Q8TCJ2

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession STT3B_HUMAN; Q8TCJ2;
Entrez ID 201595
GenBank Protein ID
GenBank Nucleotide ID
Protein Name Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B (Oligosaccharyl transferase subunit STT3B) (STT3-B) (EC 2.4.99.18) (Source of immunodominant MHC-associated peptides homolog)
Gene Name STT3B; SIMP
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionCatalytic subunit of the N-oligosaccharyl transferase (OST) complex which catalyzes the transfer of a high mannose oligosaccharide from a lipid-linked oligosaccharide donor to an asparagine residue within an Asn-X-Ser/Thr consensus motif in nascent polypeptide chains. N-glycosylation occurs cotranslationally and the complex associates with the Sec61 complex at the channel-forming translocon complex that mediates protein translocation across the endoplasmic reticulum (ER). STT3B is present in a small subset of OST complexes and mediates both cot(view all)
Sequence
(Fasta)
MAEPSAPESK HKSSLNSSPW SGLMALGNSR HGHHGPGAQC AHKAAGGAAP PKPAPAGLSG 60
GLSQPAGWQS LLSFTILFLA WLAGFSSRLF AVIRFESIIH EFDPWFNYRS THHLASHGFY 120
EFLNWFDERA WYPLGRIVGG TVYPGLMITA GLIHWILNTL NITVHIRDVC VFLAPTFSGL 180
TSISTFLLTR ELWNQGAGLL AACFIAIVPG YISRSVAGSF DNEGIAIFAL QFTYYLWVKS 240
VKTGSVFWTM CCCLSYFYMV SAWGGYVFII NLIPLHVFVL LLMQRYSKRV YIAYSTFYIV 300
GLILSMQIPF VGFQPIRTSE HMAAAGVFAL LQAYAFLQYL RDRLTKQEFQ TLFFLGVSLA 360
AGAVFLSVIY LTYTGYIAPW SGRFYSLWDT GYAKIHIPII ASVSEHQPTT WVSFFFDLHI 420
LVCTFPAGLW FCIKNINDER VFVALYAISA VYFAGVMVRL MLTLTPVVCM LSAIAFSNVF 480
EHYLGDDMKR ENPPVEDSSD EDDKRNQGNL YDKAGKVRKH ATEQEKTEEG LGPNIKSIVT 540
MLMLMLLMMF AVHCTWVTSN AYSSPSVVLA SYNHDGTRNI LDDFREAYFW LRQNTDEHAR 600
VMSWWDYGYQ IAGMANRTTL VDNNTWNNSH IALVGKAMSS NETAAYKIMR TLDVDYVLVI 660
FGGVIGYSGD DINKFLWMVR IAEGEHPKDI RESDYFTPQG EFRVDKAGSP TLLNCLMYKM 720
SYYRFGEMQL DFRTPPGFDR TRNAEIGNKD IKFKHLEEAF TSEHWLVRIY KVKAPDNRET 780
LDHKPRVTNI FPKQKYLSKK TTKRKRGYIK NKLVFKKGKK ISKKTV 827

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1GlycosylationCongenital disordersC23842455; 3888133
[Reference]: the STT3B mutation only slightly affects its glycosylation. Additional cases of STT3B-CDG may be missed by transferrin analysis and will require exome or genome sequencing.

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 1)
OMIM:615597 ; CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix
DisGeNet (Curated)
(count: 1)
C3810067; CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 16)
(view all)
13        APESKHKSSLNSSPW     dbPAF
14        PESKHKSSLNSSPWS     dbPAF
17        KHKSSLNSSPWSGLM     dbPAF
18        HKSSLNSSPWSGLMA     dbPAF
21        SLNSSPWSGLMALGN     dbPAF
29        GLMALGNSRHGHHGP     dbPAF
Acetylation
(count: 3)
10        EPSAPESKHKSSLNS     PLMD
513       NQGNLYDKAGKVRKH     PLMD
754       GNKDIKFKHLEEAFT     PLMD
Ubiquitination
(count: 18)
(view all)
10        EPSAPESKHKSSLNS     PLMD
12        SAPESKHKSSLNSSP     PLMD
504       DSSDEDDKRNQGNLY     PLMD
513       NQGNLYDKAGKVRKH     PLMD
516       NLYDKAGKVRKHATE     PLMD
526       KHATEQEKTEEGLGP     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource