6NO7: Full-length wild-type PKA RIa Holoenzyme
Crystal Structure of the full-length wild-type PKA RIa Holoenzyme. Determined by X-ray diffraction at 3.55 Å resolution. Released 24 Jul 2019.
- Method
- X-ray diffraction
- Resolution
- 3.55 Å
- Organisms
- Homo sapiens, Bos taurus
- Chains
- 8
- Atoms
- 20,128
- Mol. weight
- 335.93 kDa
- Ligands
- MG, ATP
- Released
- 24 Jul 2019
Explore 6NO7 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
6NO7 contains 124 α-helices and 134 β-strands across 8 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: 17 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-31 | 16 | |
| α-helix | 40-42 | 3 | |
| β-strand | 43-51 | 9 | 1 |
| β-strand | 56-62 | 7 | 1 |
| β-strand | 68-75 | 8 | 1 |
| α-helix | 76-81 | 6 | |
| α-helix | 85-95 | 11 | |
| β-strand | 103 | 1 | 2 |
| α-helix | 104-105 | 2 | |
| β-strand | 106-111 | 6 | 1 |
| β-strand | 115-121 | 7 | 1 |
| α-helix | 122 | 1 | |
| β-strand | 127 | 1 | 2 |
| α-helix | 128-135 | 8 | |
| α-helix | 140-159 | 20 | |
| β-strand | 162-163 | 2 | 3 |
| α-helix | 169-171 | 3 | |
| β-strand | 172-174 | 3 | 2 |
| β-strand | 180-182 | 3 | 2 |
| β-strand | 189-190 | 2 | 3 |
| β-strand | 195 | 1 | 4 |
| β-strand | 199-200 | 2 | 5 |
| α-helix | 202-204 | 3 | |
| α-helix | 207-210 | 4 | |
| β-strand | 215 | 1 | 4 |
| α-helix | 219-233 | 15 | |
| α-helix | 243-252 | 10 | |
| α-helix | 263-272 | 10 | |
| α-helix | 289-292 | 4 | |
| α-helix | 295-297 | 3 | |
| α-helix | 302-306 | 5 | |
Chain B: 14 helices, 20 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 94-97 | 4 | |
| β-strand | 98-99 | 2 | 5 |
| α-helix | 105-110 | 6 | |
| β-strand | 113-115 | 3 | 6 |
| α-helix | 120-129 | 10 | |
| α-helix | 134-137 | 4 | |
| α-helix | 141-150 | 10 | |
| β-strand | 152-156 | 5 | 7 |
| β-strand | 161-163 | 3 | 8 |
| β-strand | 168 | 1 | 9 |
| α-helix | 169 | 1 | |
| β-strand | 171-177 | 7 | 7 |
| β-strand | 180-184 | 5 | 8 |
| β-strand | 187-192 | 6 | 8 |
| β-strand | 197-198 | 2 | 7 |
| α-helix | 200-203 | 4 | |
| β-strand | 208 | 1 | 9 |
| β-strand | 212-215 | 4 | 8 |
| β-strand | 219-225 | 7 | 7 |
| α-helix | 226-249 | 24 | |
| α-helix | 252-254 | 3 | |
| α-helix | 259-268 | 10 | |
| β-strand | 270-274 | 5 | 10 |
| β-strand | 279-281 | 3 | 10 |
| β-strand | 286-287 | 2 | 11 |
| β-strand | 289-303 | 15 | 10 |
| β-strand | 310-316 | 7 | 10 |
| β-strand | 321-322 | 2 | 10 |
| α-helix | 325-327 | 3 | |
| β-strand | 331-332 | 2 | 11 |
| β-strand | 336-349 | 14 | 10 |
| α-helix | 350-357 | 8 | |
| α-helix | 360-364 | 5 | |
| α-helix | 368-373 | 6 | |
Chain C: 17 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-31 | 16 | |
| α-helix | 40-42 | 3 | |
| β-strand | 43-51 | 9 | 12 |
| β-strand | 56-62 | 7 | 12 |
| β-strand | 68-75 | 8 | 12 |
| α-helix | 76-81 | 6 | |
| α-helix | 85-95 | 11 | |
| β-strand | 103 | 1 | 13 |
| α-helix | 104-105 | 2 | |
| β-strand | 106-111 | 6 | 12 |
| β-strand | 115-121 | 7 | 12 |
| α-helix | 122 | 1 | |
| β-strand | 127 | 1 | 13 |
| α-helix | 128-135 | 8 | |
| α-helix | 140-159 | 20 | |
| β-strand | 162-163 | 2 | 14 |
| α-helix | 169-171 | 3 | |
| β-strand | 172-174 | 3 | 13 |
| β-strand | 180-182 | 3 | 13 |
| β-strand | 189-190 | 2 | 14 |
| β-strand | 195 | 1 | 15 |
| β-strand | 199-200 | 2 | 16 |
| α-helix | 202-204 | 3 | |
| α-helix | 207-210 | 4 | |
| β-strand | 215 | 1 | 15 |
| α-helix | 218-233 | 16 | |
| α-helix | 243-252 | 10 | |
| α-helix | 263-272 | 10 | |
| α-helix | 289-292 | 4 | |
| α-helix | 295-297 | 3 | |
| α-helix | 302-306 | 5 | |
Chain D: 13 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 94-97 | 4 | |
| β-strand | 98-99 | 2 | 16 |
| α-helix | 105-110 | 6 | |
| α-helix | 120-130 | 11 | |
| α-helix | 141-150 | 10 | |
| β-strand | 152-156 | 5 | 17 |
| β-strand | 161-163 | 3 | 18 |
| β-strand | 165 | 1 | 19 |
| β-strand | 168 | 1 | 20 |
| α-helix | 169 | 1 | |
| β-strand | 171-177 | 7 | 17 |
| β-strand | 180-184 | 5 | 18 |
| β-strand | 187-192 | 6 | 18 |
| β-strand | 197-198 | 2 | 17 |
| α-helix | 200-203 | 4 | |
| β-strand | 208 | 1 | 20 |
| β-strand | 209 | 1 | 19 |
| β-strand | 212-215 | 4 | 18 |
| β-strand | 219-225 | 7 | 17 |
| α-helix | 226-249 | 24 | |
| α-helix | 252-254 | 3 | |
| α-helix | 259-268 | 10 | |
| β-strand | 270-274 | 5 | 21 |
| β-strand | 279-281 | 3 | 21 |
| β-strand | 286-287 | 2 | 22 |
| β-strand | 289-303 | 15 | 21 |
| β-strand | 310-316 | 7 | 21 |
| β-strand | 321-322 | 2 | 21 |
| α-helix | 325-327 | 3 | |
| β-strand | 331-332 | 2 | 22 |
| β-strand | 336-349 | 14 | 21 |
| α-helix | 350-357 | 8 | |
| α-helix | 360-364 | 5 | |
| α-helix | 368-373 | 6 | |
Chain E: 18 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-31 | 16 | |
| α-helix | 40-42 | 3 | |
| β-strand | 43-51 | 9 | 23 |
| β-strand | 56-62 | 7 | 23 |
| β-strand | 68-75 | 8 | 23 |
| α-helix | 76-81 | 6 | |
| α-helix | 85-96 | 12 | |
| α-helix | 104-105 | 2 | |
| β-strand | 106-111 | 6 | 23 |
| β-strand | 115-120 | 6 | 23 |
| β-strand | 127 | 1 | 24 |
| α-helix | 128-135 | 8 | |
| α-helix | 140-159 | 20 | |
| β-strand | 162-163 | 2 | 25 |
| α-helix | 169-171 | 3 | |
| β-strand | 172-174 | 3 | 24 |
| β-strand | 180-182 | 3 | 24 |
| β-strand | 189-190 | 2 | 25 |
| β-strand | 195 | 1 | 26 |
| β-strand | 199-200 | 2 | 27 |
| α-helix | 202-204 | 3 | |
| α-helix | 207-210 | 4 | |
| β-strand | 215 | 1 | 26 |
| α-helix | 218-233 | 16 | |
| α-helix | 243-252 | 10 | |
| α-helix | 263-272 | 10 | |
| α-helix | 289-292 | 4 | |
| α-helix | 295-297 | 3 | |
| α-helix | 303-306 | 4 | |
| α-helix | 311-312 | 2 | |
| α-helix | 344-347 | 4 | |
Chain F: 13 helices, 20 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 95-97 | 3 | |
| β-strand | 98-99 | 2 | 27 |
| α-helix | 106-108 | 3 | |
| β-strand | 112-114 | 3 | 6 |
| α-helix | 120-130 | 11 | |
| α-helix | 134-137 | 4 | |
| α-helix | 141-150 | 10 | |
| β-strand | 152-156 | 5 | 28 |
| β-strand | 161-163 | 3 | 29 |
| β-strand | 168 | 1 | 30 |
| β-strand | 171-177 | 7 | 28 |
| β-strand | 180-184 | 5 | 29 |
| β-strand | 187-192 | 6 | 29 |
| β-strand | 197-198 | 2 | 28 |
| α-helix | 200-203 | 4 | |
| β-strand | 208 | 1 | 30 |
| β-strand | 211-215 | 5 | 29 |
| β-strand | 219-225 | 7 | 28 |
| α-helix | 226-249 | 24 | |
| α-helix | 252-254 | 3 | |
| α-helix | 259-268 | 10 | |
| β-strand | 270-274 | 5 | 31 |
| β-strand | 279-281 | 3 | 31 |
| β-strand | 286-287 | 2 | 32 |
| β-strand | 289-302 | 14 | 31 |
| β-strand | 311-316 | 6 | 31 |
| β-strand | 321-322 | 2 | 31 |
| α-helix | 325-327 | 3 | |
| β-strand | 331-332 | 2 | 32 |
| β-strand | 336-349 | 14 | 31 |
| α-helix | 351-357 | 7 | |
| α-helix | 360-364 | 5 | |
| α-helix | 368-373 | 6 | |
Chain G: 19 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 15-31 | 17 | |
| α-helix | 40-42 | 3 | |
| β-strand | 43-51 | 9 | 33 |
| β-strand | 56-62 | 7 | 33 |
| β-strand | 68-75 | 8 | 33 |
| α-helix | 76-81 | 6 | |
| α-helix | 85-96 | 12 | |
| α-helix | 104-105 | 2 | |
| β-strand | 106-111 | 6 | 33 |
| β-strand | 115-120 | 6 | 33 |
| α-helix | 121-122 | 2 | |
| β-strand | 127 | 1 | 34 |
| α-helix | 128-135 | 8 | |
| α-helix | 140-159 | 20 | |
| β-strand | 162-163 | 2 | 35 |
| α-helix | 169-171 | 3 | |
| β-strand | 172-174 | 3 | 34 |
| β-strand | 180-182 | 3 | 34 |
| α-helix | 185-187 | 3 | |
| β-strand | 189-190 | 2 | 35 |
| β-strand | 195 | 1 | 36 |
| β-strand | 199-200 | 2 | 37 |
| α-helix | 202-204 | 3 | |
| α-helix | 207-210 | 4 | |
| β-strand | 215 | 1 | 36 |
| α-helix | 219-233 | 15 | |
| α-helix | 243-252 | 10 | |
| α-helix | 263-272 | 10 | |
| α-helix | 289-292 | 4 | |
| α-helix | 295-297 | 3 | |
| α-helix | 303-306 | 4 | |
| α-helix | 344-347 | 4 | |
Chain H: 13 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 95-97 | 3 | |
| β-strand | 98-99 | 2 | 37 |
| α-helix | 106-108 | 3 | |
| α-helix | 120-130 | 11 | |
| α-helix | 134-137 | 4 | |
| α-helix | 141-150 | 10 | |
| β-strand | 152-156 | 5 | 38 |
| β-strand | 161-163 | 3 | 39 |
| β-strand | 168 | 1 | 40 |
| β-strand | 171-177 | 7 | 38 |
| β-strand | 180-184 | 5 | 39 |
| β-strand | 187-192 | 6 | 39 |
| β-strand | 197-198 | 2 | 38 |
| α-helix | 200-203 | 4 | |
| β-strand | 208 | 1 | 40 |
| β-strand | 211-215 | 5 | 39 |
| β-strand | 219-225 | 7 | 38 |
| α-helix | 226-249 | 24 | |
| α-helix | 252-254 | 3 | |
| α-helix | 259-268 | 10 | |
| β-strand | 270-274 | 5 | 41 |
| β-strand | 279-281 | 3 | 41 |
| β-strand | 286-287 | 2 | 42 |
| β-strand | 289-302 | 14 | 41 |
| β-strand | 311-316 | 6 | 41 |
| β-strand | 321-322 | 2 | 41 |
| α-helix | 324-328 | 5 | |
| β-strand | 331-332 | 2 | 42 |
| β-strand | 336-349 | 14 | 41 |
| α-helix | 351-357 | 7 | |
| α-helix | 360-364 | 5 | |
| α-helix | 368-373 | 6 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| cAMP-dependent protein kinase catalytic subunit alpha | A, C, E, G | protein | 350 | Homo sapiens | P17612 (AlphaFold model) |
| cAMP-dependent protein kinase type I-alpha regulatory subunit | B, D, F, H | protein | 380 | Bos taurus | P00514 (AlphaFold model) |
Sequence of entity 1 (A, C, E, G), FASTA
>6NO7_1 cAMP-dependent protein kinase catalytic subunit alpha (chains A, C, E, G)
GNAAAAKKGSEQESVKEFLAKAKEDFLKKWESPAQNTAHLDQFERIKTLGTGSFGRVMLV
KHKETGNHYAMKILDKQKVVKLKQIEHTLNEKRILQAVNFPFLVKLEFSFKDNSNLYMVM
EYVPGGEMFSHLRRIGRFSEPHARFYAAQIVLTFEYLHSLDLIYRDLKPENLLIDQQGYI
QVTDFGFAKRVKGRTWTLCGTPEYLAPEIILSKGYNKAVDWWALGVLIYEMAAGYPPFFA
DQPIQIYEKIVSGKVRFPSHFSSDLKDLLRNLLQVDLTKRFGNLKNGVNDIKNHKWFATT
DWIAIYQRKVEAPFIPKFKGPGDTSNFDDYEEEEIRVSINEKCGKEFSEF
Sequence of entity 2 (B, D, F, H), FASTA
>6NO7_2 cAMP-dependent protein kinase type I-alpha regulatory subunit (chains B, D, F, H)
MASGTTASEEERSLRECELYVQKHNIQALLKDSIVQLCTARPERPMAFLREYFEKLEKEE
AKQIQNLQKAGSRADSREDEISPPPPNPVVKGRRRRGAISAEVYTEEDAASYVRKVIPKD
YKTMAALAKAIEKNVLFSHLDDNERSDIFDAMFPVSFIAGETVIQQGDEGDNFYVIDQGE
MDVYVNNEWATSVGEGGSFGELALIYGTPRAATVKAKTNVKLWGIDRDSYRRILMGSTLR
KRKMYEEFLSKVSILESLDKWERLTVADALEPVQFEDGQKIVVQGEPGDEFFIILEGSAA
VLQRRSENEEFVEVGRLGPSDYFGEIALLMNRPRAATVVARGPLKCVKLDRPRFERVLGP
CSDILKRNIQQYNSFVSLSV
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| MG | Magnesium ion | Mg | 4 |
| ATP | Adenosine-5'-triphosphate | C10 H16 N5 O13 P3 | 2 |
Primary citation
Two PKA RI alpha holoenzyme states define ATP as an isoform-specific orthosteric inhibitor that competes with the allosteric activator, cAMP. Lu, T.W., Wu, J., Aoto, P.C. et al. Proc Natl Acad Sci U S A (2019) 116:16347-16356. DOI 10.1073/pnas.1906036116 · PubMed
Other PDB entries of the same protein (UniProt P17612 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 4WB8 1.55 Å, Crystal structure of human cAMP-dependent protein kinase A (catalytic alpha subunit),…
- 3OVV 1.58 Å, Human cAMP-dependent protein kinase in complex with an inhibitor
- 3POO 1.6 Å, human cAMP-dependent protein kinase in complex with an inhibitor
- 4WB5 1.64 Å, Crystal structure of human cAMP-dependent protein kinase A (catalytic alpha subunit)
- 6QJ7 1.69 Å, Difluorophenyl diacylhydrazides: Potent inhibitors of Serum- and…
- 3AMA 1.75 Å, Protein kinase A sixfold mutant model of Aurora B with inhibitor JNJ-7706621
- 4UJ1 1.77 Å, Protein Kinase A in complex with an Inhibitor
- 5IZJ 1.85 Å, Complex of PKA with the bisubstrate protein kinase inhibitor ARC-1411
- 4UJ9 1.87 Å, Protein Kinase A in complex with an Inhibitor
- 3OWP 1.88 Å, Human cAMP-dependent protein kinase in complex with an inhibitor
- 6FRX 1.88 Å, PKA variant as Aurora B mimic in complex with a dianilinopyrimidine inhibitor
- 5BX6 1.89 Å, PKA in complex with a halogenated phthalazinone fragment compound.
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