Crystal structure of therapeutic mAB AR20.5 in complex with MUC1 peptide. Determined by X-ray diffraction at 1.97 Å resolution. Released 11 Jan 2017.
Explore 5T6P in 3D Show helices and sheets RCSB PDB PDBe
5T6P contains 28 α-helices and 90 β-strands across 6 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 | 4-7 | 4 | 1 |
| β-strand | 10-14 | 5 | 2 |
| β-strand | 19-25 | 7 | 1 |
| β-strand | 30 | 1 | 3 |
| β-strand | 36 | 1 | 3 |
| β-strand | 38-43 | 6 | 2 |
| β-strand | 50-54 | 5 | 2 |
| β-strand | 58-59 | 2 | 2 |
| α-helix | 60 | 1 | |
| β-strand | 67-72 | 6 | 1 |
| β-strand | 75-80 | 6 | 1 |
| α-helix | 85-87 | 3 | |
| β-strand | 89-95 | 7 | 2 |
| α-helix | 101 | 1 | |
| β-strand | 102-103 | 2 | 2 |
| β-strand | 107-112 | 6 | 2 |
| β-strand | 116 | 1 | 4 |
| β-strand | 119-123 | 5 | 5 |
| α-helix | 124-126 | 3 | |
| α-helix | 127-132 | 6 | |
| β-strand | 134-144 | 11 | 5 |
| β-strand | 145 | 1 | 4 |
| β-strand | 150-155 | 6 | 6 |
| β-strand | 158-160 | 3 | 6 |
| β-strand | 164-168 | 5 | 5 |
| α-helix | 169-172 | 4 | |
| β-strand | 178-187 | 10 | 5 |
| α-helix | 188-191 | 4 | |
| β-strand | 196-202 | 7 | 6 |
| β-strand | 210-215 | 6 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 7 |
| β-strand | 10-12 | 3 | 8 |
| β-strand | 18-25 | 8 | 7 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 8 |
| β-strand | 45-51 | 7 | 8 |
| β-strand | 59 | 1 | 8 |
| β-strand | 69-73 | 5 | 7 |
| β-strand | 78-83 | 6 | 7 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 8 |
| β-strand | 103-106 | 4 | 8 |
| β-strand | 110-114 | 5 | 8 |
| α-helix | 118-119 | 2 | |
| β-strand | 120 | 1 | 9 |
| α-helix | 121-122 | 2 | |
| β-strand | 123-127 | 5 | 10 |
| β-strand | 139-148 | 10 | 10 |
| β-strand | 149 | 1 | 9 |
| β-strand | 154-157 | 4 | 11 |
| α-helix | 158-160 | 3 | |
| β-strand | 162 | 1 | 11 |
| β-strand | 166-168 | 3 | 10 |
| α-helix | 169-171 | 3 | |
| β-strand | 172-174 | 3 | 10 |
| β-strand | 177-186 | 10 | 10 |
| β-strand | 197-202 | 6 | 11 |
| β-strand | 207-212 | 6 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 12 |
| β-strand | 10-14 | 5 | 13 |
| β-strand | 19-25 | 7 | 12 |
| β-strand | 30 | 1 | 14 |
| β-strand | 36 | 1 | 14 |
| β-strand | 38-43 | 6 | 13 |
| β-strand | 49-54 | 6 | 13 |
| β-strand | 58-59 | 2 | 13 |
| α-helix | 60 | 1 | |
| β-strand | 67-72 | 6 | 12 |
| β-strand | 75-80 | 6 | 12 |
| α-helix | 85-87 | 3 | |
| β-strand | 89-95 | 7 | 13 |
| α-helix | 101 | 1 | |
| β-strand | 102-103 | 2 | 13 |
| β-strand | 107-112 | 6 | 13 |
| β-strand | 116 | 1 | 15 |
| β-strand | 119-123 | 5 | 16 |
| α-helix | 124-126 | 3 | |
| α-helix | 127-132 | 6 | |
| β-strand | 134-144 | 11 | 16 |
| β-strand | 145 | 1 | 15 |
| β-strand | 150-155 | 6 | 17 |
| β-strand | 158-160 | 3 | 17 |
| β-strand | 164-168 | 5 | 16 |
| α-helix | 169-172 | 4 | |
| β-strand | 178-187 | 10 | 16 |
| α-helix | 188-191 | 4 | |
| β-strand | 196-203 | 8 | 17 |
| β-strand | 206-215 | 10 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-7 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Fab fragment AR20.5 - Light Chain | A, C | protein | 216 | Mus musculus | |
| Fab Fragment - Heavy Chain | B, D | protein | 215 | Mus musculus | |
| MUC1 Peptide Fragment | E, F | protein | 8 | Homo sapiens | P15941 (AlphaFold model) |
>5T6P_1 Fab fragment AR20.5 - Light Chain (chains A, C) DVLMTQTPLSLPVSLGDQASISCRSSQTIVHSNGKIYLEWYLQKPGQSPKLLIYRVSKRF SGVPDRFSGSGSGTDFTLKISRVEAEDLGVYYCFQGSHVPWTFGGGTKLEIKRADAAPTV SIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSM SSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNR
>5T6P_2 Fab Fragment - Heavy Chain (chains B, D) EVKLVESGGGLVAPGGSLKLSCAASGFTFSSYPMSWVRQTPEKRLEWVAYINNGGGNPYY PDTVKGRFTISRDNAKNTLYLQMSSLKSEDTAIYYCIRQYYGFDYWGQGTTLTVSSAKTT PPSVYPLAPGSAAQTNSMVTLGCLVKGYFPEPVTVTWNSGSLSSGVHTFPAVLQSDLYTL SSSVTVPSSTWPSETVTCNVAHPASSTKVDKKIVP
>5T6P_3 MUC1 Peptide Fragment (chains E, F) APDTRPAP
Glycosylation of MUC1 influences the binding of a therapeutic antibody by altering the conformational equilibrium of the antigen. Movahedin, M., Brooks, T.M., Supekar, N.T. et al. Glycobiology (2017) 27:677-687. DOI 10.1093/glycob/cww131 · PubMed
Other PDB entries of the same protein (UniProt P15941 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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