Crystal structure of the peptide-bound form of HisMab-1 Fv-clasp. Determined by X-ray diffraction at 2.39 Å resolution. Released 17 Dec 2025.
Explore 9VX3 in 3D Show helices and sheets RCSB PDB PDBe
9VX3 contains 21 α-helices and 52 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 | 3-7 | 5 | 1 |
| β-strand | 11-12 | 2 | 2 |
| β-strand | 18-25 | 8 | 1 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 3 |
| β-strand | 45-52 | 8 | 3 |
| β-strand | 56-59 | 4 | 3 |
| α-helix | 61-63 | 3 | |
| β-strand | 64 | 1 | 1 |
| β-strand | 67-72 | 6 | 1 |
| α-helix | 73-75 | 3 | |
| β-strand | 77-82 | 6 | 1 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-95 | 8 | 3 |
| β-strand | 100-103 | 4 | 3 |
| β-strand | 107-109 | 3 | 3 |
| β-strand | 110-111 | 2 | 2 |
| α-helix | 119-122 | 4 | |
| α-helix | 125-163 | 39 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 4 |
| β-strand | 10 | 1 | 5 |
| β-strand | 19-25 | 7 | 4 |
| β-strand | 30-30A | 2 | 6 |
| β-strand | 30F-31 | 2 | 6 |
| β-strand | 33-38 | 6 | 5 |
| β-strand | 45-49 | 5 | 5 |
| β-strand | 53-54 | 2 | 5 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 4 |
| β-strand | 70-75 | 6 | 4 |
| α-helix | 80-82 | 3 | |
| β-strand | 85-90 | 6 | 5 |
| α-helix | 96 | 1 | |
| β-strand | 98 | 1 | 5 |
| β-strand | 102-103 | 2 | 5 |
| α-helix | 120-156 | 37 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 7 |
| β-strand | 11-12 | 2 | 8 |
| β-strand | 17-25 | 9 | 7 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 9 |
| β-strand | 45-52 | 8 | 9 |
| β-strand | 56-59 | 4 | 9 |
| α-helix | 61-63 | 3 | |
| β-strand | 64 | 1 | 7 |
| β-strand | 67-72 | 6 | 7 |
| β-strand | 77-82A | 7 | 7 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-95 | 8 | 9 |
| β-strand | 100-103 | 4 | 9 |
| β-strand | 107-109 | 3 | 9 |
| β-strand | 110-111 | 2 | 8 |
| α-helix | 117-120 | 4 | |
| α-helix | 125-163 | 39 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 10 |
| β-strand | 10-13 | 4 | 9 |
| β-strand | 19-25 | 7 | 10 |
| β-strand | 30-30A | 2 | 11 |
| β-strand | 30F-31 | 2 | 11 |
| β-strand | 33-38 | 6 | 9 |
| α-helix | 43-44 | 2 | |
| β-strand | 45-49 | 5 | 9 |
| β-strand | 53-54 | 2 | 9 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 10 |
| β-strand | 70-75 | 6 | 10 |
| α-helix | 80-82 | 3 | |
| β-strand | 85-90 | 6 | 9 |
| α-helix | 96 | 1 | |
| β-strand | 97-98 | 2 | 9 |
| β-strand | 102-106 | 5 | 9 |
| α-helix | 120-148 | 29 | |
| α-helix | 150-156 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| HisMab-1VH(S112C),Serine/threonine-protein kinase 4 18kDa subunit | A, D | protein | 175 | Mus musculus, Homo sapiens | Q13043 (AlphaFold model) |
| HisMab-1VL,Serine/threonine-protein kinase 4 18kDa subunit | B, E | protein | 167 | Mus musculus, Homo sapiens | Q13043 (AlphaFold model) |
| Polyhistidine peptide | C, F | protein | 6 | synthetic construct |
>9VX3_1 HisMab-1VH(S112C),Serine/threonine-protein kinase 4 18kDa subunit (chains A, D) GREVQLQQFGAELVKPGASVKISCKASGYTFTDYNMDWVKQSHGKSLEWIGDINPNYDST VYNQKFKGKATLTVDKSSSTAYMELRSLTSEDTAIYYCARDGAYAMDHWGQGTSVTVCSG SDYEFLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQSKRQPILDAIEAKGTLLG
>9VX3_2 HisMab-1VL,Serine/threonine-protein kinase 4 18kDa subunit (chains B, E) GRDIVMTQSPSSLSVSAGEKVTMSCKSSQSLLNSGHQKNYLAWYQQKPGQPPKLLISGAS TRESGVPDRFTGSGSGTDFTLTISSVQAEDLAVYYCQNDHRYPLTFGAGTKLELKRGSDY EFLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQCKRQPILDAIEAK
>9VX3_3 Polyhistidine peptide (chains C, F) HHHHHH
Functional and Structural Characterization of a Novel Anti-His-tag Antibody, HisMab-1. Hitomi, N., Hoshi, S., Kaneko, M.K. et al. J Mol Biol (2025) 438:169574-169574. DOI 10.1016/j.jmb.2025.169574 · PubMed
Other PDB entries of the same protein (UniProt Q13043 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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