9VX3: Peptide-bound form of HisMab-1 Fv-clasp

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.

Method
X-ray diffraction
Resolution
2.39 Å
Organisms
Mus musculus, Homo sapiens, synthetic construct
Chains
6
Atoms
5,230
Mol. weight
78.54 kDa
Released
17 Dec 2025

Explore 9VX3 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 6 helices, 13 β-strands

ElementResiduesLengthSheet
β-strand3-751
β-strand11-1222
β-strand18-2581
α-helix29-313
β-strand33-3973
β-strand45-5283
β-strand56-5943
α-helix61-633
β-strand6411
β-strand67-7261
α-helix73-753
β-strand77-8261
α-helix84-863
β-strand88-9583
β-strand100-10343
β-strand107-10933
β-strand110-11122
α-helix119-1224
α-helix125-16339
Chain B: 4 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand4-744
β-strand1015
β-strand19-2574
β-strand30-30A26
β-strand30F-3126
β-strand33-3865
β-strand45-4955
β-strand53-5425
α-helix551
β-strand62-6764
β-strand70-7564
α-helix80-823
β-strand85-9065
α-helix961
β-strand9815
β-strand102-10325
α-helix120-15637
Chain D: 5 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand3-757
β-strand11-1228
β-strand17-2597
α-helix29-313
β-strand33-3979
β-strand45-5289
β-strand56-5949
α-helix61-633
β-strand6417
β-strand67-7267
β-strand77-82A77
α-helix84-863
β-strand88-9589
β-strand100-10349
β-strand107-10939
β-strand110-11128
α-helix117-1204
α-helix125-16339
Chain E: 6 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand4-7410
β-strand10-1349
β-strand19-25710
β-strand30-30A211
β-strand30F-31211
β-strand33-3869
α-helix43-442
β-strand45-4959
β-strand53-5429
α-helix551
β-strand62-67610
β-strand70-75610
α-helix80-823
β-strand85-9069
α-helix961
β-strand97-9829
β-strand102-10659
α-helix120-14829
α-helix150-1567

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
HisMab-1VH(S112C),Serine/threonine-protein kinase 4 18kDa subunitA, Dprotein175Mus musculus, Homo sapiensQ13043 (AlphaFold model)
HisMab-1VL,Serine/threonine-protein kinase 4 18kDa subunitB, Eprotein167Mus musculus, Homo sapiensQ13043 (AlphaFold model)
Polyhistidine peptideC, Fprotein6synthetic construct
Sequence of entity 1 (A, D), FASTA
>9VX3_1 HisMab-1VH(S112C),Serine/threonine-protein kinase 4 18kDa subunit (chains A, D)
GREVQLQQFGAELVKPGASVKISCKASGYTFTDYNMDWVKQSHGKSLEWIGDINPNYDST
VYNQKFKGKATLTVDKSSSTAYMELRSLTSEDTAIYYCARDGAYAMDHWGQGTSVTVCSG
SDYEFLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQSKRQPILDAIEAKGTLLG
Sequence of entity 2 (B, E), FASTA
>9VX3_2 HisMab-1VL,Serine/threonine-protein kinase 4 18kDa subunit (chains B, E)
GRDIVMTQSPSSLSVSAGEKVTMSCKSSQSLLNSGHQKNYLAWYQQKPGQPPKLLISGAS
TRESGVPDRFTGSGSGTDFTLTISSVQAEDLAVYYCQNDHRYPLTFGAGTKLELKRGSDY
EFLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQCKRQPILDAIEAK
Sequence of entity 3 (C, F), FASTA
>9VX3_3 Polyhistidine peptide (chains C, F)
HHHHHH

Primary citation

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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