7EG2: ApoAequorin complex with (S)-daCTZ

Crystal structure of the apoAequorin complex with (S)-daCTZ. Determined by X-ray diffraction at 2.22 Å resolution. Released 23 Jun 2021.

Method
X-ray diffraction
Resolution
2.22 Å
Organism
Aequorea victoria
Chains
16
Atoms
26,432
Mol. weight
367.91 kDa
Ligands
J2X
Released
23 Jun 2021

Explore 7EG2 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7EG2 contains 173 α-helices and 72 β-strands across 16 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, 5 β-strands

ElementResiduesLengthSheet
β-strand-111
α-helix10-2314
β-strand30-3232
α-helix33-4614
α-helix52-6817
β-strand76-7832
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-12423
α-helix126-13611
α-helix142-15110
β-strand160-16123
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain B: 11 helices, 5 β-strands
ElementResiduesLengthSheet
β-strand-114
α-helix10-2314
β-strand30-3235
α-helix33-4614
α-helix52-6817
β-strand76-7835
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-12426
α-helix126-13611
α-helix142-15110
β-strand160-16126
α-helix162-1698
α-helix170-1745
α-helix178-1803
Chain C: 11 helices, 4 β-strands
ElementResiduesLengthSheet
α-helix10-2314
β-strand30-3237
α-helix33-4614
α-helix52-6716
β-strand76-7837
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-12428
α-helix126-13611
α-helix142-15110
β-strand160-16128
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain D: 11 helices, 5 β-strands
ElementResiduesLengthSheet
β-strand419
α-helix10-2314
β-strand30-32310
α-helix33-4614
α-helix52-6716
β-strand76-78310
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-124211
α-helix126-13611
α-helix142-15110
β-strand160-161211
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain E: 11 helices, 5 β-strands
ElementResiduesLengthSheet
β-strand-1112
α-helix10-2314
β-strand30-32313
α-helix33-4614
α-helix52-6716
β-strand76-78313
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-124214
α-helix126-13611
α-helix142-15110
β-strand160-161214
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain F: 12 helices, 4 β-strands
ElementResiduesLengthSheet
α-helix10-2314
β-strand30-32315
α-helix33-4210
α-helix43-475
α-helix52-6817
β-strand76-78315
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-124216
α-helix126-13611
α-helix142-15110
β-strand160-161216
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain G: 10 helices, 5 β-strands
ElementResiduesLengthSheet
β-strand411
α-helix10-2314
β-strand30-32317
α-helix33-4614
α-helix52-6716
β-strand76-78317
α-helix79-9820
α-helix104-11613
β-strand123-124218
α-helix126-13611
α-helix142-15110
β-strand160-161218
α-helix162-1698
α-helix170-1756
α-helix178-1803
Chain H: 11 helices, 5 β-strands
ElementResiduesLengthSheet
β-strand414
α-helix10-2314
β-strand30-32319
α-helix33-4614
α-helix52-6817
β-strand76-78319
α-helix79-9820
α-helix101-1033
α-helix104-11613
β-strand123-124220
α-helix126-13611
α-helix144-1518
β-strand160-161220
α-helix162-1698
α-helix170-1745
α-helix178-1803

6 more chain groups are not listed. Open the entry in the viewer and use the sequence panel to see them.

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Aequorin-2A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, Pprotein198Aequorea victoriaP02592 (AlphaFold model)
Sequence of entity 1 (A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P), FASTA
>7EG2_1 Aequorin-2 (chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P)
ANSHHHHHHGKLTSDFDNPRWIGRHKHMFNFLDVNHNGKISLDEMVYKASDIVINNLGAT
PEQAKRHKDAVEAFFGGAGMKYGVETDWPAYIEGWKKLATDELEKYAKNEPTLIRIWGDA
LFDIVDKDQNGAITLDEWKAYTKAAGIIQSSEDCEETFRVCDIDESGQLDVDEMTRQHLG
FWYTMDPACEKLYGGAVP

Ligands and cofactors

IDNameFormulaCopies
J2X(2~{S})-2-(hydroxymethyl)-6-(4-hydroxyphenyl)-2-[(4-hydroxyphenyl)methyl]-4-(ph…C30 H26 O416

Primary citation

Chiral deaza-coelenterazine analogs for probing a substrate-binding site in the Ca2+-binding photoprotein aequorin. Inouye, S., Sumida, Y., Tomabechi, Y. et al. PLoS One (2021) 16:e0251743-e0251743. DOI 10.1371/journal.pone.0251743 · PubMed

Other PDB entries of the same protein (UniProt P02592 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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