KEGG   Homo sapiens (human): 35
Entry
35                CDS       T01001                                 
Symbol
ACADS, ACAD3, SCAD
Name
(RefSeq) acyl-CoA dehydrogenase short chain
  KO
K00248  butyryl-CoA dehydrogenase [EC:1.3.8.1]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00071  Fatty acid degradation
hsa00280  Valine, leucine and isoleucine degradation
hsa00410  beta-Alanine metabolism
hsa00640  Propanoate metabolism
hsa00650  Butanoate metabolism
hsa01100  Metabolic pathways
hsa01200  Carbon metabolism
hsa01212  Fatty acid metabolism
Network
nt06020  beta-Oxidation in mitochondria
nt06024  Valine, leucine and isoleucine degradation
  Element
N00804  beta-Oxidation
N00852  Valine degradation
N00856  Isoleucine degradation
Disease
H00525  Disorders of mitochondrial fatty-acid oxidation
H01980  SCAD deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09101 Carbohydrate metabolism
   00640 Propanoate metabolism
    35 (ACADS)
   00650 Butanoate metabolism
    35 (ACADS)
  09103 Lipid metabolism
   00071 Fatty acid degradation
    35 (ACADS)
  09105 Amino acid metabolism
   00280 Valine, leucine and isoleucine degradation
    35 (ACADS)
  09106 Metabolism of other amino acids
   00410 beta-Alanine metabolism
    35 (ACADS)
Enzymes [BR:hsa01000]
 1. Oxidoreductases
  1.3  Acting on the CH-CH group of donors
   1.3.8  With a flavin as acceptor
    1.3.8.1  short-chain acyl-CoA dehydrogenase
     35 (ACADS)
SSDB
Motif
Pfam: Acyl-CoA_dh_1 Acyl-CoA_dh_N Acyl-CoA_dh_M Acyl-CoA_dh_2 HpaB_N
Other DBs
NCBI-GeneID: 35
NCBI-ProteinID: NP_000008
OMIM: 606885
HGNC: 90
Ensembl: ENSG00000122971
UniProt: P16219 E5KSD5
Structure
LinkDB
Position
12:120725826..120740008
AA seq 412 aa
MAAALLARASGPARRALCPRAWRQLHTIYQSVELPETHQMLLQTCRDFAEKELFPIAAQV
DKEHLFPAAQVKKMGGLGLLAMDVPEELGGAGLDYLAYAIAMEEISRGCASTGVIMSVNN
SLYLGPILKFGSKEQKQAWVTPFTSGDKIGCFALSEPGNGSDAGAASTTARAEGDSWVLN
GTKAWITNAWEASAAVVFASTDRALQNKGISAFLVPMPTPGLTLGKKEDKLGIRGSSTAN
LIFEDCRIPKDSILGEPGMGFKIAMQTLDMGRIGIASQALGIAQTALDCAVNYAENRMAF
GAPLTKLQVIQFKLADMALALESARLLTWRAAMLKDNKKPFIKEAAMAKLAASEAATAIS
HQAIQILGGMGYVTEMPAERHYRDARITEIYEGTSEIQRLVIAGHLLRSYRS
NT seq 1239 nt   +upstreamnt  +downstreamnt
atggccgccgcgctgctcgcccgggcctcgggccctgcccgcagagctctctgtcctagg
gcctggcggcagttacacaccatctaccagtctgtggaactgcccgagacacaccagatg
ttgctccagacatgccgggactttgccgagaaggagttgtttcccattgcagcccaggtg
gataaggaacatctcttcccagcggctcaggtgaagaagatgggcgggcttgggcttctg
gccatggacgtgcccgaggagcttggcggtgctggcctcgattacctggcctacgccatc
gccatggaggagatcagccgtggctgcgcctccaccggagtcatcatgagtgtcaacaac
tctctctacctggggcccatcttgaagtttggctccaaggagcagaagcaggcgtgggtc
acgcctttcaccagtggtgacaaaattggctgctttgccctcagcgaaccagggaacggc
agtgatgcaggagctgcgtccaccaccgcccgggccgagggcgactcatgggttctgaat
ggaaccaaagcctggatcaccaatgcctgggaggcttcggctgccgtggtctttgccagc
acggacagagccctgcaaaacaagggcatcagtgccttcctggtccccatgccaacgcct
gggctcacgttggggaagaaagaagacaagctgggcatccggggctcatccacggccaac
ctcatctttgaggactgtcgcatccccaaggacagcatcctgggggagccagggatgggc
ttcaagatagccatgcaaaccctggacatgggccgcatcggcatcgcctcccaggccctg
ggcattgcccagaccgccctcgattgtgctgtgaactacgctgagaatcgcatggccttc
ggggcgcccctcaccaagctccaggtcatccagttcaagttggcagacatggccctggcc
ctggagagtgcccggctgctgacctggcgcgctgccatgctgaaggataacaagaagcct
ttcatcaaggaggcagccatggccaagctggccgcctcggaggccgcgaccgccatcagc
caccaggccatccagatcctgggcggcatgggctacgtgacagagatgccggcagagcgg
cactaccgcgacgcccgcatcactgagatctacgagggcaccagcgaaatccagcggctg
gtgatcgccgggcatctgctcaggagctaccggagctga

KEGG   Homo sapiens (human): 27034
Entry
27034             CDS       T01001                                 
Symbol
ACAD8, ACAD-8, ARC42, IBDH
Name
(RefSeq) acyl-CoA dehydrogenase family member 8
  KO
K11538  isobutyryl-CoA dehydrogenase [EC:1.3.99.-]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00280  Valine, leucine and isoleucine degradation
hsa01100  Metabolic pathways
Network
nt06024  Valine, leucine and isoleucine degradation
  Element
N00852  Valine degradation
Disease
H01279  Isobutyryl-CoA dehydrogenase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09105 Amino acid metabolism
   00280 Valine, leucine and isoleucine degradation
    27034 (ACAD8)
SSDB
Motif
Pfam: Acyl-CoA_dh_1 Acyl-CoA_dh_N Acyl-CoA_dh_M Acyl-CoA_dh_2
Other DBs
NCBI-GeneID: 27034
NCBI-ProteinID: NP_055199
OMIM: 604773
HGNC: 87
Ensembl: ENSG00000151498
UniProt: Q9UKU7
Structure
LinkDB
Position
11:134253568..134265855
AA seq 415 aa
MLWSGCRRFGARLGCLPGGLRVLVQTGHRSLTSCIDPSMGLNEEQKEFQKVAFDFAAREM
APNMAEWDQKELFPVDVMRKAAQLGFGGVYIQTDVGGSGLSRLDTSVIFEALATGCTSTT
AYISIHNMCAWMIDSFGNEEQRHKFCPPLCTMEKFASYCLTEPGSGSDAASLLTSAKKQG
DHYILNGSKAFISGAGESDIYVVMCRTGGPGPKGISCIVVEKGTPGLSFGKKEKKVGWNS
QPTRAVIFEDCAVPVANRIGSEGQGFLIAVRGLNGGRINIASCSLGAAHASVILTRDHLN
VRKQFGEPLASNQYLQFTLADMATRLVAARLMVRNAAVALQEERKDAVALCSMAKLFATD
ECFAICNQALQMHGGYGYLKDYAVQQYVRDSRVHQILEGSNEVMRILISRSLLQE
NT seq 1248 nt   +upstreamnt  +downstreamnt
atgctgtggagcggctgccggcgtttcggggcgcgcctcggctgcctgcccggcggtctc
cgggtcctcgtccagaccggccaccggagcttgacctcctgcatcgacccttccatggga
cttaatgaagagcagaaagaatttcaaaaagtggcctttgactttgctgcccgagagatg
gctccaaatatggcagagtgggaccagaaggagctgttcccagtggatgtgatgcggaag
gcagcccagctaggcttcggaggggtctacatacaaacagatgtgggcgggtctgggctg
tcacgtcttgatacctctgtcatttttgaagccttggctacaggctgcaccagcaccaca
gcctatataagcatccacaacatgtgtgcctggatgattgatagcttcggaaatgaggaa
cagaggcacaaattttgcccaccgctctgtaccatggagaagtttgcttcctactgcctc
actgaaccaggaagtgggagtgatgctgcctctcttctgacctccgctaagaaacaggga
gatcattacatcctcaatggctccaaggccttcatcagtggtgctggtgagtcagacatc
tatgtggtcatgtgccgaacaggaggaccaggccccaagggcatctcatgcatagttgtt
gagaaggggacccctggcctcagctttggcaagaaggagaaaaaggtggggtggaactcc
cagccaacacgagctgtgatcttcgaagactgtgctgtccctgtggccaacagaattggg
agcgaggggcagggcttcctcattgccgtgagaggactgaacggagggaggatcaatatt
gcttcctgctccctgggggctgcccacgcctctgtcatcctcacccgagaccacctcaat
gtccggaagcagtttggagagcctctggccagtaaccagtacttgcaattcacactggct
gatatggcaacaaggctggtggccgcgcggctgatggtccgcaatgcagcagtggctctg
caggaggagaggaaggatgcagtggccttgtgctccatggccaagctctttgctacagat
gaatgctttgccatctgcaaccaggccttgcagatgcacgggggctacggctacctgaag
gattacgctgttcagcagtacgtgcgggactccagggtccaccagattctagaaggtagc
aatgaagtgatgaggatactgatctctagaagcctgcttcaggagtag

KEGG   Homo sapiens (human): 34
Entry
34                CDS       T01001                                 
Symbol
ACADM, ACAD1, MCAD, MCADH
Name
(RefSeq) acyl-CoA dehydrogenase medium chain
  KO
K00249  acyl-CoA dehydrogenase [EC:1.3.8.7]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00071  Fatty acid degradation
hsa00280  Valine, leucine and isoleucine degradation
hsa01100  Metabolic pathways
hsa01212  Fatty acid metabolism
hsa03320  PPAR signaling pathway
hsa04936  Alcoholic liver disease
Module
hsa_M00036  Leucine degradation, leucine => acetoacetate + acetyl-CoA
hsa_M00087  beta-Oxidation
Network
nt06020  beta-Oxidation in mitochondria
nt06024  Valine, leucine and isoleucine degradation
  Element
N00804  beta-Oxidation
N00851  Leucine degradation
N00852  Valine degradation
N00856  Isoleucine degradation
Disease
H00488  MCAD deficiency
H00525  Disorders of mitochondrial fatty-acid oxidation
H01400  Secondary hyperammonemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09103 Lipid metabolism
   00071 Fatty acid degradation
    34 (ACADM)
  09105 Amino acid metabolism
   00280 Valine, leucine and isoleucine degradation
    34 (ACADM)
 09150 Organismal Systems
  09152 Endocrine system
   03320 PPAR signaling pathway
    34 (ACADM)
 09160 Human Diseases
  09167 Endocrine and metabolic disease
   04936 Alcoholic liver disease
    34 (ACADM)
Enzymes [BR:hsa01000]
 1. Oxidoreductases
  1.3  Acting on the CH-CH group of donors
   1.3.8  With a flavin as acceptor
    1.3.8.7  medium-chain acyl-CoA dehydrogenase
     34 (ACADM)
SSDB
Motif
Pfam: Acyl-CoA_dh_1 Acyl-CoA_dh_N Acyl-CoA_dh_M Acyl-CoA_dh_2 HpaB_N
Other DBs
NCBI-GeneID: 34
NCBI-ProteinID: NP_000007
OMIM: 607008
HGNC: 89
Ensembl: ENSG00000117054
UniProt: P11310 A0A0S2Z366
Structure
LinkDB
Position
1:75724709..75763679
AA seq 421 aa
MAAGFGRCCRVLRSISRFHWRSQHTKANRQREPGLGFSFEFTEQQKEFQATARKFAREEI
IPVAAEYDKTGEYPVPLIRRAWELGLMNTHIPENCGGLGLGTFDACLISEELAYGCTGVQ
TAIEGNSLGQMPIIIAGNDQQKKKYLGRMTEEPLMCAYCVTEPGAGSDVAGIKTKAEKKG
DEYIINGQKMWITNGGKANWYFLLARSDPDPKAPANKAFTGFIVEADTPGIQIGRKELNM
GQRCSDTRGIVFEDVKVPKENVLIGDGAGFKVAMGAFDKTRPVVAAGAVGLAQRALDEAT
KYALERKTFGKLLVEHQAISFMLAEMAMKVELARMSYQRAAWEVDSGRRNTYYASIAKAF
AGDIANQLATDAVQILGGNGFNTEYPVEKLMRDAKIYQIYEGTSQIQRLIVAREHIDKYK
N
NT seq 1266 nt   +upstreamnt  +downstreamnt
atggcagcggggttcgggcgatgctgcagggtcctgagaagtatttctcgttttcattgg
agatcacagcatacaaaagccaatcgacaacgtgaaccaggattaggatttagttttgag
ttcaccgaacagcagaaagaatttcaagctactgctcgtaaatttgccagagaggaaatc
atcccagtggctgcagaatatgataaaactggtgaatatccagtccccctaattagaaga
gcctgggaacttggtttaatgaacacacacattccagagaactgtggaggtcttggactt
ggaacttttgatgcttgtttaattagtgaagaattggcttatggatgtacaggggttcag
actgctattgaaggaaattctttggggcaaatgcctattattattgctggaaatgatcaa
caaaagaagaagtatttggggagaatgactgaggagccattgatgtgtgcttattgtgta
acagaacctggagcaggctctgatgtagctggtataaagaccaaagcagaaaagaaagga
gatgagtatattattaatggtcagaagatgtggataaccaacggaggaaaagctaattgg
tattttttattggcacgttctgatccagatcctaaagctcctgctaataaagcctttact
ggattcattgtggaagcagataccccaggaattcagattgggagaaaggaattaaacatg
ggccagcgatgttcagatactagaggaattgtcttcgaagatgtgaaagtgcctaaagaa
aatgttttaattggtgacggagctggtttcaaagttgcaatgggagcttttgataaaacc
agacctgtagtagctgctggtgctgttggattagcacaaagagctttggatgaagctacc
aagtatgccctggaaaggaaaactttcggaaagctacttgtagagcaccaagcaatatca
tttatgctggctgaaatggcaatgaaagttgaactagctagaatgagttaccagagagca
gcttgggaggttgattctggtcgtcgaaatacctattatgcttctattgcaaaggcattt
gctggagatattgcaaatcagttagctactgatgctgtgcagatacttggaggcaatgga
tttaatacagaatatcctgtagaaaaactaatgagggatgccaaaatctatcagatttat
gaaggtacttcacaaattcaaagacttattgtagcccgtgaacacattgacaagtacaaa
aattaa

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