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dbo:ChemicalCompound wikidata:Q11173 dbo:ChemicalSubstance n59:ChemicalObject owl:Thing umbel-rc:ChemicalSubstanceType
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天冬氨酸 アスパラギン酸 Asparaginezuur Ασπαραγινικό οξύ Aspartic acid Аспарагінова кислота Àcid aspàrtic Ácido aspártico Azido aspartiko Asam aspartat Asparaginsäure Ácido aspártico Asparaginsyra Kyselina asparagová Аспарагиновая кислота Kwas asparaginowy Ácido Aspártico Aigéad aspartach Aspartata acido Acido aspartico 아스파르트산 Acide aspartique حمض الأسبارتيك
rdfs:comment
天门冬氨酸(aspartic acid,可簡寫為Asp或D,通常简称天冬氨酸,药学中多简称门冬氨酸)是一种α-氨基酸,其化學式為HOOCCH2CH(NH2)COOH。天冬氨酸的L-異構物是20种蛋白胺基酸之一,即蛋白質的构造单位。它的密碼子是GAU和GAC。它与谷氨酸同為酸性氨基酸。天冬氨酸普遍存在于生物合成作用中。 Azido aspartikoa (Asp) proteinen osagaia den 20 aminoazido ez esentzialetako bat da. Azido 2-aminobutanedioiko honen formula kimikoa HO2CCH(NH2)CH2CO2H da eta GAU eta GAC kodonen bidez adierazten da. pH fisiologikoan karga negatiboa du, aminoazido azidoa baita. Bere albo katea polarra eta kargaduna da. Azido aspartikoa beste aminoazido batzuen aitzindaria da, hala nola, metionina, treonina, isoleuzina eta lisina. Gainera, proteinen osagaia izateaz gain, neurotransmisore bezala ere aritzen da. O ácido aspártico ou o 2-amino-butanóic ou aspartato (forma iônica) apresenta um pka de 2,01 a 0°C, suas constantes de dissociação são: pK1 = 1.92 (COOH); pK2 =3.87 (COOH); pK3 = 9.87 (amino) e o ponto isoeletrico é 2.98. https://pubchem.ncbi.nlm.nih.gov/compound/L-aspartic_acid#section=Tophttps://www.ebah.com.br/content/ABAAAAemUAL/acido-aspartico-fenilalanina 아스파르트산(영어: Aspartic acid, Asp, D) 또는 아스파트산은 음이온의 이름인 아스파르테이트(이온 형태 aspartate)로 알려져 있는 20개의 중요한 아미노산의 하나이다. 20개의 아미노산들이 그렇듯이, 아스파르트산을 일컫는 두가지 생략형이 있다. 하나는 Asp(3글자)이며, 또 하나는 D(1글자)이다. 때때로 아스파라긴과 합쳐서 Asx(3글자) 또는 B(1글자)로 나타내기도 한다.이름에서 알 수 있다시피, 아스파르트산은 아스파라긴과 유사하게 생긴 카르복실산이다. 아스파르트산은 포유류에게 있어서 비필수 아미노산이다. 아스파르트산은 또한 요소사이클의 반응산물이며, 당신생성에 관여한다.비록 그리 강력한 증거가 존재하지는 않지만, 신경전달물질로서 아스파르트산은 피로를 억제해서 지구력을 증가시킬 수도 있다.아스파르트산을 지정하는 코돈은 GAU와 GAC이다. L’acide aspartique (abréviations IUPAC-IUBMB : Asp et D), est un acide α-aminé dont l'énantiomère L est l'un des 22 acides aminés protéinogènes, encodé sur les ARN messagers par les codons GAU et GAC. Il est caractérisé par la présence d'un groupe carboxyle –COOH à l'extrémité de sa chaîne latérale, lui conférant un point isoélectrique de 2,77, ce qui en fait le résidu le plus acide dans les protéines. Son anion et base conjuguée est l'aspartate et son rayon de van der Waals vaut 291 pm. حمض الأسبارتيك (يختصر ب Asp أو D ) هو حمض ألفا-أميني قطبي ثنائي الكربوكسيل، وهو من الأحماض الأمينية غير الأساسية ورمزه الوراثي هو GAU و GAC· الأسبارتات هو أنيون حمض الأسبارتيك· عند الثدييات هو غير أساسي، يدخل في دورة اليوريا، يشارك في دورة تخليق الجلوكوز و يلعب دور في تركيب البيريميدين·هو ناقل عصبي محفز للمخ في شكله الميثيلي، حيث يفعل مستقبلات N-méthyl-D-aspartate) NMDA) التي هي مستقبلات للجلوتامات، لكن بحدة أقل من هذا الأخير· Asam aspartat (atau sering disebut aspartat saja, karena terionisasi di dalam sel), merupakan satu dari 20 asam amino penyusun protein. Asparagin merupakan asam amino analognya karena terbentuk melalui aminasi aspartat pada satu gugus hidroksilnya. Asam aspartat bersifat asam, dan dapat digolongkan sebagan asam karboksilat. Bagi mamalia aspartat tidaklah esensial. Fungsinya diketahui sebagai pembangkit neurotransmisi di otak dan saraf otot. Diduga, aspartat berperan dalam daya tahan terhadap kepenatan. Senyawa ini juga merupakan produk dari dan terlibat dalam glukoneogenesis. Asparagina acido aŭ aspartata acido (L-(+)-asparagina acido) (simbolo Asp aŭ D; Asx aŭ B por aspartata acido aŭ asparagino) COOHCH2CHNH2COOH estas unu el la 20 proteinogeneraj aminoacidoj. La acida anjono estas nomata kiel aspartat-jono. Kyselina asparagová (Asp, D) je biogenní aminokyselina vyskytující se v organismu ve formě své , která se nazývá aspartát. Obsahuje karboxylovou skupinu, je tudíž kyselá, a hydrofilní. Kyselina asparagová je součástí bílkovin, během proteosyntézy je kódována triplety GAU a GAC. Kyselina asparagová, přesněji řečeno karboxylová skupina v jejím postranním řetězci, je katalytickou skupinou aspartátových proteáz. Aspartát může fungovat také jako neurotransmiter, společně s glutamátem je hlavní excitační neurotransmiter mozku a míchy.[zdroj?] Aspartic acid (symbol Asp or D; the ionic form is known as aspartate), is an α-amino acid that is used in the biosynthesis of proteins. Like all other amino acids, it contains an amino group and a carboxylic acid. Its α-amino group is in the protonated –NH+3 form under physiological conditions, while its α-carboxylic acid group is deprotonated −COO− under physiological conditions. Aspartic acid has an acidic side chain (CH2COOH) which reacts with other amino acids, enzymes and proteins in the body. Under physiological conditions (pH 7.4) in proteins the side chain usually occurs as the negatively charged aspartate form, −COO−. It is a non-essential amino acid in humans, meaning the body can synthesize it as needed. It is encoded by the codons GAU and GAC. Kwas asparaginowy (łac. Acidum asparticum; skróty: Asp lub D; skróty „Asx” lub „B” oznaczają „kwas asparaginowy lub asparagina”, czyli Asx = [Asp lub Asn]) – organiczny związek chemiczny z grupy aminokwasów białkowych o charakterze kwasowym. Anion karboksylowy tego kwasu (forma anionowa przeważa w warunkach fizjologicznych) to asparaginian. Аспарагиновая кислота (аминоянтарная кислота, аспартат, аминобутандиовая кислота, 2-аминобутандиовая кислота, сокр.: Asp, D) — алифатическая заменимая аминокислота, одна из 20 протеиногенных аминокислот организма. Встречается во всех организмах в свободном виде и в составе белков. Кроме того, выполняет роль нейромедиатора в центральной нервной системе. El ácido aspártico o su forma ionizada, el aspartato (símbolos Asp y D) es uno de los veinte aminoácidos con los que las células forman las proteínas. En el ARN se encuentra codificado por los codones GAU o GAC.Presenta un grupo carboxilo (-COOH) en el extremo de la cadena lateral. Su fórmula química es HO2CCH(NH2)CH2CO2H. Is éard is aigéad aspartach ná α-aimínaigéad leis an fhoirmle cheimiceach HO2CCH(NH2)CH2CO2H. Tá eolas ar an ainian carbocsaileach den aigéid aspartaigh mar aspartáit. Is ceann de na 20 aimínaigéad próitéingineach í an L-isiméir, i.e., bloic tógála na próitéine. Is iad GAU agus GAC a chódáin. Το L-Ασπαραγινικό οξύ είναι ένα από τα 22 πρωτεϊνογόνα αμινοξέα. Στο επίπεδο της μοριακής γενετικής, τα κωδικόνιά του είναι GAU και GAC. Είναι ένα α-αμινοδιοξύ με σύντομο συντακτικό τύπο HOOCCH2CH(NH2)COOH. Τα καρβοξυλικά ανιόντα, τα άλατα και και οι εστέρες του ασπαραγικού οξέος είναι γνωστά ως «ασπαραγικά». Το ασπαραγινικό οξύ και το γλουταμινικό οξύ ταξινομούνται στα «όξινα αμινοξέα». Το ελεύθερο ασπαραγινικό οξύ έχει pKa1 = 3,9, αλλά όταν βρίσκεται μέσα ένα πεπτίδιο το pKa του εξαρτάται σε μεγάλο βαθμό από το τοπικό του περιβάλλον. Ένα pKa ως και 14 δεν είναι τελείως ασυνήθιστο. Το ασπαραγινικό ανιόν είναι διαδεδομένο στη βιοσύνθεση. Όπως συμβαίνει με όλα τα αμινοξέα, η παρουσία όξινων πρωτονίων εξαρτάται από το τοπικό περιβάλλον και το pH του διαλύματος. Asparaginsäure, abgekürzt Asp oder D, ist in ihrer natürlichen L-Form eine der proteinogenen α-Aminosäuren. Wie die anderen Aminosäuren liegt Asparaginsäure im Körper normalerweise zwitterionisch vor. Zusätzlich ist jedoch die zweite Carboxygruppe deprotoniert, darum wird in der Biochemie statt L-Asparaginsäure oft die Bezeichnung L-Aspartat verwendet. L'acido aspartico è un amminoacido utilizzato degli esseri viventi per la sintesi delle proteine. Viene indicato comunemente con le sigle D o Asp ed è codificato sull’RNA messaggero dai codoni GAU e GAC. È coinvolto anche nel ciclo dell'urea ed è inserito fra gli amminoacidi gluconeogenici in quanto, per transamminazione, si trasforma in ossalacetato. アスパラギン酸(アスパラギンさん、aspartic acid)とは、アミノ酸のひとつで、2-アミノブタン二酸のこと。略号は Asp あるいは D。光学異性体としてL体とD体の両方が存在する。アスパラギンの加水分解物から単離され、由来とその構造からこの名がついた。 酸性極性側鎖アミノ酸に分類される。L体のアスパラギン酸は蛋白質を構成するアミノ酸のひとつ。非必須アミノ酸で、グリコーゲン生産性を持つ。うま味成分のひとつ。 致死量はLD50=16g/kgである。 Asparaginezuur (afgekort tot Asp of D) is een van de twintig natuurlijk voorkomende aminozuren die de bouwstenen zijn van eiwitten. De stof komt voor als kleurloze schilferige of naaldvormige kristallen, die slecht oplosbaar zijn in water. In de biologische omgeving is de stof vooral bekend onder de naam aspartaat, omdat in fysiologische omstandigheden dit de overheersende vorm is. Ook zouten en esters van asparaginezuur worden aspartaten genoemd. Asparaginezuur wordt gecodeerd door de codons GAU en GAC. L'àcid aspàrtic, (símbols Asp i D). Un dels vint-i-un aminoàcids amb què les cèl·lules formen les proteïnes. Els seus codons són GAU o GAC. Presenta un grup carboxil (-COOH) en l'extrem de la cadena lateral. * A pH fisiològic té càrrega negativa, per la qual cosa també és denominat aspartat. * Pertany al grup d'aminoàcids amb cadenes laterals polars carregades. * Pot ser sintetitzat pels humans. * La seua biosíntesi té lloc per transaminació de l'àcid oxalacètic, un producte intermedi del cicle de Krebs. Asparaginsyra (förkortas Asp eller D), är en av de 20 aminosyrorna som är byggstenar i proteiner. Dess sidokedja är sur. Syrans anjon, salter och estrar kallas aspartat. Asparaginsyra är liksom glutaminsyra en icke-essentiell, polär, sur aminosyra. Den finns oftast i L-form, men också i D-form. På syntetisk väg framställs ofta blandformer (olika DL-former). I kroppen kan den bildas via bland annat ureacykeln samt deltar i glukoneogenesen. Under matsmältningsprocessen bryts asparaginsyran ner av (den mänskliga) kroppen till ett antal olika svavelföreningar. O ácido aspártico (cuja forma iónica é conhecida como aspartato) é um dos aminoácidos codificados pelo código genético, sendo portanto um dos componentes das proteínas dos seres vivos.É um aminoácido não essencial em mamíferos, tendo uma possível função de neurotransmissor excitatório no cérebro. Como tal, existem indicações que o ácido aspártico possa conferir resistência à fadiga. É também um metabolito do ciclo da ureia e participa na gluconeogénese e pode ser neurotóxico. O aspartato faz também parte do adoçante aspartame. Аспарагі́нова кислота́ (аспартова, аміноянтарна кислота) COOHCH2CHNH2COOH — амінокислота, один з проміжних продуктів азотистого обміну у тварин і рослин. Амід аспарагінової кислоти аспарагін є важливим продуктом азотистого обміну у рослин, резервом азоту; знешкоджує аміак, що утворюється в процесі перетворення білків. Аспарагінова кислота стимулює синтез білка, знижує рівень аміаку в крові, нормалізує роботу печінки.
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Aspartic acid
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Aspartic acid
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3
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March 2017
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Skeletal formula of (L)-aspartic acid
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L-Asparaginsäure - L-Aspartic acid.svg
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Systematic: 2-Aminobutanedioic acid Trivial: Aspartic acid
dbp:othernames
Asparaginic acid Asparagic acid Aminosuccinic acid
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+
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Is this Total addressable market or Serviceable available market?
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addressable market
dbo:abstract
Asparaginsäure, abgekürzt Asp oder D, ist in ihrer natürlichen L-Form eine der proteinogenen α-Aminosäuren. Wie die anderen Aminosäuren liegt Asparaginsäure im Körper normalerweise zwitterionisch vor. Zusätzlich ist jedoch die zweite Carboxygruppe deprotoniert, darum wird in der Biochemie statt L-Asparaginsäure oft die Bezeichnung L-Aspartat verwendet. L'àcid aspàrtic, (símbols Asp i D). Un dels vint-i-un aminoàcids amb què les cèl·lules formen les proteïnes. Els seus codons són GAU o GAC. Presenta un grup carboxil (-COOH) en l'extrem de la cadena lateral. * A pH fisiològic té càrrega negativa, per la qual cosa també és denominat aspartat. * Pertany al grup d'aminoàcids amb cadenes laterals polars carregades. * Pot ser sintetitzat pels humans. * La seua biosíntesi té lloc per transaminació de l'àcid oxalacètic, un producte intermedi del cicle de Krebs. Το L-Ασπαραγινικό οξύ είναι ένα από τα 22 πρωτεϊνογόνα αμινοξέα. Στο επίπεδο της μοριακής γενετικής, τα κωδικόνιά του είναι GAU και GAC. Είναι ένα α-αμινοδιοξύ με σύντομο συντακτικό τύπο HOOCCH2CH(NH2)COOH. Τα καρβοξυλικά ανιόντα, τα άλατα και και οι εστέρες του ασπαραγικού οξέος είναι γνωστά ως «ασπαραγικά». Το ασπαραγινικό οξύ και το γλουταμινικό οξύ ταξινομούνται στα «όξινα αμινοξέα». Το ελεύθερο ασπαραγινικό οξύ έχει pKa1 = 3,9, αλλά όταν βρίσκεται μέσα ένα πεπτίδιο το pKa του εξαρτάται σε μεγάλο βαθμό από το τοπικό του περιβάλλον. Ένα pKa ως και 14 δεν είναι τελείως ασυνήθιστο. Το ασπαραγινικό ανιόν είναι διαδεδομένο στη βιοσύνθεση. Όπως συμβαίνει με όλα τα αμινοξέα, η παρουσία όξινων πρωτονίων εξαρτάται από το τοπικό περιβάλλον και το pH του διαλύματος. Asam aspartat (atau sering disebut aspartat saja, karena terionisasi di dalam sel), merupakan satu dari 20 asam amino penyusun protein. Asparagin merupakan asam amino analognya karena terbentuk melalui aminasi aspartat pada satu gugus hidroksilnya. Asam aspartat bersifat asam, dan dapat digolongkan sebagan asam karboksilat. Bagi mamalia aspartat tidaklah esensial. Fungsinya diketahui sebagai pembangkit neurotransmisi di otak dan saraf otot. Diduga, aspartat berperan dalam daya tahan terhadap kepenatan. Senyawa ini juga merupakan produk dari dan terlibat dalam glukoneogenesis. 天门冬氨酸(aspartic acid,可簡寫為Asp或D,通常简称天冬氨酸,药学中多简称门冬氨酸)是一种α-氨基酸,其化學式為HOOCCH2CH(NH2)COOH。天冬氨酸的L-異構物是20种蛋白胺基酸之一,即蛋白質的构造单位。它的密碼子是GAU和GAC。它与谷氨酸同為酸性氨基酸。天冬氨酸普遍存在于生物合成作用中。 O ácido aspártico (cuja forma iónica é conhecida como aspartato) é um dos aminoácidos codificados pelo código genético, sendo portanto um dos componentes das proteínas dos seres vivos.É um aminoácido não essencial em mamíferos, tendo uma possível função de neurotransmissor excitatório no cérebro. Como tal, existem indicações que o ácido aspártico possa conferir resistência à fadiga. É também um metabolito do ciclo da ureia e participa na gluconeogénese e pode ser neurotóxico. O aspartato faz também parte do adoçante aspartame. El ácido aspártico o su forma ionizada, el aspartato (símbolos Asp y D) es uno de los veinte aminoácidos con los que las células forman las proteínas. En el ARN se encuentra codificado por los codones GAU o GAC.Presenta un grupo carboxilo (-COOH) en el extremo de la cadena lateral. Su fórmula química es HO2CCH(NH2)CH2CO2H. A pH fisiológico, tiene una carga negativa (es ácido); pertenece al grupo de aminoácidos con cadenas laterales polares cargadas. No es un aminoácido esencial ya que puede ser sintetizado por el organismo humano.Su biosíntesis tiene lugar por transaminación del ácido oxalacético, un metabolito intermediario del ciclo de Krebs. アスパラギン酸(アスパラギンさん、aspartic acid)とは、アミノ酸のひとつで、2-アミノブタン二酸のこと。略号は Asp あるいは D。光学異性体としてL体とD体の両方が存在する。アスパラギンの加水分解物から単離され、由来とその構造からこの名がついた。 酸性極性側鎖アミノ酸に分類される。L体のアスパラギン酸は蛋白質を構成するアミノ酸のひとつ。非必須アミノ酸で、グリコーゲン生産性を持つ。うま味成分のひとつ。 致死量はLD50=16g/kgである。 Аспарагиновая кислота (аминоянтарная кислота, аспартат, аминобутандиовая кислота, 2-аминобутандиовая кислота, сокр.: Asp, D) — алифатическая заменимая аминокислота, одна из 20 протеиногенных аминокислот организма. Встречается во всех организмах в свободном виде и в составе белков. Кроме того, выполняет роль нейромедиатора в центральной нервной системе. Is éard is aigéad aspartach ná α-aimínaigéad leis an fhoirmle cheimiceach HO2CCH(NH2)CH2CO2H. Tá eolas ar an ainian carbocsaileach den aigéid aspartaigh mar aspartáit. Is ceann de na 20 aimínaigéad próitéingineach í an L-isiméir, i.e., bloic tógála na próitéine. Is iad GAU agus GAC a chódáin. O ácido aspártico ou o 2-amino-butanóic ou aspartato (forma iônica) apresenta um pka de 2,01 a 0°C, suas constantes de dissociação são: pK1 = 1.92 (COOH); pK2 =3.87 (COOH); pK3 = 9.87 (amino) e o ponto isoeletrico é 2.98. O ácido aspártico é classificado como aminoácido não essencial, isto quer dizer que em condições fisiológicas normais, os seres vivos são capazes de sintetizar essa molécula. Em mamíferos, o aspartato é produzido a partir do glutamato e oxaloacetato. A enzima responsável por esta reação é a aspartato aminotransferase que, como o nome indica, transfere um grupo amina do glutamato para o oxaloacetato para formar aspartato, o outro produto da reação é o α-cetoglutarato. Este processo ocorre na matriz mitocondrial. Esse aminoácido é precurssor de diversas moleculas como proteínas, oligopeptideos, purinas, pirimidinas, ácidos nucleios, entre outras. Além de participar do ciclo da ureia e da gluconeogénese. Atuar também como neurotransmissor excitatório no cérebro. Alguns estudos relatam que o ácido aspártico pode conferir resistência à fadiga. As plantas também são capazes de sintetizar aspartato. Após a fixação de CO2 sob a forma de oxaloacetato, este sofre transaminação com um outro aminoácido, originando aspartato e o α-cetoácido correspondente. Algumas plantas usam o aspartato como transportador de CO2; neste caso, a reação de transaminação inversa ocorre, formando-se oxaloacetato que é depois reduzido a malato (este origina subsequentemente CO2). Em bactérias, o aspartato origina os aminoácidos metionina, treonina e lisina.No campo industral é utilizado juntamente com a fenilalanina formando assim o aspartame, um aditivo alimentar que pode substituir o açúcar comum. Adoça cerca de 200 vezes mais do que a sacarose, além de apresentar uma densidade menor. Diversos estudos demonstraram que o aspartame apresenta propriedade neurotoxicas, além de provocar diversos tipos de câncer, reações alérgicas alimentares, enxaquecas; náusea, diabetes (o aspartame em indivíduos diabéticos pode favorecer as complicaces como neuropatia, retinopatia, catarata e pode provocar mal controle glicêmico), espasmos musculares, depressão, epilepsia dentre outros. https://pubchem.ncbi.nlm.nih.gov/compound/L-aspartic_acid#section=Tophttps://www.ebah.com.br/content/ABAAAAemUAL/acido-aspartico-fenilalanina L'acido aspartico è un amminoacido utilizzato degli esseri viventi per la sintesi delle proteine. Viene indicato comunemente con le sigle D o Asp ed è codificato sull’RNA messaggero dai codoni GAU e GAC. È coinvolto anche nel ciclo dell'urea ed è inserito fra gli amminoacidi gluconeogenici in quanto, per transamminazione, si trasforma in ossalacetato. Asparagina acido aŭ aspartata acido (L-(+)-asparagina acido) (simbolo Asp aŭ D; Asx aŭ B por aspartata acido aŭ asparagino) COOHCH2CHNH2COOH estas unu el la 20 proteinogeneraj aminoacidoj. La acida anjono estas nomata kiel aspartat-jono. Aspartic acid (symbol Asp or D; the ionic form is known as aspartate), is an α-amino acid that is used in the biosynthesis of proteins. Like all other amino acids, it contains an amino group and a carboxylic acid. Its α-amino group is in the protonated –NH+3 form under physiological conditions, while its α-carboxylic acid group is deprotonated −COO− under physiological conditions. Aspartic acid has an acidic side chain (CH2COOH) which reacts with other amino acids, enzymes and proteins in the body. Under physiological conditions (pH 7.4) in proteins the side chain usually occurs as the negatively charged aspartate form, −COO−. It is a non-essential amino acid in humans, meaning the body can synthesize it as needed. It is encoded by the codons GAU and GAC. D-Aspartate is one of two D-amino acids commonly found in mammals.[3] In proteins aspartate sidechains are often hydrogen bonded to form asx turns or asx motifs, which frequently occur at the N-termini of alpha helices. The L-isomer of Asp is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. Aspartic acid, like glutamic acid, is classified as an acidic amino acid, with a pKa of 3.9, however in a peptide this is highly dependent on the local environment, and could be as high as 14. Asp is pervasive in biosynthesis. Asparaginsyra (förkortas Asp eller D), är en av de 20 aminosyrorna som är byggstenar i proteiner. Dess sidokedja är sur. Syrans anjon, salter och estrar kallas aspartat. Asparaginsyra är liksom glutaminsyra en icke-essentiell, polär, sur aminosyra. Den finns oftast i L-form, men också i D-form. På syntetisk väg framställs ofta blandformer (olika DL-former). I kroppen kan den bildas via bland annat ureacykeln samt deltar i glukoneogenesen. Exogent förekommer den i sockerväxter, vissa grönsaker (bland annat i sparris som gett syran dess namn), samt i kemiska sötningsmedel. Den kan agera som signalsubstans via NMDA-receptorn. Under matsmältningsprocessen bryts asparaginsyran ner av (den mänskliga) kroppen till ett antal olika svavelföreningar. I den genetiska koden kodas asparaginsyra av två kodon: GAU och GAC. Asparaginsyra spelar en viktig roll i människans ämnesomsättning, eftersom den vid enzymkatalyserad transaminering kan omvandlas till oxalacetat vilken i sin tur reagerar i citronsyracykeln. Asparaginsyra har en molmassa på 133,1 Da, och är därmed en medelstor aminosyra. Den genomsnittliga förekomsten av asparaginsyra i protein är 5,5 %. Aminosyran asparaginsyra (Asp, D) ska inte förväxlas med den nära besläktade aminosyran asparagin (Asn, N). I sidokedjan på asparagin (Asn, N) har hydroxylgruppen på karbonylkolet i asparaginsyra bytts ut mot en aminogrupp. Syrakonstanten pKa för karboxylgruppens sidokedja är 3,90. Den isoelektriska punkten för hela aminosyran är ca 3. Kwas asparaginowy (łac. Acidum asparticum; skróty: Asp lub D; skróty „Asx” lub „B” oznaczają „kwas asparaginowy lub asparagina”, czyli Asx = [Asp lub Asn]) – organiczny związek chemiczny z grupy aminokwasów białkowych o charakterze kwasowym. Anion karboksylowy tego kwasu (forma anionowa przeważa w warunkach fizjologicznych) to asparaginian. 아스파르트산(영어: Aspartic acid, Asp, D) 또는 아스파트산은 음이온의 이름인 아스파르테이트(이온 형태 aspartate)로 알려져 있는 20개의 중요한 아미노산의 하나이다. 20개의 아미노산들이 그렇듯이, 아스파르트산을 일컫는 두가지 생략형이 있다. 하나는 Asp(3글자)이며, 또 하나는 D(1글자)이다. 때때로 아스파라긴과 합쳐서 Asx(3글자) 또는 B(1글자)로 나타내기도 한다.이름에서 알 수 있다시피, 아스파르트산은 아스파라긴과 유사하게 생긴 카르복실산이다. 아스파르트산은 포유류에게 있어서 비필수 아미노산이다. 아스파르트산은 또한 요소사이클의 반응산물이며, 당신생성에 관여한다.비록 그리 강력한 증거가 존재하지는 않지만, 신경전달물질로서 아스파르트산은 피로를 억제해서 지구력을 증가시킬 수도 있다.아스파르트산을 지정하는 코돈은 GAU와 GAC이다. Kyselina asparagová (Asp, D) je biogenní aminokyselina vyskytující se v organismu ve formě své , která se nazývá aspartát. Obsahuje karboxylovou skupinu, je tudíž kyselá, a hydrofilní. Kyselina asparagová je součástí bílkovin, během proteosyntézy je kódována triplety GAU a GAC. Kyselina asparagová, přesněji řečeno karboxylová skupina v jejím postranním řetězci, je katalytickou skupinou aspartátových proteáz. Kromě své úlohy v metabolismu je také substrátem pro mnoho biochemických pochodů – je intermediátem močovinového cyklu a jedním z hlavních substrátů pro syntézu purinových i pyrimidinových bází. U rostlin a mikroorganismů je též prekurzor při syntéze esenciálních aminokyselin methioninu, threoninu, isoleucinu a lysinu. Další významná role kyseliny asparagové je v tzv. malát-aspartátovém člunku, sledu chemických reakcí, při kterých se přenášejí přes membránu mitochondrií. Z aspartátu též může být fixací dusíku syntetizována aminokyselina asparagin. Aspartát může fungovat také jako neurotransmiter, společně s glutamátem je hlavní excitační neurotransmiter mozku a míchy.[zdroj?] Kromě klasické L-formy aspartátu je významná i jeho D-forma, která se vyskytuje v neuronech a žlázách s vnitřní sekrecí, její funkce ale není dobře prozkoumaná. حمض الأسبارتيك (يختصر ب Asp أو D ) هو حمض ألفا-أميني قطبي ثنائي الكربوكسيل، وهو من الأحماض الأمينية غير الأساسية ورمزه الوراثي هو GAU و GAC· الأسبارتات هو أنيون حمض الأسبارتيك· عند الثدييات هو غير أساسي، يدخل في دورة اليوريا، يشارك في دورة تخليق الجلوكوز و يلعب دور في تركيب البيريميدين·هو ناقل عصبي محفز للمخ في شكله الميثيلي، حيث يفعل مستقبلات N-méthyl-D-aspartate) NMDA) التي هي مستقبلات للجلوتامات، لكن بحدة أقل من هذا الأخير· L’acide aspartique (abréviations IUPAC-IUBMB : Asp et D), est un acide α-aminé dont l'énantiomère L est l'un des 22 acides aminés protéinogènes, encodé sur les ARN messagers par les codons GAU et GAC. Il est caractérisé par la présence d'un groupe carboxyle –COOH à l'extrémité de sa chaîne latérale, lui conférant un point isoélectrique de 2,77, ce qui en fait le résidu le plus acide dans les protéines. Son anion et base conjuguée est l'aspartate et son rayon de van der Waals vaut 291 pm. Il s'agit d'un acide dicarboxylique, et donc d'une molécule polaire. Chez les mammifères, il est non essentiel. C'est un métabolite du cycle de l'urée. Аспарагі́нова кислота́ (аспартова, аміноянтарна кислота) COOHCH2CHNH2COOH — амінокислота, один з проміжних продуктів азотистого обміну у тварин і рослин. Амід аспарагінової кислоти аспарагін є важливим продуктом азотистого обміну у рослин, резервом азоту; знешкоджує аміак, що утворюється в процесі перетворення білків. Аспарагінова кислота стимулює синтез білка, знижує рівень аміаку в крові, нормалізує роботу печінки. Azido aspartikoa (Asp) proteinen osagaia den 20 aminoazido ez esentzialetako bat da. Azido 2-aminobutanedioiko honen formula kimikoa HO2CCH(NH2)CH2CO2H da eta GAU eta GAC kodonen bidez adierazten da. pH fisiologikoan karga negatiboa du, aminoazido azidoa baita. Bere albo katea polarra eta kargaduna da. Azido aspartikoa beste aminoazido batzuen aitzindaria da, hala nola, metionina, treonina, isoleuzina eta lisina. Gainera, proteinen osagaia izateaz gain, neurotransmisore bezala ere aritzen da. Asparaginezuur (afgekort tot Asp of D) is een van de twintig natuurlijk voorkomende aminozuren die de bouwstenen zijn van eiwitten. De stof komt voor als kleurloze schilferige of naaldvormige kristallen, die slecht oplosbaar zijn in water. In de biologische omgeving is de stof vooral bekend onder de naam aspartaat, omdat in fysiologische omstandigheden dit de overheersende vorm is. Ook zouten en esters van asparaginezuur worden aspartaten genoemd. Asparaginezuur wordt gecodeerd door de codons GAU en GAC.
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Asparagic acid Asparaginic acid Aminosuccinic acid
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Systematic: 2-Aminobutanedioic acid Trivial: Aspartic acid
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dbr:Protein_metabolism
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Proteinogenic_amino_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:TMEM101
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:TMEM176B
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:TMEM81
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Molecular_paleontology
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:MT-TD
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:POLD1
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Ribonucleotide
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphatidate_phosphatase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphoenolpyruvate_carboxylase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphoglycolate_phosphatase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phospholipase_D
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphomimetics
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphoprotein
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phosphorylation
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Phytaspase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:PiggyBac_Transposable_Element_Derived_5
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Poly_(ADP-ribose)_polymerase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Urea_cycle
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Serine_O-acetyltransferase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Serine_protease
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Vesicular_monoamine_transporter
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Vegetarian_and_vegan_dog_diet
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Peritrich_nuclear_code
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Transmembrane_protein_251
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:STK24
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Shimeji
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:RNA_Tie_Club
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Wilson_disease_protein
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Properdin_deficiency
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Tachykinin_receptor_1
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Oxidosqualene_cyclase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:PNGase_F
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Pantothenate_kinase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Walker_motifs
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
n44:spiroplasma_code
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Sphingomyelin_phosphodiesterase
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:TRPV6
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:SAAL1
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:SARS-CoV-2_lineage_B.1.617
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:SMIM23
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
n26:_As–Az
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Sericin
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Vosoritide
dbo:wikiPageWikiLink
dbr:Aspartic_acid
Subject Item
dbr:Spizellomyces_punctatus
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dbr:Aspartic_acid
Subject Item
dbr:L-Aspartic_Acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:L-aspartate
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dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:L-aspartic_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Aminosuccinic_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Asparagic_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Asparagine_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Asparaginic_acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Asparate
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dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Aspartate
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dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Aspartic
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Aspartyl
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dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:Calcium_aspartate
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dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
dbr:1-Aspartic_Acid
dbo:wikiPageWikiLink
dbr:Aspartic_acid
dbo:wikiPageRedirects
dbr:Aspartic_acid
Subject Item
wikipedia-en:Aspartic_acid
foaf:primaryTopic
dbr:Aspartic_acid