Mannose-binding protein C

Summary
UniProt ID
P11226
Gene Symbol
  • MBL2
  • COLEC1
  • MBL
Organism
Homo sapiens (human)
External Links
GlyGen
P11226
PubChem
P11226
The Human Metabolome Database
HMDBP02647
Annotation
Keyword
  • 3D-structure
  • Calcium
  • Coiled coil
  • Collagen
  • Complement activation lectin pathway
  • Complement pathway
  • Direct protein sequencing
  • Disulfide bond
  • Hydroxylation
  • Mannose-binding
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
Gene Ontology (GO)
Sequence
MSLFPSLPLLLLSMVAASYSETVTCEDAQKTCPAVIACSSPGINGFPGKDGRDGTKGEKGEPGQGLRGLQGPPGKLGPPGNPGPSGSPGPKGQKGDPGKSPDGDSSLAASERKALQTEMARIKKWLTFSLGKQVGNKFFLTNGEIMTFEKVKALCVKFQASVATPRNAAENGAIQNLIKEEAFLGITDEKTEGQFVDLTGNRLTYTNWNEGEPNNAGSDEDCVLLLKNGQWNDVPCSTSHLAVCEFPI
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
171
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Disease
Displaying entries 61 - 70 of 444 in total
DO ID Disease Name Source
DOID:0110275 autosomal recessive limb-girdle muscular dystrophy type 2A
DOID:0110276 autosomal recessive limb-girdle muscular dystrophy type 2B
DOID:0110277 autosomal recessive limb-girdle muscular dystrophy type 2C
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E
DOID:0110280 autosomal recessive limb-girdle muscular dystrophy type 2F
DOID:0110281 autosomal recessive limb-girdle muscular dystrophy type 2G
DOID:0110282 autosomal recessive limb-girdle muscular dystrophy type 2H
DOID:0110283 autosomal recessive limb-girdle muscular dystrophy type 2J
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L

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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: August 19, 2024