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Subject Item
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Subject Item
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Subject Item
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Triptofano Tryptophan Tryptofan تريبتوفان Triptofano Tryptofan 트립토판 Triptófano Tryptophan Tryptophane 色氨酸 Триптофан Τρυπτοφάνη Triptofan Tryptofaan Triptofano トリプトファン Triptofano Tryptofan Triptòfan Триптофан
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Триптофа́н (β-(β-індоліл)-α-амінопропіонова кислота) — незамінна амінокислота. Кодується тільки одним кодоном — UGG. L-стереоізомер входить до складу гамаглобулінів, фібриногену, казеїну та інших білків. Триптофан є провітаміном. Triptofan (bahasa Inggris: tryptophan, TRP, W) merupakan satu dari 20 asam amino penyusun protein yang bersifat esensial bagi manusia. Bentuk yang umum pada mamalia adalah, seperti asam amino lainnya, L-triptofan. Meskipun demikian D-triptofan ditemukan pula di alam (contohnya adalah pada bisa ular laut ). El triptófano (abreviado como Trp o W) (también, triptofano) es un aminoácido esencial en la nutrición humana. Es uno de los 20 aminoácidos incluidos en el código genético (codón UGG). Se clasifica entre los aminoácidos apolares, también llamados hidrófobos. Se caracteriza por una cadena lateral con el grupo indol. Es esencial para promover la liberación del neurotransmisor serotonina, involucrado en la regulación del sueño y el placer. Su punto isoeléctrico se ubica a pH=5.89. La falta de triptófano puede contribuir negativamente a cuadros de ansiedad, insomnio y estrés.[cita requerida] 色氨酸(英語:Tryptophan, 縮寫Trp或W)是22個標準氨基酸之一,人體不能合成的必需氨基酸,因此它須從食物中汲取。它的標準遺傳密碼的密碼子編碼為UGG,只有L-立體異構體色氨酸有構造或酶活蛋白質的作用,R-立體異構體則偶爾在自然產生的肽中發現。色氨酸的明顯結構式特徵是,它含有吲哚官能團。它是血清素(亦称“5-羟色胺”)的前體,血清素是重要的神經递质。還能合成菸鹼素。 Η τρυπτοφάνη είναι ένα από τα 22 πρωτεϊνογόνα αμινοξέα και ένα (από τα 8) για την ανθρώπινη διατροφή. Κωδικοποιείται στον γενετικό κώδικα με το κωδικόνιο UGG. Μόνο το L-στερεοϊσομερές της τρυπτοφάνης χρησιμοποιείται σε ή σε ένζυμα, αλλά η D-τρυπτοφάνη βρίσκεται περιστασιακά σε πεπτίδια φυσικής παραγωγής (για παράδειγμα θαλάσσιο δηλητηριώδες πεπτίδιο , contryphan). Το χαρακτηριστικό δομικό χαρακτηριστικό της τρυπτοφάνης είναι ότι περιέχει μια λειτουργική ομάδα, στην πλευρική της αλυσίδα. Είναι ένα απαραίτητο αμινοξύ, όπως επιδεικνύεται από τα αυξητικά αποτελέσματα της χορήγησής της σε αρουραίους. التريبتوفان أو التربتوفان هو حمض أميني ضروري،أي لا يمكن تخليقه في الجسم بل يجب الحصول عليه من مصدر خارجي كالغذاء، يمتلك سلسة جانبية هي أكبر سلسلة جانبية عطرية (أروماتية) في الأحماض الأمينية ألفا وهذه السلسلة مكونة من حلقتين إحداهما سداسية والأخرى خماسية يشكل النيتروجين أحد أركانها وهو يصنف من الأحماض الأمينية الكبيرة الكارهة للماء (large hydrophoboic amino acids). وللحمض الصيغة الجزيئية C11H12N2O2 .وللحمض دور تكوين الناقل العصبي المهيج سيروتونين عن طريق نزع مجموعة الكاربوكسيل من التربتوفان. Tryptofan (förkortas Trp eller W) är inom biokemi en av de 20 aminosyror som är byggstenar i proteiner. Den tillhör gruppen opolära, hydrofoba aminosyror och är en av de essentiella aminosyrorna, som kroppen inte själv kan tillverka, och som därför måste tillföras i födan. Bara L-stereoisomeren av tryptofan används som strukturellt enzymprotein; D-stereoisomeren är vanligast förekommande i naturligt producerade peptider. Det utmärkande strukturella kännetecknet för tryptofan är att den har en indol-grupp. Den är en av de två aminosyror som motsvaras av endast ett kodon (UGG) i den genetiska koden. Tryptofaan (afgekort als Trp of W) is een groot, hydrofoob aminozuur dat zich kenmerkt door zijn indool-bevattende zijketen. Het is een van de ruim twintig natuurlijk voorkomende aminozuren die voor de eiwitsynthese worden gebruikt. Tryptofaan behoort tot de categorie essentieel aminozuur, wat inhoudt dat het niet kan worden gevormd door het menselijk lichaam en dus via de voeding moet worden opgenomen. Tryptofan (zkratky: Trp, W) je jednou z 20 proteinogenních aminokyselin. Řadí se k , aromatickým aminokyselinám (resp. k aminokyselinám s nepolárním, aromatickým postranním řetězcem). Jeho strukturní základ tvoří indol. Patří mezi esenciální aminokyseliny, lidské tělo ho neumí syntetizovat. Koduje ho kodon UGG, jedná se o vzácnější aminokyselinu s průměrným zastoupením v proteinech 1,4 %. Il triptofano è un amminoacido poco polare, il suo gruppo laterale è un indolile. È alla base del gruppo di composti delle triptamine. È una molecola chirale. L'enantiomero L è uno dei 20 amminoacidi ordinari. Poiché l'organismo umano non è in grado di sintetizzarlo, deve essere ricavato dagli alimenti e pertanto è classificato tra gli amminoacidi essenziali. Oltre a partecipare alla costituzione delle proteine dell'organismo, interviene in numerose reazioni chimiche, in particolare nella sintesi di serotonina e di acido nicotinico. El triptòfan (abreviat Trp o W) és un aminoàcid essencial en la nutrició humana. És un dels 20 aminoàcids inclosos en el codi genètic (codó UGG). És considerat un aminoàcid no polar i hidrofòbic: * Fórmula molecular: C11H12N₂O₂ * Massa molecular: 204,23 * Punt isoelèctric: pH = 5,89 * Nombre CAS: 73-22-3 Hopkins i Cole van descobrir el triptòfan a principis dels anys 1900 després d'aïllar-lo de la proteïna de la caseïna, i Ellinger i Flamand van determinar la seva estructura molecular poc temps després. Le tryptophane (abréviations IUPAC-IUBMB : Trp et W) est un acide α-aminé dont l'énantiomère L est l'un des 22 acides aminés protéinogènes et l'un des 9 acides aminés essentiels pour l'humain. Il est encodé sur les ARN messagers par le codon UGG. C'est l'acide aminé protéinogène le plus rare composant uniquement 1,3 % des acides aminés totaux des vertébrés et 1,1% de ceux des protéines. 트립토판(영어: tryptophan)은 인간영양에 필요한 필수 아미노산이다. 트립토판은 유전코드로 암호화된 20여개의 아미노산 중 하나로, 지정 코돈은 UGG이다. 포유류 단백질에서 오직 L형 트립토판만이 등장하지만, 때때로 D형 트립토판도 해안 생명체의 독성 펩티드인 과 같은 자연물질들에서 발견된다. 트립토판의 주목할 만한 구조적 특징은 (indole-)를 포함하고 있다는 점이다. Triptofano (α-Amino-β-Indolilpropionacido, IUPAC: 2-amino-3-(1H-indol-3-il)-propionacido) (simbolo Trp aŭ W) estas aminoacido kun aromata strukturo sur la flanka ĉeno. Ĝi apartenas al esencaj aminoacidoj, t.e. ĝin ne povas produkti la homa korpo kaj pro tio necesas akiri ĝin per manĝaĵo . Ĝi apartenas al la 20 proteinaj aminoacidoj, el kiuj la proteinoj de la homa korpo konstruiĝas. Plantoj kaj mikroorganismoj povas ĝin produkti. Triptofanoa (Trp) proteinen osagaia den aminoazido esentzialetako bat da, beraz dieta bidez hartu beharrekoa. Azido 2-amino-3-(1H-indol-3-il)propioniko honen formula kimikoa HO2CCH2(NH2)CH2(C8NH6) da eta UGG kodonaren bidez adierazten da. Molekula hidrofobikoa da, hau da, uretan disolbaezina albo katean indol talde bat duelako. Gainera, serotonina neurotransmisorearen askapenerako ezinbestekoa da. Honi esker, antsietatea, insomnioa eta estresa erregulatzen dira. Триптофа́н (β-(β-индолил)-α-аминопропионовая кислота, сокр.: Три, Трп, Trp, W) — ароматическая альфа-аминокислота. Существует в двух оптически изомерных формах, L и D, и в виде рацемата (рацемической смеси) (DL). L-триптофан является протеиногенной аминокислотой и входит в состав белков всех известных живых организмов. Относится к ряду гидрофобных аминокислот, поскольку содержит ароматическое ядро индола. Участвует в гидрофобных и стэкинг-взаимодействиях. トリプトファン (Tryptophan) はアミノ酸の一種である。ヒトにおける9つの必須アミノ酸の内の1つ。 系統名 2-アミノ-3-(インドリル)プロピオン酸。略号はTrpまたはW。 側鎖にインドール環を持ち、芳香族アミノ酸に分類される。蛋白質構成アミノ酸である。糖原性・ケト原性の両方を持つ。多くのタンパク質中に見出されるが、含量は低い。ナイアシンの体内活性物質であるNAD(H)をはじめ、セロトニン・メラトニンといったホルモン、キヌレニン等生体色素、また植物において重要な成長ホルモンであるインドール酢酸の前駆体、インドールアルカロイド(トリプタミン類)などの前駆体として重要である。 O triptofano é um aminoácido utilizado na biossíntese de proteínas, sendo codificado pelo codão UGG. Ele contém, como todo aminoácido, um grupo amino (básico) e um grupo carboxilo (ácido); sua cadeia lateral consiste num indol, o que faz dele um aminoácido aromático e apolar. No pH fisiológico, o triptofano é um zwitterion: o grupo amino (pKa = 9.39) encontra-se protonado (–NH3+) e o grupo carboxila (pKa = 2.38) encontra-se deprotonado ( –COO−). Absorve luz ultravioleta. Tryptofan (nazwa skrótowa Trp) – organiczny związek chemiczny z grupy aminokwasów białkowych. Jest obojętny elektrycznie; jego łańcuch boczny oparty jest na szkielecie indolu. Wchodzi w skład białek (białka mleka, białka krwi), należy do aminokwasów niezbędnych (nie może być syntetyzowany w organizmie człowieka i musi być dostarczany z pożywieniem). Zdolność do jego syntezy mają niektóre rośliny i bakterie. Rozpuszczalny w tłuszczach, gorącym alkoholu i mocnych zasadach. Tryptofan jest obok metioniny jednym z dwóch aminokwasów kodowanych zawsze tym samym kodonem – UGG. Tryptophan (symbol Trp or W)is an α-amino acid that is used in the biosynthesis of proteins. Tryptophan contains an α-amino group, an α-carboxylic acid group, and a side chain indole, making it a polar molecule with a non-polar aromatic beta carbon substituent. It is essential in humans, meaning that the body cannot synthesize it and it must be obtained from the diet. Tryptophan is also a precursor to the neurotransmitter serotonin, the hormone melatonin, and vitamin B3. It is encoded by the codon UGG. Tryptophan, abgekürzt Trp oder W, ist in der L-Form (siehe Fischer-Projektion) eine proteinogene α-Aminosäure mit einem aromatischen Indol-Ringsystem. Gemeinsam mit Phenylalanin, Tyrosin und Histidin zählt Tryptophan daher zu den aromatischen Aminosäuren. Es gehört zu den essentiellen Aminosäuren, kann also vom menschlichen Körper nicht gebildet und muss mit der Nahrung zugeführt werden.
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Skeletal formula of (L)-tryptophan
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dbo:abstract
El triptófano (abreviado como Trp o W) (también, triptofano) es un aminoácido esencial en la nutrición humana. Es uno de los 20 aminoácidos incluidos en el código genético (codón UGG). Se clasifica entre los aminoácidos apolares, también llamados hidrófobos. Se caracteriza por una cadena lateral con el grupo indol. Es esencial para promover la liberación del neurotransmisor serotonina, involucrado en la regulación del sueño y el placer. Su punto isoeléctrico se ubica a pH=5.89. La falta de triptófano puede contribuir negativamente a cuadros de ansiedad, insomnio y estrés.[cita requerida] Le tryptophane (abréviations IUPAC-IUBMB : Trp et W) est un acide α-aminé dont l'énantiomère L est l'un des 22 acides aminés protéinogènes et l'un des 9 acides aminés essentiels pour l'humain. Il est encodé sur les ARN messagers par le codon UGG. C'est l'acide aminé protéinogène le plus rare composant uniquement 1,3 % des acides aminés totaux des vertébrés et 1,1% de ceux des protéines. 트립토판(영어: tryptophan)은 인간영양에 필요한 필수 아미노산이다. 트립토판은 유전코드로 암호화된 20여개의 아미노산 중 하나로, 지정 코돈은 UGG이다. 포유류 단백질에서 오직 L형 트립토판만이 등장하지만, 때때로 D형 트립토판도 해안 생명체의 독성 펩티드인 과 같은 자연물질들에서 발견된다. 트립토판의 주목할 만한 구조적 특징은 (indole-)를 포함하고 있다는 점이다. Triptofanoa (Trp) proteinen osagaia den aminoazido esentzialetako bat da, beraz dieta bidez hartu beharrekoa. Azido 2-amino-3-(1H-indol-3-il)propioniko honen formula kimikoa HO2CCH2(NH2)CH2(C8NH6) da eta UGG kodonaren bidez adierazten da. Molekula hidrofobikoa da, hau da, uretan disolbaezina albo katean indol talde bat duelako. Gainera, serotonina neurotransmisorearen askapenerako ezinbestekoa da. Honi esker, antsietatea, insomnioa eta estresa erregulatzen dira. Η τρυπτοφάνη είναι ένα από τα 22 πρωτεϊνογόνα αμινοξέα και ένα (από τα 8) για την ανθρώπινη διατροφή. Κωδικοποιείται στον γενετικό κώδικα με το κωδικόνιο UGG. Μόνο το L-στερεοϊσομερές της τρυπτοφάνης χρησιμοποιείται σε ή σε ένζυμα, αλλά η D-τρυπτοφάνη βρίσκεται περιστασιακά σε πεπτίδια φυσικής παραγωγής (για παράδειγμα θαλάσσιο δηλητηριώδες πεπτίδιο , contryphan). Το χαρακτηριστικό δομικό χαρακτηριστικό της τρυπτοφάνης είναι ότι περιέχει μια λειτουργική ομάδα, στην πλευρική της αλυσίδα. Είναι ένα απαραίτητο αμινοξύ, όπως επιδεικνύεται από τα αυξητικά αποτελέσματα της χορήγησής της σε αρουραίους. Tryptofan (nazwa skrótowa Trp) – organiczny związek chemiczny z grupy aminokwasów białkowych. Jest obojętny elektrycznie; jego łańcuch boczny oparty jest na szkielecie indolu. Wchodzi w skład białek (białka mleka, białka krwi), należy do aminokwasów niezbędnych (nie może być syntetyzowany w organizmie człowieka i musi być dostarczany z pożywieniem). Zdolność do jego syntezy mają niektóre rośliny i bakterie. Przemiany tryptofanu są źródłem istotnych związków, m.in. tryptaminy, serotoniny (w organizmie zachodzi przemiana Trp → 5-hydroksytryptofan → serotonina), melatoniny, niacyny i roślinnych hormonów wzrostu (auksyn). Rozpuszczalny w tłuszczach, gorącym alkoholu i mocnych zasadach. Tryptofan jest obok metioniny jednym z dwóch aminokwasów kodowanych zawsze tym samym kodonem – UGG. Triptofan (bahasa Inggris: tryptophan, TRP, W) merupakan satu dari 20 asam amino penyusun protein yang bersifat esensial bagi manusia. Bentuk yang umum pada mamalia adalah, seperti asam amino lainnya, L-triptofan. Meskipun demikian D-triptofan ditemukan pula di alam (contohnya adalah pada bisa ular laut ). التريبتوفان أو التربتوفان هو حمض أميني ضروري،أي لا يمكن تخليقه في الجسم بل يجب الحصول عليه من مصدر خارجي كالغذاء، يمتلك سلسة جانبية هي أكبر سلسلة جانبية عطرية (أروماتية) في الأحماض الأمينية ألفا وهذه السلسلة مكونة من حلقتين إحداهما سداسية والأخرى خماسية يشكل النيتروجين أحد أركانها وهو يصنف من الأحماض الأمينية الكبيرة الكارهة للماء (large hydrophoboic amino acids). وللحمض الصيغة الجزيئية C11H12N2O2 .وللحمض دور تكوين الناقل العصبي المهيج سيروتونين عن طريق نزع مجموعة الكاربوكسيل من التربتوفان. トリプトファン (Tryptophan) はアミノ酸の一種である。ヒトにおける9つの必須アミノ酸の内の1つ。 系統名 2-アミノ-3-(インドリル)プロピオン酸。略号はTrpまたはW。 側鎖にインドール環を持ち、芳香族アミノ酸に分類される。蛋白質構成アミノ酸である。糖原性・ケト原性の両方を持つ。多くのタンパク質中に見出されるが、含量は低い。ナイアシンの体内活性物質であるNAD(H)をはじめ、セロトニン・メラトニンといったホルモン、キヌレニン等生体色素、また植物において重要な成長ホルモンであるインドール酢酸の前駆体、インドールアルカロイド(トリプタミン類)などの前駆体として重要である。 Tryptofan (förkortas Trp eller W) är inom biokemi en av de 20 aminosyror som är byggstenar i proteiner. Den tillhör gruppen opolära, hydrofoba aminosyror och är en av de essentiella aminosyrorna, som kroppen inte själv kan tillverka, och som därför måste tillföras i födan. Bara L-stereoisomeren av tryptofan används som strukturellt enzymprotein; D-stereoisomeren är vanligast förekommande i naturligt producerade peptider. Det utmärkande strukturella kännetecknet för tryptofan är att den har en indol-grupp. Den är en av de två aminosyror som motsvaras av endast ett kodon (UGG) i den genetiska koden. Tryptofan är också ett utgångsämne (substrat) vid kroppens tillverkning av serotonin och melatonin som har betydelse för sömn, avslappning och stämningsläge och även blodkärlssammandragande. Tryptofan kan även användas för bildning av niacin. I mat finns tryptofan i proteinrik föda, främst i kött och hårdost men även i mjölk och spannmål (se havregryn). Vissa nötter och frön har en hög halt av tryptofan; särskilt kan nämnas pumpafrökärnor och chiafrön. Kynurenin bildas i omsättningen av tryptofan. Hos växter, svampar och bakterier är tryptofan substrat för biosyntesen av indolättiksyra. Tryptophan (symbol Trp or W)is an α-amino acid that is used in the biosynthesis of proteins. Tryptophan contains an α-amino group, an α-carboxylic acid group, and a side chain indole, making it a polar molecule with a non-polar aromatic beta carbon substituent. It is essential in humans, meaning that the body cannot synthesize it and it must be obtained from the diet. Tryptophan is also a precursor to the neurotransmitter serotonin, the hormone melatonin, and vitamin B3. It is encoded by the codon UGG. Like other amino acids, tryptophan is a zwitterion at physiological pH where the amino group is protonated (–NH+3; pKa = 9.39) and the carboxylic acid is deprotonated ( –COO−; pKa = 2.38). Humans and many animals cannot synthesize tryptophan: they need to obtain it through their diet, making it an essential amino acid. Tryptofan (zkratky: Trp, W) je jednou z 20 proteinogenních aminokyselin. Řadí se k , aromatickým aminokyselinám (resp. k aminokyselinám s nepolárním, aromatickým postranním řetězcem). Jeho strukturní základ tvoří indol. Patří mezi esenciální aminokyseliny, lidské tělo ho neumí syntetizovat. Koduje ho kodon UGG, jedná se o vzácnější aminokyselinu s průměrným zastoupením v proteinech 1,4 %. Tryptophan, abgekürzt Trp oder W, ist in der L-Form (siehe Fischer-Projektion) eine proteinogene α-Aminosäure mit einem aromatischen Indol-Ringsystem. Gemeinsam mit Phenylalanin, Tyrosin und Histidin zählt Tryptophan daher zu den aromatischen Aminosäuren. Es gehört zu den essentiellen Aminosäuren, kann also vom menschlichen Körper nicht gebildet und muss mit der Nahrung zugeführt werden. Tryptofaan (afgekort als Trp of W) is een groot, hydrofoob aminozuur dat zich kenmerkt door zijn indool-bevattende zijketen. Het is een van de ruim twintig natuurlijk voorkomende aminozuren die voor de eiwitsynthese worden gebruikt. Tryptofaan behoort tot de categorie essentieel aminozuur, wat inhoudt dat het niet kan worden gevormd door het menselijk lichaam en dus via de voeding moet worden opgenomen. Tryptofaan is een uitgangsstof voor de aanmaak van veel belangrijke indoolderivaten zoals de neurotransmitter serotonine, het hormoon melatonine en het vitamine nicotinezuur. Deze stoffen hebben invloed op stemming, zelfvertrouwen, slaap, emotie, seksuele activiteit en eetlust. Omdat tryptofaan in relatief lage concentraties in het lichaam voorkomt, is het in mindere mate beschikbaar en men vermoedt dat het een snelheidsbepalende rol speelt tijdens de eiwitsynthese. 色氨酸(英語:Tryptophan, 縮寫Trp或W)是22個標準氨基酸之一,人體不能合成的必需氨基酸,因此它須從食物中汲取。它的標準遺傳密碼的密碼子編碼為UGG,只有L-立體異構體色氨酸有構造或酶活蛋白質的作用,R-立體異構體則偶爾在自然產生的肽中發現。色氨酸的明顯結構式特徵是,它含有吲哚官能團。它是血清素(亦称“5-羟色胺”)的前體,血清素是重要的神經递质。還能合成菸鹼素。 Триптофа́н (β-(β-індоліл)-α-амінопропіонова кислота) — незамінна амінокислота. Кодується тільки одним кодоном — UGG. L-стереоізомер входить до складу гамаглобулінів, фібриногену, казеїну та інших білків. Триптофан є провітаміном. Триптофа́н (β-(β-индолил)-α-аминопропионовая кислота, сокр.: Три, Трп, Trp, W) — ароматическая альфа-аминокислота. Существует в двух оптически изомерных формах, L и D, и в виде рацемата (рацемической смеси) (DL). L-триптофан является протеиногенной аминокислотой и входит в состав белков всех известных живых организмов. Относится к ряду гидрофобных аминокислот, поскольку содержит ароматическое ядро индола. Участвует в гидрофобных и стэкинг-взаимодействиях. Triptofano (α-Amino-β-Indolilpropionacido, IUPAC: 2-amino-3-(1H-indol-3-il)-propionacido) (simbolo Trp aŭ W) estas aminoacido kun aromata strukturo sur la flanka ĉeno. Ĝi apartenas al esencaj aminoacidoj, t.e. ĝin ne povas produkti la homa korpo kaj pro tio necesas akiri ĝin per manĝaĵo . Ĝi apartenas al la 20 proteinaj aminoacidoj, el kiuj la proteinoj de la homa korpo konstruiĝas. Plantoj kaj mikroorganismoj povas ĝin produkti. El triptòfan (abreviat Trp o W) és un aminoàcid essencial en la nutrició humana. És un dels 20 aminoàcids inclosos en el codi genètic (codó UGG). És considerat un aminoàcid no polar i hidrofòbic: * Fórmula molecular: C11H12N₂O₂ * Massa molecular: 204,23 * Punt isoelèctric: pH = 5,89 * Nombre CAS: 73-22-3 Hopkins i Cole van descobrir el triptòfan a principis dels anys 1900 després d'aïllar-lo de la proteïna de la caseïna, i Ellinger i Flamand van determinar la seva estructura molecular poc temps després. El triptòfan és també un precursor de la serotonina, un neurotransmissor de la melatonina, una hormona neural. La molècula del triptòfan és quiral, per la qual cosa el triptòfan racèmic és una barreja equimolar dels enantiòmers òptics L(-)-triptòfan i D(+)-triptòfan (el signe entre parèntesis indica si és levogir o dextrogir). El primer d'aquests estereoisòmers és el que forma part de les proteïnes i, a més, mostra activitat farmacològica rellevant. El triptòfan és un dels vuit aminoàcids essencials, aquells que no es poden sintetitzar en el cos humà i han de ser subministrats per la dieta. Algunes fonts comunes de triptòfan són la civada, la banana, les prunes seques, la llet, la tonyina, el formatge, el pa, el pollastre, el gall dindi, els cacauets i la xocolata. O triptofano é um aminoácido utilizado na biossíntese de proteínas, sendo codificado pelo codão UGG. Ele contém, como todo aminoácido, um grupo amino (básico) e um grupo carboxilo (ácido); sua cadeia lateral consiste num indol, o que faz dele um aminoácido aromático e apolar. No pH fisiológico, o triptofano é um zwitterion: o grupo amino (pKa = 9.39) encontra-se protonado (–NH3+) e o grupo carboxila (pKa = 2.38) encontra-se deprotonado ( –COO−). Absorve luz ultravioleta. Em seres humanos, este aminoácido é essencial, o que significa que não pode ser sintetizado: precisa compor a dieta. Além disso, ele é o precursor da serotonina e da melatonina. Il triptofano è un amminoacido poco polare, il suo gruppo laterale è un indolile. È alla base del gruppo di composti delle triptamine. È una molecola chirale. L'enantiomero L è uno dei 20 amminoacidi ordinari. Poiché l'organismo umano non è in grado di sintetizzarlo, deve essere ricavato dagli alimenti e pertanto è classificato tra gli amminoacidi essenziali. Oltre a partecipare alla costituzione delle proteine dell'organismo, interviene in numerose reazioni chimiche, in particolare nella sintesi di serotonina e di acido nicotinico. Come altri amminoacidi, il triptofano si trova in forma zwitterionica al pH fisiologico in cui il gruppo amminico è protonato (–NH3+; pKa = 9,41) e il gruppo carbossilico è deprotonato (–COO−; pKa = 2,46). Il triptofano presenta inoltre delle spiccate proprietà di fluorescenza, con un assorbimento massimo a 280 nm e un picco di emissione solvatocromico che può cadere dai 300 ai 350 nm circa a seconda della polarità del suo intorno.
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Tabernaemontanine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Tadalafil
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:PRPSAP2
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Shikimate_dehydrogenase
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Salkowski's_test
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Diethyltryptamine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:CD86
dbo:wikiPageWikiLink
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Subject Item
dbr:CD98
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Phenylalanine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Phosphoribosyl_pyrophosphate
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:IAEDANS
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indican
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indigo_dye
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indole-3-acetic_acid
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indole-3-carbaldehyde
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indolizidine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indolyl-3-acryloylglycine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Indoxyl_sulfate
dbo:wikiPageWikiLink
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Subject Item
dbr:Kitten
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Kynurenine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Kynurenine_3-monooxygenase
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Methionine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Buchnera_aphidicola
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Neuroendocrine_tumor
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dbr:Tryptophan
Subject Item
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dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:Oligopeptide_P11-4
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
dbr:Scytonemin
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dbr:Tryptophan
Subject Item
dbr:Serine
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbr:Tryptophan
Subject Item
dbr:Shikimic_acid
dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
dbr:UGG
dbo:wikiPageWikiLink
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Subject Item
dbr:Very_short_patch_repair
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
dbr:Toxoplasma_gondii
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dbr:Tryptophan
Subject Item
dbr:WWE_protein_domain
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
dbr:Tryptophan
Subject Item
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Subject Item
dbr:IRF5
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:MYH6
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Subject Item
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Subject Item
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Subject Item
dbr:Substituted_tryptamine
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:SERPINA2
dbo:wikiPageWikiLink
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:TPH1
dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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dbo:wikiPageWikiLink
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:Tryptophan_2-C-methyltransferase
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
dbr:(2S)-2-amino-3-(1H-indol-3-yl)propanoic_acid
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
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Subject Item
wikipedia-en:Tryptophan
foaf:primaryTopic
dbr:Tryptophan