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Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (MAN1B1)

Homo sapiens — UniProt Q9UKM7

Gene: MAN1B1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (MAN1B1) is a protein from Homo sapiens identified by UniProt accession Q9UKM7, 699 residues long. MolForge cross-references it against 0 known binders and 47 disease associations.

  • UniProt accession: Q9UKM7; gene symbol MAN1B1.
  • Organism: Homo sapiens.
  • Length: 699 amino acids.
  • Top disease associations (Open Targets): Rafiq syndrome, autosomal recessive non-syndromic intellectual disability and X-linked non-syndromic intellectual disability.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameEndoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase
UniProt accessionQ9UKM7
GeneMAN1B1
OrganismHomo sapiens
Length699 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (47)

Diseases linked to this target (Open Targets).

  • Rafiq syndrome · score 0.74
  • autosomal recessive non-syndromic intellectual disability · score 0.58
  • X-linked non-syndromic intellectual disability · score 0.53
  • genetic disorder · score 0.50
  • MAN1B1-congenital disorder of glycosylation · score 0.46
  • COVID-19 · score 0.37
  • Global developmental delay · score 0.34
  • blood protein measurement · score 0.25
  • neurodegenerative disease · score 0.22
  • platelet count · score 0.15

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9UKM7-F1alphafoldPREDICTED80.81—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9UKM7.

Amino-acid sequence (699 residues)

MAACEGRRSG ALGSSQSDFL TPPVGGAPWA VATTVVMYPP PPPPPHRDFI SVTLSFGENY DNSKSWRRRS CWRKWKQLSR LQRNMILFLL AFLLFCGLLF YINLADHWKA LAFRLEEEQK MRPEIAGLKP ANPPVLPAPQ KADTDPENLP EISSQKTQRH IQRGPPHLQI RPPSQDLKDG TQEEATKRQE APVDPRPEGD PQRTVISWRG AVIEPEQGTE LPSRRAEVPT KPPLPPARTQ GTPVHLNYRQ KGVIDVFLHA WKGYRKFAWG HDELKPVSRS FSEWFGLGLT LIDALDTMWI LGLRKEFEEA RKWVSKKLHF EKDVDVNLFE STIRILGGLL SAYHLSGDSL FLRKAEDFGN RLMPAFRTPS KIPYSDVNIG TGVAHPPRWT SDSTVAEVTS IQLEFRELSR LTGDKKFQEA VEKVTQHIHG LSGKKDGLVP MFINTHSGLF THLGVFTLGA RADSYYEYLL KQWIQGGKQE TQLLEDYVEA IEGVRTHLLR HSEPSKLTFV GELAHGRFSA KMDHLVCFLP GTLALGVYHG LPASHMELAQ ELMETCYQMN RQMETGLSPE IVHFNLYPQP GRRDVEVKPA DRHNLLRPET VESLFYLYRV TGDRKYQDWG WEILQSFSRF TRVPSGGYSS INNVQDPQKP EPRDKMESFF LGETLKYLFL LFSDDPNLLS LDAYVFNTEA HPLPIWTPA

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with MAN1B1?

The strongest Open Targets associations for MAN1B1 are Rafiq syndrome, autosomal recessive non-syndromic intellectual disability, X-linked non-syndromic intellectual disability, genetic disorder and MAN1B1-congenital disorder of glycosylation.

How long is the MAN1B1 protein?

The Homo sapiens MAN1B1 protein (UniProt Q9UKM7) is 699 amino acids long.

Browse: Targets: M · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9UKM7
GeneMAN1B1
OrganismHomo sapiens
Length699
Binders0
Diseases47
View on UniProt