3GJD: LeuT with bound OG

Crystal Structure of LeuT with bound OG. Determined by X-ray diffraction at 2.0 Å resolution. Released 28 Apr 2009.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Aquifex aeolicus
Chains
1
Atoms
4,263
Mol. weight
59.58 kDa
Ligands
LEU, BOG
Released
28 Apr 2009

Explore 3GJD in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3GJD contains 38 α-helices and 4 β-strands across 1 chain. 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: 38 helices, 4 β-strands

ElementResiduesLengthSheet
α-helix11-2212
α-helix251
α-helix26-305
α-helix31-377
α-helix41-5010
α-helix51-555
α-helix56-7015
α-helix77-848
α-helix88-947
α-helix96-12429
α-helix137-15216
β-strand16111
α-helix166-18318
α-helix1861
α-helix187-1926
α-helix193-21422
β-strand217-21822
β-strand221-22222
α-helix223-2308
α-helix235-2373
α-helix241-25515
α-helix261-2666
α-helix276-28712
α-helix288-2947
α-helix295-30612
α-helix308-31710
α-helix321-3266
α-helix327-3326
α-helix337-37034
α-helix375-39521
β-strand39611
α-helix399-4057
α-helix406-4116
α-helix412-4209
α-helix421-4277
α-helix429-4379
α-helix443-4453
α-helix447-4504
α-helix451-4555
α-helix456-47015
α-helix472-4776
α-helix483-51331

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
TransporterAprotein515Aquifex aeolicusO67854 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3GJD_1 Transporter (chains A)
MEVKREHWATRLGLILAMAGNAVGLGNFLRFPVQAAENGGGAFMIPYIIAFLLVGIPLMW
IEWAMGRYGGAQGHGTTPAIFYLLWRNRFAKILGVFGLWIPLVVAIYYVYIESWTLGFAI
KFLVGLVPEPPPNATDPDSILRPFKEFLYSYIGVPKGDEPILKPSLFAYIVFLITMFINV
SILIRGISKGIERFAKIAMPTLFILAVFLVIRVFLLETPNGTAADGLNFLWTPDFEKLKD
PGVWIAAVGQIFFTLSLGFGAIITYASYVRKDQDIVLSGLTAATLNEKAEVILGGSISIP
AAVAFFGVANAVAIAKAGAFNLGFITLPAIFSQTAGGTFLGFLWFFLLFFAGLTSSIAIM
QPMIAFLEDELKLSRKHAVLWTAAIVFFSAHLVMFLNKSLDEMDFWAGTIGVVFFGLTEL
IIFFWIFGADKAWEEINRGGIIKVPRIYYYVMRYITPAFLAVLLVVWAREYIPKIMEETH
WTVWITRFYIIGLFLFLTFLVFLAERRRNHESAGT

Ligands and cofactors

IDNameFormulaCopies
LEULeucineC6 H13 N O21
BOGoctyl beta-D-glucopyranosideC14 H28 O66

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

Primary citation

Binding of an octylglucoside detergent molecule in the second substrate (S2) site of LeuT establishes an inhibitor-bound conformation. Quick, M., Winther, A.M.L., Shi, L. et al. Proc Natl Acad Sci U S A (2009) 106:5563-5568. DOI 10.1073/pnas.0811322106 · PubMed

Other PDB entries of the same protein (UniProt O67854 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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