X-ray structure of Drosophila dopamine transporter in complex with reboxetine. Determined by X-ray diffraction at 3.0 Å resolution. Released 13 May 2015.
Explore 4XNX in 3D Show helices and sheets RCSB PDB PDBe
4XNX contains 53 α-helices and 49 β-strands across 3 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 | 33-44 | 12 | |
| α-helix | 48-51 | 4 | |
| α-helix | 53-60 | 8 | |
| α-helix | 62-65 | 4 | |
| α-helix | 66-72 | 7 | |
| α-helix | 73-77 | 5 | |
| α-helix | 78-91 | 14 | |
| α-helix | 95-102 | 8 | |
| α-helix | 104-106 | 3 | |
| α-helix | 108-136 | 29 | |
| β-strand | 158 | 1 | 1 |
| β-strand | 210 | 1 | 1 |
| α-helix | 211-214 | 4 | |
| α-helix | 215-221 | 7 | |
| α-helix | 223-225 | 3 | |
| β-strand | 235 | 1 | 2 |
| α-helix | 237-254 | 18 | |
| α-helix | 258-284 | 27 | |
| α-helix | 289-297 | 9 | |
| α-helix | 301-303 | 3 | |
| α-helix | 307-321 | 15 | |
| α-helix | 327-332 | 6 | |
| α-helix | 341-373 | 33 | |
| α-helix | 378-381 | 4 | |
| α-helix | 385-387 | 3 | |
| α-helix | 388-392 | 5 | |
| α-helix | 393-399 | 7 | |
| α-helix | 403-436 | 34 | |
| α-helix | 438-441 | 4 | |
| α-helix | 444-459 | 16 | |
| α-helix | 460-462 | 3 | |
| β-strand | 464 | 1 | 2 |
| α-helix | 467-477 | 11 | |
| α-helix | 482-492 | 11 | |
| α-helix | 493-497 | 5 | |
| α-helix | 500-511 | 12 | |
| α-helix | 514-516 | 3 | |
| α-helix | 517-521 | 5 | |
| α-helix | 522-526 | 5 | |
| α-helix | 527-540 | 14 | |
| β-strand | 546-547 | 2 | 3 |
| β-strand | 550-551 | 2 | 3 |
| α-helix | 554-568 | 15 | |
| α-helix | 570-580 | 11 | |
| α-helix | 586-593 | 8 | |
| α-helix | 597-600 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 9 |
| β-strand | 11-12 | 2 | 10 |
| β-strand | 17-25 | 9 | 9 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 11 |
| β-strand | 45-51 | 7 | 11 |
| β-strand | 58-60 | 3 | 11 |
| β-strand | 65 | 1 | 9 |
| β-strand | 68-73 | 6 | 9 |
| β-strand | 78-84 | 7 | 9 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-98 | 7 | 11 |
| β-strand | 108-109 | 2 | 11 |
| β-strand | 113-115 | 3 | 11 |
| β-strand | 116-117 | 2 | 10 |
| α-helix | 120-122 | 3 | |
| β-strand | 123 | 1 | 12 |
| β-strand | 126-130 | 5 | 13 |
| β-strand | 141-151 | 11 | 13 |
| β-strand | 152 | 1 | 12 |
| β-strand | 157-160 | 4 | 14 |
| β-strand | 169-171 | 3 | 13 |
| α-helix | 172-174 | 3 | |
| β-strand | 175-177 | 3 | 13 |
| β-strand | 180-190 | 11 | 13 |
| β-strand | 199-205 | 7 | 14 |
| β-strand | 210-216 | 7 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3 | 1 | |
| β-strand | 4-7 | 4 | 4 |
| β-strand | 10-13 | 4 | 5 |
| β-strand | 19-29 | 11 | 4 |
| α-helix | 31-33 | 3 | |
| β-strand | 34-39 | 6 | 5 |
| β-strand | 46-50 | 5 | 5 |
| β-strand | 54-55 | 2 | 5 |
| β-strand | 63-76 | 14 | 4 |
| α-helix | 81-83 | 3 | |
| β-strand | 86-91 | 6 | 5 |
| α-helix | 97 | 1 | |
| β-strand | 98-99 | 2 | 5 |
| β-strand | 103-107 | 5 | 5 |
| β-strand | 112 | 1 | 6 |
| β-strand | 115-119 | 5 | 7 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-127 | 5 | |
| β-strand | 130-140 | 11 | 7 |
| β-strand | 141 | 1 | 6 |
| β-strand | 146-151 | 6 | 8 |
| β-strand | 154-156 | 3 | 8 |
| β-strand | 160-164 | 5 | 7 |
| α-helix | 165-168 | 4 | |
| β-strand | 174-183 | 10 | 7 |
| α-helix | 184-187 | 4 | |
| β-strand | 192-198 | 7 | 8 |
| α-helix | 205 | 1 | |
| β-strand | 206-211 | 6 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Transporter | A | protein | 536 | Drosophila melanogaster | Q7K4Y6 (AlphaFold model) |
| antibody fragment light chain | L | protein | 214 | Mus musculus | |
| Antibody fragment heavy chain | H | protein | 240 | Mus musculus |
>4XNX_1 Transporter (chains A) DERETWSGKVDFLLSVIGFAVDLANVWRFPYLCYKNGGGAFLVPYGIMLAVGGIPLFYME LALGQHNRKGAITCWGRLVPLFKGIGYAVVLIAFYVDFYYNVIIAWSLRFFFASFTNSLP WTSCNNIWNTPNCRPFEGHVEGFQSAASEYFNRYILELNRSEGIHDLGAIKWDMALCLLI VYLICYFSLWKGISTSGKVVWFTALFPYAVLLILLIRGLTLPGSFLGIQYYLTPNFSAIY KAEVWVDAATQVFFSLGPGFGVLLAYASYNKYHNNVYKDALLTSFINSATSFIAGFVIFS VLGYMAHTLGVRIEDVATEGPGLVFVVYPAAIATMPASTFWALIFFMMLATLGLDSSFGG SEAIITALSDEFPKIKRNRELFVAGLFSLYFVVGLASCTQGGFYFFHLLDRYAAGYSILV AVFFEAIAVSWIYGTNRFSEDIRDMIGFPPGRYWQVCWRFVAPIFLLFITVYGLIGYEPL TYADYVYPSWANALGWCIAGSSVVMIPAVAIFKLLSTPGSLRQRFTILTTPWRDQQ
>4XNX_2 antibody fragment light chain (chains L) ENVLTQSPAIMSTSPGEKVTMTCRASSSVGSSYLHWYQQKSGASPKLWIYSTSNLASGVP ARFSGSGSGTSYSLTISSVEAEDAATYYCQQFSGYPLTFGSGTKLEMKRADAAPTVSIFP PSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTL TLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
>4XNX_3 Antibody fragment heavy chain (chains H) MNFGLRLVFLVLILKGVQCEVQLVESGGGLVKPGGSLKLSCAASGFTFSSYAMSWVRQSP EKRLEWVAEISSGGRYIYYSDTVTGRFTISRDNARNILHLEMSSLRSEDTAMYYCARGEV RQRGFDYWGQGTTLTVSSAKTTAPSVYPLAPVCGDTTGSSVTLGCLVKGYFPEPVTLTWN SGSLSSGVHTFPAVLQSDLYTLSSSVTVTSSTWPSQSITCNVAHPASSTKVDKKIEPRGP
| ID | Name | Formula | Copies |
|---|---|---|---|
| 41X | (2R)-2-[(R)-(2-ethoxyphenoxy)(phenyl)methyl]morpholine | C19 H23 N O3 | 1 |
| CLR | Cholesterol | C27 H46 O | 2 |
Water and common crystallization additives (CL, NA) are not listed.
X-ray structures of Drosophila dopamine transporter in complex with nisoxetine and reboxetine. Penmatsa, A., Wang, K.H., Gouaux, E. Nat Struct Mol Biol (2015) 22:506-508. DOI 10.1038/nsmb.3029 · PubMed
Other PDB entries of the same protein (UniProt Q7K4Y6 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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