{"metadata":{"accession":"PF05653","entry_id":null,"type":"family","go_terms":null,"source_database":"pfam","member_databases":null,"integrated":"IPR008521","hierarchy":null,"name":{"name":"Magnesium transporter NIPA","short":"Mg_trans_NIPA"},"description":[{"text":"<p>NIPA (nonimprinted in Prader-Willi/Angelman syndrome) is a family of integral membrane proteins which function as magnesium transporters [[cite:PUB00057506],[cite:PUB00057507]].</p>","llm":false,"checked":false,"updated":false}],"wikipedia":null,"literature":{"PUB00057506":{"PMID":17166836,"ISBN":null,"volume":"282","issue":"11","year":2007,"title":"NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter.","URL":null,"raw_pages":"8060-8","medline_journal":"J Biol Chem","ISO_journal":"J. Biol. Chem.","authors":["Goytain A","Hines RM","El-Husseini A","Quamme GA."],"DOI_URL":"http://dx.doi.org/10.1074/jbc.M610314200"},"PUB00057507":{"PMID":18667602,"ISBN":null,"volume":"295","issue":"4","year":2008,"title":"Functional characterization of NIPA2, a selective Mg2+ transporter.","URL":null,"raw_pages":"C944-53","medline_journal":"Am J Physiol Cell Physiol","ISO_journal":"Am. J. Physiol., Cell Physiol.","authors":["Goytain A","Hines RM","Quamme GA."],"DOI_URL":"http://dx.doi.org/10.1152/ajpcell.00091.2008"}},"set_info":{"accession":"CL0184","name":"DMT"},"overlaps_with":null,"counters":{"subfamilies":0,"domain_architectures":227,"interactions":0,"matches":22921,"pathways":0,"proteins":21330,"proteomes":4521,"sets":1,"structural_models":{"alphafold":17719},"structures":0,"taxa":10148},"entry_annotations":{"hmm":0,"logo":0,"alignment:seed":5,"alignment:full":17565},"cross_references":{},"is_llm":false,"is_reviewed_llm":false,"is_updated_llm":false,"representative_structure":null}}