Fibrinogen alpha chain [Cleaved into: Fibrinopeptide A; Fibrinogen alpha chain]

Summary
UniProt ID
P02671
Gene Symbol
FGA
Gene ID
2243
Organism
Homo sapiens (human)
GlycoProtDB
GPDB0011303
GlyConnect
GlyGen
P02671
PubChem
P02671
The Human Metabolome Database
HMDBP13512
RaftProt
P02671
Re-Glyco
P02671
Annotation
Keyword
3D-structure Adaptive immunity Alternative splicing Amyloid Amyloidosis Blood coagulation Calcium Coiled coil Direct protein sequencing Disease variant Disulfide bond Glycoprotein Hydroxylation Innate immunity Isopeptide bond Metal-binding Phosphoprotein Proteomics identification Reference proteome Secreted Signal
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Sequence
MFSMRIVCLVLSVVGTAWTADSGEGDFLAEGGGVRGPRVVERHQSACKDSDWPFCSDEDWNYKCPSGCRMKGLIDEVNQDFTNRINKLKNSLFEYQKNNKDSHSLTTNIMEILRGDFSSANNRDNTYNRVSEDLRSRIEVLKRKVIEKVQHIQLLQKNVRAQLVDMKRLEVDIDIKIRSCRGSCSRALAREVDLKDYEDQQKQLEQVIAKDLLPSRDRQHLPLIKMKPVPDLVPGNFKSQLQKVPPEWKALTDMPQMRMELERPGGNEITRGGSTSYGTGSETESPRNPSSAGSWNSGSSGPGSTGNRNPGSSGTGGTATWKPGSSGPGSTGSWNSGSSGTGSTGNQNPGSPRPGSTGTWNPGSSERGSAGHWTSESSVSGSTGQWHSESGSFRPDSPGSGNARPNNPDWGTFEEVSGNVSPGTRREYHTEKLVTSKGDKELRTGKEKVTSGSTTTTRRSCSKTVTKTVIGPDGHKEVTKEVVTSEDGSDCPEAMDLGTLSGIGTLDGFRHRHPDEAAFFDTASTGKTFPGFFSPMLGEFVSETESRGSESGIFTNTKESSSHHPGIAEFPSRGKSSSYSKQFTSSTSYNRGDSTFESKSYKMADEAGSEADHEGTHSTKRGHAKSRPVRDCDDVLQTHPSGTQSGIFNIKLPGSSKIFSVYCDQETSLGGWLLIQQRMDGSLNFNRTWQDYKRGFGSLNDEGEGEFWLGNDYLHLLTQRGSVLRVELEDWAGNEAYAEYHFRVGSEAEGYALQVSSYEGTAGDALIEGSVEEGAEYTSHNNMQFSTFDRDADQWEENCAEVYGGGWWYNNCQAANLNGIYYPGGSYDPRNNSPYEIENGVVWVSFRGADYSLRAVRMKIRPLVTQ
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying entries 1 - 10 of 22 in total
Pathway Name Organism
Aggregated β-amyloid interacts with fibrinogen Homo sapiens
Amyloid fiber formation Homo sapiens
ER-Phagosome pathway Homo sapiens
Fibrin formation Homo sapiens
GRB2:SOS provides linkage to MAPK signaling for Integrins Homo sapiens
IRAK4 deficiency (TLR2/4) Homo sapiens
Integrin cell surface interactions Homo sapiens
Integrin signaling Homo sapiens
MAP2K and MAPK activation Homo sapiens
MyD88 deficiency (TLR2/4) Homo sapiens
Disease
Displaying all 4 entries
DO ID Disease Name Source
DOID:2236 congenital afibrinogenemia
DOID:0112313 brain small vessel disease
DOID:2452 thrombophilia
DOID:0050636 hereditary systemic amyloidosis 2

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026