Structure of Lck in complex with a compound discovered by Virtual Fragment Linking. Determined by X-ray diffraction at 1.72 Å resolution. Released 23 Oct 2013.
Explore 4C3F in 3D Show helices and sheets RCSB PDB PDBe
4C3F contains 18 α-helices and 10 β-strands across 1 chain. 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 |
|---|---|---|---|
| β-strand | 239 | 1 | 1 |
| α-helix | 242-244 | 3 | |
| β-strand | 245-254 | 10 | 1 |
| β-strand | 257-264 | 8 | 1 |
| β-strand | 268-275 | 8 | 1 |
| α-helix | 276 | 1 | |
| α-helix | 282-294 | 13 | |
| β-strand | 300 | 1 | 2 |
| α-helix | 301-302 | 2 | |
| β-strand | 303-307 | 5 | 1 |
| α-helix | 312 | 1 | |
| β-strand | 313-317 | 5 | 1 |
| β-strand | 323 | 1 | 2 |
| α-helix | 324-327 | 4 | |
| α-helix | 331-334 | 4 | |
| α-helix | 338-357 | 20 | |
| α-helix | 367-369 | 3 | |
| β-strand | 370-372 | 3 | 2 |
| β-strand | 378-380 | 3 | 2 |
| α-helix | 409-414 | 6 | |
| α-helix | 419-434 | 16 | |
| α-helix | 438-439 | 2 | |
| α-helix | 446-454 | 9 | |
| α-helix | 459-462 | 4 | |
| α-helix | 467-476 | 10 | |
| α-helix | 481-483 | 3 | |
| α-helix | 485-486 | 2 | |
| α-helix | 487-495 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Tyrosine-protein kinase lck | A | protein | 267 | HOMO SAPIENS | P06239 (AlphaFold model) |
>4C3F_1 TYROSINE-PROTEIN KINASE LCK (chains A) GPEWEVPRETLKLVERLGAGQFGEVWMGYYNGHTKVAVKSLKQGSMSPDAFLAEANLMKQ LQHQRLVRLYAVVTQEPIYIITEYMENGSLVDFLKTPSGIKLTINKLLDMAAQIAEGMAF IEERNYIHRNLRAANILVSDTLSCKIADFGLARLIEDNEYTAREGAKFPIKWTAPEAINY GTFTIKSDVWSFGILLTEIVTHGRIPYPGMTNPEVIQNLERGYRMVRPDNCPEELYQLMR LCWKERPEDRPTFDYLRSVLEDFFTAT
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7KW | N-phenyl-4-(5-phenyl-1H-pyrazol-4-yl)pyrimidin-2-amine | C19 H15 N5 | 1 |
Efficient search of chemical space: navigating from fragments to structurally diverse chemotypes. Wassermann, A.M., Kutchukian, P.S., Lounkine, E. et al. J Med Chem (2013) 56:8879-8891. DOI 10.1021/jm401309q · PubMed
Other PDB entries of the same protein (UniProt P06239 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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