Crystal structure of mouse Cryptochrome 1 in complex with compound KL201. Determined by X-ray diffraction at 2.1 Å resolution. Released 10 Jun 2020.
Explore 6LUE in 3D Show helices and sheets RCSB PDB PDBe
6LUE contains 67 α-helices and 20 β-strands across 2 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 |
|---|---|---|---|
| β-strand | 4-9 | 6 | 1 |
| α-helix | 19-25 | 7 | |
| β-strand | 30-37 | 8 | 1 |
| α-helix | 49-68 | 20 | |
| β-strand | 73-77 | 5 | 1 |
| α-helix | 80-90 | 11 | |
| β-strand | 95-99 | 5 | 1 |
| α-helix | 104-120 | 17 | |
| β-strand | 123-127 | 5 | 1 |
| α-helix | 135-141 | 7 | |
| α-helix | 150-159 | 10 | |
| α-helix | 161-169 | 9 | |
| α-helix | 172-175 | 4 | |
| β-strand | 179 | 1 | 1 |
| α-helix | 186-190 | 5 | |
| α-helix | 191-194 | 4 | |
| α-helix | 196-198 | 3 | |
| α-helix | 214-228 | 15 | |
| α-helix | 242-244 | 3 | |
| α-helix | 246-247 | 2 | |
| α-helix | 252-257 | 6 | |
| α-helix | 262-275 | 14 | |
| α-helix | 284-287 | 4 | |
| α-helix | 288-300 | 13 | |
| α-helix | 316-317 | 2 | |
| β-strand | 321 | 1 | 2 |
| α-helix | 324-331 | 8 | |
| α-helix | 338-350 | 13 | |
| α-helix | 355-363 | 9 | |
| α-helix | 364-368 | 5 | |
| β-strand | 372 | 1 | 2 |
| α-helix | 374-384 | 11 | |
| α-helix | 390-400 | 11 | |
| α-helix | 417-422 | 6 | |
| α-helix | 427-432 | 6 | |
| α-helix | 434-436 | 3 | |
| α-helix | 441-444 | 4 | |
| α-helix | 447-449 | 3 | |
| α-helix | 452-457 | 6 | |
| β-strand | 462 | 1 | 3 |
| β-strand | 466 | 1 | 3 |
| α-helix | 467-469 | 3 | |
| α-helix | 473-491 | 19 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-9 | 6 | 4 |
| α-helix | 19-25 | 7 | |
| β-strand | 30-37 | 8 | 4 |
| α-helix | 49-68 | 20 | |
| β-strand | 73-77 | 5 | 4 |
| α-helix | 80-90 | 11 | |
| β-strand | 95-99 | 5 | 4 |
| α-helix | 104-120 | 17 | |
| β-strand | 123-127 | 5 | 4 |
| α-helix | 135-141 | 7 | |
| α-helix | 150-158 | 9 | |
| α-helix | 161-170 | 10 | |
| α-helix | 172-175 | 4 | |
| β-strand | 179 | 1 | 4 |
| α-helix | 186-190 | 5 | |
| α-helix | 191-194 | 4 | |
| α-helix | 196-198 | 3 | |
| α-helix | 205-208 | 4 | |
| α-helix | 214-228 | 15 | |
| α-helix | 242-244 | 3 | |
| α-helix | 246-247 | 2 | |
| α-helix | 252-257 | 6 | |
| α-helix | 262-275 | 14 | |
| α-helix | 281-283 | 3 | |
| α-helix | 284-287 | 4 | |
| α-helix | 288-300 | 13 | |
| β-strand | 321 | 1 | 5 |
| α-helix | 324-332 | 9 | |
| α-helix | 338-350 | 13 | |
| α-helix | 355-363 | 9 | |
| α-helix | 364-368 | 5 | |
| β-strand | 372 | 1 | 5 |
| α-helix | 374-384 | 11 | |
| α-helix | 390-400 | 11 | |
| α-helix | 417-422 | 6 | |
| α-helix | 427-432 | 6 | |
| α-helix | 434-436 | 3 | |
| α-helix | 441-444 | 4 | |
| α-helix | 447-449 | 3 | |
| α-helix | 452-457 | 6 | |
| β-strand | 462 | 1 | 6 |
| β-strand | 466 | 1 | 6 |
| α-helix | 467-469 | 3 | |
| α-helix | 473-490 | 18 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Cryptochrome-1 | A, B | protein | 498 | Mus musculus | P97784 (AlphaFold model) |
>6LUE_1 Cryptochrome-1 (chains A, B) GTMGVNAVHWFRKGLRLHDNPALKECIQGADTIRCVYILDPWFAGSSNVGINRWRFLLQC LEDLDANLRKLNSRLFVIRGQPADVFPRLFKEWNITKLSIEYDSEPFGKERDAAIKKLAT EAGVEVIVRISHTLYDLDKIIELNGGQPPLTYKRFQTLVSKMEPLEMPADTITSDVIGKC MTPLSDDHDEKYGVPSLEELGFDTDGLSSAVWPGGETEALTRLERHLERKAWVANFERPR MNANSLLASPTGLSPYLRFGCLSCRLFYFKLTDLYKKVKKNSSPPLSLYGQLLWREFFYT AATNNPRFDKMEGNPICVQIPWDKNPEALAKWAEGRTGFPWIDAIMTQLRQEGWIHHLAR HAVACFLTRGDLWISWEEGMKVFEELLLDADWSINAGSWMWLSCSSFFQQFFHCYCPVGF GRRTDPNGDYIRRYLPVLRGFPAKYIYDPWNAPEGIQKVAKCLIGVNYPKPMVNHAEASR LNIERMKQIYQQLSRYRG
| ID | Name | Formula | Copies |
|---|---|---|---|
| EUL | 2-bromanyl-N-(5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-4-yl)benzamide | C17 H14 Br N3 O S | 2 |
An Isoform-Selective Modulator of Cryptochrome 1 Regulates Circadian Rhythms in Mammals. Miller, S., Aikawa, Y., Sugiyama, A. et al. Cell Chem Biol (2020) 27:1192-1198.e5. DOI 10.1016/j.chembiol.2020.05.008 · PubMed
Other PDB entries of the same protein (UniProt P97784 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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