9IUT: Cancer-specific anti-HER2 antibody H2Mab-250

Crystal structure of cancer-specific anti-HER2 antibody H2Mab-250 in complex with epitope peptide. Determined by X-ray diffraction at 2.09 Å resolution. Released 4 Jun 2025.

Method
X-ray diffraction
Resolution
2.09 Å
Organisms
Mus musculus, Homo sapiens
Chains
6
Atoms
5,671
Mol. weight
77.96 kDa
Released
4 Jun 2025

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

Secondary structure: helices and β-sheets

9IUT contains 24 α-helices and 50 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: 4 helices, 12 β-strands

ElementResiduesLengthSheet
β-strand3-751
β-strand11-1222
β-strand18-2581
α-helix29-313
β-strand34-3963
β-strand45-5173
β-strand57-5823
β-strand67-7261
β-strand77-8261
α-helix84-863
β-strand88-9363
β-strand10313
β-strand107-10933
β-strand110-11122
α-helix118-1225
α-helix125-16137
Chain B: 7 helices, 13 β-strands
ElementResiduesLengthSheet
α-helix1-33
β-strand4-744
β-strand10-1345
β-strand19-2574
β-strand3016
β-strand3116
β-strand33-3865
β-strand45-4955
β-strand53-5425
α-helix551
β-strand62-6764
β-strand70-7564
α-helix80-823
β-strand84-9075
α-helix971
β-strand9815
α-helix991
β-strand102-10655
α-helix115-1173
α-helix120-15738
Chain D: 6 helices, 12 β-strands
ElementResiduesLengthSheet
β-strand3-757
β-strand11-1228
β-strand17-2597
α-helix29-313
β-strand34-3969
β-strand45-5179
β-strand57-5829
β-strand67-7267
α-helix73-753
β-strand77-82A77
α-helix84-863
β-strand88-9369
β-strand10319
β-strand107-10939
β-strand110-11128
α-helix112-1132
α-helix118-1225
α-helix125-16137
Chain E: 7 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand4-7410
β-strand10-12311
β-strand19-25710
β-strand30112
β-strand31112
β-strand33-38611
β-strand44-49611
β-strand53-54211
α-helix551
β-strand62-67610
β-strand70-75610
α-helix80-823
β-strand84-90711
α-helix971
β-strand98111
α-helix991
β-strand102-105411
α-helix113-1175
α-helix120-1289
α-helix130-15829

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
H2Mab-250 VH(S112C)-SARAHA, Dprotein169Mus musculus
H2Mab-250 VL-SARAH(S37C)B, Eprotein171Mus musculus
H2Mab-250 epitope peptideC, Fprotein8Homo sapiensP04626 (AlphaFold model)
Sequence of entity 1 (A, D), FASTA
>9IUT_1 H2Mab-250 VH(S112C)-SARAH (chains A, D)
GREVQLVESGGGLVQPGGSLKLSCAASGFTFSNYGMSWVRQTPDRRLELVATINNNGGGT
YYPDSVKGRFTISRDNAKNTLYLQMSSLKSEDTAMYYCTSPGLLWDAWGAGTTVTVCSGS
DYEFLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQSKRQPILDAIEAK
Sequence of entity 2 (B, E), FASTA
>9IUT_2 H2Mab-250 VL-SARAH(S37C) (chains B, E)
GRDVVMTQTPLTLSVSIGQPASISCKSSQSLLDSDGRTYLNWLLQRPGQSPKRLIYLVSK
LDSGAPDRFTGSGSGTDFTLKISRVEAEDLGVYYCWQGTHFPQTFGGGTKLEIKRGSDYE
FLKSWTVEDLQKRLLALDPMMEQEIEEIRQKYQCKRQPILDAIEAKGTLLG
Sequence of entity 3 (C, F), FASTA
>9IUT_3 H2Mab-250 epitope peptide (chains C, F)
MPIWKFPD

Primary citation

Preferential tumor targeting of HER2 by iPSC-derived CAR T cells engineered to overcome multiple barriers to solid tumor efficacy. Hosking, M.P., Shirinbak, S., Omilusik, K. et al. Cell Stem Cell (2025) 32:1087-1101.e4. DOI 10.1016/j.stem.2025.05.007 · 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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