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  1. Article ; Online: Primate protein-ligand interfaces exhibit significant conservation and unveil human-specific evolutionary drivers.

    King, Sean B / Singh, Mona

    PLoS computational biology

    2023  Volume 19, Issue 3, Page(s) e1010966

    Abstract: Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, ... ...

    Abstract Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, alterations in the sites that participate in these interactions may be of critical importance. To uncover the extent to which these sites evolve across primates, we built a structurally-derived dataset of ~4,200 one-to-one orthologous sequence groups across 18 primate species, consisting of ~68,000 ligand-binding sites that interact with DNA, RNA, small molecules, ions, or peptides. Using this dataset, we identify functionally important patterns of conservation and variation within the amino acid residues that facilitate protein-ligand interactions across the primate phylogeny. We uncover that interaction sites are significantly more conserved than other sites, and that sites binding DNA and RNA further exhibit the lowest levels of variation. We also show that the subset of ligand-binding sites that do vary are enriched in components of gene regulatory pathways and uncover several instances of human-specific ligand-binding site changes within transcription factors. Altogether, our results suggest that ligand-binding sites have experienced selective pressure in primates and propose that variation in these sites may have an outsized effect on phenotypic variation in primates through pleiotropic effects on gene regulation.
    MeSH term(s) Animals ; Humans ; Ligands ; Evolution, Molecular ; Primates/genetics ; Phylogeny ; DNA/genetics ; Binding Sites/genetics ; RNA
    Chemical Substances Ligands ; DNA (9007-49-2) ; RNA (63231-63-0)
    Language English
    Publishing date 2023-03-23
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2193340-6
    ISSN 1553-7358 ; 1553-734X
    ISSN (online) 1553-7358
    ISSN 1553-734X
    DOI 10.1371/journal.pcbi.1010966
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Primate protein-ligand interfaces exhibit significant conservation and unveil human-specific evolutionary drivers

    Sean B. King / Mona Singh

    PLoS Computational Biology, Vol 19, Iss

    2023  Volume 3

    Abstract: Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, ... ...

    Abstract Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, alterations in the sites that participate in these interactions may be of critical importance. To uncover the extent to which these sites evolve across primates, we built a structurally-derived dataset of ~4,200 one-to-one orthologous sequence groups across 18 primate species, consisting of ~68,000 ligand-binding sites that interact with DNA, RNA, small molecules, ions, or peptides. Using this dataset, we identify functionally important patterns of conservation and variation within the amino acid residues that facilitate protein-ligand interactions across the primate phylogeny. We uncover that interaction sites are significantly more conserved than other sites, and that sites binding DNA and RNA further exhibit the lowest levels of variation. We also show that the subset of ligand-binding sites that do vary are enriched in components of gene regulatory pathways and uncover several instances of human-specific ligand-binding site changes within transcription factors. Altogether, our results suggest that ligand-binding sites have experienced selective pressure in primates and propose that variation in these sites may have an outsized effect on phenotypic variation in primates through pleiotropic effects on gene regulation. Author summary Humans are very similar to other primates with respect to their genome sequences, yet exhibit striking phenotypic differences. We hypothesized that changes in a small number of important positions within the protein coding region of the genome may contribute to these phenotypic differences. We focused our study on evaluating the evolution of sites within proteins that interact with ligands, as variation at these sites has outsized potential for broader downstream effects. To uncover the extent to which ligand-binding sites have ...
    Keywords Biology (General) ; QH301-705.5
    Subject code 612
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Primate protein-ligand interfaces exhibit significant conservation and unveil human-specific evolutionary drivers.

    Sean B King / Mona Singh

    PLoS Computational Biology, Vol 19, Iss 3, p e

    2023  Volume 1010966

    Abstract: Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, ... ...

    Abstract Despite the vast phenotypic differences observed across primates, their protein products are largely similar to each other at the sequence level. We hypothesized that, since proteins accomplish all their functions via interactions with other molecules, alterations in the sites that participate in these interactions may be of critical importance. To uncover the extent to which these sites evolve across primates, we built a structurally-derived dataset of ~4,200 one-to-one orthologous sequence groups across 18 primate species, consisting of ~68,000 ligand-binding sites that interact with DNA, RNA, small molecules, ions, or peptides. Using this dataset, we identify functionally important patterns of conservation and variation within the amino acid residues that facilitate protein-ligand interactions across the primate phylogeny. We uncover that interaction sites are significantly more conserved than other sites, and that sites binding DNA and RNA further exhibit the lowest levels of variation. We also show that the subset of ligand-binding sites that do vary are enriched in components of gene regulatory pathways and uncover several instances of human-specific ligand-binding site changes within transcription factors. Altogether, our results suggest that ligand-binding sites have experienced selective pressure in primates and propose that variation in these sites may have an outsized effect on phenotypic variation in primates through pleiotropic effects on gene regulation.
    Keywords Biology (General) ; QH301-705.5
    Subject code 612
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Comparative genomic analysis reveals varying levels of mammalian adaptation to coronavirus infections.

    King, Sean B / Singh, Mona

    PLoS computational biology

    2021  Volume 17, Issue 11, Page(s) e1009560

    Abstract: Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful ...

    Abstract Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful in identifying additional reservoirs of potentially dangerous coronaviruses. We reasoned that if a clade of species has been repeatedly exposed to a virus, then their proteins relevant for viral entry may exhibit adaptations that affect host susceptibility or response. We perform comparative analyses across the mammalian phylogeny of angiotensin-converting enzyme 2 (ACE2), the cellular receptor for SARS-CoV-2, in order to uncover evidence for selection acting at its binding interface with the SARS-CoV-2 spike protein. We uncover that in rodents there is evidence for adaptive amino acid substitutions at positions comprising the ACE2-spike interaction interface, whereas the variation within ACE2 proteins in primates and some other mammalian clades is not consistent with evolutionary adaptations. We also analyze aminopeptidase N (APN), the receptor for the human coronavirus 229E, a virus that causes the common cold, and find evidence for adaptation in primates. Altogether, our results suggest that the rodent and primate lineages may have had ancient exposures to viruses similar to SARS-CoV-2 and HCoV-229E, respectively.
    MeSH term(s) Adaptation, Physiological/genetics ; Amino Acid Substitution ; Angiotensin-Converting Enzyme 2/genetics ; Angiotensin-Converting Enzyme 2/physiology ; Animals ; CD13 Antigens/genetics ; CD13 Antigens/physiology ; COVID-19/genetics ; COVID-19/virology ; Common Cold/genetics ; Common Cold/virology ; Computational Biology ; Coronavirus 229E, Human/genetics ; Coronavirus 229E, Human/physiology ; Coronavirus Infections/genetics ; Coronavirus Infections/virology ; Evolution, Molecular ; Genomics ; Host Microbial Interactions/genetics ; Host Microbial Interactions/physiology ; Host Specificity/genetics ; Host Specificity/physiology ; Humans ; Mammals/genetics ; Mammals/virology ; Phylogeny ; Protein Interaction Domains and Motifs/genetics ; Receptors, Virus/genetics ; Receptors, Virus/physiology ; SARS-CoV-2/genetics ; SARS-CoV-2/physiology ; Selection, Genetic ; Spike Glycoprotein, Coronavirus/genetics ; Spike Glycoprotein, Coronavirus/physiology ; Virus Internalization
    Chemical Substances Receptors, Virus ; Spike Glycoprotein, Coronavirus ; spike protein, SARS-CoV-2 ; CD13 Antigens (EC 3.4.11.2) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Language English
    Publishing date 2021-11-18
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2193340-6
    ISSN 1553-7358 ; 1553-734X
    ISSN (online) 1553-7358
    ISSN 1553-734X
    DOI 10.1371/journal.pcbi.1009560
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Comparative genomic analysis reveals varying levels of mammalian adaptation to coronavirus infections

    Sean B. King / Mona Singh

    PLoS Computational Biology, Vol 17, Iss

    2021  Volume 11

    Abstract: Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful ...

    Abstract Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful in identifying additional reservoirs of potentially dangerous coronaviruses. We reasoned that if a clade of species has been repeatedly exposed to a virus, then their proteins relevant for viral entry may exhibit adaptations that affect host susceptibility or response. We perform comparative analyses across the mammalian phylogeny of angiotensin-converting enzyme 2 (ACE2), the cellular receptor for SARS-CoV-2, in order to uncover evidence for selection acting at its binding interface with the SARS-CoV-2 spike protein. We uncover that in rodents there is evidence for adaptive amino acid substitutions at positions comprising the ACE2-spike interaction interface, whereas the variation within ACE2 proteins in primates and some other mammalian clades is not consistent with evolutionary adaptations. We also analyze aminopeptidase N (APN), the receptor for the human coronavirus 229E, a virus that causes the common cold, and find evidence for adaptation in primates. Altogether, our results suggest that the rodent and primate lineages may have had ancient exposures to viruses similar to SARS-CoV-2 and HCoV-229E, respectively. Author summary SARS-like coronaviruses, such as SARS-CoV and SARS-CoV-2, are a class of pathogens that have been a significant threat to human health. Across the animal kingdom, we see considerable differences in the severity of symptoms caused by these types of viruses. Previous research has shown adaptations to SARS-like viruses in known viral vectors such as Chinese Horseshoe bats. Uncovering evidence of adaptations to SARS-like viral infections in proteins of other hosts would shed light on whether additional mammalian clades have been previously exposed to these viruses. In our study, we characterize the evolution of the mammalian host receptor ...
    Keywords Biology (General) ; QH301-705.5
    Subject code 572
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Comparative genomic analysis reveals varying levels of mammalian adaptation to coronavirus infections.

    Sean B King / Mona Singh

    PLoS Computational Biology, Vol 17, Iss 11, p e

    2021  Volume 1009560

    Abstract: Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful ...

    Abstract Severe acute respiratory coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, is of zoonotic origin. Evolutionary analyses assessing whether coronaviruses similar to SARS-CoV-2 infected ancestral species of modern-day animal hosts could be useful in identifying additional reservoirs of potentially dangerous coronaviruses. We reasoned that if a clade of species has been repeatedly exposed to a virus, then their proteins relevant for viral entry may exhibit adaptations that affect host susceptibility or response. We perform comparative analyses across the mammalian phylogeny of angiotensin-converting enzyme 2 (ACE2), the cellular receptor for SARS-CoV-2, in order to uncover evidence for selection acting at its binding interface with the SARS-CoV-2 spike protein. We uncover that in rodents there is evidence for adaptive amino acid substitutions at positions comprising the ACE2-spike interaction interface, whereas the variation within ACE2 proteins in primates and some other mammalian clades is not consistent with evolutionary adaptations. We also analyze aminopeptidase N (APN), the receptor for the human coronavirus 229E, a virus that causes the common cold, and find evidence for adaptation in primates. Altogether, our results suggest that the rodent and primate lineages may have had ancient exposures to viruses similar to SARS-CoV-2 and HCoV-229E, respectively.
    Keywords Biology (General) ; QH301-705.5
    Subject code 572
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: Shifting Redox Reaction Equilibria on Demand Using an Orthogonal Redox Cofactor.

    Aspacio, Derek / Zhang, Yulai / Cui, Youtian / King, Edward / Black, William B / Perea, Sean / Luu, Emma / Siegel, Justin B / Li, Han

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Natural metabolism relies on chemical compartmentalization of two redox cofactors, ... ...

    Abstract Natural metabolism relies on chemical compartmentalization of two redox cofactors, NAD
    Language English
    Publishing date 2023-08-30
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.08.29.555398
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Outcomes in Pediatric Burn Patients With Additional Trauma-Related Injuries.

    Sljivic, Sanja / Agala, Chris B / McLean, Sean E / Williams, Felicia N / Nizamani, Rabia / Meyer, Anthony A / King, Booker T

    The American surgeon

    2023  Volume 89, Issue 7, Page(s) 3229–3231

    Abstract: The addition of trauma to burn injuries may result in higher morbidity and mortality. The purpose of this study was to evaluate the outcomes of pediatric patients with a combination of burn and trauma injuries, and included all pediatric Burn only, ... ...

    Abstract The addition of trauma to burn injuries may result in higher morbidity and mortality. The purpose of this study was to evaluate the outcomes of pediatric patients with a combination of burn and trauma injuries, and included all pediatric Burn only, Trauma only, and combined Burn-Trauma patients admitted between 2011 and 2020. Mean length of stay, ICU length of stay, and ventilator days were highest for the Burn-Trauma group. The odds of mortality were almost 13 times higher for the Burn-Trauma group when compared to the Burn only group (
    MeSH term(s) Humans ; Child ; Length of Stay ; Burns/complications ; Burns/therapy ; Burns/epidemiology ; Hospitalization ; Retrospective Studies
    Language English
    Publishing date 2023-02-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 202465-2
    ISSN 1555-9823 ; 0003-1348
    ISSN (online) 1555-9823
    ISSN 0003-1348
    DOI 10.1177/00031348231157849
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Correction: Elevated ATGL in colon cancer cells and cancer stem cells promotes metabolic and tumorigenic reprogramming reinforced by obesity.

    Iftikhar, Rida / Penrose, Harrison M / King, Angelle N / Samudre, Joshua S / Collins, Morgan E / Hartono, Alifiani B / Lee, Sean B / Lau, Frank / Baddoo, Melody / Flemington, Erik F / Crawford, Susan E / Savkovic, Suzana D

    Oncogenesis

    2022  Volume 11, Issue 1, Page(s) 14

    Language English
    Publishing date 2022-03-15
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 2674437-5
    ISSN 2157-9024
    ISSN 2157-9024
    DOI 10.1038/s41389-022-00388-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: FARS2

    Forman, Eva B / Gorman, Kathleen M / Ennis, Sean / King, Mary D

    Journal of child neurology

    2019  Volume 34, Issue 10, Page(s) 621

    Abstract: Herein we present two siblings with hereditary spastic paraplegia caused by novel compound heterozygous variant and deletion ... ...

    Abstract Herein we present two siblings with hereditary spastic paraplegia caused by novel compound heterozygous variant and deletion in
    MeSH term(s) Adolescent ; Child ; Disease Progression ; Dysphonia/genetics ; Female ; Heterozygote ; Humans ; Male ; Mitochondrial Proteins/genetics ; Mutation, Missense ; Phenotype ; Phenylalanine-tRNA Ligase/genetics ; Siblings ; Spastic Paraplegia, Hereditary/genetics
    Chemical Substances Mitochondrial Proteins ; FARS2 protein, human (EC 6.1.1.20) ; Phenylalanine-tRNA Ligase (EC 6.1.1.20)
    Language English
    Publishing date 2019-05-19
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 639288-x
    ISSN 1708-8283 ; 0883-0738
    ISSN (online) 1708-8283
    ISSN 0883-0738
    DOI 10.1177/0883073819846805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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