Crystal structure of a chimeric fusion of human DnaJ (Hsp40) and cAMP-dependent protein kinase A (catalytic alpha subunit). Determined by X-ray diffraction at 1.9 Å resolution. Released 21 Jan 2015.
Explore 4WB7 in 3D Show helices and sheets RCSB PDB PDBe
4WB7 contains 45 α-helices and 26 β-strands across 4 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-8 | 5 | |
| α-helix | 16-30 | 15 | |
| α-helix | 40-54 | 15 | |
| α-helix | 57-86 | 30 | |
| α-helix | 95-97 | 3 | |
| β-strand | 98-106 | 9 | 1 |
| β-strand | 111-117 | 7 | 1 |
| β-strand | 123-130 | 8 | 1 |
| α-helix | 131-136 | 6 | |
| α-helix | 140-150 | 11 | |
| β-strand | 158 | 1 | 2 |
| β-strand | 161-166 | 6 | 1 |
| β-strand | 170-176 | 7 | 1 |
| α-helix | 177 | 1 | |
| β-strand | 182 | 1 | 2 |
| α-helix | 183-190 | 8 | |
| α-helix | 195-214 | 20 | |
| β-strand | 217-218 | 2 | 3 |
| α-helix | 224-226 | 3 | |
| β-strand | 227-229 | 3 | 2 |
| β-strand | 235-237 | 3 | 2 |
| β-strand | 244-245 | 2 | 3 |
| β-strand | 250 | 1 | 4 |
| α-helix | 257-259 | 3 | |
| α-helix | 262-265 | 4 | |
| β-strand | 270 | 1 | 4 |
| α-helix | 273-288 | 16 | |
| α-helix | 298-307 | 10 | |
| α-helix | 318-327 | 10 | |
| α-helix | 332-334 | 3 | |
| α-helix | 344-347 | 4 | |
| α-helix | 350-352 | 3 | |
| α-helix | 357-361 | 5 | |
| α-helix | 366-367 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-8 | 5 | |
| α-helix | 16-30 | 15 | |
| α-helix | 40-54 | 15 | |
| α-helix | 57-86 | 30 | |
| α-helix | 95-97 | 3 | |
| β-strand | 98-106 | 9 | 5 |
| β-strand | 111-117 | 7 | 5 |
| β-strand | 123-130 | 8 | 5 |
| α-helix | 131-136 | 6 | |
| α-helix | 140-150 | 11 | |
| β-strand | 158 | 1 | 6 |
| β-strand | 161-166 | 6 | 5 |
| β-strand | 170-176 | 7 | 5 |
| β-strand | 182 | 1 | 6 |
| α-helix | 183-190 | 8 | |
| α-helix | 195-214 | 20 | |
| β-strand | 217-218 | 2 | 7 |
| α-helix | 224-226 | 3 | |
| β-strand | 227-229 | 3 | 6 |
| β-strand | 235-237 | 3 | 6 |
| β-strand | 244-245 | 2 | 7 |
| β-strand | 250 | 1 | 8 |
| α-helix | 257-259 | 3 | |
| α-helix | 262-265 | 4 | |
| β-strand | 270 | 1 | 8 |
| α-helix | 273-288 | 16 | |
| α-helix | 298-307 | 10 | |
| α-helix | 318-327 | 10 | |
| α-helix | 332-334 | 3 | |
| α-helix | 344-347 | 4 | |
| α-helix | 350-352 | 3 | |
| α-helix | 357-361 | 5 | |
| α-helix | 366-367 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 6-11 | 6 | |
| α-helix | 20-22 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 6-13 | 8 | |
| α-helix | 20-22 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alpha | A, B | protein | 405 | Homo sapiens | P17612 (AlphaFold model), P25685 (AlphaFold model) |
| PKI (5-24) | I, J | protein | 20 | Homo sapiens | P61925 (AlphaFold model) |
>4WB7_1 DnaJ homolog subfamily B member 1,cAMP-dependent protein kinase catalytic subunit alpha (chains A, B) GKDYYQTLGLARGASDEEIKRAYRRQALRYHPDKNKEPGAEEKFKEIAEAYDVLSDPRKR EIFDRYGEEVKEFLAKAKEDFLKKWESPAQNTAHLDQFERIKTLGTGSFGRVMLVKHKET GNHYAMKILDKQKVVKLKQIEHTLNEKRILQAVNFPFLVKLEFSFKDNSNLYMVMEYVPG GEMFSHLRRIGRFSEPHARFYAAQIVLTFEYLHSLDLIYRDLKPENLLIDQQGYIQVTDF GFAKRVKGRTWTLCGTPEYLAPEIILSKGYNKAVDWWALGVLIYEMAAGYPPFFADQPIQ IYEKIVSGKVRFPSHFSSDLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATTDWIAI YQRKVEAPFIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF
>4WB7_2 PKI (5-24) (chains I, J) TTYADFIASGRTGRRNAIHD
Structural insights into mis-regulation of protein kinase A in human tumors. Cheung, J., Ginter, C., Cassidy, M. et al. Proc Natl Acad Sci U S A (2015) 112:1374-1379. DOI 10.1073/pnas.1424206112 · PubMed
Other PDB entries of the same protein (UniProt P17612 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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