6MKR: 5287 TCR

5287 TCR bound to IAb Padi4. Determined by X-ray diffraction at 3.35 Å resolution. Released 3 Jul 2019.

Method
X-ray diffraction
Resolution
3.35 Å
Organism
Mus musculus
Chains
4
Atoms
5,982
Mol. weight
95.21 kDa
Released
3 Jul 2019

Explore 6MKR in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6MKR contains 23 α-helices and 79 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: 5 helices, 21 β-strands

ElementResiduesLengthSheet
β-strand3-4210
β-strand9-13511
β-strand18-24710
β-strand31-37711
β-strand44-50711
β-strand55-58410
β-strand61-66610
β-strand71-76610
α-helix81-833
β-strand86-89411
β-strand90112
β-strand92111
α-helix94-963
β-strand103112
β-strand107-112611
β-strand121-125513
β-strand126114
β-strand135-139513
α-helix146-1472
β-strand156-157213
α-helix158-1603
β-strand161-164415
β-strand171-174415
β-strand176-178313
α-helix186-1927
β-strand200113
Chain B: 6 helices, 26 β-strands
ElementResiduesLengthSheet
β-strand2-5416
β-strand8-12517
β-strand17116
β-strand20-23416
β-strand29-36817
β-strand40-491017
β-strand52-55417
β-strand62-65416
β-strand71-76616
α-helix81-833
β-strand85-92817
β-strand100-101217
β-strand105-110617
α-helix113-1153
β-strand117118
β-strand120-124519
β-strand125114
α-helix126-1272
α-helix128-1336
β-strand136-1461119
β-strand147118
β-strand151-157720
β-strand160-161220
β-strand166-168319
β-strand173-174219
β-strand184-1931019
α-helix194-1974
β-strand203-210820
β-strand213121
α-helix224-2252
β-strand227121
β-strand230-236720
Chain C: 4 helices, 16 β-strands
ElementResiduesLengthSheet
β-strand4-15121
β-strand19-2681
β-strand29-3571
β-strand40-4341
α-helix46-516
β-strand5312
α-helix57-7620
α-helix80-845
β-strand8513
β-strand88-9364
β-strand103-112104
β-strand11313
β-strand11815
β-strand133-13424
α-helix136-1372
β-strand138-13924
β-strand145-15394
β-strand164-16526
β-strand16615
β-strand174-17526
Chain D: 8 helices, 16 β-strands
ElementResiduesLengthSheet
β-strand-2412
α-helix-18--163
β-strand7-18121
β-strand23-32101
β-strand35-4171
β-strand47-4931
α-helix54-6310
α-helix65-7410
α-helix75-806
α-helix81-822
α-helix83-875
α-helix91-933
β-strand9617
β-strand99-10468
β-strand114-12188
β-strand12417
β-strand129-13469
β-strand13819
β-strand143-14538
α-helix146-1483
β-strand149-15028
β-strand156-16498
β-strand171-17779
β-strand185-19069

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
H-2 class II histocompatibility antigen, A-B alpha chainCprotein179Mus musculusP14434 (AlphaFold model)
Padi 4 (92-105) peptide and MHC Class II IAb beta chainDprotein217Mus musculusP14483 (AlphaFold model), Q9Z183 (AlphaFold model)
5287 TCR alpha chainAprotein208Mus musculus
5287 TCR beta chainBprotein239Mus musculus
Sequence of entity 1 (C), FASTA
>6MKR_1 H-2 class II histocompatibility antigen, A-B alpha chain (chains C)
IEADHVGTYGISVYQSPGDIGQYTFEFDGDELFYVDLDKKETVWMLPEFGQLASFDPQGG
LQNIAVVKHNLGVLTKRSNSTPATNEAPQATVFPKSPVLLGQPNTLICFVDNIFPPVINI
TWLRNSKSVADGVYETSFFVNRDYSFHKLSYLTFIPSDDDIYDCKVEHWGLEEPVLKHW
Sequence of entity 2 (D), FASTA
>6MKR_2 Padi 4 (92-105) peptide and MHC Class II IAb beta chain (chains D)
RVSYYGPKTSPVQGGGGSLVPRGSGGGGSERHFVYQFMGECYFTNGTQRIRYVTRYIYNR
EEYVRYDSDVGEHRAVTELGRPDAEYWNSQPEILERTRAELDTVCRHNYEGPETHTSLRR
LEQPNVVISLSRTEALNHHNTLVCSVTDFYPAKIKVRWFRNGQEETVGVSSTQLIRNGDW
TFQVLVMLEMTPRRGEVYTCHVEHPSLKSPITVEWRA
Sequence of entity 3 (A), FASTA
>6MKR_3 5287 TCR alpha chain (chains A)
MQQVRQSPQSLTVWEGETAILNCSYENSAFDYFPWYQQFPGEGPALLISILSVSDKKEDG
RFTIFFNKREKKLSLHIADSQPGDSATYFCAASETGANTGKLTFGHGTILRVHPNIQNPD
PAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKCVLDMRSMDFKSNSAVAWS
NKSDFACANAFNNSIIPEDTFFPSPESS
Sequence of entity 4 (B), FASTA
>6MKR_4 5287 TCR beta chain (chains B)
AVTQSPRNKVAVTGGKVTLSCNQTNNHNNMYWYRQDTGHGLRLIHYSYGAGSTEKGDIPD
GYKASRPSQENFSLILELATPSQTSVYFCASGDFWGDTLYFGAGTRLSVLEDLKNVFPPE
VAVFEPSEAEISHTQKATLVCLATGFYPDHVELSWWVNGKEVHSGVCTDPQPLKEQPALN
DSRYALSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQIVSAEAWGRA

Primary citation

A temporal thymic selection switch and ligand binding kinetics constrain neonatal Foxp3+Tregcell development. Stadinski, B.D., Blevins, S.J., Spidale, N.A. et al. Nat Immunol (2019) 20:1046-1058. DOI 10.1038/s41590-019-0414-1 · PubMed

Other PDB entries of the same protein (UniProt P14434 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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