Structural basis of trans-inhibition in a molybdate/tungstate ABC transporter

Science. 2008 Jul 11;321(5886):246-50. doi: 10.1126/science.1156213. Epub 2008 May 29.


Transport across cellular membranes is an essential process that is catalyzed by diverse membrane transport proteins. The turnover rates of certain transporters are inhibited by their substrates in a process termed trans-inhibition, whose structural basis is poorly understood. We present the crystal structure of a molybdate/tungstate ABC transporter (ModBC) from Methanosarcina acetivorans in a trans-inhibited state. The regulatory domains of the nucleotide-binding subunits are in close contact and provide two oxyanion binding pockets at the shared interface. By specifically binding to these pockets, molybdate or tungstate prevent adenosine triphosphatase activity and lock the transporter in an inward-facing conformation, with the catalytic motifs of the nucleotide-binding domains separated. This allosteric effect prevents the transporter from switching between the inward-facing and the outward-facing states, thus interfering with the alternating access and release mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters / antagonists & inhibitors*
  • ATP-Binding Cassette Transporters / chemistry*
  • ATP-Binding Cassette Transporters / metabolism
  • Adenosine Triphosphatases / metabolism
  • Adenosine Triphosphate / metabolism
  • Amino Acid Motifs
  • Amino Acid Sequence
  • Archaeal Proteins / antagonists & inhibitors
  • Archaeal Proteins / chemistry*
  • Archaeal Proteins / metabolism
  • Binding Sites
  • Catalytic Domain
  • Crystallography, X-Ray
  • Methanosarcina / chemistry*
  • Models, Molecular
  • Molecular Sequence Data
  • Molybdenum / metabolism*
  • Protein Conformation
  • Protein Folding
  • Protein Structure, Tertiary
  • Tungsten Compounds / metabolism*


  • ATP-Binding Cassette Transporters
  • Archaeal Proteins
  • Tungsten Compounds
  • molybdate
  • Molybdenum
  • Adenosine Triphosphate
  • Adenosine Triphosphatases
  • tungstate

Associated data

  • PDB/3D31