4.4 Article

Identification of two-histidines one-carboxylate binding motifs in proteins amenable to facial coordination to metals

Journal

METALLOMICS
Volume 4, Issue 4, Pages 379-388

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2mt20010d

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Funding

  1. SNF [FN 200020_126366, PDFMP2_127457]
  2. NCCR nanosciences from SNF
  3. Professur fur Molecular Bionics
  4. Swiss National Science Foundation (SNF) [PDFMP2_127457] Funding Source: Swiss National Science Foundation (SNF)

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Among natural metalloenzymes, the facial two-histidines one-carboxylate binding motif (FTM) is a widely represented first coordination sphere motif present in the active site of a variety of metalloenzymes. A PDB search revealed a total of 1685 structures bearing such FTMs bound to a metal. Sixty statistically representative FTMs were selected and used as template for the identification of structurally characterized proteins bearing these three amino acids in a propitious environment for binding to a transition metal. This geometrical superposition search, carried out using the STAMPS software, returned 2320 hits. While most consisted of either apo-FTMs or bore strong sequence homology to known FTMs, seven such structures lying within a cavity were identified as novel and viable scaffolds for the creation of artificial metalloenzymes bearing an FTM.

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