Protein ID | OphauG2|2361 |
Gene name | |
Location | Contig_184:13878..15633 |
Strand | + |
Gene length (bp) | 1755 |
Transcript length (bp) | 1602 |
Coding sequence length (bp) | 1602 |
Protein length (aa) | 534 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF07994 | NAD_binding_5 | Myo-inositol-1-phosphate synthase | 1.8E-144 | 78 | 515 |
PF01658 | Inos-1-P_synth | Myo-inositol-1-phosphate synthase | 2.3E-40 | 330 | 443 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q54N49|INO1_DICDI | Inositol-3-phosphate synthase OS=Dictyostelium discoideum GN=ino1 PE=3 SV=1 | 24 | 532 | 0.0E+00 |
sp|Q6FQI1|INO1_CANGA | Inositol-3-phosphate synthase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=INO1 PE=3 SV=1 | 14 | 532 | 0.0E+00 |
sp|P11986|INO1_YEAST | Inositol-3-phosphate synthase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INO1 PE=1 SV=3 | 24 | 533 | 0.0E+00 |
sp|P42800|INO1_CANAL | Inositol-3-phosphate synthase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=INO1 PE=3 SV=1 | 29 | 532 | 0.0E+00 |
sp|P42802|INO1_CITPA | Inositol-3-phosphate synthase OS=Citrus paradisi PE=3 SV=1 | 24 | 531 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q54N49|INO1_DICDI | Inositol-3-phosphate synthase OS=Dictyostelium discoideum GN=ino1 PE=3 SV=1 | 24 | 532 | 0.0E+00 |
sp|Q6FQI1|INO1_CANGA | Inositol-3-phosphate synthase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=INO1 PE=3 SV=1 | 14 | 532 | 0.0E+00 |
sp|P11986|INO1_YEAST | Inositol-3-phosphate synthase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=INO1 PE=1 SV=3 | 24 | 533 | 0.0E+00 |
sp|P42800|INO1_CANAL | Inositol-3-phosphate synthase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=INO1 PE=3 SV=1 | 29 | 532 | 0.0E+00 |
sp|P42802|INO1_CITPA | Inositol-3-phosphate synthase OS=Citrus paradisi PE=3 SV=1 | 24 | 531 | 0.0E+00 |
sp|O97477|INO1_DROME | Inositol-3-phosphate synthase OS=Drosophila melanogaster GN=Inos PE=1 SV=1 | 18 | 532 | 0.0E+00 |
sp|Q9NPH2|INO1_HUMAN | Inositol-3-phosphate synthase 1 OS=Homo sapiens GN=ISYNA1 PE=1 SV=1 | 22 | 532 | 0.0E+00 |
sp|Q2NL29|INO1_BOVIN | Inositol-3-phosphate synthase 1 OS=Bos taurus GN=ISYNA1 PE=2 SV=1 | 25 | 532 | 0.0E+00 |
sp|Q9JHU9|INO1_MOUSE | Inositol-3-phosphate synthase 1 OS=Mus musculus GN=Isyna1 PE=1 SV=1 | 22 | 532 | 0.0E+00 |
sp|Q4R6E3|INO1_MACFA | Inositol-3-phosphate synthase 1 OS=Macaca fascicularis GN=ISYNA1 PE=2 SV=1 | 22 | 532 | 0.0E+00 |
sp|Q6AYK3|INO1_RAT | Inositol-3-phosphate synthase 1 OS=Rattus norvegicus GN=Isyna1 PE=3 SV=2 | 22 | 532 | 0.0E+00 |
sp|Q7ZXY0|INO1A_XENLA | Inositol-3-phosphate synthase 1-A OS=Xenopus laevis GN=isyna1-a PE=2 SV=1 | 25 | 532 | 0.0E+00 |
sp|Q6DDT1|INO1B_XENLA | Inositol-3-phosphate synthase 1-B OS=Xenopus laevis GN=isyna1-b PE=2 SV=2 | 25 | 532 | 0.0E+00 |
sp|Q41107|INO1_PHAVU | Inositol-3-phosphate synthase OS=Phaseolus vulgaris PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|Q38862|INO2_ARATH | Inositol-3-phosphate synthase isozyme 2 OS=Arabidopsis thaliana GN=IPS2 PE=1 SV=2 | 24 | 531 | 0.0E+00 |
sp|O65195|INO1_HORVU | Inositol-3-phosphate synthase OS=Hordeum vulgare PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|P42801|INO1_ARATH | Inositol-3-phosphate synthase isozyme 1 OS=Arabidopsis thaliana GN=IPS1 PE=1 SV=3 | 24 | 531 | 0.0E+00 |
sp|Q9FPK7|INO1_MAIZE | Inositol-3-phosphate synthase OS=Zea mays PE=2 SV=2 | 24 | 531 | 0.0E+00 |
sp|O64437|INO1_ORYSJ | Inositol-3-phosphate synthase OS=Oryza sativa subsp. japonica GN=INO1 PE=2 SV=2 | 24 | 531 | 0.0E+00 |
sp|Q40271|INO1_MESCR | Inositol-3-phosphate synthase OS=Mesembryanthemum crystallinum PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|Q96348|INO1_BRANA | Inositol-3-phosphate synthase OS=Brassica napus PE=2 SV=2 | 24 | 531 | 0.0E+00 |
sp|Q9LX12|INO3_ARATH | Probable inositol 3-phosphate synthase isozyme 3 OS=Arabidopsis thaliana GN=IPS3 PE=1 SV=1 | 24 | 531 | 0.0E+00 |
sp|P42803|INO1_SPIPO | Inositol-3-phosphate synthase OS=Spirodela polyrhiza GN=TUR1 PE=2 SV=1 | 25 | 531 | 0.0E+00 |
sp|Q9S7U0|INO1_WHEAT | Inositol-3-phosphate synthase OS=Triticum aestivum GN=MIPS PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|Q9LW96|INO1_TOBAC | Inositol-3-phosphate synthase OS=Nicotiana tabacum PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|Q9FYV1|INO1_SESIN | Inositol-3-phosphate synthase OS=Sesamum indicum PE=2 SV=1 | 24 | 531 | 0.0E+00 |
sp|Q9SSV4|INO1_NICPA | Inositol-3-phosphate synthase OS=Nicotiana paniculata GN=INPS1 PE=2 SV=1 | 24 | 531 | 0.0E+00 |
GO Term | Description | Terminal node |
---|---|---|
GO:0008654 | phospholipid biosynthetic process | Yes |
GO:0004512 | inositol-3-phosphate synthase activity | Yes |
GO:0006021 | inositol biosynthetic process | Yes |
GO:0044238 | primary metabolic process | No |
GO:0006793 | phosphorus metabolic process | No |
GO:0044281 | small molecule metabolic process | No |
GO:0044255 | cellular lipid metabolic process | No |
GO:0046165 | alcohol biosynthetic process | No |
GO:0008610 | lipid biosynthetic process | No |
GO:1901617 | organic hydroxy compound biosynthetic process | No |
GO:0005975 | carbohydrate metabolic process | No |
GO:0008150 | biological_process | No |
GO:0008152 | metabolic process | No |
GO:0009058 | biosynthetic process | No |
GO:1901576 | organic substance biosynthetic process | No |
GO:0006066 | alcohol metabolic process | No |
GO:0019637 | organophosphate metabolic process | No |
GO:0009987 | cellular process | No |
GO:0044283 | small molecule biosynthetic process | No |
GO:0046173 | polyol biosynthetic process | No |
GO:0090407 | organophosphate biosynthetic process | No |
GO:0006629 | lipid metabolic process | No |
GO:0003824 | catalytic activity | No |
GO:0006020 | inositol metabolic process | No |
GO:0044237 | cellular metabolic process | No |
GO:0019751 | polyol metabolic process | No |
GO:1901615 | organic hydroxy compound metabolic process | No |
GO:0016051 | carbohydrate biosynthetic process | No |
GO:0016853 | isomerase activity | No |
GO:0003674 | molecular_function | No |
GO:0006644 | phospholipid metabolic process | No |
GO:0034637 | cellular carbohydrate biosynthetic process | No |
GO:0044249 | cellular biosynthetic process | No |
GO:0071704 | organic substance metabolic process | No |
GO:0044262 | cellular carbohydrate metabolic process | No |
GO:0006796 | phosphate-containing compound metabolic process | No |
GO:0016872 | intramolecular lyase activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 20 | 0.45 |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >OphauG2|2361 MAPHAQVSTPSANAVSTRPNNSGSFVVNSPNVSYSDSDIKSTYTYRTTRVETDAQGQLVATPNEVVYDFKTDRRV PRVGMMLVGWGGNNGTTVTAGILANRRGLVWQTKEGPRAANYYGSVVMGSTMKLGSERGTNKDVNVPFHSVLPMV HPNDLVIGGWDISKMNLSQAMDRAQVLEPTLKAQVSKEMAEMVPLPSIYYPDFIAANQEDRADNIIAGDRASMAH VEHLRRDIRDFKERNGLDKVIVMWTANTERYAHVLAGVNDTADNLLRAIEQGHAEVSPSTVFAVACILEQTPFIN GSPQNTFVPGAIELAEAKGAFIGGDDFKSGQTKMKSALVDFLINAGIKLTSIASYNHLGNNDGKNLSSQKQFRSK EISKSNVVDDMVEANSVLYAKGEHPDHCVVIKYMPAVADNKRALDEYYAEIFLGGHQTISLFNICEDSLLASPLI IDLVLLAEMMTRIQWKLSGASGGYKNFHSVLSVLSYMLKAPMTPPGTPVVNSLAKQRAALTNIFRACVGLEPESD MTLEHKLF* |
Coding | >OphauG2|2361 ATGGCTCCCCACGCGCAGGTCAGCACGCCTTCGGCCAATGCCGTCAGCACCCGACCCAACAACAGCGGCTCCTTT GTCGTCAACTCGCCCAATGTCAGCTACAGCGACAGCGACATCAAGTCGACGTACACGTACCGCACCACCCGCGTC GAGACGGACGCCCAGGGCCAGCTGGTGGCGACGCCCAACGAGGTGGTCTACGACTTCAAGACGGACCGCCGCGTG CCTCGAGTCGGCATGATGCTCGTGGGCTGGGGCGGCAACAACGGCACCACCGTCACGGCCGGCATCCTGGCCAAT CGCCGCGGGCTCGTCTGGCAGACCAAGGAGGGCCCTCGCGCCGCCAATTACTACGGATCCGTCGTCATGGGCTCC ACCATGAAGCTGGGCAGCGAGCGCGGCACCAACAAGGACGTCAATGTGCCCTTCCACAGCGTCTTGCCCATGGTG CACCCCAACGACCTCGTCATTGGCGGCTGGGACATTAGCAAGATGAATCTGTCCCAGGCCATGGACCGCGCCCAG GTGCTGGAGCCGACTCTCAAAGCCCAGGTGTCCAAGGAAATGGCCGAGATGGTGCCGCTGCCCTCCATCTACTAC CCGGACTTTATTGCCGCCAACCAGGAGGACCGGGCCGACAATATCATTGCGGGCGACCGGGCGTCCATGGCCCAC GTCGAGCATCTGCGCCGCGACATCCGCGACTTCAAGGAGCGCAACGGGCTCGACAAGGTCATTGTCATGTGGACG GCCAACACGGAGCGCTACGCCCATGTGCTGGCGGGCGTCAACGACACGGCCGACAATCTGCTGCGCGCCATTGAG CAGGGCCACGCCGAGGTGTCGCCGTCAACCGTCTTTGCCGTGGCGTGCATTCTCGAGCAGACGCCCTTTATCAAT GGCTCGCCGCAAAACACCTTTGTGCCGGGAGCCATTGAGCTGGCCGAGGCCAAGGGCGCCTTTATCGGCGGCGAC GACTTCAAGTCGGGCCAGACCAAGATGAAGTCGGCCCTCGTCGACTTTCTCATCAACGCCGGCATCAAACTGACC TCCATCGCCAGCTACAACCACTTGGGCAACAATGACGGCAAGAACCTGAGCTCGCAGAAGCAGTTCCGCTCCAAG GAGATTTCAAAGTCCAACGTGGTTGACGACATGGTCGAGGCCAACTCCGTGCTCTATGCCAAGGGGGAGCACCCG GACCACTGCGTCGTCATCAAGTACATGCCCGCCGTGGCCGACAACAAGCGCGCTCTCGACGAGTACTATGCCGAG ATTTTCCTGGGCGGACACCAGACCATTTCCCTCTTCAACATTTGCGAAGATTCTCTATTGGCGTCGCCACTCATC ATCGACCTCGTCCTTCTGGCCGAGATGATGACGCGCATCCAGTGGAAGCTGTCGGGTGCCTCGGGCGGCTACAAA AACTTCCACAGCGTGCTCAGCGTGCTCAGCTACATGCTCAAGGCGCCCATGACGCCTCCTGGCACGCCCGTCGTC AACTCGCTGGCAAAGCAACGCGCTGCATTGACCAACATCTTTCGGGCTTGCGTTGGCCTGGAGCCTGAGTCGGAC ATGACGCTTGAACACAAGCTCTTTTAA |
Transcript | >OphauG2|2361 ATGGCTCCCCACGCGCAGGTCAGCACGCCTTCGGCCAATGCCGTCAGCACCCGACCCAACAACAGCGGCTCCTTT GTCGTCAACTCGCCCAATGTCAGCTACAGCGACAGCGACATCAAGTCGACGTACACGTACCGCACCACCCGCGTC GAGACGGACGCCCAGGGCCAGCTGGTGGCGACGCCCAACGAGGTGGTCTACGACTTCAAGACGGACCGCCGCGTG CCTCGAGTCGGCATGATGCTCGTGGGCTGGGGCGGCAACAACGGCACCACCGTCACGGCCGGCATCCTGGCCAAT CGCCGCGGGCTCGTCTGGCAGACCAAGGAGGGCCCTCGCGCCGCCAATTACTACGGATCCGTCGTCATGGGCTCC ACCATGAAGCTGGGCAGCGAGCGCGGCACCAACAAGGACGTCAATGTGCCCTTCCACAGCGTCTTGCCCATGGTG CACCCCAACGACCTCGTCATTGGCGGCTGGGACATTAGCAAGATGAATCTGTCCCAGGCCATGGACCGCGCCCAG GTGCTGGAGCCGACTCTCAAAGCCCAGGTGTCCAAGGAAATGGCCGAGATGGTGCCGCTGCCCTCCATCTACTAC CCGGACTTTATTGCCGCCAACCAGGAGGACCGGGCCGACAATATCATTGCGGGCGACCGGGCGTCCATGGCCCAC GTCGAGCATCTGCGCCGCGACATCCGCGACTTCAAGGAGCGCAACGGGCTCGACAAGGTCATTGTCATGTGGACG GCCAACACGGAGCGCTACGCCCATGTGCTGGCGGGCGTCAACGACACGGCCGACAATCTGCTGCGCGCCATTGAG CAGGGCCACGCCGAGGTGTCGCCGTCAACCGTCTTTGCCGTGGCGTGCATTCTCGAGCAGACGCCCTTTATCAAT GGCTCGCCGCAAAACACCTTTGTGCCGGGAGCCATTGAGCTGGCCGAGGCCAAGGGCGCCTTTATCGGCGGCGAC GACTTCAAGTCGGGCCAGACCAAGATGAAGTCGGCCCTCGTCGACTTTCTCATCAACGCCGGCATCAAACTGACC TCCATCGCCAGCTACAACCACTTGGGCAACAATGACGGCAAGAACCTGAGCTCGCAGAAGCAGTTCCGCTCCAAG GAGATTTCAAAGTCCAACGTGGTTGACGACATGGTCGAGGCCAACTCCGTGCTCTATGCCAAGGGGGAGCACCCG GACCACTGCGTCGTCATCAAGTACATGCCCGCCGTGGCCGACAACAAGCGCGCTCTCGACGAGTACTATGCCGAG ATTTTCCTGGGCGGACACCAGACCATTTCCCTCTTCAACATTTGCGAAGATTCTCTATTGGCGTCGCCACTCATC ATCGACCTCGTCCTTCTGGCCGAGATGATGACGCGCATCCAGTGGAAGCTGTCGGGTGCCTCGGGCGGCTACAAA AACTTCCACAGCGTGCTCAGCGTGCTCAGCTACATGCTCAAGGCGCCCATGACGCCTCCTGGCACGCCCGTCGTC AACTCGCTGGCAAAGCAACGCGCTGCATTGACCAACATCTTTCGGGCTTGCGTTGGCCTGGAGCCTGAGTCGGAC ATGACGCTTGAACACAAGCTCTTTTAA |
Gene | >OphauG2|2361 ATGGCTCCCCACGCGCAGGTCAGCACGCCTTCGGCCAATGCCGTCAGCACCCGACCCAACAACAGCGGCTCCTTT GTCGTCAACTCGCCCAATGTCAGCTACAGCGACAGCGACATCAAGTCGACGTACACGTACCGCACCACCCGCGTC GAGACGGACGCCCAGGGCCAGCTGGTGGCGACGCCCAACGAGGTGGTCTACGACTTCAAGACGGACCGCCGCGTG CCTCGAGTCGGCATGATGCTCGTGGGCTGGGGCGGCAACAACGGCACCACCGTCACGGCCGGCATCCTGGCCAAT CGCCGCGGGCTCGTCTGGCAGACCAAGGAGGGCCCTCGCGCCGCCAATTACTACGGATCCGTCGTCATGGGCTCC ACCATGAAGCTGGGCAGCGAGCGCGGCACCAACAAGGACGTCAATGTGCCCTTCCACAGCGTCTTGCCCATGGTG CACCCCAACGACCTCGTCATTGGCGGCTGGGACATTAGCAAGATGAATCTGTCCCAGGCCATGGACCGCGCCCAG GTGCTGGAGCCGACTCTCAAAGCCCAGGTGTCCAAGGAAATGGCCGAGATGGTGCCGCTGCCCTCCATCTACTAC CCGGACTTTATTGCCGCCAACCAGGAGGACCGGGCCGACAATATCATTGCGGGCGACCGGGCGTCCATGGCCCAC GTCGAGCATCTGCGCCGCGACATCCGCGACTTCAAGGAGCGCAACGGGCTCGACAAGGTCATTGTCATGTGGACG GCCAACACGGAGCGCTACGCCCATGTGCTGGCGGGCGTCAACGACACGGCCGACAATCTGCTGCGCGCCATTGAG CAGGGCCACGCCGAGGTGTCGCCGTCAACCGTCTTTGCCGTGGCGTGCATTCTCGAGCAGACGCCCTTTATCAAT GGCTCGCCGCAAAACACCTTTGTGCCGGGAGCCATTGAGCTGGCCGAGGCCAAGGGCGCCTTTATCGGCGGCGAC GACTTCAAGTCGGGCCAGACCAAGATGAAGTCGGCCCTCGTCGACTTTCTCATCAACGCCGGCATCAAACTGACC TCCATCGCCAGCTACAACCACTTGGGCAACAATGACGGCAAGAACCTGAGCTCGCAGAAGCAGTTCCGCTCCAAG GAGATTTCAAAGTCCAACGTGGTTGACGACATGGTCGAGGCCAACTCCGTGCTCTATGCCAAGGGGGAGCACCCG GACCACTGCGTCGTCATCAAGTACATGCCCGCCGTGGCCGACAACAAGCGCGCTCTCGACGAGTACTATGCCGAG ATTTTCCTGGGCGGACACCAGACCATTTCGTGAGTTTTTTCCCCCCTCTTTTTTTATCTTTTTTCTTTTCTTTTC TTTTCTTTTTTCTTTTCCTTTTTTTCCTTTTTTCTTTTTTCTCTCCTCTCTCTTCTTTGATGCCCTCGCACTAGT CCCAGCAGTCACTGACCCTTTGCGCCGCGCAGCCTCTTCAACATTTGCGAAGATTCTCTATTGGCGTCGCCACTC ATCATCGACCTCGTCCTTCTGGCCGAGATGATGACGCGCATCCAGTGGAAGCTGTCGGGTGCCTCGGGCGGCTAC AAAAACTTCCACAGCGTGCTCAGCGTGCTCAGCTACATGCTCAAGGCGCCCATGACGCCTCCTGGCACGCCCGTC GTCAACTCGCTGGCAAAGCAACGCGCTGCATTGACCAACATCTTTCGGGCTTGCGTTGGCCTGGAGCCTGAGTCG GACATGACGCTTGAACACAAGCTCTTTTAA |