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- {{Infobox protein family | OPM protein = ...4 KB (604 words) - 00:13, 14 December 2023
- ..., a fragment structure (represented by a "paradigm" fragment chosen from a protein in the PDB) and optionally, a 4-dimensional tensor of pairwise sequence cov ...ach family contained a single known structure (parent) from the Brookhaven protein Data Bank. These were a subset of the PDBSelect-25 list, having no more tha ...4 KB (635 words) - 23:36, 25 April 2024
- Human protein [[DTYMK]] contains this domain. ...structure|structures]] have been solved for this class of enzymes, with [[Protein Data Bank|PDB]] accession codes {{PDB link|1E2D}}, {{PDB link|1E2E}}, {{PDB ...4 KB (530 words) - 07:28, 29 November 2023
- ...linked. In simpler terms, it helps scientists understand which parts of a protein are working together and how they have changed over evolutionary time.<ref> ...Ranganathan group] on the [[GPCR]], [[serine protease]] and [[hemoglobin]] families also showed energetic coupling in sparse networks of residues that cooperat ...9 KB (1,282 words) - 21:09, 6 February 2025
- This article discusses the protein domains that make up the SAM synthetase enzyme and how these domains contri ...Roth A, Washietl S, Wen J, Kellis M, Breaker R, Pedersen JS | title = New families of human regulatory RNA structures identified by comparative analysis of ve ...9 KB (1,170 words) - 18:37, 31 May 2024
- ...erase superfamily with a large set of manually-annotated proteins |journal=Protein Sci. Biochem. | year=2022 |volume= 31 |issue= 4 |pages= 864–881 |pmid=35049 ==Families== ...10 KB (1,320 words) - 00:20, 30 January 2025
- ...essible surface area''' or '''relative solvent accessibility (RSA)''' of a protein residue is a measure of [[Solvent exposure|residue solvent exposure]]. It c ASA and hence RSA values are generally calculated from a protein structure, for example with the software DSSP.<ref name = "DSSP"> ...8 KB (888 words) - 20:45, 25 October 2023
- ...ns</math> 3-O-beta-D-galactosyl-N-acetyl-alpha-D-galactosamine + L-serine-[protein] ...de hydrolases: subfamily structure and evolutionary connections with other families | journal = Journal of Bioinformatics and Computational Biology | volume = ...5 KB (485 words) - 20:29, 28 August 2023
- ...title = Role of cysteine residues in pseudouridine synthases of different families | journal = Biochemistry | volume = 38 | issue = 40 | pages = 13106–11 | da ...3 KB (393 words) - 17:08, 26 August 2023
- ...alysis of residue coevolution captures native contacts across many protein families|journal=Proceedings of the National Academy of Sciences|date=21 November 20 ...20714458 |issn=0036-8075}}</ref> and the modeling of [[Molecular evolution|protein evolution]].<ref>{{Cite journal |last1=Rodriguez-Rivas |first1=Juan |last2= ...26 KB (3,739 words) - 01:27, 15 January 2025
- ...E'')}} that is in any nontrivial [[Minor (graph theory)#Minor-closed graph families|minor-closed graph family]] (e.g., a [[planar graph]]), if {{mvar|G}} conta ...e <math>2^{O(k)}</math>. Consequently, by composing the {{mvar|k}}-perfect families from both steps, a {{mvar|k}}-perfect family of size <math>2^{O(k)}\log |V| ...13 KB (2,065 words) - 18:58, 17 November 2024
- ...ene.<ref name="Graur_2000" /> It is much more rare to see major changes in protein function, such as subunit structure or substrate and ligand affinity, as a ...a vivid example of neofunctionalization. The development of an antifreeze protein from an ancestral Sialic Acid Synthase (SAS) gene illustrates the acquisiti ...13 KB (1,737 words) - 20:18, 7 February 2025
- ...probabilistic suffix trees: statistical modeling and prediction of protein families |journal = Bioinformatics |volume = 17|issue = 5|date = 2001|pages = 23–43 ...10 KB (1,578 words) - 23:45, 1 April 2024
- {{Redirect|Root symbol|the root symbols for gene and protein families|Gene nomenclature#Symbol and name}} ...9 KB (1,377 words) - 16:31, 20 February 2025
- ...ix multiplication and applications of mathematics to biology, particularly protein folding."<ref>{{cite web|title=Sandy Davie's Home page|website=School of Ma ...al|doi=10.1016/0167-2789(93)90047-5|title=Period-doubling in two-parameter families|year=1993|last1=Davie|first1=A.M.|last2=Dutta|first2=T.K.|journal=Physica D ...9 KB (1,192 words) - 09:02, 22 August 2024
- | OPM protein= ...=en |doi=10.1007/978-3-0348-8446-4_2 |isbn=978-3-0348-8446-4}}</ref> These families are not similar in sequence or structure because they evolved independently ...38 KB (5,443 words) - 16:28, 19 January 2025
- ...aloop]] is a four-base pairs hairpin RNA structure. There are three common families of tetraloop in ribosomal RNA: '''UNCG''', '''GNRA''', and '''CUUG''' (''N' The quaternary structure of nucleic acids is similar to that of [[protein quaternary structure]]. Although some of the concepts are not exactly the s ...18 KB (2,739 words) - 17:16, 5 December 2024
- ...7" /> DEC2 inhibits [[CLOCK]]/[[BMAL1]] activation of PER, through protein-protein interaction or competition for the [[E-box]] transcriptional elements.<ref ...caused a short sleep phenotype. NPSR1 is a [[G protein-coupled receptor|G-protein coupled receptor]] that plays a role in [[arousal]] and sleep behaviors. Th ...28 KB (3,848 words) - 13:06, 4 April 2024
- ...emical Technology |access-date=22 October 2015}}</ref> structural biology, protein dynamics,<ref>{{cite news |date=30 April 2015 |title=Waking proteins up fro ...equency pulses for homonuclear decoupling in solid-state NMR, allowing new families of decoupling sequences.<ref>{{cite journal |last1=Sakellariou |first1=Dimi ...30 KB (3,981 words) - 12:19, 14 December 2024
- ...anson J, Paliwal K, Zhou Y | title = Sixty-five years of the long march in protein secondary structure prediction: the final stretch? | journal = Briefings in * Comparing and aligning RNA, protein, and DNA sequences. ...70 KB (9,251 words) - 08:48, 6 January 2025