• 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

与少毛症相关的脂肪酶H(LIPH基因)蛋白临床显著变异体的计算机表征与分析

In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis.

作者信息

Khan Hamza Ali, Asif Muhammad Umair, Ijaz Muhammad Khurram, Alharbi Metab, Ali Yasir, Ahmad Faisal, Azhar Ramsha, Ahmad Sajjad, Irfan Muhammad, Javed Maryana, Naseer Noorulain, Aziz Abdul

机构信息

Department of Computer Science and Bioinformatics, Khushal Khan Khattak University, Karak 27200, Pakistan.

Basic Health Unit, 196 RB, Faisalabad 38000, Pakistan.

出版信息

Pharmaceuticals (Basel). 2023 May 29;16(6):803. doi: 10.3390/ph16060803.

DOI:10.3390/ph16060803
PMID:37375751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10302509/
Abstract

Hypotrichosis is an uncommon type of alopecia (hair loss) characterized by coarse scalp hair caused by the reduced or fully terminated activity of the Lipase-H (LIPH) enzyme. LIPH gene mutations contribute to the development of irregular or non-functional proteins. Because several cellular processes, including cell maturation and proliferation, are inhibited when this enzyme is inactive, the hair follicles become structurally unreliable, undeveloped, and immature. This results in brittle hair, as well as altered hair shaft development and structure. Because of these nsSNPs, the protein's structure and/or function may be altered. Given the difficulty in discovering functional SNPs in genes associated with disease, it is possible to assess potential functional SNPs before conducting broader population investigations. As a result, in our in silico analysis, we separated potentially hazardous nsSNPs of the LIPH gene from benign representatives using a variety of sequencing and architecture-based bioinformatics approaches. Using seven prediction algorithms, 9 out of a total of 215 nsSNPs were shown to be the most likely to cause harm. In order to distinguish between potentially harmful and benign nsSNPs of the LIPH gene, in our in silico investigation, we employed a range of sequence- and architecture-based bioinformatics techniques. Three nsSNPs (W108R, C246S, and H248N) were chosen as potentially harmful. The present findings will likely be helpful in future large population-based studies, as well as in drug discovery, particularly in the creation of personalized medicine, since this study provides an initial thorough investigation of the functional nsSNPs of LIPH.

摘要

少毛症是一种罕见的脱发类型,其特征是头皮毛发粗糙,这是由脂肪酶-H(LIPH)酶的活性降低或完全终止引起的。LIPH基因突变导致不规则或无功能蛋白质的产生。由于当这种酶无活性时,包括细胞成熟和增殖在内的几个细胞过程会受到抑制,毛囊在结构上变得不可靠、未发育成熟。这导致头发变脆,以及毛干发育和结构改变。由于这些非同义单核苷酸多态性(nsSNPs),蛋白质的结构和/或功能可能会发生改变。鉴于在与疾病相关的基因中发现功能性单核苷酸多态性存在困难,在进行更广泛的人群调查之前,可以评估潜在的功能性单核苷酸多态性。因此,在我们的计算机模拟分析中,我们使用了多种基于测序和结构的生物信息学方法,将LIPH基因潜在有害的nsSNPs与良性的区分开来。使用七种预测算法,在总共215个nsSNPs中,有9个被证明最有可能造成危害。为了区分LIPH基因潜在有害和良性的nsSNPs,在我们的计算机模拟研究中,我们采用了一系列基于序列和结构的生物信息学技术。选择了三个nsSNPs(W108R、C246S和H248N)作为潜在有害的。本研究结果可能会对未来基于大规模人群的研究以及药物发现有所帮助,特别是在个性化医疗的创建方面,因为这项研究对LIPH的功能性nsSNPs进行了初步的全面调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/062f5c0b7d18/pharmaceuticals-16-00803-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/d425e41467b7/pharmaceuticals-16-00803-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/cf4a2ca42577/pharmaceuticals-16-00803-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/d58f5b748ac6/pharmaceuticals-16-00803-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/1078729fd0cc/pharmaceuticals-16-00803-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/19d421fc5048/pharmaceuticals-16-00803-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/497e073bbd33/pharmaceuticals-16-00803-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/062f5c0b7d18/pharmaceuticals-16-00803-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/d425e41467b7/pharmaceuticals-16-00803-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/cf4a2ca42577/pharmaceuticals-16-00803-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/d58f5b748ac6/pharmaceuticals-16-00803-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/1078729fd0cc/pharmaceuticals-16-00803-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/19d421fc5048/pharmaceuticals-16-00803-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/497e073bbd33/pharmaceuticals-16-00803-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f46/10302509/062f5c0b7d18/pharmaceuticals-16-00803-g007.jpg

相似文献

1
In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis.与少毛症相关的脂肪酶H(LIPH基因)蛋白临床显著变异体的计算机表征与分析
Pharmaceuticals (Basel). 2023 May 29;16(6):803. doi: 10.3390/ph16060803.
2
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).脂肪酶H(LIPH)基因中的新型错义突变导致常染色体隐性少毛症(LAH2)。
J Dermatol Sci. 2009 Apr;54(1):12-6. doi: 10.1016/j.jdermsci.2008.12.001. Epub 2009 Jan 23.
3
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.LPAR6 和 LIPH 基因突变导致巴基斯坦 17 个近亲家族常染色体隐性性少毛症/羊毛状发。
Clin Exp Dermatol. 2011 Aug;36(6):652-4. doi: 10.1111/j.1365-2230.2011.04014.x. Epub 2011 Mar 21.
4
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis.常染色体隐性遗传性羊毛状毛发/毛发稀少症家族中脂肪酶h基因的奠基者突变
J Invest Dermatol. 2009 Aug;129(8):1927-34. doi: 10.1038/jid.2009.19. Epub 2009 Mar 5.
5
Novel small-insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis.一名患有常染色体隐性遗传性羊毛状发/毛发稀少症患者的LIPH基因存在新型小插入突变。
J Dermatol. 2020 Dec;47(12):1445-1449. doi: 10.1111/1346-8138.15581. Epub 2020 Sep 9.
6
Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair/hypotrichosis in Japan and the genotype/phenotype correlations.在日本导致常染色体隐性遗传性羊毛状发/毛发稀少的高度流行的LIPH基因创始突变及基因型/表型相关性
PLoS One. 2014 Feb 19;9(2):e89261. doi: 10.1371/journal.pone.0089261. eCollection 2014.
7
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth.导致单纯性少毛症的LIPH突变的体外分析:证实脂肪酶H和溶血磷脂酸在毛发生长中作用的证据
J Invest Dermatol. 2009 Dec;129(12):2772-6. doi: 10.1038/jid.2009.154. Epub 2009 Jun 18.
8
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.LIPH和LPAR6基因中的新型序列变异是近亲家庭中常染色体隐性遗传性羊毛状毛发/毛发稀少症的基础。
Congenit Anom (Kyoto). 2018 Jan;58(1):24-28. doi: 10.1111/cga.12226. Epub 2017 Jun 12.
9
Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies.孤立性常染色体隐性羊毛状发/毛发稀少症:遗传学、发病机制和治疗。
J Eur Acad Dermatol Venereol. 2021 Sep;35(9):1788-1796. doi: 10.1111/jdv.17350. Epub 2021 Jun 4.
10
Novel mutations in the lipase H gene lead to secretion defects of LIPH in Chinese patients with autosomal recessive woolly hair/hypotrichosis (ARWH/HT).脂肪酶H基因的新型突变导致中国常染色体隐性遗传性羊毛状发/毛发稀少症(ARWH/HT)患者中LIPH的分泌缺陷。
Mutagenesis. 2017 Dec 31;32(6):599-606. doi: 10.1093/mutage/gex043.

本文引用的文献

1
Fragment-Based Approaches Identified Tecovirimat-Competitive Novel Drug Candidate for Targeting the F13 Protein of the Monkeypox Virus.基于片段的方法鉴定了特考韦瑞玛特竞争性新型药物候选物,用于靶向猴痘病毒的 F13 蛋白。
Viruses. 2023 Feb 19;15(2):570. doi: 10.3390/v15020570.
2
Structural Evaluation and Conformational Dynamics of Mutation Provoking Postaxial Polydactyly Type A.引发A型轴后多指畸形的突变的结构评估与构象动力学
Bioengineering (Basel). 2022 Dec 1;9(12):749. doi: 10.3390/bioengineering9120749.
3
Identification of novel peptide inhibitors for the KRas-G12C variant to prevent oncogenic signaling.
鉴定用于KRas-G12C变体的新型肽抑制剂以预防致癌信号传导。
J Biomol Struct Dyn. 2023 Oct-Nov;41(18):8866-8875. doi: 10.1080/07391102.2022.2138550. Epub 2022 Oct 27.
4
Molecular Insights into the Role of Pathogenic nsSNPs in Gene Provoking Neurodevelopmental Disorders.致病性 nsSNPs 在引发神经发育障碍的基因中的作用的分子见解。
Genes (Basel). 2022 Jul 26;13(8):1332. doi: 10.3390/genes13081332.
5
A comprehensive genomic study, mutation screening, phylogenetic and statistical analysis of SARS-CoV-2 and its variant omicron among different countries.一项针对 SARS-CoV-2 及其不同国家变异株奥密克戎的全基因组研究、突变筛查、系统进化和统计学分析。
J Infect Public Health. 2022 Aug;15(8):878-891. doi: 10.1016/j.jiph.2022.07.002. Epub 2022 Jul 8.
6
A lesson for the maestro of the replication fork: Targeting the protein-binding interface of proliferating cell nuclear antigen for anticancer therapy.给复制叉大师的一课:靶向增殖细胞核抗原的蛋白质结合界面用于抗癌治疗。
J Cell Biochem. 2022 Jun;123(6):1091-1102. doi: 10.1002/jcb.30265. Epub 2022 Apr 29.
7
Computational screening and analysis of deleterious nsSNPs in human 14ARF ( gene) protein using molecular dynamic simulation approach.运用分子动力学模拟方法对人类 14ARF(基因)蛋白中的有害 nsSNP 进行计算筛选和分析。
J Biomol Struct Dyn. 2023 Jun;41(9):3964-3975. doi: 10.1080/07391102.2022.2059570. Epub 2022 Apr 21.
8
Mechanistic behavior and subtle key events during DNA clamp opening and closing in T4 bacteriophage.T4 噬菌体 DNA 夹打开和关闭过程中的机械行为和微妙关键事件。
Int J Biol Macromol. 2022 May 31;208:11-19. doi: 10.1016/j.ijbiomac.2022.03.021. Epub 2022 Mar 8.
9
Prediction of disease-associated nsSNPs by integrating multi-scale ResNet models with deep feature fusion.通过整合多尺度 ResNet 模型与深度特征融合来预测疾病相关的 nsSNPs。
Brief Bioinform. 2022 Jan 17;23(1). doi: 10.1093/bib/bbab530.
10
Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19.全基因组分析揭示了 SARS-CoV-2 病毒密码子使用模式的全球异质性,表明 COVID-19 具有全球差异性。
Biomolecules. 2021 Jun 18;11(6):912. doi: 10.3390/biom11060912.