NMR in structural genomics to increase structural coverage of the protein universe

Author(s):  
Pedro Serrano ◽  
Samit K. Dutta ◽  
Andrew Proudfoot ◽  
Biswaranjan Mohanty ◽  
Lukas Susac ◽  
...  
2014 ◽  
Vol 111 (10) ◽  
pp. 3733-3738 ◽  
Author(s):  
Kamil Khafizov ◽  
Carlos Madrid-Aliste ◽  
Steven C. Almo ◽  
Andras Fiser

The exponential growth of protein sequence data provides an ever-expanding body of unannotated and misannotated proteins. The National Institutes of Health-supported Protein Structure Initiative and related worldwide structural genomics efforts facilitate functional annotation of proteins through structural characterization. Recently there have been profound changes in the taxonomic composition of sequence databases, which are effectively redefining the scope and contribution of these large-scale structure-based efforts. The faster-growing bacterial genomic entries have overtaken the eukaryotic entries over the last 5 y, but also have become more redundant. Despite the enormous increase in the number of sequences, the overall structural coverage of proteins—including proteins for which reliable homology models can be generated—on the residue level has increased from 30% to 40% over the last 10 y. Structural genomics efforts contributed ∼50% of this new structural coverage, despite determining only ∼10% of all new structures. Based on current trends, it is expected that ∼55% structural coverage (the level required for significant functional insight) will be achieved within 15 y, whereas without structural genomics efforts, realizing this goal will take approximately twice as long.


FEBS Journal ◽  
2016 ◽  
Vol 283 (21) ◽  
pp. 3870-3881 ◽  
Author(s):  
Pedro Serrano ◽  
Samit K. Dutta ◽  
Andrew Proudfoot ◽  
Biswaranjan Mohanty ◽  
Lukas Susac ◽  
...  

2007 ◽  
Vol 17 (3) ◽  
pp. 347-353 ◽  
Author(s):  
Marek Grabowski ◽  
Andrzej Joachimiak ◽  
Zbyszek Otwinowski ◽  
Wladek Minor

2014 ◽  
Vol 70 (a1) ◽  
pp. C1148-C1148
Author(s):  
Marc-André Elsliger ◽  
Ashley Deacon ◽  
Adam Godzik ◽  
Scott Lesley ◽  
Keith Hodgson ◽  
...  

For over a decade, the Joint Center for Structural Genomics (JCSG.org) has been at the forefront of developing tools and methodologies that enable the application of high-throughput structural biology (HTBSB) approaches to a broad range of challenging biological and biomedical problems. In PSI:Biology (2010-2015) to meet the challenges and embrace the opportunities that arise from our Partnerships projects, we have leveraged our gene-to-structure pipeline to explore challenging projects focused on structural characterization of interaction networks involved in stem cell regulation, T-cell activation and nuclear receptor signaling. These highly collaborative efforts have enabled development of systematic and integrative approaches for identifying and investigating networks of key multi-domain eukaryotic proteins and higher order assemblies of multi-component eukaryotic protein/protein and protein/nucleic acid complexes. In parallel, our biomedical theme project has focused on investigating host/microbe interactions of the microbial communities that inhabit specific niches and environments of the human body, e.g. the human gut microbiome. These efforts to date have been centered on secreted proteins from commensal bacteria in the human gut. The symbiotic relationship and influence on human development, physiology, immunity, and nutrition represent an exciting new frontier for HTBSB where we can investigate how these microorganisms contribute to human health as well as to disease. The JCSG also strives to promote widespread use of PSI resources, materials, methodologies and data to the general scientific community, via Community Nominated Target (CNT) projects and development and use of new technologies and methodologies. We also continue to contribute to the original PSI mission of structural coverage of the expanding protein universe. Supported by NIH U54-GM094586.


Sign in / Sign up

Export Citation Format

Share Document