Crystal structure of the single-chain Fv (scFv) fragment of an anti-ErbB2 antibody chA21 in complex with residues 1-192 of ErbB2 extracellular domain. Determined by X-ray diffraction at 2.45 Å resolution. Released 28 Apr 2010.
Explore 3H3B in 3D Show helices and sheets RCSB PDB PDBe
3H3B contains 28 α-helices and 84 β-strands across 4 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 | 3-5 | 3 | 1 |
| α-helix | 12-14 | 3 | |
| α-helix | 17-28 | 12 | |
| β-strand | 33-35 | 3 | 1 |
| β-strand | 38-41 | 4 | 2 |
| α-helix | 50-52 | 3 | |
| β-strand | 57-58 | 2 | 1 |
| β-strand | 62-65 | 4 | 2 |
| β-strand | 71-73 | 3 | 3 |
| β-strand | 79-80 | 2 | 1 |
| β-strand | 86 | 1 | 2 |
| β-strand | 90-95 | 6 | 2 |
| β-strand | 98 | 1 | 4 |
| α-helix | 105-107 | 3 | |
| β-strand | 114 | 1 | 4 |
| β-strand | 117-119 | 3 | 3 |
| β-strand | 125-126 | 2 | 1 |
| β-strand | 130-134 | 5 | 2 |
| α-helix | 147-150 | 4 | |
| β-strand | 151 | 1 | 1 |
| β-strand | 160-162 | 3 | 2 |
| α-helix | 169-174 | 6 | |
| β-strand | 182 | 1 | 5 |
| β-strand | 190 | 1 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-5 | 3 | 6 |
| α-helix | 12-14 | 3 | |
| α-helix | 17-28 | 12 | |
| β-strand | 33-35 | 3 | 6 |
| β-strand | 38-41 | 4 | 7 |
| α-helix | 50-52 | 3 | |
| β-strand | 57-58 | 2 | 6 |
| β-strand | 62-65 | 4 | 7 |
| β-strand | 71-73 | 3 | 8 |
| β-strand | 79-80 | 2 | 6 |
| β-strand | 86 | 1 | 7 |
| β-strand | 90-95 | 6 | 7 |
| β-strand | 98 | 1 | 9 |
| β-strand | 114 | 1 | 9 |
| β-strand | 117-119 | 3 | 8 |
| β-strand | 125-126 | 2 | 6 |
| β-strand | 130-134 | 5 | 7 |
| α-helix | 142-144 | 3 | |
| α-helix | 147-150 | 4 | |
| β-strand | 151 | 1 | 6 |
| β-strand | 160-162 | 3 | 7 |
| α-helix | 169-174 | 6 | |
| β-strand | 182 | 1 | 10 |
| α-helix | 187-189 | 3 | |
| β-strand | 190 | 1 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 0-2 | 3 | |
| β-strand | 4-7 | 4 | 11 |
| β-strand | 10-12 | 3 | 12 |
| β-strand | 19-25 | 7 | 11 |
| β-strand | 30-31 | 2 | 13 |
| β-strand | 36-37 | 2 | 13 |
| β-strand | 39-44 | 6 | 12 |
| β-strand | 51-55 | 5 | 12 |
| β-strand | 59-60 | 2 | 12 |
| α-helix | 61 | 1 | |
| β-strand | 68-73 | 6 | 11 |
| β-strand | 76-81 | 6 | 11 |
| α-helix | 86-88 | 3 | |
| β-strand | 91-96 | 6 | 12 |
| α-helix | 102 | 1 | |
| β-strand | 103-104 | 2 | 12 |
| β-strand | 108-111 | 4 | 12 |
| β-strand | 137-140 | 4 | 14 |
| α-helix | 141-143 | 3 | |
| β-strand | 144-146 | 3 | 15 |
| β-strand | 152-159 | 8 | 14 |
| α-helix | 163-165 | 3 | |
| β-strand | 167-173 | 7 | 15 |
| β-strand | 180-186 | 7 | 15 |
| β-strand | 192-194 | 3 | 15 |
| α-helix | 196-198 | 3 | |
| β-strand | 202-207 | 6 | 14 |
| β-strand | 212-217 | 6 | 14 |
| α-helix | 222-224 | 3 | |
| β-strand | 226-233 | 8 | 15 |
| α-helix | 236-238 | 3 | |
| β-strand | 241-244 | 4 | 15 |
| β-strand | 248-252 | 5 | 15 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | -1-3 | 5 | |
| β-strand | 4-7 | 4 | 16 |
| β-strand | 10-13 | 4 | 17 |
| β-strand | 19-25 | 7 | 16 |
| β-strand | 30-31 | 2 | 18 |
| β-strand | 36-37 | 2 | 18 |
| β-strand | 39-44 | 6 | 17 |
| β-strand | 51-55 | 5 | 17 |
| β-strand | 59-60 | 2 | 17 |
| α-helix | 61 | 1 | |
| β-strand | 68-73 | 6 | 16 |
| β-strand | 76-81 | 6 | 16 |
| β-strand | 91-96 | 6 | 17 |
| α-helix | 102 | 1 | |
| β-strand | 103-104 | 2 | 17 |
| β-strand | 108-112 | 5 | 17 |
| β-strand | 137-140 | 4 | 19 |
| β-strand | 144-146 | 3 | 20 |
| β-strand | 152-159 | 8 | 19 |
| α-helix | 163-165 | 3 | |
| β-strand | 167-173 | 7 | 20 |
| β-strand | 180-186 | 7 | 20 |
| β-strand | 192-194 | 3 | 20 |
| β-strand | 202-207 | 6 | 19 |
| β-strand | 212-217 | 6 | 19 |
| α-helix | 222-224 | 3 | |
| β-strand | 226-233 | 8 | 20 |
| α-helix | 236-238 | 3 | |
| β-strand | 241-244 | 4 | 20 |
| β-strand | 248-252 | 5 | 20 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Receptor tyrosine-protein kinase erbB-2 | A, B | protein | 194 | Homo sapiens | P04626 (AlphaFold model) |
| anti-ErbB2 antibody chA21 | C, D | protein | 259 | Mus musculus |
>3H3B_1 Receptor tyrosine-protein kinase erbB-2 (chains A, B) GSTQVCTGTDMKLRLPASPETHLDMLRHLYQGCQVVQGNLELTYLPTNASLSFLQDIQEV QGYVLIAHNQVRQVPLQRLRIVRGTQLFEDNYALAVLDNGDPLNNTTPVTGASPGGLREL QLRSLTEILKGGVLIQRNPQLCYQDTILWKDIFHKNNQLALTLIDTNRSRACHPCSPMCK GSRCWGESSEDCQS
>3H3B_2 anti-ErbB2 antibody chA21 (chains C, D) AAQPADIVLTQTPSSLPVSVGEKVTMTCKSSQTLLYSNNQKNYLAWYQQKPGQSPKLLIS WAFTRKSGVPDRFTGSGSGTDFTLTIGSVKAEDLAVYYCQQYSNYPWTFGGGTRLEIKRG GGGSGGGGSGGGGSGGGGSEVQLQQSGPEVVKTGASVKISCKASGYSFTGYFINWVKKNS GKSPEWIGHISSSYATSTYNQKFKNKAAFTVDTSSSTAFMQLNSLTSEDSAVYYCVRSGN YEEYAMDYWGQGTSVTVSS
Structural Insights into the Down-regulation of Overexpressed p185her2/neu Protein of Transformed Cells by the Antibody chA21. Zhou, H., Zha, Z., Liu, Y. et al. J Biol Chem (2011) 286:31676-31683. DOI 10.1074/jbc.M111.235184 · PubMed
Other PDB entries of the same protein (UniProt P04626 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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