› 2lf3

Solution NMR

Solution NMR structure of HopPmaL_281_385 from Pseudomonas syringae pv. maculicola str. ES4326, Midwest Center for Structural Genomics target APC40104.5 and Northeast Structural Genomics Consortium target PsT2A

Released:
DOI: 10.2210/pdb2lf3/pdb
PDB entry 2lf3 coloured by chain, ensemble of 20 models, front view.
PDB entry 2lf3 coloured by chain, ensemble of 20 models, side view.
PDB entry 2lf3 coloured by chain, ensemble of 20 models, top view.
Source organism: Pseudomonas syringae pv. maculicola
Primary publication:
Structural analysis of HopPmaL reveals the presence of a second adaptor domain common to the HopAB family of Pseudomonas syringae type III effectors.
Singer AU, Wu B, Yee A, Houliston S, Xu X, Cui H, Skarina T, Garcia M, Semesi A, Arrowsmith CH, Savchenko A
Biochemistry 51 1-3 (2012)
PMID: 22191472

Function and Biology Details

Biochemical function:
  • not assigned
Biological process:
  • not assigned
Cellular component:
  • not assigned
Sequence domains:

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-186015 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Effector protein hopAB3 Chain: A
Molecule details ›
Chain: A
Length: 107 amino acids
Theoretical weight: 11.77 KDa
Source organism: Pseudomonas syringae pv. maculicola
Expression system: Escherichia coli
UniProt:
  • Canonical: Q8RP04 (Residues: 281-385; Coverage: 27%)
Gene names: hopAB3, hopPmaL
Sequence domains: Avirulence AvrPtoB, BAK1-binding domain
Structure domains: Effector protein HopAB, BAK1-interacting domain

Ligands and Environments

No bound ligands
No modified residues

Experiments and Validation Details

Entry percentile scores
Chemical shift assignment: 92%
Refinement method: simulated annealing
Expression system: Escherichia coli

Quick links

Citations

2 review citations

On the front line: structural insights into plant-pathogen interactions.
Wirthmueller et al. (2013)
1 more

2 mentions without citation

Hydroxyethylamine Based Phthalimides as New Class of Plasmepsin Hits: Design, Synthesis and Antimalarial Evaluation.
Singh et al. (2015)
1 more