about
UDP-glucose glycoprotein glucosyltransferase 1Lectin, mannose binding 1Magnesium transporter 1Beta-1,4-N-acetyl-galactosaminyltransferase 2Valosin containing proteinDefender against cell death 1UDP-glucose glycoprotein glucosyltransferase 2Fucosyltransferase 8Ubiquitin conjugating enzyme E2 G2Multiple coagulation factor deficiency 2, ER cargo receptor complex subunitALG8 alpha-1,3-glucosyltransferaseDolichyl-phosphate mannosyltransferase subunit 1, catalyticDolichyl-phosphate mannosyltransferase subunit 3, regulatoryOligosaccharyltransferase complex non-catalytic subunitNudix hydrolase 14Chromosome 20 open reading frame 173STT3 oligosaccharyltransferase complex catalytic subunit AAlpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferaseAlpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferaseOligosaccharyltransferase complex subunit 4, non-catalyticDolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunitRibophorin IRibophorin IISTT3 oligosaccharyltransferase complex catalytic subunit BAsialoglycoprotein receptor 1Asialoglycoprotein receptor 2Dolichyl-phosphate mannosyltransferase subunit 2, regulatoryUbiquitin conjugating enzyme E2 J1ST6 beta-galactoside alpha-2,6-sialyltransferase 1ST3 beta-galactoside alpha-2,3-sialyltransferase 3ST6 beta-galactoside alpha-2,6-sialyltransferase 2ST3 beta-galactoside alpha-2,3-sialyltransferase 1ST3 beta-galactoside alpha-2,3-sialyltransferase 4ST3 beta-galactoside alpha-2,3-sialyltransferase 2ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2
P682
Ribophorin I acts as a substrate-specific facilitator of N-glycosylationThe human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant proteinMutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain developmentOxidoreductase activity is necessary for N-glycosylation of cysteine-proximal acceptor sites in glycoproteinsOST4 is a subunit of the mammalian oligosaccharyltransferase required for efficient N-glycosylationMammalian cells lacking either the cotranslational or posttranslocational oligosaccharyltransferase complex display substrate-dependent defects in asparagine linked glycosylation
P921
Q21102408-82B81AA4-7808-4CD5-A29F-780D3B98B667Q21103045-8784BDA7-55DE-4B48-847C-915591EFBD11Q21107967-7A3E6144-72C1-4DC5-BD5E-FCFEEAA70251Q21107967-7FEC53D1-9967-46E7-8C7B-1327E9A71E34Q21107967-E2FAEAF7-D8B6-40EF-A432-428F6F0C37ADQ21108269-CA54FC11-F807-447E-B3D9-EF8FA87282B8Q21109279-DCB58C4C-A8F0-4794-A807-09A60EC712BFQ21110825-3FB319FC-3AF1-4569-9043-54CEB0EB7098Q21110825-52DA5FC5-4B4F-4EAA-ACAC-F23B8723C747Q21111588-8467192F-DDA6-463C-A332-40E5EB0E8409Q21112469-1C0FD693-EB03-4DBC-A706-D3F7377DEAC5Q21112620-97495E56-926A-41DD-8883-13F2E7080612Q21113638-84F1A2D2-5B66-4A80-B053-859D299C960FQ21113858-8B571A38-5B02-463D-91D9-3DC557D91C4FQ21114290-0F520876-4E2A-44DE-A2A4-4EFD69B300EEQ21114311-0B4F064A-4B65-4260-A314-D90660E08304Q21115854-E0883EBA-8A14-4E76-9B41-17E166F98E1CQ21116642-6921493C-0CF8-4F58-AE9B-8EAD513CF0E5Q21117381-2E497AEA-FFEF-48BB-A469-74D91D2F0DB3Q21119173-2E159FC5-A2D1-4735-8CDD-9505AC76D938Q21119173-F26CA0F0-7E63-4C4F-9DB1-65D3046994FBQ21119441-9EB10042-4D43-4938-9AAE-C03CB7091C65Q21119445-3A4B0F50-C7F0-4B9B-811B-77CA838EE171Q21119445-3D01334E-8451-4EFC-AC59-FD1B420AFD7BQ21119631-F0A33AF8-4288-4AA7-9905-04689977D13DQ21119632-0FC76323-D1E1-4288-8EDA-554716EDB56BQ21119632-D048600F-5865-4E7C-81B8-B850793A4412Q21119632-D09F2A87-7015-40D9-BB4E-4AC1407E8F82Q21120565-61B6ACDF-B10F-49E3-A6FA-E3F187D39DDCQ21120565-BC4F17B9-D014-4CBE-8A55-D11956BC9E7DQ21120566-473DF2BD-7B03-4B24-AD24-A9856B8BB6F5Q21120566-EE64773C-FB3F-417A-9C02-67D287CFD4F2Q21126478-3275435F-221A-4593-8176-367C5654AAEEQ21126478-5E145722-1F68-45C0-8E4B-0557D0662AE6Q21130024-36BCCCA4-94F2-483F-A501-E8E372F7FCB2Q21130027-A5352C07-AE8C-4B53-9BBB-11BD51A6CCB7Q21132620-5BDE0A6C-6AE6-4F94-990F-AD8DAE7B2379Q21135863-B569CF4A-7653-4E61-B2C5-034B08441F30Q21136000-B08A4513-AAE8-42FC-A4A6-F0B40A119206Q21136000-DE75974A-C4E9-4DAA-A411-906BE1E4F084
P682
description
The glycosylation of protein v ...... also occur. This modification
@en
biologisch proces
@nl
name
protein N-linked glycosylation via asparagine
@en
type
label
protein N-linked glycosylation via asparagine
@en
altLabel
GO:0018279
@en
protein amino acid N-linked glycosylation via asparagine
@en
prefLabel
protein N-linked glycosylation via asparagine
@en
P2888
P686
GO:0018279