
PMC:7594251 / 35973-36955
Annnotations
LitCovid-PD-FMA-UBERON
{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T43243","span":{"begin":193,"end":201},"obj":"Body_part"},{"id":"T42194","span":{"begin":397,"end":404},"obj":"Body_part"}],"attributes":[{"id":"A49478","pred":"fma_id","subj":"T43243","obj":"http://purl.org/sig/ont/fma/fma67257"},{"id":"A16049","pred":"fma_id","subj":"T42194","obj":"http://purl.org/sig/ont/fma/fma67257"}],"text":"T2 measurements of ligands are also useful for determining the binding nature of a small molecule. The T2 values of small molecules are quite large compared to those of bigger molecules (i.e., proteins) mostly because macromolecules have more spin-spin diffusion [175]. Bound ligands will, therefore, display shorter T2 values than non-binding ligands because they interact with the target (i.e., protein), adopting similar vibrational and rotational energies to the target [176]. This interaction is represented by the resonance line broadening in the binding ligand’s spectrum when a receptor is introduced into the sample [156]. Given the sizable difference of T2 values of binding and non-binding ligands, one can utilize 1D relaxation-edited experiments to distinguish the binding ligands from the non-binding ligands efficiently and effectively based on the differences in the T2 values [167]. These and other related relaxation edited experiments prove useful in drug design."}
LitCovid-PD-CLO
{"project":"LitCovid-PD-CLO","denotations":[{"id":"T88676","span":{"begin":0,"end":2},"obj":"http://purl.obolibrary.org/obo/CLO_0050160"},{"id":"T90343","span":{"begin":81,"end":82},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T92264","span":{"begin":103,"end":105},"obj":"http://purl.obolibrary.org/obo/CLO_0050160"},{"id":"T51742","span":{"begin":317,"end":319},"obj":"http://purl.obolibrary.org/obo/CLO_0050160"},{"id":"T65081","span":{"begin":584,"end":585},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T76730","span":{"begin":664,"end":666},"obj":"http://purl.obolibrary.org/obo/CLO_0050160"},{"id":"T85793","span":{"begin":883,"end":885},"obj":"http://purl.obolibrary.org/obo/CLO_0050160"}],"text":"T2 measurements of ligands are also useful for determining the binding nature of a small molecule. The T2 values of small molecules are quite large compared to those of bigger molecules (i.e., proteins) mostly because macromolecules have more spin-spin diffusion [175]. Bound ligands will, therefore, display shorter T2 values than non-binding ligands because they interact with the target (i.e., protein), adopting similar vibrational and rotational energies to the target [176]. This interaction is represented by the resonance line broadening in the binding ligand’s spectrum when a receptor is introduced into the sample [156]. Given the sizable difference of T2 values of binding and non-binding ligands, one can utilize 1D relaxation-edited experiments to distinguish the binding ligands from the non-binding ligands efficiently and effectively based on the differences in the T2 values [167]. These and other related relaxation edited experiments prove useful in drug design."}
LitCovid-PD-CHEBI
{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T351","span":{"begin":0,"end":2},"obj":"Chemical"},{"id":"T353","span":{"begin":19,"end":26},"obj":"Chemical"},{"id":"T354","span":{"begin":89,"end":97},"obj":"Chemical"},{"id":"T355","span":{"begin":103,"end":105},"obj":"Chemical"},{"id":"T357","span":{"begin":122,"end":131},"obj":"Chemical"},{"id":"T358","span":{"begin":176,"end":185},"obj":"Chemical"},{"id":"T359","span":{"begin":193,"end":201},"obj":"Chemical"},{"id":"T360","span":{"begin":218,"end":232},"obj":"Chemical"},{"id":"T361","span":{"begin":276,"end":283},"obj":"Chemical"},{"id":"T362","span":{"begin":317,"end":319},"obj":"Chemical"},{"id":"T364","span":{"begin":344,"end":351},"obj":"Chemical"},{"id":"T365","span":{"begin":397,"end":404},"obj":"Chemical"},{"id":"T366","span":{"begin":664,"end":666},"obj":"Chemical"},{"id":"T368","span":{"begin":701,"end":708},"obj":"Chemical"},{"id":"T369","span":{"begin":786,"end":793},"obj":"Chemical"},{"id":"T370","span":{"begin":815,"end":822},"obj":"Chemical"},{"id":"T371","span":{"begin":883,"end":885},"obj":"Chemical"},{"id":"T373","span":{"begin":970,"end":974},"obj":"Chemical"}],"attributes":[{"id":"A351","pred":"chebi_id","subj":"T351","obj":"http://purl.obolibrary.org/obo/CHEBI_29298"},{"id":"A352","pred":"chebi_id","subj":"T351","obj":"http://purl.obolibrary.org/obo/CHEBI_75710"},{"id":"A353","pred":"chebi_id","subj":"T353","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A354","pred":"chebi_id","subj":"T354","obj":"http://purl.obolibrary.org/obo/CHEBI_25367"},{"id":"A355","pred":"chebi_id","subj":"T355","obj":"http://purl.obolibrary.org/obo/CHEBI_29298"},{"id":"A356","pred":"chebi_id","subj":"T355","obj":"http://purl.obolibrary.org/obo/CHEBI_75710"},{"id":"A357","pred":"chebi_id","subj":"T357","obj":"http://purl.obolibrary.org/obo/CHEBI_25367"},{"id":"A358","pred":"chebi_id","subj":"T358","obj":"http://purl.obolibrary.org/obo/CHEBI_25367"},{"id":"A359","pred":"chebi_id","subj":"T359","obj":"http://purl.obolibrary.org/obo/CHEBI_36080"},{"id":"A360","pred":"chebi_id","subj":"T360","obj":"http://purl.obolibrary.org/obo/CHEBI_33839"},{"id":"A361","pred":"chebi_id","subj":"T361","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A362","pred":"chebi_id","subj":"T362","obj":"http://purl.obolibrary.org/obo/CHEBI_29298"},{"id":"A363","pred":"chebi_id","subj":"T362","obj":"http://purl.obolibrary.org/obo/CHEBI_75710"},{"id":"A364","pred":"chebi_id","subj":"T364","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A365","pred":"chebi_id","subj":"T365","obj":"http://purl.obolibrary.org/obo/CHEBI_36080"},{"id":"A366","pred":"chebi_id","subj":"T366","obj":"http://purl.obolibrary.org/obo/CHEBI_29298"},{"id":"A367","pred":"chebi_id","subj":"T366","obj":"http://purl.obolibrary.org/obo/CHEBI_75710"},{"id":"A368","pred":"chebi_id","subj":"T368","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A369","pred":"chebi_id","subj":"T369","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A370","pred":"chebi_id","subj":"T370","obj":"http://purl.obolibrary.org/obo/CHEBI_52214"},{"id":"A371","pred":"chebi_id","subj":"T371","obj":"http://purl.obolibrary.org/obo/CHEBI_29298"},{"id":"A372","pred":"chebi_id","subj":"T371","obj":"http://purl.obolibrary.org/obo/CHEBI_75710"},{"id":"A373","pred":"chebi_id","subj":"T373","obj":"http://purl.obolibrary.org/obo/CHEBI_23888"}],"text":"T2 measurements of ligands are also useful for determining the binding nature of a small molecule. The T2 values of small molecules are quite large compared to those of bigger molecules (i.e., proteins) mostly because macromolecules have more spin-spin diffusion [175]. Bound ligands will, therefore, display shorter T2 values than non-binding ligands because they interact with the target (i.e., protein), adopting similar vibrational and rotational energies to the target [176]. This interaction is represented by the resonance line broadening in the binding ligand’s spectrum when a receptor is introduced into the sample [156]. Given the sizable difference of T2 values of binding and non-binding ligands, one can utilize 1D relaxation-edited experiments to distinguish the binding ligands from the non-binding ligands efficiently and effectively based on the differences in the T2 values [167]. These and other related relaxation edited experiments prove useful in drug design."}
LitCovid-PubTator
{"project":"LitCovid-PubTator","denotations":[{"id":"514","span":{"begin":248,"end":252},"obj":"Gene"},{"id":"515","span":{"begin":243,"end":247},"obj":"Gene"}],"attributes":[{"id":"A514","pred":"tao:has_database_id","subj":"514","obj":"Gene:10927"},{"id":"A515","pred":"tao:has_database_id","subj":"515","obj":"Gene:10927"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"T2 measurements of ligands are also useful for determining the binding nature of a small molecule. The T2 values of small molecules are quite large compared to those of bigger molecules (i.e., proteins) mostly because macromolecules have more spin-spin diffusion [175]. Bound ligands will, therefore, display shorter T2 values than non-binding ligands because they interact with the target (i.e., protein), adopting similar vibrational and rotational energies to the target [176]. This interaction is represented by the resonance line broadening in the binding ligand’s spectrum when a receptor is introduced into the sample [156]. Given the sizable difference of T2 values of binding and non-binding ligands, one can utilize 1D relaxation-edited experiments to distinguish the binding ligands from the non-binding ligands efficiently and effectively based on the differences in the T2 values [167]. These and other related relaxation edited experiments prove useful in drug design."}
LitCovid-sentences
{"project":"LitCovid-sentences","denotations":[{"id":"T250","span":{"begin":0,"end":98},"obj":"Sentence"},{"id":"T251","span":{"begin":99,"end":269},"obj":"Sentence"},{"id":"T252","span":{"begin":270,"end":480},"obj":"Sentence"},{"id":"T253","span":{"begin":481,"end":631},"obj":"Sentence"},{"id":"T254","span":{"begin":632,"end":899},"obj":"Sentence"},{"id":"T255","span":{"begin":900,"end":982},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"T2 measurements of ligands are also useful for determining the binding nature of a small molecule. The T2 values of small molecules are quite large compared to those of bigger molecules (i.e., proteins) mostly because macromolecules have more spin-spin diffusion [175]. Bound ligands will, therefore, display shorter T2 values than non-binding ligands because they interact with the target (i.e., protein), adopting similar vibrational and rotational energies to the target [176]. This interaction is represented by the resonance line broadening in the binding ligand’s spectrum when a receptor is introduced into the sample [156]. Given the sizable difference of T2 values of binding and non-binding ligands, one can utilize 1D relaxation-edited experiments to distinguish the binding ligands from the non-binding ligands efficiently and effectively based on the differences in the T2 values [167]. These and other related relaxation edited experiments prove useful in drug design."}