Serin

Serin
Rumus rangka Rumus rangka L-serin	Serin dina pH pisiologis L-serin zwitterion
Modél bal jeung tongkat	Modél ngeusi rohang
Wasta
	Wasta IUPAC Serine
	Wasta lian Asam 2-amino-3-hidroxipropanoat
Pananda
Nomer CAS	L: 56-45-1 ; D/L: 302-84-1 ; D: 312-84-5 ;
Modél 3D (JSmol)	L: Gambar interaktif; D/L Zwitterion: Gambar interaktif;
ChEBI	L: CHEBI:17115 ;
ChEMBL	L: ChEMBL11298 ;
ChemSpider	L: 5736 ; D/L: 597 ; D: 64231 ;
DrugBank	L: DB00133 ;
ECHA InfoCard	100.000.250
Nomer EC	206-130-6
IUPHAR/BPS	L: 726;
KEGG	L: C00065; D: C00740;
PubChem CID	L: 5951; D/L: 617; D: 71077;
UNII	L: 452VLY9402 ; D/L: 00PAR1C66F ; D: 1K77H2Z9B1 ;
CompTox Dashboard (EPA)	L: DTXSID60883230 ;
	InChI InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m0/s1 Key: MTCFGRXMJLQNBG-REOHCLBHSA-N ; D/L: Key: MTCFGRXMJLQNBG-UHFFFAOYSA-N; D: Key: MTCFGRXMJLQNBG-UWTATZPHSA-N;
	SMILES L: C([C@@H](C(=O)O)N)O; D/L Zwitterion: C([C@@H](C(=O)[O-])[NH3+])O;
Sipat
Rumus kimia	C3H7NO3
Massa molar	105093 g·mol−1
Panampilan	kristal atawa tipung bodas
Dénsitas	1.603 g/cm3 (22 °C)
Titik lebur	246 °C (475 °F; 519 K) decomposes
Kelarutan dina cai	soluble
Kaasaman (pKa)	2.21 (carboxyl), 9.15 (amino)
	Iwal disebutkeun séjén, data nu dipidangkeun keur matéri dina kaayaan baku (dina 25 °C, 100 kPa).
	Rujukan kotak info

Serin atawa serina (lambang Ser atawa S)^[3]^[4] nyaéta asam α-amino anu dipaké dina biosintésis protéin anu ngandung hiji gugus α-amino (wangun kaprotonan −NH+3 dina kaayaan biologis), hiji gugus karboxil (wangun deprotonasi −COO⁻ dina kaayaan biologis), jeung hiji ranté gigir gugus hidroximétil, ku kituna kagolong asam amino polar. Serin bisa disintésis sacara pisiologis, jadi kaasup asam amino non-ésénsial. Serin dikode ku kodon UCU, UCC, UCA, UCG, AGU, jeung AGC.

Baca ogé édit

Rujukan édit

↑ Dawson, R.M.C., et al., Data for Biochemical Research, Oxford, Clarendon Press, 1959.
↑ Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. C-512. ISBN 0-8493-0462-8.
↑ "Nomenclature and Symbolism for Amino Acids and Peptides". IUPAC-IUB Joint Commission on Biochemical Nomenclature. 1983. Diarsipkan dari versi asli tanggal 9 October 2008. Diakses tanggal 5 March 2018.
↑ Citakan:IUPAC-IUB amino acids 1983.

Tutumbu kaluar édit

Serine MS Spectrum

Citakan:Neurotransmitter

[1] Dawson, R.M.C., et al., Data for Biochemical Research, Oxford, Clarendon Press, 1959.

[2] Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. C-512. ISBN 0-8493-0462-8.

[3] "Nomenclature and Symbolism for Amino Acids and Peptides". IUPAC-IUB Joint Commission on Biochemical Nomenclature. 1983. Diarsipkan dari versi asli tanggal 9 October 2008. Diakses tanggal 5 March 2018.

[4] Citakan:IUPAC-IUB amino acids 1983.

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