• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

SNP@Domain:蛋白质结构域结构和序列中单个核苷酸多态性(SNP)的网络资源。

SNP@Domain: a web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences.

作者信息

Han Areum, Kang Hyo Jin, Cho Yoobok, Lee Sunghoon, Kim Young Joo, Gong Sungsam

机构信息

National Genome Information Center (NGIC), Korea Research Institute of Bioscience and Biotechnology, 52 Eoeun-dong, Yuseong-guDaejeon 305-333, Korea.

出版信息

Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W642-4. doi: 10.1093/nar/gkl323.

DOI:10.1093/nar/gkl323
PMID:16845090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1538855/
Abstract

The single nucleotide polymorphisms (SNPs) in conserved protein regions have been thought to be strong candidates that alter protein functions. Thus, we have developed SNP@Domain, a web resource, to identify SNPs within human protein domains. We annotated SNPs from dbSNP with protein structure-based as well as sequence-based domains: (i) structure-based using SCOP and (ii) sequence-based using Pfam to avoid conflicts from two domain assignment methodologies. Users can investigate SNPs within protein domains with 2D and 3D maps. We expect this visual annotation of SNPs within protein domains will help scientists select and interpret SNPs associated with diseases. A web interface for the SNP@Domain is freely available at http://snpnavigator.net/ and from http://bioportal.net/.

摘要

保守蛋白区域中的单核苷酸多态性(SNP)被认为是改变蛋白功能的有力候选因素。因此,我们开发了一个网络资源SNP@Domain,用于识别人类蛋白结构域内的SNP。我们使用基于蛋白质结构以及基于序列的结构域对来自dbSNP的SNP进行注释:(i)基于结构的使用SCOP,(ii)基于序列的使用Pfam,以避免两种结构域分配方法产生冲突。用户可以通过二维和三维图谱研究蛋白结构域内的SNP。我们期望这种对蛋白结构域内SNP的可视化注释将有助于科学家选择和解释与疾病相关的SNP。SNP@Domain的网络界面可从http://snpnavigator.net/和http://bioportal.net/免费获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55f/1538855/1db9961e66e3/gkl323f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55f/1538855/76c1e4791b09/gkl323f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55f/1538855/1db9961e66e3/gkl323f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55f/1538855/76c1e4791b09/gkl323f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55f/1538855/1db9961e66e3/gkl323f2.jpg

相似文献

1
SNP@Domain: a web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences.SNP@Domain:蛋白质结构域结构和序列中单个核苷酸多态性(SNP)的网络资源。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W642-4. doi: 10.1093/nar/gkl323.
2
SNP mining porcine ESTs with MAVIANT, a novel tool for SNP evaluation and annotation.利用MAVIANT挖掘猪EST中的单核苷酸多态性,MAVIANT是一种用于单核苷酸多态性评估和注释的新型工具。
Bioinformatics. 2007 Jul 1;23(13):i387-91. doi: 10.1093/bioinformatics/btm192.
3
MyHits: a new interactive resource for protein annotation and domain identification.MyHits:一种用于蛋白质注释和结构域识别的新型交互式资源。
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W332-5. doi: 10.1093/nar/gkh479.
4
LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.LS-SNP:基于多信息源的编码非同义单核苷酸多态性的大规模注释
Bioinformatics. 2005 Jun 15;21(12):2814-20. doi: 10.1093/bioinformatics/bti442. Epub 2005 Apr 12.
5
The ProDom database of protein domain families: more emphasis on 3D.蛋白质结构域家族的ProDom数据库:更注重三维结构。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D212-5. doi: 10.1093/nar/gki034.
6
SNP-VISTA: an interactive SNP visualization tool.SNP-VISTA:一种交互式单核苷酸多态性可视化工具。
BMC Bioinformatics. 2005 Dec 8;6:292. doi: 10.1186/1471-2105-6-292.
7
Single nucleotide polymorphism discovery in barley using autoSNPdb.利用自动单核苷酸多态性数据库(autoSNPdb)在大麦中发现单核苷酸多态性
Plant Biotechnol J. 2009 May;7(4):326-33. doi: 10.1111/j.1467-7652.2009.00407.x.
8
Dynamic programming for single nucleotide polymorphism ID identification in systematic association studies.系统关联研究中单核苷酸多态性 ID 识别的动态规划。
Kaohsiung J Med Sci. 2009 Apr;25(4):165-76. doi: 10.1016/S1607-551X(09)70057-9.
9
PicSNP: a browsable catalog of nonsynonymous single nucleotide polymorphisms in the human genome.PicSNP:人类基因组中非同义单核苷酸多态性的可浏览目录。
Biochem Biophys Res Commun. 2001 Sep 14;287(1):288-91. doi: 10.1006/bbrc.2001.5576.
10
Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms.非同义编码区单核苷酸多态性的大规模分析
Bioinformatics. 2004 May 1;20(7):1006-14. doi: 10.1093/bioinformatics/bth029. Epub 2004 Jan 29.

引用本文的文献

1
Prediction and prioritization of rare oncogenic mutations in the cancer Kinome using novel features and multiple classifiers.利用新特征和多分类器对癌症激酶组中罕见致癌突变进行预测和优先级排序。
PLoS Comput Biol. 2014 Apr 17;10(4):e1003545. doi: 10.1371/journal.pcbi.1003545. eCollection 2014 Apr.
2
Towards precision medicine: advances in computational approaches for the analysis of human variants.迈向精准医学:人类变异分析的计算方法进展。
J Mol Biol. 2013 Nov 1;425(21):4047-63. doi: 10.1016/j.jmb.2013.08.008. Epub 2013 Aug 17.
3
Meet me halfway: when genomics meets structural bioinformatics.

本文引用的文献

1
SNPs3D: candidate gene and SNP selection for association studies.SNPs3D:用于关联研究的候选基因和单核苷酸多态性选择
BMC Bioinformatics. 2006 Mar 22;7:166. doi: 10.1186/1471-2105-7-166.
2
nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms.nsSNPAnalyzer:识别与疾病相关的非同义单核苷酸多态性
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W480-2. doi: 10.1093/nar/gki372.
3
MutDB services: interactive structural analysis of mutation data.MutDB服务:突变数据的交互式结构分析
折衷方案:基因组学与结构生物信息学相遇。
J Cardiovasc Transl Res. 2011 Jun;4(3):281-303. doi: 10.1007/s12265-011-9259-1. Epub 2011 Feb 25.
4
CanProVar: a human cancer proteome variation database.CanProVar:一个人类癌症蛋白质组变异数据库。
Hum Mutat. 2010 Mar;31(3):219-28. doi: 10.1002/humu.21176.
5
Inferring selection on amino acid preference in protein domains.推断蛋白质结构域中氨基酸偏好性的选择作用。
Mol Biol Evol. 2009 Mar;26(3):527-36. doi: 10.1093/molbev/msn286. Epub 2008 Dec 18.
6
An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.一种用于研究单核苷酸多态性与疾病的集成数据库-管道系统。
BMC Bioinformatics. 2008 Dec 12;9 Suppl 12(Suppl 12):S19. doi: 10.1186/1471-2105-9-S12-S19.
7
SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions.SNP@启动子:一个关于假定启动子区域内人类单核苷酸多态性(SNP)的数据库。
BMC Bioinformatics. 2008;9 Suppl 1(Suppl 1):S2. doi: 10.1186/1471-2105-9-S1-S2.
8
Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.结构单核苷酸多态性(StSNP):一个用于在蛋白质结构上对非同义单核苷酸多态性进行映射和建模并与代谢途径相联系的网络服务器。
Nucleic Acids Res. 2007 Jul;35(Web Server issue):W384-92. doi: 10.1093/nar/gkm232. Epub 2007 May 30.
9
SNP@Ethnos: a database of ethnically variant single-nucleotide polymorphisms.SNP@Ethnos:一个关于种族特异性单核苷酸多态性的数据库。
Nucleic Acids Res. 2007 Jan;35(Database issue):D711-5. doi: 10.1093/nar/gkl962. Epub 2006 Nov 28.
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W311-4. doi: 10.1093/nar/gki404.
4
Comparative mapping of sequence-based and structure-based protein domains.基于序列和基于结构的蛋白质结构域的比较图谱
BMC Bioinformatics. 2005 Mar 25;6:77. doi: 10.1186/1471-2105-6-77.
5
SNPNB: analyzing neighboring-nucleotide biases on single nucleotide polymorphisms (SNPs).SNPNB:分析单核苷酸多态性(SNP)上的相邻核苷酸偏差。
Bioinformatics. 2005 May 15;21(10):2517-9. doi: 10.1093/bioinformatics/bti377. Epub 2005 Mar 15.
6
Selecton: a server for detecting evolutionary forces at a single amino-acid site.选择器:用于检测单个氨基酸位点进化力的服务器。
Bioinformatics. 2005 May 1;21(9):2101-3. doi: 10.1093/bioinformatics/bti259. Epub 2005 Jan 12.
7
SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs.SNPeffect:一个映射人类非同义编码单核苷酸多态性分子表型效应的数据库。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D527-32. doi: 10.1093/nar/gki086.
8
FESD: a Functional Element SNPs Database in human.FESD:人类功能性元件单核苷酸多态性数据库。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D518-22. doi: 10.1093/nar/gki082.
9
Ensembl 2005.Ensembl 2005。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D447-53. doi: 10.1093/nar/gki138.
10
Target SNP selection in complex disease association studies.复杂疾病关联研究中的目标单核苷酸多态性选择
BMC Bioinformatics. 2004 Jul 12;5:92. doi: 10.1186/1471-2105-5-92.