NIH MBI Laboratory for Structural Genomics and Proteomics

Servers

•3DCA
•Crystallization Notebook Server
•daps
•Diffraction anisotropy server
•Diffusion Accessibility
•DPANN: Fold recognition -> Protein Function
•ERRAT: Structure Analysis
•FAD or NADP binding Rossmann fold detector
•FIBERS: Diffraction Data Anaylsis
•Fold Recognition
•HotPatch
•iFunc: Protein Function
•Internal Repeat Finder
•LATTICE: Diffraction Data Analysis
•MOMENT: Sequence Analysis
•MTBreg: database
•PROKNOW: Protein Function
•PROLINKS:Proteome Navigator
•Protein Triples
•RACC: Rare Codon Caculator
•Rosetta: Protein Function
•SAVES: MetaServer Structure Analysis
•SER: Surface Entropy Reduction
•TwinTest: Diffraction Data Analysis
•Twin detection with improved robustness
•Verify_3D: Structure Analysis
Group Members
Principal InvestigatorsAssociates
James Bowie Jeff Abramson
David Eisenberg Rob Clubb
Feng Guo Juli Feigon
Todd Yeates Wayne Hubbell
Joan Valentine
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The central goal of the NIH-UCLA program project is to understand the basis of protein self-recognition in health and disease, and to use X-ray crystallographic solutions to solve frontier problems in molecular recognition.


Recent Structures Solved

PDB Name
2B5A C.BclI, Control Element of the BclI Restriction-Modification System
2FGY Beta Carbonic Anhydrase from the Carboxysomal Shell of Halothiobacillus neapolitanus (CsoSCA)
2A7X Crystal Structure of A Pantothenate synthetase complexed with AMP
2A84 Crystal structure of A Pantothenate synthetase complexed with ATP
2A86 Crystal structure of A Pantothenate synthetase complexed with AMP and beta-alanine
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