Crystal Structure of Human DNA ligase IV-Artemis Complex (Native). Determined by X-ray diffraction at 2.55 Å resolution. Released 3 Apr 2013.
Explore 3W1G in 3D Show helices and sheets RCSB PDB PDBe
3W1G contains 33 α-helices and 29 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 |
|---|---|---|---|
| α-helix | 10-12 | 3 | |
| β-strand | 15 | 1 | 1 |
| α-helix | 16-28 | 13 | |
| α-helix | 32-54 | 23 | |
| α-helix | 65-71 | 7 | |
| α-helix | 73-75 | 3 | |
| α-helix | 86-97 | 12 | |
| α-helix | 104-110 | 7 | |
| α-helix | 125-136 | 12 | |
| α-helix | 139-141 | 3 | |
| β-strand | 144 | 1 | 1 |
| α-helix | 145-160 | 16 | |
| α-helix | 164-176 | 13 | |
| α-helix | 180-191 | 12 | |
| α-helix | 200-207 | 8 | |
| α-helix | 211-217 | 7 | |
| α-helix | 221-227 | 7 | |
| α-helix | 245-249 | 5 | |
| β-strand | 250-253 | 4 | 2 |
| α-helix | 256-258 | 3 | |
| α-helix | 259-262 | 4 | |
| β-strand | 268-272 | 5 | 2 |
| β-strand | 277-284 | 8 | 3 |
| β-strand | 287-292 | 6 | 3 |
| β-strand | 297 | 1 | 3 |
| α-helix | 299-302 | 4 | |
| α-helix | 312-315 | 4 | |
| α-helix | 316-318 | 3 | |
| β-strand | 319 | 1 | 4 |
| β-strand | 325-336 | 12 | 3 |
| β-strand | 341-343 | 3 | 3 |
| α-helix | 344 | 1 | |
| α-helix | 351-356 | 6 | |
| β-strand | 361-372 | 12 | 3 |
| β-strand | 375-376 | 2 | 3 |
| α-helix | 382-392 | 11 | |
| β-strand | 393 | 1 | 4 |
| β-strand | 396 | 1 | 3 |
| β-strand | 400-402 | 3 | 3 |
| α-helix | 403-404 | 2 | |
| β-strand | 405-408 | 4 | 2 |
| α-helix | 411-423 | 13 | |
| β-strand | 429-432 | 4 | 2 |
| α-helix | 436-438 | 3 | |
| β-strand | 443-450 | 8 | 2 |
| β-strand | 462-471 | 10 | 5 |
| β-strand | 480-488 | 9 | 5 |
| β-strand | 500-507 | 8 | 5 |
| α-helix | 513-522 | 10 | |
| β-strand | 527-528 | 2 | 5 |
| β-strand | 538-539 | 2 | 5 |
| β-strand | 547-548 | 2 | 5 |
| α-helix | 551-553 | 3 | |
| β-strand | 556-560 | 5 | 5 |
| β-strand | 563-566 | 4 | 6 |
| β-strand | 574-577 | 4 | 6 |
| β-strand | 580-585 | 6 | 5 |
| α-helix | 590-592 | 3 | |
| α-helix | 593-594 | 2 | |
| β-strand | 595 | 1 | 5 |
| α-helix | 596-603 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 490-493 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| DNA ligase 4 | A | protein | 610 | Homo sapiens | P49917 (AlphaFold model) |
| Artemis-derived peptide | B | protein | 11 | Homo sapiens | Q96SD1 (AlphaFold model) |
>3W1G_1 DNA ligase 4 (chains A) TMAASQTSQTVASHVPFADLCSTLERIQKSKGRAEKIRHFREFLDSWRKFHDALHKNHKD VTDSFYPAMRLILPQLERERMAYGIKETMLAKLYIELLNLPRDGKDALKLLNYRTPTGTH GDAGDFAMIAYFVLKPRCLQKGSLTIQQVNDLLDSIASNNSAKRKDLIKKSLLQLITQSS ALEQKWLIRMIIKDLKLGVSQQTIFSVFHNDAAELHNVTTDLEKVCRQLHDPSVGLSDIS ITLFSAFKPMLAAIADIEHIEKDMKHQSFYIETKLDGERMQMHKDGDVYKYFSRNGYNYT DQFGASPTEGSLTPFIHNAFKADIQICILDGEMMAYNPNTQTFMQKGTKFDIKRMVEDSD LQTCYCVFDVLMVNNKKLGHETLRKRYEILSSIFTPIPGRIEIVQKTQAHTKNEVIDALN EAIDKREEGIMVKQPLSIYKPDKRGEGWLKIKPEYVSGLMDELDILIVGGYWGKGSRGGM MSHFLCAVAEKPPPGEKPSVFHTLSRVGSGCTMKELYDLGLKLAKYWKPFHRKAPPSSIL CGTEKPEVYIEPCNSVIVQIKAAEIVPSDMYKTGCTLRFPRIEKIRDDKEWHECMTLDDL EQLRGKASGK
>3W1G_2 Artemis-derived peptide (chains B) DVPQWEVFFKR
| ID | Name | Formula | Copies |
|---|---|---|---|
| ATP | Adenosine-5'-triphosphate | C10 H16 N5 O13 P3 | 1 |
Water and common crystallization additives (SO4) are not listed.
Structure of the catalytic region of DNA ligase IV in complex with an artemis fragment sheds light on double-strand break repair. Ochi, T., Gu, X., Blundell, T.L. Structure (2013) 21:672-679. DOI 10.1016/j.str.2013.02.014 · PubMed
Other PDB entries of the same protein (UniProt P49917 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 3W1G directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.