5MOL: Human IgE-Fc crystal structure

Human IgE-Fc crystal structure. Determined by X-ray diffraction at 1.75 Å resolution. Released 10 Jan 2018.

Method
X-ray diffraction
Resolution
1.75 Å
Organism
Homo sapiens
Chains
2
Atoms
5,750
Mol. weight
75.75 kDa
Ligands
PG0, AE3
Released
10 Jan 2018

Explore 5MOL in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5MOL contains 37 α-helices and 52 β-strands across 2 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: 18 helices, 26 β-strands

ElementResiduesLengthSheet
β-strand235-23951
α-helix240-2412
α-helix246-2483
β-strand250-259111
β-strand264-27072
β-strand273-27422
α-helix275-2762
α-helix277-2793
β-strand280-28781
β-strand290-300111
α-helix301-3055
β-strand310-31672
β-strand319-32572
α-helix327-3304
α-helix333-3353
β-strand337-34043
α-helix341-3444
α-helix3451
α-helix346-3516
β-strand355-36393
α-helix369-3702
β-strand371-37664
β-strand388-39143
β-strand397-40483
α-helix407-4115
β-strand416-42164
β-strand429-43354
β-strand44115
α-helix442-4432
β-strand444-44966
α-helix450-4534
β-strand459-469116
β-strand47015
β-strand475-48067
β-strand483-48427
α-helix485-4862
α-helix487-4893
β-strand490-49236
α-helix493-4953
β-strand496-49726
β-strand503-512106
α-helix513-5186
β-strand522-52767
β-strand536-54167
Chain B: 19 helices, 26 β-strands
ElementResiduesLengthSheet
α-helix226-2283
β-strand234-23961
α-helix240-2412
α-helix246-2483
β-strand250-259111
β-strand264-27078
β-strand273-27428
α-helix275-2762
α-helix277-2793
β-strand280-28781
β-strand290-300111
α-helix301-3055
β-strand310-31678
β-strand319-32578
α-helix327-3304
α-helix333-3364
β-strand337-34049
α-helix341-3444
α-helix345-3495
β-strand355-36399
α-helix3641
α-helix368-3703
β-strand371-376610
α-helix380-3856
β-strand386-39169
β-strand397-40489
α-helix407-4115
β-strand416-421610
β-strand429-433510
β-strand441111
α-helix442-4432
β-strand444-449612
α-helix450-4523
β-strand459-4691112
β-strand470111
β-strand475-480613
β-strand483-484213
α-helix487-4893
β-strand490-492312
α-helix493-4953
β-strand496-497212
β-strand503-5121012
α-helix513-5186
β-strand522-527613
β-strand536-541613

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ig epsilon chain C regionA, Bprotein327Homo sapiensP01854 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5MOL_1 Ig epsilon chain C region (chains A, B)
DIVASRDFTPPTVKILQSSCDGGGHFPPTIQLLCLVSGYTPGTIQITWLEDGQVMDVDLS
TASTTQEGELASTQSELTLSQKHWLSDRTYTCQVTYQGHTFEDSTKKCADSNPRGVSAYL
SRPSPFDLFIRKSPTITCLVVDLAPSKGTVQLTWSRASGKPVNHSTRKEEKQRNGTLTVT
STLPVGTRDWIEGETYQCRVTHPHLPRALMRSTTKTSGPRAAPEVYAFATPEWPGSRDKR
TLACLIQNFMPEDISVQWLHNEVQLPDARHSTTQPRKTKGSGFFVFSRLEVTRAEWEQKD
EFICRAVHEAASPSQTVQRAVSVNPGK

Ligands and cofactors

IDNameFormulaCopies
PG02-(2-methoxyethoxy)ethanolC5 H12 O32
AE32-(2-ethoxyethoxy)ethanolC6 H14 O31

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

Primary citation

Thermal sensitivity and flexibility of the C epsilon 3 domains in immunoglobulin E. Dore, K.A., Davies, A.M., Drinkwater, N. et al. Biochim Biophys Acta (2017) 1865:1336-1347. DOI 10.1016/j.bbapap.2017.08.005 · PubMed

Other PDB entries of the same protein (UniProt P01854 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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