Structure of rat neuronal nitric oxide synthase heme domain in complex with N2-((3-((2-aminoquinolin-7-yl)methoxy)phenoxy)methyl)pyridine-2,6-diamine. Determined by X-ray diffraction at 1.73 Å resolution. Released 14 Sept 2022.
Explore 7S3Z in 3D Show helices and sheets RCSB PDB PDBe
7S3Z contains 52 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 | 301-304 | 4 | 1 |
| β-strand | 305 | 1 | 2 |
| β-strand | 311-314 | 4 | 1 |
| α-helix | 316-319 | 4 | |
| β-strand | 331 | 1 | 3 |
| α-helix | 348-350 | 3 | |
| α-helix | 351-368 | 18 | |
| α-helix | 375-391 | 17 | |
| α-helix | 398-410 | 13 | |
| α-helix | 418-420 | 3 | |
| β-strand | 425-428 | 4 | 4 |
| α-helix | 435-450 | 16 | |
| α-helix | 451-453 | 3 | |
| β-strand | 458-461 | 4 | 4 |
| α-helix | 462-465 | 4 | |
| β-strand | 473-474 | 2 | 5 |
| β-strand | 478 | 1 | 4 |
| β-strand | 482 | 1 | 6 |
| β-strand | 484-486 | 3 | 7 |
| β-strand | 492-494 | 3 | 7 |
| α-helix | 496-498 | 3 | |
| α-helix | 499-506 | 8 | |
| β-strand | 519 | 1 | 6 |
| α-helix | 520-521 | 2 | |
| β-strand | 522-525 | 4 | 5 |
| α-helix | 529-531 | 3 | |
| β-strand | 532-534 | 3 | 5 |
| α-helix | 535-537 | 3 | |
| α-helix | 538-540 | 3 | |
| β-strand | 543-545 | 3 | 8 |
| α-helix | 552-557 | 6 | |
| β-strand | 560-562 | 3 | 8 |
| β-strand | 566-567 | 2 | 4 |
| β-strand | 571-574 | 4 | 9 |
| β-strand | 577-579 | 3 | 9 |
| β-strand | 584-585 | 2 | 4 |
| β-strand | 588-589 | 2 | 10 |
| α-helix | 590-591 | 2 | |
| α-helix | 592-597 | 6 | |
| α-helix | 598-599 | 2 | |
| α-helix | 607-613 | 7 | |
| α-helix | 621-623 | 3 | |
| α-helix | 625-643 | 19 | |
| β-strand | 648-649 | 2 | 10 |
| α-helix | 651-669 | 19 | |
| α-helix | 676-679 | 4 | |
| α-helix | 685-687 | 3 | |
| α-helix | 689-692 | 4 | |
| β-strand | 693 | 1 | 2 |
| β-strand | 697 | 1 | 11 |
| β-strand | 703-705 | 3 | 9 |
| α-helix | 710-712 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 301-304 | 4 | 12 |
| β-strand | 305 | 1 | 13 |
| β-strand | 311-314 | 4 | 12 |
| α-helix | 316-319 | 4 | |
| β-strand | 331 | 1 | 11 |
| α-helix | 351-368 | 18 | |
| α-helix | 375-391 | 17 | |
| α-helix | 398-410 | 13 | |
| α-helix | 418-420 | 3 | |
| β-strand | 425-428 | 4 | 14 |
| α-helix | 435-450 | 16 | |
| α-helix | 451-453 | 3 | |
| β-strand | 458-461 | 4 | 14 |
| α-helix | 462-465 | 4 | |
| β-strand | 473-474 | 2 | 15 |
| β-strand | 478 | 1 | 14 |
| β-strand | 482 | 1 | 16 |
| β-strand | 484-486 | 3 | 17 |
| β-strand | 492-494 | 3 | 17 |
| α-helix | 496-498 | 3 | |
| α-helix | 499-507 | 9 | |
| α-helix | 518 | 1 | |
| β-strand | 519 | 1 | 16 |
| α-helix | 520-521 | 2 | |
| β-strand | 522-525 | 4 | 15 |
| α-helix | 529-531 | 3 | |
| β-strand | 532-534 | 3 | 15 |
| α-helix | 538-540 | 3 | |
| β-strand | 543-545 | 3 | 18 |
| α-helix | 552-557 | 6 | |
| β-strand | 560-562 | 3 | 18 |
| β-strand | 566-567 | 2 | 14 |
| β-strand | 571-574 | 4 | 19 |
| β-strand | 577-579 | 3 | 19 |
| β-strand | 584-585 | 2 | 14 |
| β-strand | 588-589 | 2 | 20 |
| α-helix | 590-591 | 2 | |
| α-helix | 592-597 | 6 | |
| α-helix | 598-599 | 2 | |
| α-helix | 607-613 | 7 | |
| α-helix | 621-623 | 3 | |
| α-helix | 625-643 | 19 | |
| β-strand | 648-649 | 2 | 20 |
| α-helix | 651-669 | 19 | |
| α-helix | 676-679 | 4 | |
| α-helix | 685-687 | 3 | |
| β-strand | 693 | 1 | 13 |
| β-strand | 697 | 1 | 3 |
| β-strand | 703-705 | 3 | 19 |
| α-helix | 710-713 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Nitric oxide synthase, brain | A, B | protein | 422 | Rattus norvegicus | P29476 (AlphaFold model) |
>7S3Z_1 Nitric oxide synthase, brain (chains A, B) CPRFLKVKNWETDVVLTDTLHLKSTLETGCTEHICMGSIMLPSQHTRKPEDVRTKDQLFP LAKEFLDQYYSSIKRFGSKAHMDRLEEVNKEIESTSTYQLKDTELIYGAKHAWRNASRCV GRIQWSKLQVFDARDCTTAHGMFNYICNHVKYATNKGNLRSAITIFPQRTDGKHDFRVWN SQLIRYAGYKQPDGSTLGDPANVQFTEICIQQGWKAPRGRFDVLPLLLQANGNDPELFQI PPELVLEVPIRHPKFDWFKDLGLKWYGLPAVSNMLLEIGGLEFSACPFSGWYMGTEIGVR DYCDNSRYNILEEVAKKMDLDMRKTSSLWKDQALVEINIAVLYSFQSDKVTIVDHHSATE SFIKHMENEYRCRGGCPADWVWIVPPMSGSITPVFHQEMLNYRLTPSFEYQPDPWNTHVW KG
| ID | Name | Formula | Copies |
|---|---|---|---|
| HEM | Protoporphyrin IX containing FE | C34 H32 Fe N4 O4 | 2 |
| H4B | 5,6,7,8-tetrahydrobiopterin | C9 H15 N5 O3 | 2 |
| V0P | 7-{[3-(2-{[(6-aminopyridin-2-yl)methyl]amino}ethoxy)phenoxy]methyl}quinolin-2-a… | C24 H25 N5 O2 | 2 |
| ZN | Zinc ion | Zn | 1 |
Water and common crystallization additives (ACT) are not listed.
Selective anti-MRSA inhibitors targeting bacterial nitric oxide synthase. Lewis, M.C., Weerawarna, P.M., Li, H. et al. To be published.
Other PDB entries of the same protein (UniProt P29476 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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