Homo sapiens (human): 285362 Help Entry 285362            CDS       T01001                                  Symbol SUMF1, AAPA3037, FGE, UNQ3037 Name (RefSeq) sulfatase modifying factor 1   KO K13444   formylglycine-generating enzyme [EC:1.8.3.7] Organism hsa  Homo sapiens (human) Pathway hsa04142   Lysosome Disease H00272   Multiple sulfatase deficiency H00423   Sphingolipidosis Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04142 Lysosome     285362 (SUMF1) Enzymes [BR:hsa01000]  1. Oxidoreductases   1.8  Acting on a sulfur group of donors    1.8.3  With oxygen as acceptor     1.8.3.7  formylglycine-generating enzyme      285362 (SUMF1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  FGE-sulfatase Motif Other DBs NCBI-GeneID:  285362 NCBI-ProteinID:  NP_877437 OMIM:  607939 HGNC:  20376 Ensembl:  ENSG00000144455 UniProt:  Q8NBK3 Structure PDB LinkDB All DBs Position 3:complement(4034486..4467269) Genome browser AA seq 374 aa AA seqDB search MAAPALGLVCGRCPELGLVLLLLLLSLLCGAAGSQEAGTGAGAGSLAGSCGCGTPQRPGA HGSSAAAHRYSREANAPGPVPGERQLAHSKMVPIPAGVFTMGTDDPQIKQDGEAPARRVT IDAFYMDAYEVSNTEFEKFVNSTGYLTEAEKFGDSFVFEGMLSEQVKTNIQQAVAAAPWW LPVKGANWRHPEGPDSTILHRPDHPVLHVSWNDAVAYCTWAGKRLPTEAEWEYSCRGGLH NRLFPWGNKLQPKGQHYANIWQGEFPVTNTGEDGFQGTAPVDAFPPNGYGLYNIVGNAWE WTSDWWTVHHSVEETLNPKGPPSGKDRVKKGGSYMCHRSYCYRYRCAARSQNTPDSSASN LGFRCAADRLPTMD NT seq 1125 nt NT seq  +upstreamnt  +downstreamnt atggctgcgcccgcactagggctggtgtgtggacgttgccctgagctgggtctcgtcctc ttgctgctgctgctctcgctgctgtgtggagcggcagggagccaggaggccgggaccggt gcgggcgcggggtcccttgcgggttcttgcggctgcggcacgccccagcggcctggcgcc catggcagttcggcagccgctcaccgatactcgcgggaggctaacgctccgggccccgta cccggagagcggcaactcgcgcactcaaagatggtccccatccctgctggagtatttaca atgggcacagatgatcctcagataaagcaggatggggaagcacctgcgaggagagttact attgatgccttttacatggatgcctatgaagtcagtaatactgaatttgagaagtttgtg aactcaactggctatttgacagaggctgagaagtttggcgactcctttgtctttgaaggc atgttgagtgagcaagtgaagaccaatattcaacaggcagttgcagctgctccctggtgg ttacctgtgaaaggcgctaactggagacacccagaagggcctgactctactattctgcac aggccggatcatccagttctccatgtgtcctggaatgatgcggttgcctactgcacttgg gcagggaagcggctgcccacggaagctgagtgggaatacagctgtcgaggaggcctgcat aatagacttttcccctggggcaacaaactgcagcccaaaggccagcattatgccaacatt tggcagggcgagtttccggtgaccaacactggtgaggatggcttccaaggaactgcgcct gttgatgccttccctcccaatggttatggcttatacaacatagtggggaacgcatgggaa tggacttcagactggtggactgttcatcattctgttgaagaaacgcttaacccaaaaggt cccccttctgggaaagaccgagtgaagaaaggtggatcctacatgtgccataggtcttat tgttacaggtatcgctgtgctgctcggagccagaacacacctgatagctctgcttcgaat ctgggattccgctgtgcagccgaccgcctgcccactatggactga

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