X-ray structure of a Drosophila dopamine transporter with subsiteB mutations (D121G/S426M) in S-duloxetine bound form. Determined by X-ray diffraction at 3.0 Å resolution. Released 17 Feb 2021.
Explore 6M38 in 3D Show helices and sheets RCSB PDB PDBe
6M38 contains 54 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 | 53-59 | 7 | |
| α-helix | 62-65 | 4 | |
| α-helix | 66-72 | 7 | |
| α-helix | 73-77 | 5 | |
| α-helix | 78-91 | 14 | |
| α-helix | 95-100 | 6 | |
| α-helix | 104-106 | 3 | |
| α-helix | 107-120 | 14 | |
| α-helix | 124-137 | 14 | |
| α-helix | 144-146 | 3 | |
| β-strand | 158 | 1 | 1 |
| β-strand | 210 | 1 | 1 |
| α-helix | 211-214 | 4 | |
| α-helix | 215-220 | 6 | |
| α-helix | 223-225 | 3 | |
| β-strand | 235 | 1 | 2 |
| α-helix | 237-254 | 18 | |
| α-helix | 258-285 | 28 | |
| α-helix | 289-297 | 9 | |
| α-helix | 307-320 | 14 | |
| α-helix | 327-332 | 6 | |
| α-helix | 341-369 | 29 | |
| α-helix | 370-374 | 5 | |
| α-helix | 378-381 | 4 | |
| α-helix | 386-387 | 2 | |
| α-helix | 388-392 | 5 | |
| α-helix | 393-399 | 7 | |
| α-helix | 403-434 | 32 | |
| α-helix | 438-441 | 4 | |
| α-helix | 444-459 | 16 | |
| α-helix | 460-463 | 4 | |
| β-strand | 464 | 1 | 2 |
| α-helix | 467-477 | 11 | |
| α-helix | 481-492 | 12 | |
| α-helix | 493-499 | 7 | |
| 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 | 570-579 | 10 | |
| α-helix | 586-593 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 9 |
| β-strand | 11-12 | 2 | 10 |
| β-strand | 18-25 | 8 | 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 | 69-73 | 5 | 9 |
| β-strand | 78-83 | 6 | 9 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-98 | 7 | 11 |
| α-helix | 102-104 | 3 | |
| β-strand | 108-109 | 2 | 11 |
| β-strand | 113-115 | 3 | 11 |
| β-strand | 116-117 | 2 | 10 |
| 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 |
| α-helix | 161-163 | 3 | |
| β-strand | 165 | 1 | 14 |
| β-strand | 169-177 | 9 | 13 |
| β-strand | 180-190 | 11 | 13 |
| β-strand | 200-205 | 6 | 14 |
| α-helix | 206-208 | 3 | |
| β-strand | 210-215 | 6 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 4 |
| β-strand | 10-13 | 4 | 5 |
| β-strand | 19-25 | 7 | 4 |
| α-helix | 31-33 | 3 | |
| β-strand | 34-39 | 6 | 5 |
| β-strand | 45-50 | 6 | 5 |
| β-strand | 54-55 | 2 | 5 |
| β-strand | 63-68 | 6 | 4 |
| β-strand | 71-76 | 6 | 4 |
| α-helix | 81-83 | 3 | |
| β-strand | 85-91 | 7 | 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 | 123-128 | 6 | |
| 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 | 184-188 | 5 | |
| β-strand | 192-198 | 7 | 8 |
| α-helix | 205 | 1 | |
| β-strand | 206-211 | 6 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Sodium-dependent dopamine transporter | A | protein | 534 | Drosophila melanogaster | Q7K4Y6 (AlphaFold model) |
| Antibody fragment 9D5 light chain | L | protein | 214 | Mus musculus | |
| Antibody fragment 9D5 heavy chain | H | protein | 219 | Mus musculus |
>6M38_1 Sodium-dependent dopamine transporter (chains A) DERETWSGKVDFLLSVIGFAVDLANVWRFPYLCYKNGGGAFLVPYGIMLAVGGIPLFYME LALGQHNRKGAITCWGRLVPLFKGIGYAVVLIAFYVGFYYNVIIAWSLRFFFASFTNSLP WTSCNNIWNTPNCRPFEGHVEGFQSAASEYFNRYILELNRSEGIHDLGAIKWDMALCLLI VYLICYFSLWKGISTSGKVVWFTALFPYAVLLILLIRGLTLPGSFLGIQYYLTPNFSAIY KAEVWVDAATQVFFSLGPGFGVLLAYASYNKYHNNVYKDALLTSFINSATSFIAGFVIFS VLGYMAHTLGVRIEDVATEGPGLVFVVYPAAIATMPASTFWALIFFMMLATLGLDSSFGG MEAIITALSDEFPKIKRNRELFVAGLFSLYFVVGLASCTQGGFYFFHLLDRYAAGYSILV AVFFEAIAVSWIYGTNRFSEDIRDMIGFPPGRYWQVCWRFVAPIFLLFITVYGLIGYEPL TYADYVYPSWANALGWCIAGSSVVMIPAVAIFKLLSTPGSLRQRFTILTTPWRD
>6M38_2 Antibody fragment 9D5 light chain (chains L) ENVLTQSPAIMSTSPGEKVTMTCRASSSVGSSYLHWYQQKSGASPKLWIYSTSNLASGVP ARFSGSGSGTSYSLTISSVEAEDAATYYCQQFSGYPLTFGSGTKLEMKRADAAPTVSIFP PSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTL TLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
>6M38_3 Antibody fragment 9D5 heavy chain (chains H) EVQLVESGGGLVKPGGSLKLSCAASGFTFSSYAMSWVRQSPEKRLEWVAEISSGGRYIYY SDTVTGRFTISRDNARNILHLEMSSLRSEDTAMYYCARGEVRQRGFDYWGQGTTLTVSSA KTTAPSVYPLAPVCGDTTGSSVTLGCLVKGYFPEPVTLTWNSGSLSSGVHTFPAVLQSDL YTLSSSVTVTSSTWPSQSITCNVAHPASSTKVDKKIEPR
| ID | Name | Formula | Copies |
|---|---|---|---|
| 29E | (3S)-N-methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine | C18 H19 N O S | 1 |
| Y01 | Cholesterol hemisuccinate | C31 H50 O4 | 1 |
| DMU | Decyl-beta-D-maltopyranoside | C22 H42 O11 | 1 |
| CLR | Cholesterol | C27 H46 O | 1 |
Water and common crystallization additives (NA, CL) are not listed.
Structural basis of norepinephrine recognition and transport inhibition in neurotransmitter transporters. Pidathala, S., Mallela, A.K., Joseph, D. et al. Nat Commun (2021) 12:2199-2199. DOI 10.1038/s41467-021-22385-9 · 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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