KEGG   Homo sapiens (human): 686
Entry
686               CDS       T01001                                 
Symbol
BTD
Name
(RefSeq) biotinidase
  KO
K01435  biotinidase [EC:3.5.1.12]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00780  Biotin metabolism
hsa01100  Metabolic pathways
hsa04977  Vitamin digestion and absorption
Disease
H01182  Biotinidase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09108 Metabolism of cofactors and vitamins
   00780 Biotin metabolism
    686 (BTD)
 09150 Organismal Systems
  09154 Digestive system
   04977 Vitamin digestion and absorption
    686 (BTD)
Enzymes [BR:hsa01000]
 3. Hydrolases
  3.5  Acting on carbon-nitrogen bonds, other than peptide bonds
   3.5.1  In linear amides
    3.5.1.12  biotinidase
     686 (BTD)
SSDB
Motif
Pfam: Vanin_C CN_hydrolase
Other DBs
NCBI-GeneID: 686
NCBI-ProteinID: NP_001268652
OMIM: 609019
HGNC: 1122
Ensembl: ENSG00000169814
UniProt: P43251
Position
3:15601361..15722516
AA seq 523 aa
MSGARSKLALFLCGCYVVALGAHTGEESVADHHEAEYYVAAVYEHPSILSLNPLALISRQ
EALELMNQNLDIYEQQVMTAAQKDVQIIVFPEDGIHGFNFTRTSIYPFLDFMPSPQVVRW
NPCLEPHRFNDTEVLQRLSCMAIRGDMFLVANLGTKEPCHSSDPRCPKDGRYQFNTNVVF
SNNGTLVDRYRKHNLYFEAAFDVPLKVDLITFDTPFAGRFGIFTCFDILFFDPAIRVLRD
YKVKHVVYPTAWMNQLPLLAAIEIQKAFAVAFGINVLAANVHHPVLGMTGSGIHTPLESF
WYHDMENPKSHLIIAQVAKNPVGLIGAENATGETDPSHSKFLKILSGDPYCEKDAQEVHC
DEATKWNVNAPPTFHSEMMYDNFTLVPVWGKEGYLHVCSNGLCCYLLYERPTLSKELYAL
GVFDGLHTVHGTYYIQVCALVRCGGLGFDTCGQEITEATGIFEFHLWGNFSTSYIFPLFL
TSGMTLEVPDQLGWENDHYFLRKSRLSSGLVTAALYGRLYERD
NT seq 1572 nt   +upstreamnt  +downstreamnt
atgtctggagccagaagtaagcttgctcttttcctctgcggctgttacgtggttgccctg
ggagcccacaccggggaggagagcgtggctgaccatcacgaggctgaatattatgtggct
gccgtgtatgagcatccatccatcctgagtctgaaccctctggctctcatcagccgccaa
gaggccttggagctcatgaaccagaaccttgacatctatgaacagcaagtgatgactgca
gcccaaaaggatgtacagattatagtgtttccagaagatggcattcatggattcaacttt
acaagaacatccatttatccatttttggacttcatgccgtctccccaggtggtcaggtgg
aacccatgcctggagcctcaccgcttcaatgacacagaggtgctccagcgcctgagttgt
atggccatcaggggagatatgttcttggtggccaatcttgggacaaaggagccttgtcat
agcagtgacccaaggtgcccaaaagatgggagataccagttcaacacaaatgtcgtgttc
agcaataatggaacccttgttgaccgctaccgtaaacacaacctctactttgaggcagca
ttcgatgttcctcttaaagtggatctcatcacctttgataccccctttgctggcaggttt
ggcatcttcacatgctttgatatattgttctttgaccctgccatcagagtcctcagagac
tacaaggtgaagcatgttgtgtacccaactgcctggatgaaccagctcccactcttggca
gcaattgagattcagaaagcttttgctgttgcctttggcatcaacgttctggcagctaat
gtccaccacccagttctggggatgacaggaagtggcatacacacccctctggagtccttt
tggtaccatgacatggaaaatcccaaaagtcaccttataattgcccaggtggccaaaaat
ccagtgggtctcattggtgcagagaatgcaacaggtgaaacggacccatcccatagtaag
tttttaaaaattttgtcaggcgatccgtactgtgagaaggatgctcaggaagtccactgt
gatgaggccaccaagtggaacgtgaatgctcctcccacatttcactctgagatgatgtat
gacaatttcaccctggtccctgtctggggaaaggaaggctatctccacgtctgttccaat
ggcctctgctgttatttactttacgagaggcccaccttatccaaagagctgtatgccctg
ggggtctttgatgggcttcacacagtacatggcacttactacatccaagtgtgtgccctg
gtcaggtgtgggggtcttggcttcgacacctgtggacaggaaatcacagaggccacgggg
atatttgagtttcacctgtggggcaacttcagtacttcctatatctttcctttgtttctg
acctcagggatgaccctagaagtccctgaccagcttggctgggagaatgaccactatttc
ctgaggaaaagtaggctgtcctctgggctggtgacggcggctctctatgggcgcttgtat
gagagggactag

  All links  
Disease (2)   
   OMIM (2)   
Gene (17)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (43)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (41)   
DNA sequence (83)   
   RefSeq(nuc) (43)   
   GenBank (20)   
   EMBL (20)   
Protein domain (2)   
   Pfam (2)   
All databases (147)   

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