8ES8: PN45545 TCR-CD3
CryoEM structure of PN45545 TCR-CD3 in complex with HLA-A2 MAGEA4 (230-239). Determined by electron microscopy at 2.65 Å resolution. Released 3 May 2023.
- Method
- Electron microscopy
- Resolution
- 2.65 Å
- Organism
- Homo sapiens
- Chains
- 11
- Atoms
- 11,976
- Mol. weight
- 242.05 kDa
- Ligands
- NAG, Y01
- Released
- 3 May 2023
Explore 8ES8 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8ES8 contains 37 α-helices and 110 β-strands across 10 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: 6 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-5 | 3 | 9 |
| β-strand | 11-14 | 4 | 10 |
| β-strand | 19-21 | 3 | 9 |
| β-strand | 24-26 | 3 | 9 |
| β-strand | 32-39 | 8 | 11 |
| β-strand | 46-52 | 7 | 11 |
| β-strand | 60-61 | 2 | 9 |
| β-strand | 64-69 | 6 | 9 |
| β-strand | 74-79 | 6 | 9 |
| α-helix | 84-86 | 3 | |
| β-strand | 89-96 | 8 | 11 |
| β-strand | 106-107 | 2 | 11 |
| β-strand | 111-112 | 2 | 11 |
| β-strand | 113-116 | 4 | 10 |
| α-helix | 117 | 1 | |
| β-strand | 125-128 | 4 | 12 |
| α-helix | 129-131 | 3 | |
| β-strand | 138-143 | 6 | 12 |
| β-strand | 159-161 | 3 | 12 |
| α-helix | 162-164 | 3 | |
| β-strand | 165-169 | 5 | 12 |
| β-strand | 174-183 | 10 | 12 |
| β-strand | 204 | 1 | 12 |
| α-helix | 214-219 | 6 | |
| α-helix | 225-256 | 32 | |
Chain B: 7 helices, 26 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-6 | 3 | 13 |
| β-strand | 10-14 | 5 | 14 |
| β-strand | 19-21 | 3 | 15 |
| β-strand | 23-25 | 3 | 13 |
| β-strand | 31-38 | 8 | 14 |
| β-strand | 42-49 | 8 | 14 |
| β-strand | 56-57 | 2 | 14 |
| β-strand | 64-67 | 4 | 15 |
| β-strand | 73 | 1 | 13 |
| β-strand | 75-78 | 4 | 15 |
| α-helix | 83-85 | 3 | |
| β-strand | 87-94 | 8 | 14 |
| β-strand | 104-105 | 2 | 14 |
| β-strand | 109-114 | 6 | 14 |
| α-helix | 117-119 | 3 | |
| β-strand | 121 | 1 | 16 |
| β-strand | 124-128 | 5 | 17 |
| α-helix | 129-131 | 3 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-150 | 11 | 17 |
| β-strand | 151 | 1 | 16 |
| β-strand | 155-161 | 7 | 18 |
| β-strand | 164-166 | 3 | 18 |
| β-strand | 170-172 | 3 | 17 |
| β-strand | 177-178 | 2 | 17 |
| β-strand | 188-197 | 10 | 17 |
| α-helix | 198-201 | 4 | |
| β-strand | 207-214 | 8 | 18 |
| β-strand | 217 | 1 | 19 |
| α-helix | 228-229 | 2 | |
| β-strand | 231 | 1 | 19 |
| β-strand | 233-240 | 8 | 18 |
| α-helix | 249-288 | 40 | |
Chain D: 4 helices, 8 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 23-25 | 3 | |
| β-strand | 26-28 | 3 | 1 |
| β-strand | 32-36 | 5 | 1 |
| α-helix | 40-41 | 2 | |
| β-strand | 42-46 | 5 | 2 |
| β-strand | 50-51 | 2 | 1 |
| β-strand | 57-62 | 6 | 1 |
| α-helix | 63-65 | 3 | |
| β-strand | 68-73 | 6 | 2 |
| β-strand | 84-91 | 8 | 2 |
| β-strand | 96-98 | 3 | 3 |
| α-helix | 101-126 | 26 | |
Chain E: 2 helices, 9 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 37-41 | 5 | 8 |
| β-strand | 44-48 | 5 | 8 |
| β-strand | 57-61 | 5 | 2 |
| β-strand | 65-66 | 2 | 2 |
| β-strand | 75-77 | 3 | 8 |
| β-strand | 81-85 | 5 | 8 |
| α-helix | 89-92 | 4 | |
| β-strand | 94-100 | 7 | 2 |
| β-strand | 110-116 | 7 | 2 |
| β-strand | 122-124 | 3 | 3 |
| α-helix | 127-153 | 27 | |
Chain F: 3 helices, 9 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 37-41 | 5 | 4 |
| β-strand | 44-48 | 5 | 4 |
| β-strand | 57-61 | 5 | 5 |
| β-strand | 64-66 | 3 | 5 |
| β-strand | 75-77 | 3 | 4 |
| β-strand | 81-84 | 4 | 4 |
| α-helix | 89-92 | 4 | |
| β-strand | 94-100 | 7 | 5 |
| α-helix | 105-107 | 3 | |
| β-strand | 111-116 | 6 | 5 |
| β-strand | 122-123 | 2 | 6 |
| α-helix | 127-155 | 29 | |
Chain G: 3 helices, 8 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 31-34 | 4 | 7 |
| β-strand | 41-46 | 6 | 7 |
| β-strand | 53-57 | 5 | 5 |
| β-strand | 60-65 | 6 | 5 |
| β-strand | 71-76 | 6 | 7 |
| α-helix | 77-79 | 3 | |
| β-strand | 83-88 | 6 | 5 |
| α-helix | 93-96 | 4 | |
| β-strand | 97-102 | 6 | 5 |
| β-strand | 108-109 | 2 | 6 |
| α-helix | 112-135 | 24 | |
Chain M: 0 helices, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3 | 1 | 24 |
| β-strand | 6-11 | 6 | 25 |
| β-strand | 21-30 | 10 | 25 |
| β-strand | 31 | 1 | 24 |
| β-strand | 36-41 | 6 | 26 |
| β-strand | 44-45 | 2 | 26 |
| β-strand | 50-51 | 2 | 25 |
| β-strand | 55-56 | 2 | 25 |
| β-strand | 62-70 | 9 | 25 |
| β-strand | 78-83 | 6 | 26 |
| β-strand | 91-94 | 4 | 26 |
Chain N: 10 helices, 20 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-12 | 10 | 20 |
| α-helix | 20 | 1 | |
| β-strand | 21-28 | 8 | 20 |
| β-strand | 31-37 | 7 | 20 |
| β-strand | 46-47 | 2 | 20 |
| α-helix | 50-54 | 5 | |
| α-helix | 57-85 | 29 | |
| β-strand | 94-103 | 10 | 20 |
| β-strand | 109-118 | 10 | 20 |
| β-strand | 121-126 | 6 | 20 |
| β-strand | 133-135 | 3 | 20 |
| α-helix | 138-150 | 13 | |
| α-helix | 152-158 | 7 | |
| α-helix | 159-163 | 5 | |
| α-helix | 164-174 | 11 | |
| α-helix | 176-179 | 4 | |
| β-strand | 183 | 1 | 21 |
| α-helix | 184-185 | 2 | |
| β-strand | 186 | 1 | 22 |
| β-strand | 189-193 | 5 | 22 |
| β-strand | 198-208 | 11 | 22 |
| β-strand | 209 | 1 | 21 |
| β-strand | 214-219 | 6 | 23 |
| β-strand | 222-223 | 2 | 23 |
| β-strand | 228-230 | 3 | 22 |
| α-helix | 231-233 | 3 | |
| β-strand | 234-235 | 2 | 22 |
| β-strand | 241-250 | 10 | 22 |
| β-strand | 257-262 | 6 | 23 |
| β-strand | 272-273 | 2 | 23 |
2 more chain groups are not listed. Open the entry in the viewer and use the sequence panel to see them.
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| T-cell surface glycoprotein CD3 zeta chain | Y, Z | protein | 173 | Homo sapiens | P20963 (AlphaFold model) |
| T-cell surface glycoprotein CD3 delta chain | D | protein | 174 | Homo sapiens | P04234 (AlphaFold model) |
| T-cell surface glycoprotein CD3 epsilon chain | E, F | protein | 211 | Homo sapiens | P07766 (AlphaFold model) |
| T-cell surface glycoprotein CD3 gamma chain | G | protein | 185 | Homo sapiens | P09693 (AlphaFold model) |
| PN45545 TCR alpha chain | A | protein | 278 | Homo sapiens | |
| PN45545 TCR beta chain | B | protein | 319 | Homo sapiens | |
| MHC class I antigen | N | protein | 277 | Homo sapiens | Q861F7 |
| Beta-2-microglobulin | M | protein | 100 | Homo sapiens | P61769 |
| Melanoma-associated antigen 4 | P | protein | 10 | Homo sapiens | P43358 |
Sequence of entity 1 (Y, Z), FASTA
>8ES8_1 T-cell surface glycoprotein CD3 zeta chain (chains Y, Z)
MKWKALFTAAILQAQLPITEAQSFGLLDPKLCYLLDGILFIYGVILTALFLRVKFSRSAD
APAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPQRRKNPQEGLYNELQKDKMA
EAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPRGSGLEVLFQ
Sequence of entity 2 (D), FASTA
>8ES8_2 T-cell surface glycoprotein CD3 delta chain (chains D)
MEHSTFLSGLVLATLLSQVSPFKIPIEELEDRVFVNCNTSITWVEGTVGTLLSDITRLDL
GKRILDPRGIYRCNGTDIYKDKESTVQVHYRMCQSCVELDPATVAGIIVTDVIATLLLAL
GVFCFAGHETGRLSGAADTQALLRNDQVYQPLRDRDDAQYSHLGGNWARNKGSG
Sequence of entity 3 (E, F), FASTA
>8ES8_3 T-cell surface glycoprotein CD3 epsilon chain (chains E, F)
MGQSGTHWRVLGLCLLSVGVWGQDGNEEMGGITQTPYKVSISGTTVILTCPQYPGSEILW
QHNDKNIGGDEDDKNIGSDEDHLSLKEFSELEQSGYYVCYPRGSKPEDANFYLYLRARVC
ENCMEMDVMSVATIVIVDICITGGLLLLVYYWSKNRKAKAKPVTRGAGAGGRQRGQNKER
PPPVPNPDYEPIRKGQRDLYSGLNQRRIGSG
Sequence of entity 4 (G), FASTA
>8ES8_4 T-cell surface glycoprotein CD3 gamma chain (chains G)
MEQGKGLAVLILAIILLQGTLAQSIKGNHLVKVYDYQEDGSVLLTCDAEAKNITWFKDGK
MIGFLTEDKKKWNLGSNAKDPRGMYQCKGSQNKSKPLQVYYRMCQNCIELNAATISGFLF
AEIVSIFVLAVGVYFIAGQDGVRQSRASDKQTLLPNDQLYQPLKDREDDQYSHLQGNQLR
RNGSG
Sequence of entity 5 (A), FASTA
>8ES8_5 PN45545 TCR alpha chain (chains A)
MSLSSLLKVVTASLWLGPGIAQKITQTQPGMFVQEKEAVTLDCTYDTSDPSYGLFWYKQP
SSGEMIFLIYQGSYDQQNATEGRYSLNFQKARKSANLVISASQLGDSAMYFCAMRGGGSG
GSYIPTFGRGTSLIVHPNIQNPDPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVY
ITDKTVLDMRSMDFKSNSAVAWSNKSDFACANAFNNSIIPEDTFFPSPESSCDVKLVEKS
FETDTNLNFQNLSVIGFRILLLKVAGFNLLMTLRLWSS
Sequence of entity 6 (B), FASTA
>8ES8_6 PN45545 TCR beta chain (chains B)
MGFRLLCCVAFCLLGAGPVDVKVTQSSRYLVKRTGEKVFLECVQDMDHENMFWYRQDPGL
GLRLIYFSYDVKMKEKGDIPEGYSVSREKKERFSLILESASTNQTSMYLCASSFTGPYNS
PLHFGNGTRLTVTEDLNKVFPPEVAVFEPSEAEISHTQKATLVCLATGFFPDHVELSWWV
NGKEVHSGVSTDPQPLKEQPALNDSRYCLSSRLRVSATFWQNPRNHFRCQVQFYGLSEND
EWTQDRAKPVTQIVSAEAWGRADCGFTSVSYQQGVLSATILYEILLGKATLYAVLVSALV
LMAMVKRKDSRGRAKRGSG
Sequence of entity 7 (N), FASTA
>8ES8_7 MHC class I antigen (chains N)
MGSHSMRYFFTSVSRPGRGEPRFIAVGYVDDTQFVRFDSDAASQRMEPRAPWIEQEGPEY
WDGETRKVKAHSQTHRVDLGTLRGYYNQSEAGSHTVQRMYGCDVGSDWRFLRGYHQYAYD
GKDYIALKEDLRSWTAADMAAQTTKHKWEAAHVAEQLRAYLEGTCVEWLRRYLENGKETL
QRTDAPKTHMTHHAVSDHEATLRCWALSFYPAEITLTWQRDGEDQTQDTELVETRPAGDG
TFQKWAAVVVPSGQEQRYTCHVQHEGLPKPLTLRWEP
Sequence of entity 8 (M), FASTA
>8ES8_8 Beta-2-microglobulin (chains M)
MIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLLKNGERIEKVEHSDLSFSKD
WSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
Sequence of entity 9 (P), FASTA
>8ES8_9 Melanoma-associated antigen 4 (chains P)
GVYDGREHTV
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 5 |
| Y01 | Cholesterol hemisuccinate | C31 H50 O4 | 1 |
Primary citation
Structural analysis of cancer-relevant TCR-CD3 and peptide-MHC complexes by cryoEM. Saotome, K., Dudgeon, D., Colotti, K. et al. Nat Commun (2023) 14:2401-2401. DOI 10.1038/s41467-023-37532-7 · PubMed
Other PDB entries of the same protein (UniProt P20963 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 2OQ1 1.9 Å, Tandem SH2 domains of ZAP-70 with 19-mer zeta1 peptide
- 3IK5 2.05 Å, SIVmac239 Nef in complex with TCR zeta ITAM 1 polypeptide (A63-R80)
- 4XZ1 2.8 Å, ZAP-70-tSH2:Compound-B adduct
- 1YGR 2.9 Å, Crystal structure of the tandem phosphatase domain of RPTP CD45
- 7FJE 3.0 Å, Cryo-EM structure of a membrane protein(LL)
- 9CI8 3.01 Å, T cell receptor complex
- 8ES7 3.04 Å, CryoEM structure of PN45545 TCR-CD3 complex
- 7PHR 3.08 Å, Structure of a fully assembled T-cell receptor engaging a tumor-associated peptide-MHC I
- 9JY1 3.08 Å, delta epsilon/delta epsilon Fab-TCR tetramer
- 7FJF 3.1 Å, Cryo-EM structure of a membrane protein(CS)
- 8TW6 3.1 Å, TCR in nanodisc ND-II
- 9IRU 3.14 Å, Cryo-em structure of TCR-4B1 complex
Browse structure collections
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