Structure of murine iNOS oxygenase domain with inhibitor AR-C95791. Determined by X-ray diffraction at 2.0 Å resolution. Released 7 Oct 2008.
Explore 3E7M in 3D Show helices and sheets RCSB PDB PDBe
3E7M contains 59 α-helices and 50 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 | 79-82 | 4 | 1 |
| β-strand | 83 | 1 | 2 |
| β-strand | 89-92 | 4 | 1 |
| α-helix | 94-97 | 4 | |
| α-helix | 117-119 | 3 | |
| β-strand | 120 | 1 | 3 |
| α-helix | 127-129 | 3 | |
| α-helix | 130-145 | 16 | |
| α-helix | 153-170 | 18 | |
| α-helix | 177-189 | 13 | |
| α-helix | 197-199 | 3 | |
| β-strand | 204-207 | 4 | 4 |
| α-helix | 214-229 | 16 | |
| α-helix | 230-232 | 3 | |
| β-strand | 237-240 | 4 | 4 |
| α-helix | 242-244 | 3 | |
| β-strand | 252-253 | 2 | 5 |
| β-strand | 257 | 1 | 4 |
| β-strand | 261 | 1 | 6 |
| β-strand | 263-265 | 3 | 7 |
| β-strand | 271-273 | 3 | 7 |
| α-helix | 275-277 | 3 | |
| α-helix | 278-286 | 9 | |
| α-helix | 289-291 | 3 | |
| α-helix | 297 | 1 | |
| β-strand | 298 | 1 | 6 |
| α-helix | 299-300 | 2 | |
| β-strand | 301-304 | 4 | 5 |
| α-helix | 308-310 | 3 | |
| β-strand | 311-313 | 3 | 5 |
| α-helix | 314-316 | 3 | |
| α-helix | 317-319 | 3 | |
| β-strand | 322-324 | 3 | 8 |
| α-helix | 331-336 | 6 | |
| β-strand | 339-341 | 3 | 8 |
| β-strand | 345-346 | 2 | 4 |
| β-strand | 350-353 | 4 | 9 |
| β-strand | 356-358 | 3 | 9 |
| β-strand | 363-364 | 2 | 4 |
| β-strand | 367-368 | 2 | 10 |
| α-helix | 369-370 | 2 | |
| α-helix | 371-376 | 6 | |
| α-helix | 377-378 | 2 | |
| α-helix | 386-392 | 7 | |
| α-helix | 400-402 | 3 | |
| α-helix | 404-422 | 19 | |
| β-strand | 427-428 | 2 | 10 |
| α-helix | 430-448 | 19 | |
| α-helix | 455-458 | 4 | |
| α-helix | 464-466 | 3 | |
| α-helix | 468-471 | 4 | |
| β-strand | 472 | 1 | 2 |
| β-strand | 482-484 | 3 | 9 |
| β-strand | 485 | 1 | 3 |
| α-helix | 489-492 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 79-82 | 4 | 11 |
| β-strand | 83 | 1 | 12 |
| β-strand | 89-92 | 4 | 11 |
| α-helix | 94-97 | 4 | |
| α-helix | 117-119 | 3 | |
| β-strand | 120 | 1 | 13 |
| α-helix | 127-129 | 3 | |
| α-helix | 130-146 | 17 | |
| α-helix | 153-170 | 18 | |
| α-helix | 177-189 | 13 | |
| α-helix | 197-199 | 3 | |
| β-strand | 204-207 | 4 | 14 |
| α-helix | 214-229 | 16 | |
| α-helix | 230-232 | 3 | |
| β-strand | 237-240 | 4 | 14 |
| α-helix | 241-244 | 4 | |
| β-strand | 252-253 | 2 | 15 |
| β-strand | 257 | 1 | 14 |
| β-strand | 261 | 1 | 16 |
| β-strand | 263-265 | 3 | 17 |
| β-strand | 271-273 | 3 | 17 |
| α-helix | 275-277 | 3 | |
| α-helix | 278-286 | 9 | |
| α-helix | 297 | 1 | |
| β-strand | 298 | 1 | 16 |
| α-helix | 299-300 | 2 | |
| β-strand | 301-304 | 4 | 15 |
| α-helix | 308-310 | 3 | |
| β-strand | 311-313 | 3 | 15 |
| α-helix | 314-316 | 3 | |
| α-helix | 317-319 | 3 | |
| β-strand | 322-324 | 3 | 18 |
| α-helix | 331-336 | 6 | |
| β-strand | 339-341 | 3 | 18 |
| β-strand | 345-346 | 2 | 14 |
| β-strand | 350-353 | 4 | 19 |
| β-strand | 356-358 | 3 | 19 |
| β-strand | 363-364 | 2 | 14 |
| β-strand | 367-368 | 2 | 20 |
| α-helix | 369-370 | 2 | |
| α-helix | 371-376 | 6 | |
| α-helix | 377-378 | 2 | |
| α-helix | 386-392 | 7 | |
| α-helix | 400-402 | 3 | |
| α-helix | 404-422 | 19 | |
| β-strand | 427-428 | 2 | 20 |
| α-helix | 430-448 | 19 | |
| α-helix | 455-458 | 4 | |
| α-helix | 464-466 | 3 | |
| α-helix | 468-471 | 4 | |
| β-strand | 472 | 1 | 12 |
| β-strand | 482-484 | 3 | 19 |
| β-strand | 485 | 1 | 13 |
| α-helix | 489-491 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Nitric oxide synthase, inducible | A, B | protein | 433 | Mus musculus | P29477 (AlphaFold model) |
>3E7M_1 Nitric oxide synthase, inducible (chains A, B) LDKLHVTSTRPQYVRIKNWGSGEILHDTLHHKATSDFTCKSKSCLGSIMNPKSLTRGPRD KPTPLEELLPHAIEFINQYYGSFKEAKIEEHLARLEAVTKEIETTGTYQLTLDELIFATK MAWRNAPRCIGRIQWSNLQVFDARNCSTAQEMFQHICRHILYATNNGNIRSAITVFPQRS DGKHDFRLWNSQLIRYAGYQMPDGTIRGDAATLEFTQLCIDLGWKPRYGRFDVLPLVLQA DGQDPEVFEIPPDLVLEVTMEHPKYEWFQELGLKWYALPAVANMLLEVGGLEFPACPFNG WYMGTEIGVRDFCDTQRYNILEEVGRRMGLETHTLASLWKDRAVTEINVAVLHSFQKQNV TIMDHHTASESFMKHMQNEYRARGGCPADWIWLVPPVSGSITPVFHQEMLNYVLSPFYYY QIEPWKTHIWQNE
| ID | Name | Formula | Copies |
|---|---|---|---|
| AT2 | Ethyl 4-[(4-methylpyridin-2-yl)amino]piperidine-1-carboxylate | C14 H21 N3 O2 | 2 |
| H4B | 5,6,7,8-tetrahydrobiopterin | C9 H15 N5 O3 | 2 |
| HEM | Protoporphyrin IX containing FE | C34 H32 Fe N4 O4 | 2 |
| ZN | Zinc ion | Zn | 2 |
Water and common crystallization additives (EDO) are not listed.
Anchored plasticity opens doors for selective inhibitor design in nitric oxide synthase. Garcin, E.D., Arvai, A.S., Rosenfeld, R.J. et al. Nat Chem Biol (2008) 4:700-707. DOI 10.1038/nchembio.115 · PubMed
Other PDB entries of the same protein (UniProt P29477 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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