Homo sapiens (human): 5199 Help Entry 5199              CDS       T01001                                  Symbol CFP, BFD, PFC, PFD, PROPERDIN Name (RefSeq) complement factor properdin   KO K15412   complement factor properdin Organism hsa  Homo sapiens (human) Pathway hsa05168   Herpes simplex virus 1 infection Network nt06513  Complement cascade   Element N01494   Alternative pathway of complement cascade, C3/5 convertase formation Disease H00104   Alternative complement pathway component defects Drug target Tarperprumig:  D12823 Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09172 Infectious disease: viral    05168 Herpes simplex virus 1 infection     5199 (CFP) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TSP_1 CFP_C_TSP1 TSR TSP1_spondin Motif Other DBs NCBI-GeneID:  5199 NCBI-ProteinID:  NP_001138724 OMIM:  300383 HGNC:  8864 Ensembl:  ENSG00000126759 Pharos:  P27918(Tbio) UniProt:  P27918 A0A0S2Z4I5 Structure PDB LinkDB All DBs Position X:complement(47623282..47630305) Genome browser AA seq 469 aa AA seqDB search MITEGAQAPRLLLPPLLLLLTLPATGSDPVLCFTQYEESSGKCKGLLGGGVSVEDCCLNT AFAYQKRSGGLCQPCRSPRWSLWSTWAPCSVTCSEGSQLRYRRCVGWNGQCSGKVAPGTL EWQLQACEDQQCCPEMGGWSGWGPWEPCSVTCSKGTRTRRRACNHPAPKCGGHCPGQAQE SEACDTQQVCPTHGAWATWGPWTPCSASCHGGPHEPKETRSRKCSAPEPSQKPPGKPCPG LAYEQRRCTGLPPCPVAGGWGPWGPVSPCPVTCGLGQTMEQRTCNHPVPQHGGPFCAGDA TRTHICNTAVPCPVDGEWDSWGEWSPCIRRNMKSISCQEIPGQQSRGRTCRGRKFDGHRC AGQQQDIRHCYSIQHCPLKGSWSEWSTWGLCMPPCGPNPTRARQRLCTPLLPKYPPTVSM VEGQGEKNVTFWGRPLPRCEELQGQKLVVEEKRPCLHVPACKDPEEEEL NT seq 1410 nt NT seq  +upstreamnt  +downstreamnt atgatcacagagggagcgcaggcccctcgattgttgctgccgccgctgctcctgctgctc accctgccagccacaggctcagaccccgtgctctgcttcacccagtatgaagaatcctcc ggcaagtgcaagggcctcctggggggtggtgtcagcgtggaagactgctgtctcaacact gcctttgcctaccagaaacgtagtggtgggctctgtcagccttgcaggtccccacgatgg tccctgtggtccacatgggccccctgttcggtgacgtgctctgagggctcccagctgcgg taccggcgctgtgtgggctggaatgggcagtgctctggaaaggtggcacctgggaccctg gagtggcagctccaggcctgtgaggaccagcagtgctgtcctgagatgggcggctggtct ggctgggggccctgggagccttgctctgtcacctgctccaaagggacccggacccgcagg cgagcctgtaatcaccctgctcccaagtgtgggggccactgcccaggacaggcacaggaa tcagaggcctgtgacacccagcaggtctgccccacacacggggcctgggccacctggggc ccctggaccccctgctcagcctcctgccacggtggaccccacgaacctaaggagacacga agccgcaagtgttctgcacctgagccctcccagaaacctcctgggaagccctgcccgggg ctagcctacgagcagcggaggtgcaccggcctgccaccctgcccagtggctgggggctgg gggccttggggccctgtgagcccctgccctgtgacctgtggcctgggccagaccatggaa caacggacgtgcaatcaccctgtgccccagcatgggggccccttctgtgctggcgatgcc acccggacccacatctgcaacacagctgtgccctgccctgtggatggggagtgggactcg tggggggagtggagcccctgtatccgacggaacatgaagtccatcagctgtcaagaaatc ccgggccagcagtcacgcgggaggacctgcaggggccgcaagtttgacggacatcgatgt gccgggcaacagcaggatatccggcactgctacagcatccagcactgccccttgaaagga tcatggtcagagtggagtacctgggggctgtgcatgcccccctgtggacctaatcctacc cgtgcccgccagcgcctctgcacacccttgctccccaagtacccgcccaccgtttccatg gtcgaaggtcagggcgagaagaacgtgaccttctgggggagaccgctgccacggtgtgag gagctacaagggcagaagctggtggtggaggagaaacgaccatgtctacacgtgcctgct tgcaaagaccctgaggaagaggaactctaa

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