Magnesium transporter NIPA1 (NIPA1)

Homo sapiens — UniProt Q7RTP0

Gene: NIPA1Homo sapiensSwissProt reviewed

About Magnesium transporter NIPA1

Magnesium transporter NIPA1 (NIPA1) is a protein from Homo sapiens identified by UniProt accession Q7RTP0, 329 residues long. MolForge cross-references it against 0 known binders and 135 disease associations.

Target properties

Protein nameMagnesium transporter NIPA1
UniProt accessionQ7RTP0
GeneNIPA1
OrganismHomo sapiens
Length329 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (135)

Diseases linked to this target (Open Targets).

  • Autosomal dominant spastic paraplegia type 6 · score 0.75
  • hereditary spastic paraplegia 6 · score 0.74
  • hereditary spastic paraplegia · score 0.44
  • Spastic paraplegia · score 0.37
  • visual perception measurement · score 0.23
  • amyotrophic lateral sclerosis · score 0.19
  • genetic disorder · score 0.19
  • autosomal dominant complex spastic paraplegia · score 0.18
  • early-onset non-syndromic cataract · score 0.09
  • isolated ectopia lentis · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q7RTP0-F1alphafoldPREDICTED85.29—

Amino-acid sequence (329 residues)

MGTAAAAAAA AAAAAAGEGA RSPSPAAVSL GLGVAVVSSL VNGSTFVLQK KGIVRAKRRG TSYLTDIVWW AGTIAMAVGQ IGNFLAYTAV PTVLVTPLGA LGVPFGSILA SYLLKEKLNI LGKLGCLLSC AGSVVLIIHS PKSESVTTQA ELEEKLTNPV FVGYLCIVLL MLLLLIFWIA PAHGPTNIMV YISICSLLGS FTVPSTKGIG LAAQDILHNN PSSQRALCLC LVLLAVLGCS IIVQFRYINK ALECFDSSVF GAIYYVVFTT LVLLASAILF REWSNVGLVD FLGMACGFTT VSVGIVLIQV FKEFNFNLGE MNKSNMKTD

Explore Magnesium transporter NIPA1 with MolForge

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Quick facts

UniProtQ7RTP0
GeneNIPA1
OrganismHomo sapiens
Length329
Binders0
Diseases135
View on UniProt