7WT3: HLA-A*2402

Crystal structure of HLA-A*2402 complexed with 4-mer lipopeptide. Determined by X-ray diffraction at 1.89 Å resolution. Released 22 Jun 2022.

Method
X-ray diffraction
Resolution
1.89 Å
Organisms
Homo sapiens, synthetic construct
Chains
6
Atoms
6,236
Mol. weight
91.36 kDa
Ligands
ZN
Released
22 Jun 2022

Explore 7WT3 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7WT3 contains 21 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: 10 helices, 19 β-strands

ElementResiduesLengthSheet
β-strand2-12111
α-helix201
β-strand21-2881
β-strand31-3771
β-strand46-4721
α-helix50-545
α-helix57-8529
β-strand94-104111
β-strand109-118101
β-strand121-12661
β-strand133-13531
α-helix138-14912
α-helix152-16110
α-helix163-17412
α-helix176-1794
β-strand18312
α-helix184-1852
β-strand186-19383
β-strand198-208113
β-strand20912
β-strand214-21964
β-strand222-22324
β-strand229-23023
α-helix231-2333
β-strand234-23523
β-strand241-250103
α-helix254-2563
β-strand257-26264
β-strand270-27234
Chain B: 2 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand315
α-helix4-52
β-strand6-1166
β-strand21-30106
β-strand3115
β-strand36-4167
β-strand44-4527
β-strand50-5126
α-helix52-543
β-strand55-5626
β-strand62-7096
β-strand78-8367
β-strand91-9447
Chain D: 7 helices, 10 β-strands
ElementResiduesLengthSheet
β-strand2-12118
α-helix201
β-strand21-2888
β-strand31-3778
β-strand46-4728
α-helix50-545
α-helix57-8529
β-strand94-104118
β-strand109-118108
β-strand121-12668
β-strand133-13538
α-helix138-14912
α-helix152-16110
α-helix163-17412
α-helix231-2333
β-strand234-23529
β-strand241-24229
Chain E: 2 helices, 10 β-strands
ElementResiduesLengthSheet
β-strand3110
α-helix4-52
β-strand6-11611
β-strand21-301011
β-strand31110
β-strand36-38312
α-helix44-463
β-strand50-51211
β-strand55-56211
β-strand62-70911
β-strand81-83312
β-strand91-92212

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
MHC class I antigenA, Dprotein277Homo sapiensA0A5H2UYS3 (AlphaFold model)
Beta-2-microglobulinB, Eprotein100Homo sapiensP61769 (AlphaFold model)
4-mer lipopeptideC, Fprotein5synthetic construct
Sequence of entity 1 (A, D), FASTA
>7WT3_1 MHC class I antigen (chains A, D)
AGSHSMRYFSTSVSRPGRGEPRFIAVGYVDDTQFVRFDSDAASQRMEPRAPWIEQEGPEY
WDEETGKVKAHSQTDRENLRIALRYYNQSEAGSHTLQMMFGCDVGSDGRFLRGYHQYAYD
GKDYIALKEDLRSWTAADMAAQITKRKWEAAHVAEQQRAYLEGTCVDGLRRYLENGKETL
QRTDPPKTHMTHHPISDHEATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDG
TFQKWAAVVVPSGEEQRYTCHVQHEGLPKPLTLRWEP
Sequence of entity 2 (B, E), FASTA
>7WT3_2 Beta-2-microglobulin (chains B, E)
AIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLLKNGERIEKVEHSDLSFSKD
WSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
Sequence of entity 3 (C, F), FASTA
>7WT3_3 4-mer lipopeptide (chains C, F)
XGANF

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn3

Water and common crystallization additives (ACT, EDO, TRS) are not listed.

Primary citation

Crystal structures of N-myristoylated lipopeptide-bound HLA class I complexes indicate reorganization of B-pocket architecture upon ligand binding. Asa, M., Morita, D., Kuroha, J. et al. J Biol Chem (2022) 298:102100-102100. DOI 10.1016/j.jbc.2022.102100 · PubMed

Other PDB entries of the same protein (UniProt A0A5H2UYS3 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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