6M3Z: Sodium-dependent dopamine transporter

X-ray structure of a Drosophila dopamine transporter with NET-like mutations (D121G/S426M/F471L) in milnacipran bound form. Determined by X-ray diffraction at 3.11 Å resolution. Released 17 Feb 2021.

Method
X-ray diffraction
Resolution
3.11 Å
Organisms
Drosophila melanogaster, Mus musculus
Chains
3
Atoms
7,670
Mol. weight
109.15 kDa
Ligands
D10, F0F, CLR, Y01
Released
17 Feb 2021

Explore 6M3Z in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6M3Z contains 57 α-helices and 48 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.

Chain A: 42 helices, 6 β-strands

ElementResiduesLengthSheet
α-helix33-4412
α-helix48-514
α-helix53-597
α-helix62-654
α-helix66-727
α-helix73-775
α-helix78-9114
α-helix95-1028
α-helix104-1063
α-helix108-12417
α-helix126-13510
α-helix144-1463
β-strand157-15821
β-strand209-21021
α-helix211-2155
α-helix216-2205
α-helix223-2253
β-strand23512
α-helix237-25418
α-helix258-26811
α-helix271-28414
α-helix289-2979
α-helix301-3055
α-helix307-32115
α-helix327-3337
α-helix341-37333
α-helix378-3803
α-helix386-3872
α-helix388-3925
α-helix393-3975
α-helix403-43432
α-helix438-4425
α-helix444-45815
α-helix461-4633
β-strand46412
α-helix467-47711
α-helix481-49212
α-helix493-4997
α-helix500-51112
α-helix514-5163
α-helix517-5215
α-helix522-5265
α-helix527-54014
β-strand546-54723
β-strand550-55123
α-helix554-56815
α-helix570-57910
α-helix586-5927
Chain H: 7 helices, 22 β-strands
ElementResiduesLengthSheet
β-strand3-759
β-strand11-12210
β-strand18-2589
α-helix29-313
β-strand34-39611
β-strand45-51711
β-strand58-60311
β-strand68-7369
β-strand78-8369
α-helix88-903
β-strand92-98711
α-helix102-1043
β-strand108-109211
β-strand113-115311
β-strand116-117210
β-strand123112
α-helix124-1252
β-strand126-130513
β-strand141-1511113
β-strand152112
β-strand157-160414
α-helix161-1633
β-strand169-171313
α-helix172-1743
β-strand175-177313
β-strand180-1901113
β-strand200-205614
α-helix206-2083
β-strand210-215614
Chain L: 8 helices, 20 β-strands
ElementResiduesLengthSheet
β-strand4-744
β-strand10-1345
β-strand19-29114
α-helix31-333
β-strand34-3965
β-strand46-5055
β-strand54-5525
α-helix561
β-strand63-76144
α-helix81-833
β-strand86-9165
β-strand98-9925
β-strand103-10755
β-strand11216
β-strand115-11957
α-helix120-1223
α-helix123-1275
β-strand131-140107
β-strand14116
β-strand146-15168
β-strand154-15638
β-strand160-16457
α-helix165-1684
β-strand174-18297
α-helix184-1874
β-strand192-19878
α-helix2051
β-strand206-21168

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Sodium-dependent dopamine transporterAprotein536Drosophila melanogasterQ7K4Y6 (AlphaFold model)
Antibody fragment 9D5 Light chainLprotein214Mus musculus
Antibody fragment 9D5 heavy chainHprotein219Mus musculus
Sequence of entity 1 (A), FASTA
>6M3Z_1 Sodium-dependent dopamine transporter (chains A)
DERETWSGKVDFLLSVIGFAVDLANVWRFPYLCYKNGGGAFLVPYGIMLAVGGIPLFYME
LALGQHNRKGAITCWGRLVPLFKGIGYAVVLIAFYVGFYYNVIIAWSLRFFFASFTNSLP
WTSCNNIWNTPNCRPFEGHVEGFQSAASEYFNRYILELNRSEGIHDLGAIKWDMALCLLI
VYLICYFSLWKGISTSGKVVWFTALFPYAVLLILLIRGLTLPGSFLGIQYYLTPNFSAIY
KAEVWVDAATQVFFSLGPGFGVLLAYASYNKYHNNVYKDALLTSFINSATSFIAGFVIFS
VLGYMAHTLGVRIEDVATEGPGLVFVVYPAAIATMPASTFWALIFFMMLATLGLDSSFGG
MEAIITALSDEFPKIKRNRELFVAGLFSLYFVVGLASCTQGGFYFLHLLDRYAAGYSILV
AVFFEAIAVSWIYGTNRFSEDIRDMIGFPPGRYWQVCWRFVAPIFLLFITVYGLIGYEPL
TYADYVYPSWANALGWCIAGSSVVMIPAVAIFKLLSTPGSLRQRFTILTTPWRDQQ
Sequence of entity 2 (L), FASTA
>6M3Z_2 Antibody fragment 9D5 Light chain (chains L)
ENVLTQSPAIMSTSPGEKVTMTCRASSSVGSSYLHWYQQKSGASPKLWIYSTSNLASGVP
ARFSGSGSGTSYSLTISSVEAEDAATYYCQQFSGYPLTFGSGTKLEMKRADAAPTVSIFP
PSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTL
TLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
Sequence of entity 3 (H), FASTA
>6M3Z_3 Antibody fragment 9D5 heavy chain (chains H)
EVQLVESGGGLVKPGGSLKLSCAASGFTFSSYAMSWVRQSPEKRLEWVAEISSGGRYIYY
SDTVTGRFTISRDNARNILHLEMSSLRSEDTAMYYCARGEVRQRGFDYWGQGTTLTVSSA
KTTAPSVYPLAPVCGDTTGSSVTLGCLVKGYFPEPVTLTWNSGSLSSGVHTFPAVLQSDL
YTLSSSVTVTSSTWPSQSITCNVAHPASSTKVDKKIEPR

Ligands and cofactors

IDNameFormulaCopies
D10DecaneC10 H221
F0F(1R,2S)-2-(aminomethyl)-N,N-diethyl-1-phenyl-cyclopropane-1-carboxamideC15 H22 N2 O1
CLRCholesterolC27 H46 O1
Y01Cholesterol hemisuccinateC31 H50 O41

Water and common crystallization additives (NA, CL, GOL) are not listed.

Primary citation

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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