7LFJ: Histocompatibility 2, M region locus 3

Model of MHC class ib H2-M3 with mouse ND1 N-terminal heptapeptide, ala mutant, refined at 1.70 Å resolution. Determined by X-ray diffraction at 1.7 Å resolution. Released 14 Jul 2021.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Mus musculus
Chains
6
Atoms
6,739
Mol. weight
90.72 kDa
Ligands
NAG
Released
14 Jul 2021

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

Secondary structure: helices and β-sheets

7LFJ contains 27 α-helices and 60 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: 11 helices, 19 β-strands

ElementResiduesLengthSheet
β-strand3-12101
α-helix15-162
β-strand22-2871
β-strand31-3991
β-strand42-4761
α-helix50-545
α-helix57-8428
β-strand94-103101
β-strand109-118101
β-strand121-12661
β-strand133-13531
α-helix138-15013
α-helix153-1597
α-helix160-1645
α-helix165-17410
α-helix176-1794
β-strand18312
α-helix184-1852
β-strand186-19383
β-strand199-208103
β-strand20912
β-strand214-21964
β-strand222-22324
β-strand229-23023
α-helix231-2333
β-strand234-23523
β-strand241-24993
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: 11 helices, 19 β-strands
ElementResiduesLengthSheet
β-strand3-12108
β-strand22-2878
β-strand31-3998
β-strand42-4768
α-helix50-545
α-helix57-8428
β-strand94-103108
β-strand109-118108
β-strand121-12668
β-strand133-13538
α-helix138-15013
α-helix153-1597
α-helix160-1645
α-helix165-17410
α-helix176-1794
β-strand18319
α-helix184-1852
β-strand186-193810
β-strand198-2081110
β-strand20919
β-strand214-219611
β-strand222-223211
α-helix225-2273
β-strand229-230210
α-helix231-2333
β-strand234-235210
β-strand241-2501010
α-helix254-2563
β-strand257-262611
β-strand270-272311
Chain E: 3 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand3112
α-helix4-52
β-strand6-11613
β-strand21-301013
β-strand31112
β-strand36-41614
β-strand44-45214
α-helix461
β-strand50-51213
α-helix52-543
β-strand55-56213
β-strand62-70913
β-strand78-83614
β-strand91-94414

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histocompatibility 2, M region locus 3A, Dprotein282Mus musculusQ31093 (AlphaFold model)
Beta-2-microglobulinB, Eprotein99Mus musculusP01887 (AlphaFold model)
Heptapeptide from NADH-ubiquinone oxidoreductase chain 1C, Fprotein7Mus musculusP03888 (AlphaFold model)
Sequence of entity 1 (A, D), FASTA
>7LFJ_1 Histocompatibility 2, M region locus 3 (chains A, D)
GSHSLRYFHTAVSRPGRGEPQYISVGYVDDVQFQRCDSIEEIPRMEPRAPWMEKERPEYW
KELKLKVKNIAQSARANLRTLLRYYNQSEGGSHILQWMVSCEVGPDMRLLGAHYQAAYDG
SDYITLNEDLSSWTAVDMVSQITKSRLESAGTAEYFRAYVEGECLELLHRFLRNGKEILQ
RADPPKAHVAHHPRPKGDVTLRCWALGFYPADITLTWQKDEEDLTQDMELVETRPSGDGT
FQKWAAVVVPSGEEQRYTCYVHHEGLTEPLALKWRSHHHHHH
Sequence of entity 2 (B, E), FASTA
>7LFJ_2 Beta-2-microglobulin (chains B, E)
IQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVEMSDMSFSKDW
SFYILAHTEFTPTETDTYACRVKHDSMAEPKTVYWDRDM
Sequence of entity 3 (C, F), FASTA
>7LFJ_3 Heptapeptide from NADH-ubiquinone oxidoreductase chain 1 (chains C, F)
MFFINAL

Ligands and cofactors

IDNameFormulaCopies
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O61

Water and common crystallization additives (NA) are not listed.

Primary citation

Structure and dynamics of major histocompatibility class Ib molecule H2-M3 complexed with mitochondrial-derived peptides. Strand, A., Shen, S.T., Tomchick, D.R. et al. J Biomol Struct Dyn (2022) 40:10300-10312. DOI 10.1080/07391102.2021.1942214 · PubMed

Other PDB entries of the same protein (UniProt Q31093 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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