3ZNI: E3 ubiquitin-protein ligase cbl-B
Structure of phosphoTyr363-Cbl-b - UbcH5B-Ub - ZAP-70 peptide complex. Determined by X-ray diffraction at 2.21 Å resolution. Released 10 Jul 2013.
- Method
- X-ray diffraction
- Resolution
- 2.21 Å
- Organism
- HOMO SAPIENS
- Chains
- 16
- Atoms
- 20,546
- Mol. weight
- 291.87 kDa
- Ligands
- ZN, CA
- Released
- 10 Jul 2013
Explore 3ZNI in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
3ZNI contains 136 α-helices and 127 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: 22 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 43-60 | 18 | |
| α-helix | 63-65 | 3 | |
| α-helix | 74-91 | 18 | |
| α-helix | 95-102 | 8 | |
| α-helix | 105-128 | 24 | |
| α-helix | 129-133 | 5 | |
| α-helix | 138-160 | 23 | |
| α-helix | 162-164 | 3 | |
| α-helix | 168-170 | 3 | |
| α-helix | 176-186 | 11 | |
| β-strand | 191-193 | 3 | 1 |
| α-helix | 194-204 | 11 | |
| α-helix | 210-220 | 11 | |
| β-strand | 227-229 | 3 | 1 |
| α-helix | 230-239 | 10 | |
| α-helix | 243-245 | 3 | |
| α-helix | 246-250 | 5 | |
| α-helix | 251-255 | 5 | |
| β-strand | 260 | 1 | 2 |
| α-helix | 266-273 | 8 | |
| α-helix | 274-276 | 3 | |
| β-strand | 282-287 | 6 | 2 |
| β-strand | 295-300 | 6 | 2 |
| β-strand | 306-309 | 4 | 2 |
| α-helix | 316-325 | 10 | |
| β-strand | 331-332 | 2 | 2 |
| β-strand | 352-354 | 3 | 3 |
| α-helix | 357-364 | 8 | |
| β-strand | 372 | 1 | 4 |
| β-strand | 380 | 1 | 4 |
| α-helix | 381 | 1 | |
| β-strand | 383-386 | 4 | 5 |
| β-strand | 391-392 | 2 | 5 |
| α-helix | 394-402 | 9 | |
| β-strand | 417-420 | 4 | 5 |
| β-strand | 422-424 | 3 | 3 |
Chains B, F and N: 1 helix, 1 β-strand
| Element | Residues | Length | Sheet |
|---|
| β-strand | 7 | 1 | 2 |
| α-helix | 9-11 | 3 | |
Chains C and K: 6 helices, 9 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 3-15 | 13 | |
| β-strand | 21-26 | 6 | 6 |
| β-strand | 29-38 | 10 | 6 |
| α-helix | 39-40 | 2 | |
| β-strand | 49-55 | 7 | 6 |
| β-strand | 66-69 | 4 | 6 |
| β-strand | 75 | 1 | 7 |
| β-strand | 78 | 1 | 7 |
| β-strand | 83 | 1 | 6 |
| β-strand | 84 | 1 | 7 |
| β-strand | 86 | 1 | 8 |
| α-helix | 87-89 | 3 | |
| α-helix | 99-110 | 12 | |
| α-helix | 121-129 | 9 | |
| α-helix | 131-145 | 15 | |
Chain D: 3 helices, 8 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 1-6 | 6 | 9 |
| β-strand | 12-17 | 6 | 9 |
| β-strand | 22 | 1 | 10 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 9 |
| β-strand | 48-49 | 2 | 9 |
| α-helix | 50-51 | 2 | |
| β-strand | 55 | 1 | 10 |
| β-strand | 66-71 | 6 | 9 |
| β-strand | 75 | 1 | 8 |
Chain E: 24 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 41-60 | 20 | |
| α-helix | 63-65 | 3 | |
| α-helix | 74-91 | 18 | |
| α-helix | 95-102 | 8 | |
| α-helix | 105-128 | 24 | |
| α-helix | 129-133 | 5 | |
| α-helix | 138-160 | 23 | |
| α-helix | 162-164 | 3 | |
| α-helix | 168-170 | 3 | |
| α-helix | 176-186 | 11 | |
| β-strand | 191-193 | 3 | 11 |
| α-helix | 194-204 | 11 | |
| α-helix | 210-220 | 11 | |
| β-strand | 227-229 | 3 | 11 |
| α-helix | 230-239 | 10 | |
| α-helix | 243-245 | 3 | |
| α-helix | 246-250 | 5 | |
| α-helix | 251-255 | 5 | |
| β-strand | 260 | 1 | 12 |
| α-helix | 266-273 | 8 | |
| α-helix | 274-276 | 3 | |
| β-strand | 282-287 | 6 | 12 |
| β-strand | 295-300 | 6 | 12 |
| β-strand | 306-309 | 4 | 12 |
| α-helix | 316-325 | 10 | |
| β-strand | 331-332 | 2 | 12 |
| α-helix | 346-352 | 7 | |
| β-strand | 353-354 | 2 | 13 |
| α-helix | 355-356 | 2 | |
| α-helix | 357-365 | 9 | |
| β-strand | 372 | 1 | 14 |
| β-strand | 380 | 1 | 14 |
| α-helix | 381 | 1 | |
| β-strand | 383-386 | 4 | 15 |
| β-strand | 391-392 | 2 | 15 |
| α-helix | 394-402 | 9 | |
| β-strand | 417-420 | 4 | 15 |
| β-strand | 423-424 | 2 | 13 |
Chain G: 7 helices, 9 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 3-15 | 13 | |
| β-strand | 21-26 | 6 | 16 |
| β-strand | 29-38 | 10 | 16 |
| α-helix | 39-40 | 2 | |
| β-strand | 49-55 | 7 | 16 |
| α-helix | 64-65 | 2 | |
| β-strand | 66-69 | 4 | 16 |
| β-strand | 75 | 1 | 17 |
| β-strand | 78 | 1 | 17 |
| β-strand | 83 | 1 | 16 |
| β-strand | 84 | 1 | 17 |
| β-strand | 86 | 1 | 18 |
| α-helix | 87-89 | 3 | |
| α-helix | 99-109 | 11 | |
| α-helix | 121-129 | 9 | |
| α-helix | 131-145 | 15 | |
Chain H: 3 helices, 8 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 1-6 | 6 | 19 |
| β-strand | 12-17 | 6 | 19 |
| β-strand | 22 | 1 | 20 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 19 |
| β-strand | 48-49 | 2 | 19 |
| β-strand | 55 | 1 | 20 |
| α-helix | 57-59 | 3 | |
| β-strand | 66-71 | 6 | 19 |
| β-strand | 75 | 1 | 18 |
Chain I: 23 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 42-60 | 19 | |
| α-helix | 63-65 | 3 | |
| α-helix | 74-91 | 18 | |
| α-helix | 95-103 | 9 | |
| α-helix | 105-128 | 24 | |
| α-helix | 129-133 | 5 | |
| α-helix | 138-160 | 23 | |
| α-helix | 162-164 | 3 | |
| α-helix | 168-170 | 3 | |
| α-helix | 176-186 | 11 | |
| β-strand | 191-193 | 3 | 21 |
| α-helix | 194-202 | 9 | |
| α-helix | 210-220 | 11 | |
| β-strand | 227-229 | 3 | 21 |
| α-helix | 230-239 | 10 | |
| α-helix | 243-245 | 3 | |
| α-helix | 246-250 | 5 | |
| α-helix | 251-255 | 5 | |
| β-strand | 260 | 1 | 22 |
| α-helix | 266-273 | 8 | |
| α-helix | 274-276 | 3 | |
| β-strand | 282-287 | 6 | 22 |
| β-strand | 295-300 | 6 | 22 |
| β-strand | 306-309 | 4 | 22 |
| α-helix | 316-325 | 10 | |
| β-strand | 331-332 | 2 | 22 |
| α-helix | 348-351 | 4 | |
| β-strand | 352-354 | 3 | 23 |
| α-helix | 357-364 | 8 | |
| β-strand | 372 | 1 | 24 |
| β-strand | 380 | 1 | 24 |
| α-helix | 381 | 1 | |
| β-strand | 383-386 | 4 | 25 |
| β-strand | 391-392 | 2 | 25 |
| α-helix | 394-402 | 9 | |
| β-strand | 417-420 | 4 | 25 |
| β-strand | 422-424 | 3 | 23 |
4 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 |
|---|
| E3 ubiquitin-protein ligase cbl-B | A, E, I, M | protein | 394 | HOMO SAPIENS | Q13191 (AlphaFold model) |
| Tyrosine-protein kinase zap-70 | B, F, J, N | protein | 12 | HOMO SAPIENS | P43403 (AlphaFold model) |
| Ubiquitin-conjugating enzyme E2 D2 | C, G, K, O | protein | 146 | HOMO SAPIENS | P62837 (AlphaFold model) |
| Polyubiquitin-C | D, H, L, P | protein | 81 | HOMO SAPIENS | P0CG48 (AlphaFold model) |
Sequence of entity 1 (A, E, I, M), FASTA
>3ZNI_1 E3 UBIQUITIN-PROTEIN LIGASE CBL-B (chains A, E, I, M)
GSPKQAAADRRTVEKTWKLMDKVVRLCQNPKLQLKNSPPYILDILPDTYQHLRLILSKYD
DNQKLAQLSENEYFKIYIDSLMKKSKRAIRLFKEGKERMYEEQSQDRRNLTKLSLIFSHM
LAEIKAIFPNGQFQGDNFRITKADAAEFWRKFFGDKTIVPWKVFRQCLHEVHQISSGLEA
MALKSTIDLTCNDYISVFEFDIFTRLFQPWGSILRNWNFLAVTHPGYMAFLTYDEVKARL
QKYSTKPGSYIFRLSCTRLGQWAIGYVTGDGNILQTIPHNKPLFQALIDGSREGFYLYPD
GRSYNPDLTGLCEPTPHDHIKVTQEQFELYCEMGSTFQLCKICAENDKDVKIEPCGHLMC
TSCLTAWQESDGQGCPFCRCEIKGTEPIIVDPFD
Sequence of entity 2 (B, F, J, N), FASTA
>3ZNI_2 TYROSINE-PROTEIN KINASE ZAP-70 (chains B, F, J, N)
TLNSDGYTPEPA
Sequence of entity 3 (C, G, K, O), FASTA
>3ZNI_3 UBIQUITIN-CONJUGATING ENZYME E2 D2 (chains C, G, K, O)
ALKRIHKELNDLARDPPAQCRAGPVGDDMFHWQATIMGPNDSPYQGGVFFLTIHFPTDYP
FKPPKVAFTTRIYHPNINSNGSIKLDILRSQWSPALTISKVLLSICSLLCDPNPDDPLVP
EIARIYKTDREKYNRIAREWTQKYAM
Sequence of entity 4 (D, H, L, P), FASTA
>3ZNI_4 POLYUBIQUITIN-C (chains D, H, L, P)
GSGGSMQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLIFAGKQLEDGRT
LSDYNIQKESTLHLVLRLRGG
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| ZN | Zinc ion | Zn | 8 |
| CA | Calcium ion | Ca | 4 |
Water and common crystallization additives (EDO) are not listed.
Primary citation
Essentiality of a Non-Ring Element in Priming Donor Ubiquitin for Catalysis by a Monomeric E3. Dou, H., Buetow, L., Sibbet, G.J. et al. Nat Struct Mol Biol (2013) 20:982. DOI 10.1038/NSMB.2621 · PubMed
Other PDB entries of the same protein (UniProt Q13191 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 8QTG 1.42 Å, Crystal structure of CBL-b in complex with an allosteric inhibitor (compound 9)
- 8QTJ 1.52 Å, Crystal structure of Cbl-b in complex with an allosteric inhibitor (compound 30)
- 2OOA 1.56 Å, crystal structure of the UBA domain from Cbl-b ubiquitin ligase
- 9FQJ 1.56 Å, E3 ligase Cbl-b in complex with a carbamate scaffold inhibitor (compound 12)
- 9XZD 1.65 Å, E3 ubiquitin-protein ligase CBL-B in complex with compound 8
- 9I0B 1.66 Å, E3 ubiquitin ligase CBL-B in complex with inhibitor
- 2J6F 1.7 Å, N-terminal SH3 domain of cms (CD2AP human homolog) bound to cbl-B peptide
- 9XZB 1.75 Å, E3 ubiquitin-protein ligase CBL-B in complex with compound 2
- 8VW5 1.76 Å, Crystal structure of Cbl-b TKB bound to compound 2
- 10ZJ 1.77 Å, Structure of Cbl-B bound to compound 8
- 9FQH 1.79 Å, E3 ligase Cbl-b in complex with a triazolone core inhibitor (compound 1)
- 9XZC 1.8 Å, E3 ubiquitin-protein ligase CBL-B in complex with compound 6
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