRQVDLVKTKQEP
DDKRARKHVKQDSNVNEEWKSMFGSLDPPNMPQALPKGSDQEVIQTGKPPRSESSAGICV
PLSTSSQVPEVTTVQNKKPVIPVLSSTILPSTYQIRITTCKTELQQLIQQKREQCNAERI
AKQMMENAEWESKPPPPGWRPKGLLVAHLHEHKSAVNRIRVSDEHSLFATCSNDGTVKIW
NSQKMEGKTTTTRSILTYSRIGGRVKTLTFCQGSHYLAIASDNGAVQLLGIEASKLPKSP
KIHPLQSRILDQKEDGCVVDMHHFNSGAQSVLAYATVNGSLVGWDLRSSSNAWTLKHDLK
SGLITSFAVDIHQCWLCIGTSSGTMACWDMRFQLPISSHCHPSRARIRRLSMHPLYQSWV
IAAVQGNNEVSMWDMETGDRRFTLWASSAPPLSELQPSPHSVHGIYCSPADGNPILLTAG
SDMKIRFWDLAYPERSYVVAGSTSSPSVSYYRKIIEGTEVVQEIQNKQKVGPSDDTPRRG
PESLPVGHHDIITDVATFQTTQGFIVTASRDGIVKVWKSRPTTASENLYFQ
Sequence of entity 3 (C, G), FASTA
>9TW3_3 Beclin-1 (chains C, G)
MEGSKTSNNSTMQVSFVCQRCSQPLKLDTSFKILDRVTIQELTAPLLTTAQAKPGETQEE
ETNSGEEPFIETPRQDGVSRRFIPPARMMSTESANSFTLIGEASDGGTMENLSRRLKVTG
DLFDIMSGQTDVDHPLCEECTDTLLDQLDTQLNVTENECQNYKRCLEILEQMNEDDSEQL
QMELKELALEEERLIQELEDVEKNRKIVAENLEKVQAEAERLDQEEAQYQREYSEFKRQQ
LELDDELKSVENQMRYAQTQLDKLKKTNVFNATFHIWHSGQFGTINNFRLGRLPSVPVEW
NEINAAWGQTVLLLHALANKMGLKFQRYRLVPYGNHSYLESLTDKSKELPLYCSGGLRFF
WDNKFDHAMVAFLDCVQQFKEEVEKGETRFCLPYRMDVEKGKIEDTGGSGGSYSIKTQFN
SEEQWTKALKFMLTNLKWGLAWVSSQFYNK
Sequence of entity 4 (D), FASTA
>9TW3_4 Beclin 1-associated autophagy-related key regulator (chains D)
MTASPSGKGARALEAPGCGPRPLARDLVDSVDDAEGLYVAVERCPLCNTTRRRLTCAKCV
QSGDFVYFDGRDRERFIDKKERLSRLKSKQEEFQKEVLKAMEGKWITDQLRWKIMSCKMR
IEQLKQTICKGNEEMEKNSEGLLKTKEKNQKLYSRAQRHQEKKEKIQRHNRKLGDLVEKK
TIDLRSHYERLANLRRSHILELTSVIFPIEEVKTGVRDPADVSSESDSAMTSSTVSKLAE
ARRTTYLSGRWVCDDHSGDTSISITGPWISLPNNGDYSAYYSWVEEKKTTQGPDMEQSNP
AYTISAALCYATQLVNILSHILDVNLPKKLCNSEFCGENLSKQKFTRAVKKLNANILYLC
FSQHVNLDQLQPLHTLRNLMYLVSPSSEHLGRSGPFEVRADLEESMEFVDPGVAGESDES
GDERVSDEETDLGTDWENLPSPRFCDIPSQSVEVSQSQSTQASPPIASSSAGGMISSAAA
SVTSWFKAYTGHR
Sequence of entity 5 (E), FASTA
>9TW3_5 Nuclear receptor-binding factor 2 (chains E)
SHMEVMEVMEGPLNLAHQQSRRADRLLAAGKYEEAISCHKKAAAYLSEAMKLTQSEQAHL
SLELQRDSHMKQLLLIQERWKRAQ
Sequence of entity 6 (F), FASTA
>9TW3_6 Gamma-aminobutyric acid receptor-associated protein (chains F)
GSHMKFVYKEEHPFEKRRSEGEKIRKKYPDRVPVIVEKAPKARIGDLDKKKYLVPSDLTV
GQFYFLIRKRIHLRAEDALFFFVNNVIPPTSATMGQLYQEHHEEDFFLYIAYSDESVYG
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| MG | Magnesium ion | Mg | 1 |
| GDP | Guanosine-5'-diphosphate | C10 H15 N5 O11 P2 | 1 |
| MYR | Myristic acid | C14 H28 O2 | 1 |
| ZN | Zinc ion | Zn | 2 |
Primary citation
A GABARAP-PtdIns3K-C1 positive feedback loop at the heart of the phagophore nucleation. Dessus, A.N., Ohashi, Y., Bourguet, M. et al. Nat Commun (2026) 17. DOI 10.1038/s41467-026-76135-w · PubMed
Other PDB entries of the same protein (UniProt Q8NEB9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 6HOG 1.26 Å, Structure of VPS34 LIR motif bound to GABARAP
- 7RSP 1.67 Å, Structure of the VPS34 kinase domain with compound 14
- 7RSV 1.78 Å, Structure of the VPS34 kinase domain with compound 5
- 7RSJ 1.88 Å, Structure of the VPS34 kinase domain with compound 14
- 4UWH 1.93 Å, Discovery of (2S)-8-((3R)-3-Methylmorpholin-4-yl)-1-(3-methyl-2-oxo-…
- 9NIN 2.01 Å, The structure of human Vacuolar Protein Sorting 34 catalytic domain bound to RD-I-86
- 8RXR 2.06 Å, Crystal structure of VPS34 in complex with inhibitor SB02024
- 9ORM 2.06 Å, The structure of human Vacuolar Protein Sorting 34 catalytic domain bound to RD-I-137
- 6I3U 2.09 Å, Optimization of potent and selective ATM inhibitors suitable for a proof-of-concept…
- 9ZF4 2.09 Å, The structure of human Vacuolar Protein Sorting 34 catalytic domain bound to RD-II-83
- 9DKP 2.16 Å, The structure of human vacuolar protein sorting 34 catalytic domain bound to RD-I-53
- 3LS8 2.25 Å, Crystal structure of human PIK3C3 in complex with 3-[4-(4-Morpholinyl)thieno[3,2-d]pyrimi…
Browse structure collections
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