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Featured researches published by Marc Gwadz.


Nucleic Acids Research | 2011

CDD: a Conserved Domain Database for the functional annotation of proteins

Shennan Lu; John B. Anderson; Farideh Chitsaz; Myra K. Derbyshire; Carol DeWeese-Scott; Jessica H. Fong; Lewis Y. Geer; Renata C. Geer; Noreen R. Gonzales; Marc Gwadz; David I. Hurwitz; John D. Jackson; Zhaoxi Ke; Christopher J. Lanczycki; Fu-Ping Lu; Gabriele H. Marchler; Mikhail Mullokandov; Marina V. Omelchenko; Cynthia L. Robertson; James S. Song; Narmada Thanki; Roxanne A. Yamashita; Dachuan Zhang; Naigong Zhang; Chanjuan Zheng; Stephen H. Bryant

NCBI’s Conserved Domain Database (CDD) is a resource for the annotation of protein sequences with the location of conserved domain footprints, and functional sites inferred from these footprints. CDD includes manually curated domain models that make use of protein 3D structure to refine domain models and provide insights into sequence/structure/function relationships. Manually curated models are organized hierarchically if they describe domain families that are clearly related by common descent. As CDD also imports domain family models from a variety of external sources, it is a partially redundant collection. To simplify protein annotation, redundant models and models describing homologous families are clustered into superfamilies. By default, domain footprints are annotated with the corresponding superfamily designation, on top of which specific annotation may indicate high-confidence assignment of family membership. Pre-computed domain annotation is available for proteins in the Entrez/Protein dataset, and a novel interface, Batch CD-Search, allows the computation and download of annotation for large sets of protein queries. CDD can be accessed via http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml.


Nucleic Acids Research | 2015

CDD: NCBI's conserved domain database

Myra K. Derbyshire; Noreen R. Gonzales; Shennan Lu; Farideh Chitsaz; Lewis Y. Geer; Renata C. Geer; Jane He; Marc Gwadz; David I. Hurwitz; Christopher J. Lanczycki; Fu Lu; Gabriele H. Marchler; James S. Song; Narmada Thanki; Zhouxi Wang; Roxanne A. Yamashita; Dachuan Zhang; Chanjuan Zheng; Stephen H. Bryant

NCBIs CDD, the Conserved Domain Database, enters its 15th year as a public resource for the annotation of proteins with the location of conserved domain footprints. Going forward, we strive to improve the coverage and consistency of domain annotation provided by CDD. We maintain a live search system as well as an archive of pre-computed domain annotation for sequences tracked in NCBIs Entrez protein database, which can be retrieved for single sequences or in bulk. We also maintain import procedures so that CDD contains domain models and domain definitions provided by several collections available in the public domain, as well as those produced by an in-house curation effort. The curation effort aims at increasing coverage and providing finer-grained classifications of common protein domains, for which a wealth of functional and structural data has become available. CDD curation generates alignment models of representative sequence fragments, which are in agreement with domain boundaries as observed in protein 3D structure, and which model the structurally conserved cores of domain families as well as annotate conserved features. CDD can be accessed at http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml.


Nucleic Acids Research | 2004

CDD: a Conserved Domain Database for protein classification

John B. Anderson; Praveen F. Cherukuri; Carol DeWeese-Scott; Lewis Y. Geer; Marc Gwadz; Siqian He; David I. Hurwitz; John D. Jackson; Zhaoxi Ke; Christopher J. Lanczycki; Cynthia A. Liebert; Chunlei Liu; Fu Lu; Gabriele H. Marchler; Mikhail Mullokandov; Benjamin A. Shoemaker; Vahan Simonyan; James S. Song; Paul A. Thiessen; Roxanne A. Yamashita; Jodie J. Yin; Dachuan Zhang; Stephen H. Bryant

The Conserved Domain Database (CDD) is the protein classification component of NCBIs Entrez query and retrieval system. CDD is linked to other Entrez databases such as Proteins, Taxonomy and PubMed®, and can be accessed at http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=cdd. CD-Search, which is available at http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi, is a fast, interactive tool to identify conserved domains in new protein sequences. CD-Search results for protein sequences in Entrez are pre-computed to provide links between proteins and domain models, and computational annotation visible upon request. Protein–protein queries submitted to NCBIs BLAST search service at http://www.ncbi.nlm.nih.gov/BLAST are scanned for the presence of conserved domains by default. While CDD started out as essentially a mirror of publicly available domain alignment collections, such as SMART, Pfam and COG, we have continued an effort to update, and in some cases replace these models with domain hierarchies curated at the NCBI. Here, we report on the progress of the curation effort and associated improvements in the functionality of the CDD information retrieval system.


Nucleic Acids Research | 2009

CDD: specific functional annotation with the Conserved Domain Database.

John B. Anderson; Farideh Chitsaz; Myra K. Derbyshire; Carol DeWeese-Scott; Jessica H. Fong; Lewis Y. Geer; Renata C. Geer; Noreen R. Gonzales; Marc Gwadz; Siqian He; David I. Hurwitz; John D. Jackson; Zhaoxi Ke; Christopher J. Lanczycki; Cynthia A. Liebert; Chunlei Liu; Fu-er Lu; Shennan Lu; Gabriele H. Marchler; Mikhail Mullokandov; James S. Song; Asba Tasneem; Narmada Thanki; Roxanne A. Yamashita; Dachuan Zhang; Naigong Zhang; Stephen H. Bryant

NCBIs Conserved Domain Database (CDD) is a collection of multiple sequence alignments and derived database search models, which represent protein domains conserved in molecular evolution. The collection can be accessed at http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml, and is also part of NCBIs Entrez query and retrieval system, cross-linked to numerous other resources. CDD provides annotation of domain footprints and conserved functional sites on protein sequences. Precalculated domain annotation can be retrieved for protein sequences tracked in NCBIs Entrez system, and CDDs collection of models can be queried with novel protein sequences via the CD-Search service at http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi. Starting with the latest version of CDD, v2.14, information from redundant and homologous domain models is summarized at a superfamily level, and domain annotation on proteins is flagged as either ‘specific’ (identifying molecular function with high confidence) or as ‘non-specific’ (identifying superfamily membership only).


Nucleic Acids Research | 2007

CDD: a conserved domain database for interactive domain family analysis

John B. Anderson; Myra K. Derbyshire; Carol DeWeese-Scott; Noreen R. Gonzales; Marc Gwadz; Luning Hao; Siqian He; David I. Hurwitz; John D. Jackson; Zhaoxi Ke; Dmitri M. Krylov; Christopher J. Lanczycki; Cynthia A. Liebert; Chunlei Liu; Fu Lu; Shennan Lu; Gabriele H. Marchler; Mikhail Mullokandov; James S. Song; Narmada Thanki; Roxanne A. Yamashita; Jodie J. Yin; Dachuan Zhang; Stephen H. Bryant

The conserved domain database (CDD) is part of NCBIs Entrez database system and serves as a primary resource for the annotation of conserved domain footprints on protein sequences in Entrez. Entrezs global query interface can be accessed at and will search CDD and many other databases. Domain annotation for proteins in Entrez has been pre-computed and is readily available in the form of ‘Conserved Domain’ links. Novel protein sequences can be scanned against CDD using the CD-Search service; this service searches databases of CDD-derived profile models with protein sequence queries using BLAST heuristics, at . Protein query sequences submitted to NCBIs protein BLAST search service are scanned for conserved domain signatures by default. The CDD collection contains models imported from Pfam, SMART and COG, as well as domain models curated at NCBI. NCBI curated models are organized into hierarchies of domains related by common descent. Here we report on the status of the curation effort and present a novel helper application, CDTree, which enables users of the CDD resource to examine curated hierarchies. More importantly, CDD and CDTree used in concert, serve as a powerful tool in protein classification, as they allow users to analyze protein sequences in the context of domain family hierarchies.


Nucleic Acids Research | 2012

CDD: conserved domains and protein three-dimensional structure

Chanjuan Zheng; Farideh Chitsaz; Myra K. Derbyshire; Lewis Y. Geer; Renata C. Geer; Noreen R. Gonzales; Marc Gwadz; David I. Hurwitz; Christopher J. Lanczycki; Fu Lu; Shennan Lu; Gabriele H. Marchler; James S. Song; Narmada Thanki; Roxanne A. Yamashita; Dachuan Zhang; Stephen H. Bryant

CDD, the Conserved Domain Database, is part of NCBI’s Entrez query and retrieval system and is also accessible via http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml. CDD provides annotation of protein sequences with the location of conserved domain footprints and functional sites inferred from these footprints. Pre-computed annotation is available via Entrez, and interactive search services accept single protein or nucleotide queries, as well as batch submissions of protein query sequences, utilizing RPS-BLAST to rapidly identify putative matches. CDD incorporates several protein domain and full-length protein model collections, and maintains an active curation effort that aims at providing fine grained classifications for major and well-characterized protein domain families, as supported by available protein three-dimensional (3D) structure and the published literature. To this date, the majority of protein 3D structures are represented by models tracked by CDD, and CDD curators are characterizing novel families that emerge from protein structure determination efforts.


Nucleic Acids Research | 2017

CDD/SPARCLE: functional classification of proteins via subfamily domain architectures

Yu Bo; Lianyi Han; Jane He; Christopher J. Lanczycki; Shennan Lu; Farideh Chitsaz; Myra K. Derbyshire; Renata C. Geer; Noreen R. Gonzales; Marc Gwadz; David I. Hurwitz; Fu Lu; Gabriele H. Marchler; James S. Song; Narmada Thanki; Zhouxi Wang; Roxanne A. Yamashita; Dachuan Zhang; Chanjuan Zheng; Lewis Y. Geer; Stephen H. Bryant

NCBIs Conserved Domain Database (CDD) aims at annotating biomolecular sequences with the location of evolutionarily conserved protein domain footprints, and functional sites inferred from such footprints. An archive of pre-computed domain annotation is maintained for proteins tracked by NCBIs Entrez database, and live search services are offered as well. CDD curation staff supplements a comprehensive collection of protein domain and protein family models, which have been imported from external providers, with representations of selected domain families that are curated in-house and organized into hierarchical classifications of functionally distinct families and sub-families. CDD also supports comparative analyses of protein families via conserved domain architectures, and a recent curation effort focuses on providing functional characterizations of distinct subfamily architectures using SPARCLE: Subfamily Protein Architecture Labeling Engine. CDD can be accessed at https://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml.


Nucleic Acids Research | 2018

RefSeq: an update on prokaryotic genome annotation and curation

Daniel H. Haft; Michael DiCuccio; Azat Badretdin; Vyacheslav Brover; Vyacheslav Chetvernin; Kathleen O’Neill; Wenjun Li; Farideh Chitsaz; Myra K. Derbyshire; Noreen R. Gonzales; Marc Gwadz; Fu Lu; Gabriele H. Marchler; James S. Song; Narmada Thanki; Roxanne A. Yamashita; Chanjuan Zheng; Françoise Thibaud-Nissen; Lewis Y. Geer; Kim D. Pruitt

Abstract The Reference Sequence (RefSeq) project at the National Center for Biotechnology Information (NCBI) provides annotation for over 95 000 prokaryotic genomes that meet standards for sequence quality, completeness, and freedom from contamination. Genomes are annotated by a single Prokaryotic Genome Annotation Pipeline (PGAP) to provide users with a resource that is as consistent and accurate as possible. Notable recent changes include the development of a hierarchical evidence scheme, a new focus on curating annotation evidence sources, the addition and curation of protein profile hidden Markov models (HMMs), release of an updated pipeline (PGAP-4), and comprehensive re-annotation of RefSeq prokaryotic genomes. Antimicrobial resistance proteins have been reannotated comprehensively, improved structural annotation of insertion sequence transposases and selenoproteins is provided, curated complex domain architectures have given upgraded names to millions of multidomain proteins, and we introduce a new kind of annotation rule—BlastRules. Continual curation of supporting evidence, and propagation of improved names onto RefSeq proteins ensures that the functional annotation of genomes is kept current. An increasing share of our annotation now derives from HMMs and other sets of annotation rules that are portable by nature, and available for download and for reuse by other investigators. RefSeq is found at https://www.ncbi.nlm.nih.gov/refseq/.


Cancer Research | 2013

Abstract 2900: Phylogenetic classification, structural evolution, and functional divergence of the Ras superfamily of GTPases as tracked by the Conserved Domain Database (CDD)..

James S. Song; Narmada Thanki; Myra K. Derbyshire; Marc Gwadz; Noreen R. Gonzales; Stephen H. Bryant

Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC The Conserved Domain Database (CDD, http://www.ncbi.nlm.nih.gov/Structure/cdd/cdd.shtml) is part of NCBIs Entrez query and retrieval system and is a collection of annotated multiple sequence alignment (MSA) models representing ancient conserved protein domains, basic units of protein function and protein evolution.These MSA models are available as position specific score matrices (PSSMs) for fast identification of conserved domains in protein sequences via Reverse Position Specific -BLAST (RPS-BLAST), a variation of the commonly used PSI-BLAST. The domain models can be viewed and examined interactively using NCBIs CDTree/Cn3D software applications. Conserved functional annotations such as key catalytic and ligand-binding sites are displayed on protein structures sharing significant homology to the query, thereby inferring the underlying mechanism(s) of the protein domain family. Here, we present the current, functionally annotated, evolutionary classification of the Ras GTPase superfamily, including the circularly permuted Ras-like domain, and its downstream effectors such as RasGAP and RasGEF. Using CDTree/Cn3D tools, subfamilies in diverse organisms were inferred from the MSAs, phylogenetic trees, and domain architectures of the Ras superfamily. Furthermore, several subfamilies comprising of only uncharacterized protein sequences have their functions annotated by inference from the molecular and cellular functions of known related proteins having 3D structure, and based on the available literature. We demonstrate the utility of CDTree/Cn3D in studying molecular evolution of protein domain families, and in accelerating the pace of biological discovery by enabling researchers to obtain valuable clues regarding as-yet-unidentified molecular properties and mechanisms. CDTree/Cn3D software is freely available for download via the CDD website. Citation Format: James S. Song, Narmada Thanki, Myra K. Derbyshire, Marc Gwadz, Noreen R. Gonzales, Aron Marchler-Bauer, Stephen H. Bryant. Phylogenetic classification, structural evolution, and functional divergence of the Ras superfamily of GTPases as tracked by the Conserved Domain Database (CDD). [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 2900. doi:10.1158/1538-7445.AM2013-2900


F1000Research | 2017

SPARCLE: Functional characterization of proteins by domain architecture

Roxanne A. Yamashita; Lianyi Han; Jane He; Christopher J. Lanczycki; Shennan Lu; Bo Yu; Farideh Chitsaz; Myra K. Derbyshire; Renata C. Geer; Noreen R. Gonzales; Marc Gwadz; Dave Hurwitz; Fu Lu; Gabriele H. Marchler; James S. Song; Narmada Thanki; Dachuan Zhang; Christina Zheng; Lewis Y. Geer; Stephen H. Bryant

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James S. Song

National Institutes of Health

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Myra K. Derbyshire

National Institutes of Health

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Narmada Thanki

National Institutes of Health

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Noreen R. Gonzales

National Institutes of Health

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Roxanne A. Yamashita

National Institutes of Health

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Gabriele H. Marchler

National Institutes of Health

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Farideh Chitsaz

National Institutes of Health

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Stephen H. Bryant

National Institutes of Health

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Fu Lu

National Institutes of Health

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