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
| Element | Residues | Length | Sheet |
|---|
| β-strand | -1 | 1 | 1 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 2 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-68 | 17 | |
| β-strand | 76-78 | 3 | 2 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 3 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 3 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain B: 11 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | -1 | 1 | 4 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 5 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-68 | 17 | |
| β-strand | 76-78 | 3 | 5 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 6 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 6 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-174 | 5 | |
| α-helix | 178-180 | 3 | |
Chain C: 11 helices, 4 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 7 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-67 | 16 | |
| β-strand | 76-78 | 3 | 7 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 8 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 8 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain D: 11 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4 | 1 | 9 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 10 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-67 | 16 | |
| β-strand | 76-78 | 3 | 10 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 11 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 11 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain E: 11 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | -1 | 1 | 12 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 13 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-67 | 16 | |
| β-strand | 76-78 | 3 | 13 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 14 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 14 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain F: 12 helices, 4 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 15 |
| α-helix | 33-42 | 10 | |
| α-helix | 43-47 | 5 | |
| α-helix | 52-68 | 17 | |
| β-strand | 76-78 | 3 | 15 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 16 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 16 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain G: 10 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4 | 1 | 1 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 17 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-67 | 16 | |
| β-strand | 76-78 | 3 | 17 |
| α-helix | 79-98 | 20 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 18 |
| α-helix | 126-136 | 11 | |
| α-helix | 142-151 | 10 | |
| β-strand | 160-161 | 2 | 18 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-175 | 6 | |
| α-helix | 178-180 | 3 | |
Chain H: 11 helices, 5 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4 | 1 | 4 |
| α-helix | 10-23 | 14 | |
| β-strand | 30-32 | 3 | 19 |
| α-helix | 33-46 | 14 | |
| α-helix | 52-68 | 17 | |
| β-strand | 76-78 | 3 | 19 |
| α-helix | 79-98 | 20 | |
| α-helix | 101-103 | 3 | |
| α-helix | 104-116 | 13 | |
| β-strand | 123-124 | 2 | 20 |
| α-helix | 126-136 | 11 | |
| α-helix | 144-151 | 8 | |
| β-strand | 160-161 | 2 | 20 |
| α-helix | 162-169 | 8 | |
| α-helix | 170-174 | 5 | |
| α-helix | 178-180 | 3 | |
6 more chain groups are not listed. Open the entry in the viewer and use the sequence panel to see them.
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Aequorin-2 | A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P | protein | 198 | Aequorea victoria | P02592 (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
| ID | Name | Formula | Copies |
|---|
| J2X | (2~{S})-2-(hydroxymethyl)-6-(4-hydroxyphenyl)-2-[(4-hydroxyphenyl)methyl]-4-(ph… | C30 H26 O4 | 16 |
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:
- 1UHK 1.6 Å, Crystal structure of n-aequorin
- 1UHH 1.8 Å, Crystal structure of cp-aequorin
- 1UHI 1.8 Å, Crystal structure of i-aequorin
- 1UHJ 1.8 Å, Crystal structure of br-aequorin
- 7EG3 2.09 Å, Crystal structure of the apoAequorin complex with (S)-HM-daCTZ
- 5ZAB 2.15 Å, Crystal structure of cf3-aequorin
- 1EJ3 2.3 Å, Crystal structure of aequorin
Browse structure collections
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