Crystal Structure of TACE with Tryptophan Sulfonamide Derivative Inhibitor. Determined by X-ray diffraction at 2.1 Å resolution. Released 19 May 2009.
Explore 3G42 in 3D Show helices and sheets RCSB PDB PDBe
3G42 contains 50 α-helices and 42 β-strands across 4 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 | 224-231 | 8 | 1 |
| α-helix | 233-234 | 2 | |
| α-helix | 235-239 | 5 | |
| α-helix | 244-263 | 20 | |
| β-strand | 276-284 | 9 | 1 |
| α-helix | 307-309 | 3 | |
| α-helix | 314-329 | 16 | |
| β-strand | 334-339 | 6 | 1 |
| β-strand | 349-351 | 3 | 1 |
| β-strand | 369-371 | 3 | 2 |
| β-strand | 376-378 | 3 | 2 |
| β-strand | 382-386 | 5 | 1 |
| β-strand | 388-389 | 2 | 3 |
| β-strand | 392-393 | 2 | 3 |
| α-helix | 394-395 | 2 | |
| α-helix | 396-410 | 15 | |
| α-helix | 415-417 | 3 | |
| α-helix | 427-429 | 3 | |
| α-helix | 445-448 | 4 | |
| α-helix | 452-469 | 18 | |
| β-strand | 471 | 1 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 224-231 | 8 | 4 |
| α-helix | 233-234 | 2 | |
| α-helix | 235-239 | 5 | |
| α-helix | 244-263 | 20 | |
| β-strand | 276-284 | 9 | 4 |
| α-helix | 288-290 | 3 | |
| α-helix | 314-324 | 11 | |
| α-helix | 326-329 | 4 | |
| β-strand | 334-339 | 6 | 4 |
| α-helix | 344-346 | 3 | |
| β-strand | 349-351 | 3 | 4 |
| α-helix | 352-354 | 3 | |
| β-strand | 368-371 | 4 | 5 |
| β-strand | 376-379 | 4 | 5 |
| β-strand | 382-386 | 5 | 4 |
| β-strand | 388-389 | 2 | 6 |
| β-strand | 392-393 | 2 | 6 |
| α-helix | 394-395 | 2 | |
| α-helix | 396-410 | 15 | |
| α-helix | 421-423 | 3 | |
| α-helix | 427-429 | 3 | |
| α-helix | 445-448 | 4 | |
| α-helix | 452-469 | 18 | |
| β-strand | 471 | 1 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 224-231 | 8 | 7 |
| α-helix | 233-238 | 6 | |
| α-helix | 244-263 | 20 | |
| β-strand | 276-284 | 9 | 7 |
| α-helix | 288 | 1 | |
| β-strand | 289 | 1 | 8 |
| α-helix | 290 | 1 | |
| β-strand | 300 | 1 | 8 |
| α-helix | 314-324 | 11 | |
| α-helix | 326-329 | 4 | |
| β-strand | 334-339 | 6 | 7 |
| α-helix | 344-346 | 3 | |
| β-strand | 349-351 | 3 | 7 |
| β-strand | 369-371 | 3 | 9 |
| β-strand | 376-378 | 3 | 9 |
| β-strand | 382-386 | 5 | 7 |
| β-strand | 388-389 | 2 | 10 |
| β-strand | 392-393 | 2 | 10 |
| α-helix | 394-395 | 2 | |
| α-helix | 396-410 | 15 | |
| α-helix | 415-417 | 3 | |
| α-helix | 421-423 | 3 | |
| α-helix | 427-429 | 3 | |
| α-helix | 445-448 | 4 | |
| α-helix | 452-469 | 18 | |
| β-strand | 471 | 1 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 224-231 | 8 | 11 |
| α-helix | 233-238 | 6 | |
| α-helix | 244-263 | 20 | |
| β-strand | 276-284 | 9 | 11 |
| α-helix | 288-290 | 3 | |
| α-helix | 314-329 | 16 | |
| β-strand | 334-339 | 6 | 11 |
| α-helix | 344-346 | 3 | |
| β-strand | 349-351 | 3 | 11 |
| β-strand | 369-371 | 3 | 12 |
| β-strand | 376-378 | 3 | 12 |
| β-strand | 382-386 | 5 | 11 |
| β-strand | 388-389 | 2 | 13 |
| β-strand | 392-393 | 2 | 13 |
| α-helix | 394-395 | 2 | |
| α-helix | 396-410 | 15 | |
| α-helix | 421-423 | 3 | |
| α-helix | 427-429 | 3 | |
| α-helix | 445-448 | 4 | |
| α-helix | 452-469 | 18 | |
| β-strand | 471 | 1 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Adam 17 | A, B, C, D | protein | 288 | Homo sapiens | P78536 (AlphaFold model) |
>3G42_1 ADAM 17 (chains A, B, C, D) VKRRADPDPMKNTCKLLVVADHRFYRYMGRGEESTTTNYLIELIDRVDDIYRNTAWDNAG FKGYGIQIEQIRILKSPQEVKPGEKHYNMAKSYPNEEKDAWDVKMLLEQFSFDIAEEASK VCLAHLFTYQDFDMGTLGLAYVGSPRANSHGGVCPKAYYSPVGKKNIYLNSGLTSTKNYG KTILTKEADLVTTHELGHNFGAEHDPDGLAECAPNEDQGGKYVMYPIAVSGDHENNKMFS QCSKQSIYKTIESKAQECFQERSNKVCGNSRVDEGEECDPGSHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| 792 | N-{[4-(but-2-yn-1-yloxy)phenyl]sulfonyl}-5-methyl-D-tryptophan | C22 H22 N2 O5 S | 4 |
| ZN | Zinc ion | Zn | 4 |
Synthesis and activity of tryptophan sulfonamide derivatives as novel non-hydroxamate TNF-alpha converting enzyme (TACE) inhibitors. Park, K., Gopalsamy, A., Aplasca, A. et al. Bioorg Med Chem (2009) 17:3857-3865. DOI 10.1016/j.bmc.2009.04.033 · PubMed
Other PDB entries of the same protein (UniProt P78536 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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