7ZLM: SOCS2:ElonginB:ElonginC
Crystal structure of SOCS2:ElonginB:ElonginC in complex with compound MN551. Determined by X-ray diffraction at 1.79 Å resolution. Released 26 Apr 2023.
- Method
- X-ray diffraction
- Resolution
- 1.79 Å
- Organism
- Homo sapiens
- Chains
- 12
- Atoms
- 11,856
- Mol. weight
- 175.89 kDa
- Ligands
- JIH
- Released
- 26 Apr 2023
Explore 7ZLM in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
7ZLM contains 86 α-helices and 90 β-strands across 12 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: 9 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 33-46 | 14 | |
| β-strand | 49 | 1 | 1 |
| α-helix | 55-62 | 8 | |
| α-helix | 66 | 1 | |
| β-strand | 70-74 | 5 | 1 |
| β-strand | 82-88 | 7 | 1 |
| β-strand | 91-100 | 10 | 1 |
| β-strand | 103-106 | 4 | 1 |
| α-helix | 113-115 | 3 | |
| β-strand | 119 | 1 | 1 |
| α-helix | 122-134 | 13 | |
| β-strand | 155 | 1 | 1 |
| α-helix | 160-162 | 3 | |
| α-helix | 163-174 | 12 | |
| α-helix | 178-180 | 3 | |
| α-helix | 185-192 | 8 | |
Chain B: 8 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 2-9 | 8 | 2 |
| β-strand | 10 | 1 | 3 |
| β-strand | 12-19 | 8 | 2 |
| β-strand | 23 | 1 | 4 |
| α-helix | 24-35 | 12 | |
| α-helix | 39-41 | 3 | |
| β-strand | 42-46 | 5 | 2 |
| β-strand | 49-50 | 2 | 2 |
| α-helix | 51-52 | 2 | |
| β-strand | 56 | 1 | 4 |
| α-helix | 64-66 | 3 | |
| β-strand | 68 | 1 | 5 |
| β-strand | 71 | 1 | 5 |
| α-helix | 72 | 1 | |
| β-strand | 73-79 | 7 | 2 |
| β-strand | 80-81 | 2 | 6 |
| β-strand | 84-85 | 2 | 6 |
| α-helix | 86-88 | 3 | |
| β-strand | 90 | 1 | 3 |
| α-helix | 91-100 | 10 | |
| α-helix | 101-103 | 3 | |
Chains C and F: 5 helices, 3 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 18-22 | 5 | 2 |
| β-strand | 28-32 | 5 | 2 |
| α-helix | 33-36 | 4 | |
| α-helix | 40-44 | 5 | |
| β-strand | 59-61 | 3 | 2 |
| α-helix | 67-82 | 16 | |
| α-helix | 89-92 | 4 | |
| α-helix | 97-110 | 14 | |
Chain D: 8 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 33-46 | 14 | |
| β-strand | 49 | 1 | 7 |
| α-helix | 55-62 | 8 | |
| α-helix | 66 | 1 | |
| β-strand | 70-74 | 5 | 7 |
| β-strand | 82-88 | 7 | 7 |
| β-strand | 91-100 | 10 | 7 |
| β-strand | 103-106 | 4 | 7 |
| β-strand | 119 | 1 | 7 |
| α-helix | 122-134 | 13 | |
| β-strand | 155 | 1 | 7 |
| α-helix | 160-162 | 3 | |
| α-helix | 163-174 | 12 | |
| α-helix | 178-180 | 3 | |
| α-helix | 185-192 | 8 | |
Chain E: 8 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 2-9 | 8 | 8 |
| β-strand | 10 | 1 | 9 |
| β-strand | 12-19 | 8 | 8 |
| β-strand | 23 | 1 | 10 |
| α-helix | 24-35 | 12 | |
| α-helix | 39-41 | 3 | |
| β-strand | 42-46 | 5 | 8 |
| β-strand | 49-50 | 2 | 8 |
| α-helix | 51-52 | 2 | |
| β-strand | 56 | 1 | 10 |
| β-strand | 68 | 1 | 11 |
| β-strand | 71 | 1 | 11 |
| α-helix | 72 | 1 | |
| β-strand | 73-79 | 7 | 8 |
| β-strand | 80-81 | 2 | 12 |
| β-strand | 84-85 | 2 | 12 |
| α-helix | 86-88 | 3 | |
| β-strand | 90 | 1 | 9 |
| α-helix | 91-96 | 6 | |
| α-helix | 98-100 | 3 | |
| α-helix | 101-103 | 3 | |
Chain G: 9 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 33-45 | 13 | |
| β-strand | 49 | 1 | 13 |
| α-helix | 55-62 | 8 | |
| α-helix | 66 | 1 | |
| β-strand | 70-74 | 5 | 13 |
| β-strand | 82-88 | 7 | 13 |
| β-strand | 91-100 | 10 | 13 |
| β-strand | 103-106 | 4 | 13 |
| α-helix | 113-115 | 3 | |
| β-strand | 119 | 1 | 13 |
| α-helix | 122-134 | 13 | |
| β-strand | 155 | 1 | 13 |
| α-helix | 160-162 | 3 | |
| α-helix | 163-174 | 12 | |
| α-helix | 178-180 | 3 | |
| α-helix | 185-192 | 8 | |
Chain H: 9 helices, 11 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 2-9 | 8 | 14 |
| β-strand | 10 | 1 | 15 |
| β-strand | 12-19 | 8 | 14 |
| β-strand | 23 | 1 | 16 |
| α-helix | 24-35 | 12 | |
| α-helix | 39-41 | 3 | |
| β-strand | 43-46 | 4 | 14 |
| β-strand | 49-50 | 2 | 14 |
| α-helix | 51-52 | 2 | |
| β-strand | 56 | 1 | 16 |
| α-helix | 58-60 | 3 | |
| α-helix | 64-66 | 3 | |
| β-strand | 68 | 1 | 17 |
| β-strand | 71 | 1 | 17 |
| α-helix | 72 | 1 | |
| β-strand | 73-78 | 6 | 14 |
| α-helix | 85-87 | 3 | |
| β-strand | 90 | 1 | 15 |
| α-helix | 91-100 | 10 | |
| α-helix | 101-103 | 3 | |
Chain I: 5 helices, 3 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 18-22 | 5 | 14 |
| β-strand | 28-32 | 5 | 14 |
| α-helix | 33-36 | 4 | |
| α-helix | 40-45 | 6 | |
| β-strand | 59-61 | 3 | 14 |
| α-helix | 67-82 | 16 | |
| α-helix | 89-90 | 2 | |
| α-helix | 97-110 | 14 | |
3 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 |
|---|
| Suppressor of cytokine signaling 2 | A, D, G, J | protein | 169 | Homo sapiens | O14508 (AlphaFold model) |
| Elongin-B | B, E, H, K | protein | 118 | Homo sapiens | Q15370 (AlphaFold model) |
| Elongin-C | C, F, I, L | protein | 97 | Homo sapiens | Q15369 (AlphaFold model) |
Sequence of entity 1 (A, D, G, J), FASTA
>7ZLM_1 Suppressor of cytokine signaling 2 (chains A, D, G, J)
SMQAARLAKALRELGQTGWYWGSMTVNEAKEKLKEAPEGTFLIRDSSHSDYLLTISVKTS
AGPTNLRIEYQDGKFRLDSIICVKSKLKQFDSVVHLIDYYVQMCKDKRTGPEAPRNGTVH
LYLTKPLYTSAPSLQHLCRLTINKCTGAIWGLPLPTRLKDYLEEYKFQV
Sequence of entity 2 (B, E, H, K), FASTA
>7ZLM_2 Elongin-B (chains B, E, H, K)
MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGEC
GFTSQTARPQAPATVGLAFRADDTFEALCIEPFSSPPELPDVMKPQDSGSSANEQAVQ
Sequence of entity 3 (C, F, I, L), FASTA
>7ZLM_3 Elongin-C (chains C, F, I, L)
MMYVKLISSDGHEFIVKREHALTSGTIKAMLSGPGQFAENETNEVNFREIPSHVLSKVCM
YFTYKVRYTNSSTEIPEFPIAPEIALELLMAANFLDC
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| JIH | [4-[(2~{S})-3-[[3-(2-chloranylethanoylamino)phenyl]methylamino]-2-[2-(4-fluorop… | C26 H26 Cl F N3 O7 P | 4 |
Primary citation
Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2. Ramachandran, S., Makukhin, N., Haubrich, K. et al. Nat Commun (2023) 14:6345-6345. DOI 10.1038/s41467-023-41894-3 · PubMed
Other PDB entries of the same protein (UniProt O14508 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 2C9W 1.9 Å, Crystal structure of socs-2 in complex with elongin-B and elongin-C at 1.9A resolution
- 7ZLS 1.92 Å, co-crystal structure of SOCS2:ElonginB:ElonginC in complex with compound 13
- 7ZLP 1.94 Å, Crystal structure of SOCS2:ElonginB:ElonginC in complex with compound 9
- 6I5N 1.98 Å, Crystal structure of SOCS2:Elongin C:Elongin B in complex with growth hormone receptor…
- 7ZLR 2.01 Å, Crystal structure of SOCS2:ElonginB:ElonginC in complex with compound 13
- 7ZLO 2.22 Å, Crystal structure of SOCS2:ElonginB:ElonginC in complex with compound 12
- 7ZLN 2.6 Å, Crystal structure of SOCS2:ElonginB:ElonginC in complex with compound 11
- 6I4X 2.69 Å, Crystal structure of SOCS2:Elongin C:Elongin B in complex with erythropoietin receptor…
- 6I5J 2.8 Å, Crystal structure of SOCS2:Elongin C:Elongin B in complex with growth hormone receptor…
- 5BO4 2.9 Å, Structure of SOCS2:Elongin C:Elongin B from DMSO-treated crystals
- 4JGH 3.0 Å, Structure of the SOCS2-Elongin BC complex bound to an N-terminal fragment of Cullin5
- 7M6T 3.19 Å, Crystal structure of SOCS2/ElonginB/ElonginC bound to a non-canonical peptide that…
Browse structure collections
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