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AsparagineGlycineAspartate-Ammonia LigaseReceptors, GlycineGlycine AgentsGlycine Plasma Membrane Transport ProteinsAsparaginaseGlycine Dehydrogenase (Decarboxylating)Molecular Sequence DataAmino Acid SequenceAspartic AcidGlutamineAmino AcidsPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseStrychnineGlycine N-MethyltransferaseMutagenesis, Site-DirectedAspartate-tRNA LigaseRNA, Transfer, AsnMutationGlycine Decarboxylase Complex H-ProteinSoybeansBetaineGlycosylationBase SequenceKineticsGlycine Decarboxylase ComplexBinding SitesAmino Acid SubstitutionAmino Acid Transport Systems, NeutralLigasesGlycine HydroxymethyltransferaseEscherichia coliModels, MolecularStructure-Activity RelationshipAlanineSequence Homology, Amino AcidSubstrate SpecificitySarcosineCarbon-Nitrogen Ligases with Glutamine as Amide-N-DonorSerineProtein ConformationHistidineIsoaspartic AcidRecombinant ProteinsCloning, MolecularNitrogenous Group TransferasesCatalysisTaurineProtein Structure, TertiaryHydrogen-Ion ConcentrationNitrogenAmmoniaOligosaccharidesTransferasesGlycopeptidesProlineReceptors, N-Methyl-D-AspartateGlutamatesAminomethyltransferaseGlutamic AcidCell LineChromatography, High Pressure LiquidAmidohydrolasesSequence AlignmentAmino Acid OxidoreductasesPeptidesPoint MutationCarbohydratesBacterial ProteinsCarbohydrate SequenceAmidesProtein Processing, Post-TranslationalProtein BindingProtein Structure, SecondaryElectrophoresis, Polyacrylamide GelKynurenic AcidDeaminationMolecular WeightBiological TransportHydrogen BondingConserved SequencePeptide FragmentsAminobutyratesCrystallography, X-RayRNA, Transfer, Amino AcylOocytesLysineHydrolysisAmino Acid MotifsDecarboxylationCulture MediaArginineMutagenesisThreonineLiverXenopus laevisCysteinePlasmidsFabaceae

AlanineArginineAsparticAmino acid asparagineLysineProteinsPositionFormation

Alanine3

• The Flemish type is caused by replacement of the amino acid alanine with glycine at position 21 (written as Ala21Gly or A21G). (nih.gov)
• Amino acid profile in autistic children showed statistically significant lower levels of aspartic acid, glycine, β-alanine, tryptophan, lysine and proline amino acids with significantly higher asparagine amino acid derivative levels among autistic patients versus the control group (p˂0.05). (dovepress.com)
• Alanine and derivatives are compounds containing alanine or a derivative thereof resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. (ymdb.ca)

Arginine3

• NGR (asparagine-glycine-arginine) is a tripeptide present in fibronectin ( FINC_HUMAN ), fibrillin-1 ( FBN1_HUMAN ), and adeno-associated virus 2 protein capsid ( CAPSD_AAV2S ). (eu.org)
• Asparagine deamidation of NGR motif yields isoDGR (isoaspartic acid-glycine-arginine) motif. (eu.org)
• Peptides containing the asparagine-glycine-arginine (NGR) motif can target the tumor neovascular biomarker CD13/aminopeptidase N receptor. (eurekaselect.com)

Aspartic1

• In the Iowa type, the amino acid aspartic acid is switched with the amino acid asparagine at position 23 (written as Asp23Asn or D23N). (nih.gov)

Amino acid asparagine1

• In vitro, the amino acid asparagine stimulates the growth of the organism, while glycine induces hyphal formation. (medscape.com)

Lysine1

• In the Italian type, glutamic acid is replaced with the amino acid lysine (written as Glu22Lys or E22K) and in the Arctic type, glutamic acid is replaced with the amino acid glycine (written as Glu22Gly or E22G). (nih.gov)

Proteins1

• Asparagine attaches sugars to proteins. (editthis.info)

Position2

• 21 A -Gly-30 B a- l -Arg-30 B b- l -Arg-human insulin) is a modification of human insulin in which two arginines are added to the B-chain and glycine is substituted for asparagine at the A21 position of the insulin molecule. (diabetesjournals.org)
• A variant form of carbonic anhydrase I that has asparagine at position 86 replaced by glycine. (bvsalud.org)

Formation1

• T-protein, a component of the glycine cleavage system, catalyzes the formation of ammonia and 5,10-methylenetetrahydrofolate from the aminomethyl moiety of glycine attached to the lipoate cofactor of H-protein. (nih.gov)