KLTH0G10384g
highly similar to uniprot|P40495 Saccharomyces cerevisiae YIL094C LYS12 Homo-isocitrate dehydrogenase an NAD-linked mitochondrial enzyme required for the fourth step in the biosynthesis of lysine in which homo- isocitrate is oxidatively decarboxylated to alpha- ketoadipate
Element type: CDS
Element length: 1104 nucleotides,
on anti-sense strand of
Klth0G: complement(878375..879478).
Other names:
KLTH-ORF3666
Coding sequence: 368 codons.
Element length: 1104 nucleotides,
on anti-sense strand of
Klth0G: complement(878375..879478).
Other names:
KLTH-ORF3666
Coding sequence: 368 codons.
Database cross references:
EMBL: CU928171
GeneID: 8293763
GenomeReviews: CU928171_GR
Orthologs: strict determination not possible; homologs must be refined manually
EMBL: CU928171
GeneID: 8293763
GenomeReviews: CU928171_GR
Homologs and Orthologs
Homologs in protein family: GL3C0069Orthologs: strict determination not possible; homologs must be refined manually
Protein KLTH0G10384p 
highly similar to uniprot|P40495 Saccharomyces cerevisiae YIL094C LYS12 Homo-isocitrate dehydrogenase an NAD-linked mitochondrial enzyme required for the fourth step in the biosynthesis of lysine in which homo- isocitrate is oxidatively decarboxylated to alpha- ketoadipate; SubName: Full=KLTH0G10384p;
Protein domain map
Database cross references:
Gene3D: G3DSA:3.40.718.10
InterPro: IPR001804
InterPro: IPR019818
InterPro: IPR024084
KEGG: lth:KLTH0G10384g
PANTHER: PTHR11835
PROSITE: PS00470
Pfam: PF00180
RefSeq: XP_002555485.1
UniProtKB/TrEMBL: C5DMN7
UniProtKB: C5DMN7_LACTC
Phylogeny
PhylomeDB:KLTH0G10384g
Gene3D: G3DSA:3.40.718.10
InterPro: IPR001804
InterPro: IPR019818
InterPro: IPR024084
KEGG: lth:KLTH0G10384g
PANTHER: PTHR11835
PROSITE: PS00470
Pfam: PF00180
RefSeq: XP_002555485.1
UniProtKB/TrEMBL: C5DMN7
UniProtKB: C5DMN7_LACTC
Phylogeny 
PhylomeDB:KLTH0G10384gSequence data 
>KLTH0G10384g.nt ATGCTGAGAGCTTCTTTTACCCAACTGGCGCGTCGCTCCTACGCGTCCGCTTCCAAGTCT CTAACAATTGGTTTAATTCCAGGTGATGGTATCGGTAAAGAAGTGATTCCTGCGGGCAGA CAAGTTTTGGAGAACCTTTCCAGTAAGCACGGTCTGAAATTCGACTTCATCGACCTGCAG GCTGGGTGGCAGACTTTCCAGGAAACTGGAAAAGCGCTGCCAGATGAAACTATCGACATC CTGAGAAATCAGTGCCAAGGTGCTCTGTTTGGCGCTGTGCAGTCGCCAACTAACAAAGTT GAAGGCTACTCGTCACCCATTGTGGCTCTGAGGAAAAAGCTTGGGCTATATGCCAACGTA CGTCCCGTCAAGTCCGTCTTGCCACAAGAGAGACCTGTCGATATGATTATCGTGAGAGAA AACACCGAGGATCTGTACATCAAGACTGAGAAAACCTACATTGACGAAAAAACCGGCACT CGTGTTGCTGAGGCCATCAAAAGAATTTCAGAGACTGCTACCAAGAACATCGCCAACATC GCTTTGGAGATTGCTCTGCAAAGGCAGAAGGTTAACGGAGAGGCCACTTTGACTGTTACA CACAAGTCCAACGTGCTTTCTCAAAGTGACGGTTTGTTCAGAGAAGTCTGCAGACAAGTT TACGAAAGCAACAAAGACAAGTTTGGCTCTATCAAATACAACGAACAGATTGTTGACTCA ATGGTTTACAGGATGTTCAGGGAGCCAGAGTGCTTCGACGTTATTGTTGCCCCCAACTTG TATGGTGACATTTTGTCCGATGGTGCTGCTGCGCTCGTGGGTTCGCTTGGTGTCGTGCCA AGCGCCAACGTTGGCTTCGACTTTGTAGTCGGAGAGCCATGTCACGGTTCTGCCCCAGAC ATCGCGGGCAAGGGTATATCTAACCCTGTTGCGACCATCAGATCCACCGCCTTGATGTTG GAGTTTATGGGCCATCCAGAAGCTGCTCAAGACATCCACAAAGCTGTCGACGCAAACCTG CGTGACAACTCTATCAAGACACCAGACCTTGGCGGCAAATCAACTACCCAACAAGTAGTC GAAGATGTTCTCTCCAGAATGTAA
>KLTH0G10384g.cds ATGCTGAGAGCTTCTTTTACCCAACTGGCGCGTCGCTCCTACGCGTCCGCTTCCAAGTCT CTAACAATTGGTTTAATTCCAGGTGATGGTATCGGTAAAGAAGTGATTCCTGCGGGCAGA CAAGTTTTGGAGAACCTTTCCAGTAAGCACGGTCTGAAATTCGACTTCATCGACCTGCAG GCTGGGTGGCAGACTTTCCAGGAAACTGGAAAAGCGCTGCCAGATGAAACTATCGACATC CTGAGAAATCAGTGCCAAGGTGCTCTGTTTGGCGCTGTGCAGTCGCCAACTAACAAAGTT GAAGGCTACTCGTCACCCATTGTGGCTCTGAGGAAAAAGCTTGGGCTATATGCCAACGTA CGTCCCGTCAAGTCCGTCTTGCCACAAGAGAGACCTGTCGATATGATTATCGTGAGAGAA AACACCGAGGATCTGTACATCAAGACTGAGAAAACCTACATTGACGAAAAAACCGGCACT CGTGTTGCTGAGGCCATCAAAAGAATTTCAGAGACTGCTACCAAGAACATCGCCAACATC GCTTTGGAGATTGCTCTGCAAAGGCAGAAGGTTAACGGAGAGGCCACTTTGACTGTTACA CACAAGTCCAACGTGCTTTCTCAAAGTGACGGTTTGTTCAGAGAAGTCTGCAGACAAGTT TACGAAAGCAACAAAGACAAGTTTGGCTCTATCAAATACAACGAACAGATTGTTGACTCA ATGGTTTACAGGATGTTCAGGGAGCCAGAGTGCTTCGACGTTATTGTTGCCCCCAACTTG TATGGTGACATTTTGTCCGATGGTGCTGCTGCGCTCGTGGGTTCGCTTGGTGTCGTGCCA AGCGCCAACGTTGGCTTCGACTTTGTAGTCGGAGAGCCATGTCACGGTTCTGCCCCAGAC ATCGCGGGCAAGGGTATATCTAACCCTGTTGCGACCATCAGATCCACCGCCTTGATGTTG GAGTTTATGGGCCATCCAGAAGCTGCTCAAGACATCCACAAAGCTGTCGACGCAAACCTG CGTGACAACTCTATCAAGACACCAGACCTTGGCGGCAAATCAACTACCCAACAAGTAGTC GAAGATGTTCTCTCCAGAATGTAA
>KLTH0G10384g.aa MLRASFTQLARRSYASASKSLTIGLIPGDGIGKEVIPAGRQVLENLSSKHGLKFDFIDLQ AGWQTFQETGKALPDETIDILRNQCQGALFGAVQSPTNKVEGYSSPIVALRKKLGLYANV RPVKSVLPQERPVDMIIVRENTEDLYIKTEKTYIDEKTGTRVAEAIKRISETATKNIANI ALEIALQRQKVNGEATLTVTHKSNVLSQSDGLFREVCRQVYESNKDKFGSIKYNEQIVDS MVYRMFREPECFDVIVAPNLYGDILSDGAAALVGSLGVVPSANVGFDFVVGEPCHGSAPD IAGKGISNPVATIRSTALMLEFMGHPEAAQDIHKAVDANLRDNSIKTPDLGGKSTTQQVV EDVLSRM*
Legend and notes 
Lengths
The length, in codons, of coding sequences includes the stop codon, hence it is one unit longer than the protein length.
Genomic environment map
Click on the symbol of an element or a family to go to its corresponding page. Colors in the lane "protein encoding genes" indicate strandedness: shades of blue for direct orientation, shades of red for reverse orientation. Colors in the lane "protein family" are arbitrarly chosen in such a way that different protein families have different colors in the map.
Protein domain map
Domains are extracted from SwissProt files. Click on the symbol of a domain to extract the domain sequence.
Genemark image and list
Genemark computation of protein-coding potential of DNA was made from 1000 nucleotides upstream the open reading frame to 300 nucleotides downstream. Thus the open reading frame protein-coding potential appears on frame #3.
Sequences
| Color | Nucleotide sequence and Coding sequence | Predicted translation product |
| RED | start and stop codons | Initial methionine and sequence end |
| BLUE | coding sequence | protein sequence |
| grey | non-coding sequence (upstream, downstream or intron) | |
| grey | donor and acceptor splicing sites |
Home
URL: http://192.168.122.177/elt/KLTH/KLTH0G10384g