Crystal structure of mouse Cryptochrome 1 in complex with compound TH129. Determined by X-ray diffraction at 2.35 Å resolution. Released 27 Jan 2021.
Explore 7D19 in 3D Show helices and sheets RCSB PDB PDBe
7D19 contains 60 α-helices and 26 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 | 39-41 | 3 | |
| β-strand | 44 | 1 | 2 |
| α-helix | 46-48 | 3 | |
| α-helix | 49-67 | 19 | |
| β-strand | 73-77 | 5 | 1 |
| α-helix | 80-91 | 12 | |
| 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 | 164-170 | 7 | |
| 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 | 214-231 | 18 | |
| α-helix | 246-247 | 2 | |
| α-helix | 252-257 | 6 | |
| α-helix | 262-277 | 16 | |
| α-helix | 284-287 | 4 | |
| α-helix | 290-300 | 11 | |
| β-strand | 315 | 1 | 3 |
| β-strand | 321 | 1 | 4 |
| α-helix | 324-331 | 8 | |
| α-helix | 338-350 | 13 | |
| α-helix | 355-363 | 9 | |
| α-helix | 364-368 | 5 | |
| β-strand | 372 | 1 | 4 |
| α-helix | 374-384 | 11 | |
| α-helix | 390-400 | 11 | |
| β-strand | 404 | 1 | 3 |
| α-helix | 417-422 | 6 | |
| α-helix | 427-432 | 6 | |
| α-helix | 434-436 | 3 | |
| α-helix | 452-458 | 7 | |
| β-strand | 462 | 1 | 5 |
| β-strand | 466 | 1 | 5 |
| α-helix | 473-491 | 19 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-9 | 6 | 6 |
| α-helix | 19-25 | 7 | |
| β-strand | 30-37 | 8 | 6 |
| α-helix | 46-48 | 3 | |
| α-helix | 49-67 | 19 | |
| β-strand | 73-77 | 5 | 6 |
| α-helix | 80-91 | 12 | |
| β-strand | 95-99 | 5 | 6 |
| α-helix | 104-120 | 17 | |
| β-strand | 123-127 | 5 | 6 |
| α-helix | 135-141 | 7 | |
| α-helix | 150-159 | 10 | |
| α-helix | 161-170 | 10 | |
| α-helix | 172-175 | 4 | |
| β-strand | 179 | 1 | 6 |
| α-helix | 186-190 | 5 | |
| α-helix | 191-194 | 4 | |
| α-helix | 214-231 | 18 | |
| α-helix | 246-247 | 2 | |
| α-helix | 252-257 | 6 | |
| α-helix | 262-277 | 16 | |
| α-helix | 284-287 | 4 | |
| α-helix | 290-300 | 11 | |
| β-strand | 315 | 1 | 7 |
| β-strand | 321 | 1 | 8 |
| α-helix | 324-331 | 8 | |
| α-helix | 338-350 | 13 | |
| α-helix | 355-363 | 9 | |
| α-helix | 364-368 | 5 | |
| β-strand | 372 | 1 | 8 |
| α-helix | 374-384 | 11 | |
| α-helix | 390-400 | 11 | |
| β-strand | 404 | 1 | 7 |
| β-strand | 411 | 1 | 2 |
| α-helix | 417-422 | 6 | |
| α-helix | 427-432 | 6 | |
| α-helix | 434-436 | 3 | |
| α-helix | 447-449 | 3 | |
| α-helix | 452-458 | 7 | |
| β-strand | 462 | 1 | 9 |
| β-strand | 466 | 1 | 9 |
| α-helix | 467-469 | 3 | |
| α-helix | 473-488 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Cryptochrome-1 | A, B | protein | 498 | Mus musculus | P97784 (AlphaFold model) |
>7D19_1 Cryptochrome-1 (chains A, B) GTMGVNAVHWFRKGLRLHDNPALKECIQGADTIRCVYILDPWFAGSSNVGINRWRFLLQC LEDLDANLRKLNSRLFVIRGQPADVFPRLFKEWNITKLSIEYDSEPFGKERDAAIKKLAT EAGVEVIVRISHTLYDLDKIIELNGGQPPLTYKRFQTLVSKMEPLEMPADTITSDVIGKC MTPLSDDHDEKYGVPSLEELGFDTDGLSSAVWPGGETEALTRLERHLERKAWVANFERPR MNANSLLASPTGLSPYLRFGCLSCRLFYFKLTDLYKKVKKNSSPPLSLYGQLLWREFFYT AATNNPRFDKMEGNPICVQIPWDKNPEALAKWAEGRTGFPWIDAIMTQLRQEGWIHHLAR HAVACFLTRGDLWISWEEGMKVFEELLLDADWSINAGSWMWLSCSSFFQQFFHCYCPVGF GRRTDPNGDYIRRYLPVLRGFPAKYIYDPWNAPEGIQKVAKCLIGVNYPKPMVNHAEASR LNIERMKQIYQQLSRYRG
| ID | Name | Formula | Copies |
|---|---|---|---|
| GOC | N-[2-(2,4-dimethylphenyl)-4,6-dihydrothieno[3,4-c]pyrazol-3-yl]-4-(phenylcarbon… | C27 H23 N3 O2 S | 2 |
Photopharmacological Manipulation of Mammalian CRY1 for Regulation of the Circadian Clock. Kolarski, D., Miller, S., Oshima, T. et al. J Am Chem Soc (2021) 143:2078-2087. DOI 10.1021/jacs.0c12280 · 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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