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1958 1
1959 1
1961 2
1962 2
1964 2
1965 6
1966 11
1967 8
1968 5
1969 8
1970 10
1971 24
1972 17
1973 20
1974 36
1975 688
1976 666
1977 623
1978 602
1979 621
1980 736
1981 854
1982 955
1983 1187
1984 1322
1985 1533
1986 1669
1987 1835
1988 2236
1989 2469
1990 2656
1991 3020
1992 3271
1993 3372
1994 3682
1995 3780
1996 3665
1997 3776
1998 3827
1999 3959
2000 4198
2001 4292
2002 4166
2003 4191
2004 4470
2005 4516
2006 4759
2007 4740
2008 4769
2009 4601
2010 4799
2011 4840
2012 4718
2013 4353
2014 4044
2015 3850
2016 3082
2017 2807
2018 3507
2019 3577
2020 3677
2021 3697
2022 3571
2023 3424
2024 1067

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142,494 results

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Page 1
Showing results for residue h
Search for Raeside H instead (1 results)
The C-Terminal Domain of RNase H and the C-Terminus Amino Acid Residue Regulate Virus Release and Autoprocessing of a Defective HIV-1 Possessing M50I and V151I Changes in Integrase.
Imamichi T, Chen Q, Hao M, Chang W, Yang J. Imamichi T, et al. Viruses. 2022 Nov 30;14(12):2687. doi: 10.3390/v14122687. Viruses. 2022. PMID: 36560691 Free PMC article.
In the current study, we attempted to identify the critical domains or amino acid (aa) residue(s) that promote defects in HIV(IN:M50I/V151I), using a series of variants, including truncated or aa-substituted RNase H (RH) or IN. ...
In the current study, we attempted to identify the critical domains or amino acid (aa) residue(s) that promote defects in HIV( …
Asp133 Residue in NhaA Na(+)/H(+) Antiporter Is Required for Stability Cation Binding and Transport.
Rimon A, Dwivedi M, Friedler A, Padan E. Rimon A, et al. J Mol Biol. 2018 Mar 16;430(6):867-880. doi: 10.1016/j.jmb.2018.01.014. Epub 2018 Feb 2. J Mol Biol. 2018. PMID: 29410365
Na(+)/H(+) antiporters have a crucial role in pH and Na(+) homeostasis in cells. ...In this work, we show the multiple roles of Asp133 in NhaA: (i) The residue's negative charge is critical for the stability of the NhaA structure. ...
Na(+)/H(+) antiporters have a crucial role in pH and Na(+) homeostasis in cells. ...In this work, we show the multiple roles of Asp13 …
The Modus Operandi of Hydrogen Sulfide(H(2)S)-Dependent Protein Persulfidation in Higher Plants.
Corpas FJ, González-Gordo S, Muñoz-Vargas MA, Rodríguez-Ruiz M, Palma JM. Corpas FJ, et al. Antioxidants (Basel). 2021 Oct 26;10(11):1686. doi: 10.3390/antiox10111686. Antioxidants (Basel). 2021. PMID: 34829557 Free PMC article. Review.
Protein persulfidation is a post-translational modification (PTM) mediated by hydrogen sulfide (H(2)S), which affects the thiol group of cysteine residues from target proteins and can have a positive, negative or zero impact on protein function. ...However, its prec …
Protein persulfidation is a post-translational modification (PTM) mediated by hydrogen sulfide (H(2)S), which affects the thiol group …
Functioning of Yeast Pma1 H+-ATPase under Changing Charge: Role of Asp739 and Arg811 Residues.
Petrov VV. Petrov VV. Biochemistry (Mosc). 2017 Jan;82(1):46-59. doi: 10.1134/S0006297917010059. Biochemistry (Mosc). 2017. PMID: 28320286 Free article.
The plasma membrane Pma1 H+-ATPase of the yeast Saccharomyces cerevisiae contains conserved residue Asp739 located at the interface of transmembrane segment M6 and the cytosol. ...It was proposed that a strong ionic bond (salt bridge) could be formed between this …
The plasma membrane Pma1 H+-ATPase of the yeast Saccharomyces cerevisiae contains conserved residue Asp739 located at the inte …
Advancing Rational Control of Peptide-Surface Complexes.
Dasetty S, Sarupria S. Dasetty S, et al. J Phys Chem B. 2021 Mar 18;125(10):2644-2657. doi: 10.1021/acs.jpcb.0c10740. Epub 2021 Mar 4. J Phys Chem B. 2021. PMID: 33661633
In this study, we developed insights into the dependence of a residue's interaction with a surface on its neighboring residue in a tripeptide using molecular dynamics simulations. ...Our results indicate that deltaA(ads) of a tripeptide cannot be estimated as …
In this study, we developed insights into the dependence of a residue's interaction with a surface on its neighboring resid …
Possible Mechanisms of Nonenzymatic Formation of Dehydroalanine Residue Catalyzed by Dihydrogen Phosphate Ion.
Nakayoshi T, Kato K, Kurimoto E, Oda A. Nakayoshi T, et al. J Phys Chem B. 2019 Apr 18;123(15):3147-3155. doi: 10.1021/acs.jpcb.8b10386. Epub 2019 Apr 9. J Phys Chem B. 2019. PMID: 30916562
The calculated activation barrier for Dha residue formation was estimated as 30.4 kcal mol(-1). In this pathway, the catalytic H(2)PO(4)(-) interacts with the Ser residue alpha-proton, carbonyl oxygen of Ser, and C-terminal side adjacent residues, and …
The calculated activation barrier for Dha residue formation was estimated as 30.4 kcal mol(-1). In this pathway, the catalytic H …
Converting a cysteine-rich natively noncatalytic protein to an artificial hydrogenase.
Malayam Parambath S, Prakash D, Swetman W, Surakanti A, Chakraborty S. Malayam Parambath S, et al. Chem Commun (Camb). 2023 Nov 7;59(89):13325-13328. doi: 10.1039/d3cc02774k. Chem Commun (Camb). 2023. PMID: 37867329
An artificial hydrogenase is constructed when the natively noncatalytic alpha-domain of the Cys-rich protein metallothionein (MT) is assembled with Ni(II). alphaMT binds four eq. of Ni(II) in a non-cooperative manner where the addition of the 1(st) Ni(II) eq. affords the most cat …
An artificial hydrogenase is constructed when the natively noncatalytic alpha-domain of the Cys-rich protein metallothionein (MT) is assembl …
Effect of amino acids present at the carboxyl end of succinimidyl residue on the rate constants for succinimidyl hydrolysis in small peptides.
Sadakane Y, Senda S, Deguchi T, Tanaka A, Tsuruta H, Morimoto S. Sadakane Y, et al. Biochim Biophys Acta Proteins Proteom. 2020 Nov;1868(11):140496. doi: 10.1016/j.bbapap.2020.140496. Epub 2020 Jul 14. Biochim Biophys Acta Proteins Proteom. 2020. PMID: 32673742
The rate constant of succinimidyl hydrolysis in the peptide bearing a Ser residue at the carboxyl side (0.50 0.02 /h) was 3.0 times higher than that for the peptide bearing an Ala residue (0.17 0.01 /h), whereas it was just 1.2 times higher for the pep …
The rate constant of succinimidyl hydrolysis in the peptide bearing a Ser residue at the carboxyl side (0.50 0.02 /h) was 3.0 …
Nrf2:INrf2 (Keap1) signaling in oxidative stress.
Kaspar JW, Niture SK, Jaiswal AK. Kaspar JW, et al. Free Radic Biol Med. 2009 Nov 1;47(9):1304-9. doi: 10.1016/j.freeradbiomed.2009.07.035. Epub 2009 Aug 7. Free Radic Biol Med. 2009. PMID: 19666107 Free PMC article. Review.
This is followed by activation of a delayed mechanism that controls the switching off of Nrf2 activation of gene expression. GSK3beta phosphorylates Fyn at an unknown threonine residue(s), leading to the nuclear localization of Fyn. Fyn phosphorylates Nrf2 tyrosine …
This is followed by activation of a delayed mechanism that controls the switching off of Nrf2 activation of gene expression. GSK3beta phosph …
Parallel Chemoselective Profiling for Mapping Protein Structure.
Potter ZE, Lau HT, Chakraborty S, Fang L, Guttman M, Ong SE, Fowler DM, Maly DJ. Potter ZE, et al. Cell Chem Biol. 2020 Aug 20;27(8):1084-1096.e4. doi: 10.1016/j.chembiol.2020.06.014. Epub 2020 Jul 9. Cell Chem Biol. 2020. PMID: 32649906 Free PMC article.
Our method utilizes deep mutational scanning saturation mutagenesis data to install amino acid residues with specific chemistries at defined positions on the solvent-exposed surface of a protein. Differences in the extent of labeling of installed mutant residues are …
Our method utilizes deep mutational scanning saturation mutagenesis data to install amino acid residues with specific chemistries at …
142,494 results
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