X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in complex with an inhibitor and MgATP. Determined by X-ray diffraction at 2.0 Å resolution. Released 28 Aug 2013.
Explore 3VVH in 3D Show helices and sheets RCSB PDB PDBe
3VVH contains 57 α-helices and 30 β-strands across 3 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 | 65-67 | 3 | |
| β-strand | 68-76 | 9 | 1 |
| β-strand | 80-87 | 8 | 1 |
| β-strand | 92 | 1 | 2 |
| β-strand | 93-100 | 8 | 1 |
| α-helix | 105-115 | 11 | |
| α-helix | 116-120 | 5 | |
| β-strand | 126 | 1 | 3 |
| β-strand | 129-135 | 7 | 1 |
| β-strand | 138-144 | 7 | 1 |
| β-strand | 150 | 1 | 3 |
| α-helix | 151-158 | 8 | |
| α-helix | 163-184 | 22 | |
| α-helix | 193-195 | 3 | |
| β-strand | 196-198 | 3 | 3 |
| β-strand | 204-206 | 3 | 3 |
| α-helix | 213-219 | 7 | |
| α-helix | 232-235 | 4 | |
| α-helix | 243-258 | 16 | |
| α-helix | 265-266 | 2 | |
| α-helix | 269-274 | 6 | |
| α-helix | 307-309 | 3 | |
| α-helix | 310-319 | 10 | |
| α-helix | 321-323 | 3 | |
| α-helix | 332-341 | 10 | |
| α-helix | 350-351 | 2 | |
| α-helix | 352-356 | 5 | |
| α-helix | 359-366 | 8 | |
| β-strand | 369 | 1 | 4 |
| α-helix | 371-379 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 65-67 | 3 | |
| β-strand | 68-76 | 9 | 4 |
| β-strand | 80-87 | 8 | 4 |
| β-strand | 92-100 | 9 | 4 |
| α-helix | 105-115 | 11 | |
| α-helix | 116-120 | 5 | |
| β-strand | 126 | 1 | 5 |
| β-strand | 129-135 | 7 | 4 |
| β-strand | 138-144 | 7 | 4 |
| β-strand | 150 | 1 | 5 |
| α-helix | 151-158 | 8 | |
| α-helix | 163-184 | 22 | |
| α-helix | 193-195 | 3 | |
| β-strand | 196-198 | 3 | 5 |
| β-strand | 204-206 | 3 | 5 |
| α-helix | 213-219 | 7 | |
| α-helix | 221-223 | 3 | |
| α-helix | 234-236 | 3 | |
| α-helix | 238-240 | 3 | |
| α-helix | 242-258 | 17 | |
| α-helix | 265-267 | 3 | |
| α-helix | 268-274 | 7 | |
| α-helix | 310-319 | 10 | |
| α-helix | 321-323 | 3 | |
| α-helix | 325-326 | 2 | |
| α-helix | 332-341 | 10 | |
| α-helix | 352-356 | 5 | |
| α-helix | 359-366 | 8 | |
| α-helix | 371-379 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 65-67 | 3 | |
| β-strand | 68-76 | 9 | 6 |
| β-strand | 80-87 | 8 | 6 |
| β-strand | 92-100 | 9 | 6 |
| α-helix | 105-115 | 11 | |
| α-helix | 116-120 | 5 | |
| β-strand | 126 | 1 | 7 |
| β-strand | 129-135 | 7 | 6 |
| β-strand | 138-144 | 7 | 6 |
| β-strand | 150 | 1 | 7 |
| α-helix | 151-158 | 8 | |
| α-helix | 163-184 | 22 | |
| α-helix | 193-195 | 3 | |
| β-strand | 196-198 | 3 | 7 |
| β-strand | 204-206 | 3 | 7 |
| α-helix | 213-219 | 7 | |
| α-helix | 221-223 | 3 | |
| α-helix | 234-236 | 3 | |
| α-helix | 238-240 | 3 | |
| α-helix | 242-258 | 17 | |
| α-helix | 265-266 | 2 | |
| α-helix | 310-319 | 10 | |
| α-helix | 321-323 | 3 | |
| α-helix | 332-341 | 10 | |
| α-helix | 352-356 | 5 | |
| α-helix | 359-366 | 8 | |
| β-strand | 369 | 1 | 2 |
| α-helix | 371-379 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Dual specificity mitogen-activated protein kinase kinase 1 | A, B, C | protein | 341 | Homo sapiens | Q02750 (AlphaFold model) |
>3VVH_1 Dual specificity mitogen-activated protein kinase kinase 1 (chains A, B, C) MELKDDDFEKISELGAGNGGVVFKVSHKPSGLVMARKLIHLEIKPAIRNQIIRELQVLHE CNSPYIVGFYGAFYSDGEISICMEHMDGGSLDQVLKKAGRIPEQILGKVSIAVIKGLTYL REKHKIMHRDVKPSNILVNSRGEIKLCDFGVSGQLIDSMANSFVGTRSYMSPERLQGTHY SVQSDIWSMGLSLVEMAVGRYPIPPPDAKELELMFGCQVEGDAAETPPRPRTPGRPLSSY GMDSRPPMAIFELLDYIVNEPPPKLPSGVFSLEFQDFVNKCLIKNPAERADLKQLMVHAF IKRSDAEEVDFAGWLCSTIGLNQPSTPTHAAGVLEHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 3 |
| ATP | Adenosine-5'-triphosphate | C10 H16 N5 O13 P3 | 3 |
| 4BM | N-{[(2R)-2,3-dihydroxypropyl]oxy}-3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]… | C16 H14 F3 I N2 O4 | 3 |
X-ray structure of the human mitogen-activated protein kinase kinase 1 (MEK1) in complex with an inhibitor and MgATP. Kudo, N., Kato, R., Wakatsuki, S. To be published.
Other PDB entries of the same protein (UniProt Q02750 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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