6PUF: Human MAIT A-F7 TCR
Structure of human MAIT A-F7 TCR in complex with human MR1-5'D-5-OP-RU. Determined by X-ray diffraction at 1.92 Å resolution. Released 19 Feb 2020.
- Method
- X-ray diffraction
- Resolution
- 1.92 Å
- Organism
- Homo sapiens
- Chains
- 8
- Atoms
- 14,924
- Mol. weight
- 189.33 kDa
- Ligands
- 2LJ
- Released
- 19 Feb 2020
Explore 6PUF in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
6PUF contains 52 α-helices and 148 β-strands across 8 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: 10 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-12 | 10 | 1 |
| β-strand | 22-28 | 7 | 1 |
| β-strand | 31-37 | 7 | 1 |
| β-strand | 44-45 | 2 | 1 |
| α-helix | 48-51 | 4 | |
| α-helix | 56-84 | 29 | |
| β-strand | 91-100 | 10 | 1 |
| β-strand | 106-114 | 9 | 1 |
| β-strand | 117-123 | 7 | 1 |
| β-strand | 128-131 | 4 | 1 |
| α-helix | 134-144 | 11 | |
| α-helix | 147-155 | 9 | |
| α-helix | 156-160 | 5 | |
| α-helix | 161-171 | 11 | |
| α-helix | 173-176 | 4 | |
| β-strand | 180 | 1 | 2 |
| α-helix | 181-182 | 2 | |
| β-strand | 183-188 | 6 | 3 |
| β-strand | 197-205 | 9 | 3 |
| β-strand | 206 | 1 | 2 |
| β-strand | 211-216 | 6 | 4 |
| β-strand | 219-220 | 2 | 4 |
| α-helix | 222-224 | 3 | |
| β-strand | 225-227 | 3 | 3 |
| α-helix | 228-229 | 2 | |
| β-strand | 231-232 | 2 | 3 |
| β-strand | 238-245 | 8 | 3 |
| β-strand | 254-260 | 7 | 4 |
| β-strand | 263-268 | 6 | 4 |
Chain B: 2 helices, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3 | 1 | 5 |
| α-helix | 4-5 | 2 | |
| β-strand | 6-11 | 6 | 6 |
| β-strand | 21-30 | 10 | 6 |
| β-strand | 31 | 1 | 5 |
| β-strand | 36-41 | 6 | 7 |
| β-strand | 44-45 | 2 | 7 |
| β-strand | 50-51 | 2 | 6 |
| α-helix | 52-54 | 3 | |
| β-strand | 55-56 | 2 | 6 |
| β-strand | 62-70 | 9 | 6 |
| β-strand | 78-83 | 6 | 7 |
| β-strand | 91-94 | 4 | 7 |
Chain C: 10 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-12 | 10 | 8 |
| α-helix | 15-16 | 2 | |
| β-strand | 22-28 | 7 | 8 |
| β-strand | 31-37 | 7 | 8 |
| β-strand | 44-45 | 2 | 8 |
| α-helix | 48-51 | 4 | |
| α-helix | 56-84 | 29 | |
| β-strand | 91-100 | 10 | 8 |
| β-strand | 106-114 | 9 | 8 |
| β-strand | 117-123 | 7 | 8 |
| β-strand | 128-131 | 4 | 8 |
| α-helix | 134-144 | 11 | |
| α-helix | 147-155 | 9 | |
| α-helix | 156-160 | 5 | |
| α-helix | 161-171 | 11 | |
| α-helix | 173-176 | 4 | |
| β-strand | 180 | 1 | 9 |
| α-helix | 181-182 | 2 | |
| β-strand | 183-190 | 8 | 10 |
| β-strand | 196-205 | 10 | 10 |
| β-strand | 206 | 1 | 9 |
| β-strand | 211-216 | 6 | 11 |
| β-strand | 219-220 | 2 | 11 |
| α-helix | 224-225 | 2 | |
| β-strand | 226-227 | 2 | 10 |
| β-strand | 231-232 | 2 | 10 |
| β-strand | 238-245 | 8 | 10 |
| β-strand | 254-260 | 7 | 11 |
| β-strand | 263-268 | 6 | 11 |
Chain D: 5 helices, 18 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-5 | 3 | 12 |
| β-strand | 9-13 | 5 | 13 |
| β-strand | 18-25 | 8 | 12 |
| β-strand | 32-37 | 6 | 13 |
| β-strand | 44-49 | 6 | 13 |
| β-strand | 53-57 | 5 | 12 |
| β-strand | 60-65 | 6 | 12 |
| β-strand | 70-75 | 6 | 12 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-91 | 8 | 13 |
| β-strand | 97-99 | 3 | 13 |
| α-helix | 100 | 1 | |
| β-strand | 103-108 | 6 | 13 |
| β-strand | 117-121 | 5 | 14 |
| β-strand | 122 | 1 | 15 |
| β-strand | 131-135 | 5 | 14 |
| α-helix | 143-146 | 4 | |
| β-strand | 151-153 | 3 | 14 |
| α-helix | 154-156 | 3 | |
| β-strand | 157-161 | 5 | 14 |
| β-strand | 166-175 | 10 | 14 |
| α-helix | 182-184 | 3 | |
| β-strand | 196 | 1 | 14 |
Chain E: 7 helices, 27 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 16 |
| β-strand | 10-14 | 5 | 17 |
| β-strand | 19-21 | 3 | 18 |
| β-strand | 22-25 | 4 | 16 |
| β-strand | 31-37 | 7 | 17 |
| β-strand | 44-51 | 8 | 17 |
| β-strand | 54-57 | 4 | 17 |
| β-strand | 64-68 | 5 | 18 |
| β-strand | 73 | 1 | 16 |
| β-strand | 74-78 | 5 | 18 |
| α-helix | 83-85 | 3 | |
| β-strand | 87-94 | 8 | 17 |
| α-helix | 102-104 | 3 | |
| β-strand | 105-106 | 2 | 17 |
| β-strand | 110-115 | 6 | 17 |
| β-strand | 122 | 1 | 19 |
| α-helix | 123-124 | 2 | |
| β-strand | 125-129 | 5 | 20 |
| β-strand | 130 | 1 | 15 |
| α-helix | 131-132 | 2 | |
| α-helix | 133-139 | 7 | |
| β-strand | 141-151 | 11 | 20 |
| β-strand | 152 | 1 | 19 |
| β-strand | 156-162 | 7 | 21 |
| β-strand | 165-167 | 3 | 21 |
| β-strand | 171-173 | 3 | 20 |
| β-strand | 178-179 | 2 | 20 |
| β-strand | 189-198 | 10 | 20 |
| α-helix | 199-203 | 5 | |
| β-strand | 208-215 | 8 | 21 |
| β-strand | 218 | 1 | 22 |
| α-helix | 229-230 | 2 | |
| β-strand | 232 | 1 | 22 |
| β-strand | 234-241 | 8 | 21 |
Chain F: 3 helices, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3 | 1 | 23 |
| α-helix | 4-5 | 2 | |
| β-strand | 6-11 | 6 | 24 |
| β-strand | 21-30 | 10 | 24 |
| β-strand | 31 | 1 | 23 |
| β-strand | 35-41 | 7 | 25 |
| β-strand | 44-45 | 2 | 25 |
| α-helix | 46 | 1 | |
| β-strand | 50-51 | 2 | 24 |
| α-helix | 52-54 | 3 | |
| β-strand | 55-56 | 2 | 24 |
| β-strand | 62-70 | 9 | 24 |
| β-strand | 78-84 | 7 | 25 |
| β-strand | 91-94 | 4 | 25 |
Chain G: 6 helices, 17 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-5 | 3 | 26 |
| β-strand | 9-13 | 5 | 27 |
| β-strand | 18-25 | 8 | 26 |
| β-strand | 32-37 | 6 | 27 |
| β-strand | 43-49 | 7 | 27 |
| β-strand | 53-57 | 5 | 26 |
| β-strand | 60-65 | 6 | 26 |
| β-strand | 70-75 | 6 | 26 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-91 | 8 | 27 |
| β-strand | 97-99 | 3 | 27 |
| β-strand | 103-108 | 6 | 27 |
| β-strand | 117-120 | 4 | 28 |
| α-helix | 121-123 | 3 | |
| β-strand | 130-135 | 6 | 28 |
| α-helix | 143-146 | 4 | |
| β-strand | 152-153 | 2 | 28 |
| α-helix | 154-156 | 3 | |
| β-strand | 157-161 | 5 | 28 |
| α-helix | 162-164 | 3 | |
| β-strand | 166-175 | 10 | 28 |
| α-helix | 182-185 | 4 | |
| β-strand | 196 | 1 | 28 |
Chain H: 9 helices, 26 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 29 |
| β-strand | 10-14 | 5 | 30 |
| β-strand | 19-21 | 3 | 31 |
| β-strand | 22-25 | 4 | 29 |
| β-strand | 31-37 | 7 | 30 |
| β-strand | 44-51 | 8 | 30 |
| β-strand | 54-57 | 4 | 30 |
| β-strand | 65-68 | 4 | 31 |
| β-strand | 73 | 1 | 29 |
| β-strand | 74-78 | 5 | 31 |
| α-helix | 83-85 | 3 | |
| β-strand | 87-94 | 8 | 30 |
| α-helix | 102-104 | 3 | |
| β-strand | 105-106 | 2 | 30 |
| β-strand | 110-115 | 6 | 30 |
| α-helix | 118-120 | 3 | |
| β-strand | 122 | 1 | 32 |
| α-helix | 123-124 | 2 | |
| β-strand | 125-129 | 5 | 33 |
| α-helix | 130-132 | 3 | |
| α-helix | 133-139 | 7 | |
| β-strand | 141-151 | 11 | 33 |
| β-strand | 152 | 1 | 32 |
| β-strand | 156-162 | 7 | 34 |
| β-strand | 165-167 | 3 | 34 |
| β-strand | 171-173 | 3 | 33 |
| α-helix | 177 | 1 | |
| β-strand | 178-179 | 2 | 33 |
| β-strand | 189-198 | 10 | 33 |
| α-helix | 199-202 | 4 | |
| β-strand | 208-215 | 8 | 34 |
| β-strand | 218 | 1 | 35 |
| α-helix | 229-230 | 2 | |
| β-strand | 232 | 1 | 35 |
| β-strand | 234-241 | 8 | 34 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Major histocompatibility complex class I-related gene protein | A, C | protein | 271 | Homo sapiens | Q95460 (AlphaFold model) |
| Beta-2-microglobulin | B, F | protein | 100 | Homo sapiens | P61769 (AlphaFold model) |
| Human TCR alpha chain | D, G | protein | 204 | Homo sapiens | |
| Human TCR beta chain | E, H | protein | 246 | Homo sapiens | |
Sequence of entity 1 (A, C), FASTA
>6PUF_1 Major histocompatibility complex class I-related gene protein (chains A, C)
MRTHSLRYFRLGVSDPIHGVPEFISVGYVDSHPITTYDSVTRQKEPRAPWMAENLAPDHW
ERYTQLLRGWQQMFKVELKRLQRHYNHSGSHTYQRMIGCELLEDGSTTGFLQYAYDGQDF
LIFNKDTLSWLAVDNVAHTIKQAWEANQHELLYQKNWLEEECIAWLKRFLEYGKDTLQRT
EPPLVRVNRKETFPGVTALFCKAHGFYPPEIYMTWMKNGEEIVQEIDYGDILPSGDGTYQ
AWASIELDPQSSNLYSCHVEHSGVHMVLQVP
Sequence of entity 2 (B, F), FASTA
>6PUF_2 Beta-2-microglobulin (chains B, F)
MIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLLKNGERIEKVEHSDLSFSKD
WSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
Sequence of entity 3 (D, G), FASTA
>6PUF_3 Human TCR alpha chain (chains D, G)
MGQNIDQPTEMTATEGAIVQINCTYQTSGFNGLFWYQQHAGEAPTFLSYNVLDGLEEKGR
FSSFLSRSKGYSYLLLKELQMKDSASYLCAVKDSNYQLIWGAGTKLIIKPDIQNPDPAVY
QLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKCVLDMRSMDFKSNSAVAWSNKSD
FACANAFNNSIIPEDTFFPSPESS
Sequence of entity 4 (E, H), FASTA
>6PUF_4 Human TCR beta chain (chains E, H)
MNAGVTQTPKFQVLKTGQSMTLQCAQDMNHNSMYWYRQDPGMGLRLIYYSASEGTTDKGE
VPNGYNVSRLNKREFSLRLESAAPSQTSVYFCASSVWTGEGSGELFFGEGSRLTVLEDLK
NVFPPEVAVFEPSEAEISHTQKATLVCLATGFYPDHVELSWWVNGKEVHSGVCTDPQPLK
EQPALNDSRYALSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQIVSAE
AWGRAD
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| 2LJ | 1-deoxy-1-({2,6-dioxo-5-[(E)-propylideneamino]-1,2,3,6-tetrahydropyrimidin-4-yl… | C12 H20 N4 O6 | 2 |
Water and common crystallization additives (NA, GOL) are not listed.
Primary citation
The molecular basis underpinning the potency and specificity of MAIT cell antigens. Awad, W., Ler, G.J.M., Xu, W. et al. Nat Immunol (2020) 21:400-411. DOI 10.1038/s41590-020-0616-6 · PubMed
Other PDB entries of the same protein (UniProt Q95460 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 6PUD 1.8 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-5'OH-Pentyl-5-OP-U
- 6PUG 1.8 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-2`OH-Ethyl-5-OP-U
- 6PUL 1.84 Å, Structure of human MAIT A-F7 TCR in complex with human MR1 3'D-5-OP-RU
- 7ZT7 1.84 Å, Structure of E8 TCR in complex in human MR1 bound to 5FSA
- 6PUC 1.85 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-5-OP-RU
- 6PUH 1.88 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-Ribityl-less
- 6W9U 1.89 Å, Structure of human MAIT A-F7 TCR in complex with patient MR1-R9H-Ac-6-FP
- 4L4V 1.9 Å, Structure of human MAIT TCR in complex with human MR1-RL-6-Me-7-OH
- 5U6Q 1.9 Å, Structure of human MR1-3-F-SA in complex with human MAIT A-F7 TCR
- 6PUE 1.9 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-4'D-5-OP-RU
- 6PUJ 1.92 Å, Structure of human MAIT A-F7 TCR in complex with human MR1-3`OH-Propyl-5-OP-U
- 4PJE 1.95 Å, Structure of human MR1-Ac-6-FP in complex with human MAIT B-B10 TCR
Browse structure collections
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