blastp_kegg |
lcl|rcu:RCOM_1428040
|
1 |
573 |
+ |
573 |
Gaps:14 |
60.89 |
964 |
84.84 |
0.0 |
Zeta-carotene desaturase chloroplast precursor putative (EC:1.14.99.30)
|
blastp_kegg |
lcl|pop:POPTR_0005s05230g
|
1 |
573 |
+ |
573 |
Gaps:16 |
100.00 |
589 |
84.38 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100245154
|
1 |
573 |
+ |
573 |
Gaps:16 |
100.00 |
583 |
85.08 |
0.0 |
zeta-carotene desaturase chloroplastic/chromoplastic-like
|
blastp_kegg |
lcl|pop:POPTR_0013s03470g
|
1 |
573 |
+ |
573 |
Gaps:17 |
100.00 |
582 |
84.19 |
0.0 |
POPTRDRAFT_806861 hypothetical protein
|
blastp_kegg |
lcl|pmum:103318575
|
1 |
573 |
+ |
573 |
Gaps:28 |
100.00 |
571 |
86.16 |
0.0 |
PmZDS zeta-carotene desaturase chloroplastic/chromoplastic
|
blastp_kegg |
lcl|pper:PRUPE_ppa003478mg
|
1 |
573 |
+ |
573 |
Gaps:28 |
100.00 |
571 |
86.16 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103434148
|
1 |
573 |
+ |
573 |
Gaps:22 |
100.00 |
571 |
85.11 |
0.0 |
zeta-carotene desaturase chloroplastic/chromoplastic-like
|
blastp_kegg |
lcl|mdm:103451012
|
1 |
573 |
+ |
573 |
Gaps:28 |
100.00 |
571 |
84.76 |
0.0 |
zeta-carotene desaturase chloroplastic/chromoplastic
|
blastp_kegg |
lcl|cit:102577969
|
1 |
573 |
+ |
573 |
Gaps:25 |
100.00 |
570 |
84.56 |
0.0 |
CitZDS ZDS
|
blastp_kegg |
lcl|cam:101493508
|
1 |
573 |
+ |
573 |
Gaps:16 |
99.83 |
582 |
82.10 |
0.0 |
zeta-carotene desaturase chloroplastic/chromoplastic-like
|
blastp_uniprot_sprot |
sp|Q9SMJ3|ZDS_CAPAN
|
20 |
573 |
+ |
554 |
Gaps:14 |
95.58 |
588 |
82.92 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Capsicum annuum GN ZDS PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FV46|ZDS_TARER
|
8 |
573 |
+ |
566 |
Gaps:21 |
97.61 |
587 |
82.37 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Tagetes erecta PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SE20|ZDS_SOLLC
|
2 |
573 |
+ |
572 |
Gaps:18 |
99.32 |
588 |
79.62 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Solanum lycopersicum GN ZDS PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O49901|ZDS_NARPS
|
33 |
573 |
+ |
541 |
Gaps:14 |
95.64 |
574 |
83.42 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Narcissus pseudonarcissus GN ZDS1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q38893|ZDS_ARATH
|
22 |
573 |
+ |
552 |
Gaps:20 |
98.92 |
558 |
81.70 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Arabidopsis thaliana GN ZDS1 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9ZTP4|ZDS_MAIZE
|
62 |
552 |
+ |
491 |
Gaps:10 |
87.89 |
570 |
83.03 |
0.0 |
Zeta-carotene desaturase chloroplastic/chromoplastic OS Zea mays GN ZDS1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P74306|ZDS_SYNY3
|
75 |
538 |
+ |
464 |
Gaps:10 |
96.93 |
489 |
65.82 |
0.0 |
Zeta-carotene desaturase OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN crtQ PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9R6X4|ZDS_NOSS1
|
75 |
540 |
+ |
466 |
Gaps:9 |
99.16 |
479 |
61.89 |
0.0 |
Zeta-carotene desaturase OS Nostoc sp. (strain PCC 7120 / UTEX 2576) GN crtQ PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q31N27|ZDS_SYNE7
|
75 |
541 |
+ |
467 |
Gaps:9 |
98.96 |
481 |
61.13 |
0.0 |
Probable zeta-carotene desaturase OS Synechococcus elongatus (strain PCC 7942) GN zds PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q40406|CRTI_NARPS
|
65 |
556 |
+ |
492 |
Gaps:39 |
83.33 |
570 |
35.16 |
5e-77 |
Phytoene dehydrogenase chloroplastic/chromoplastic OS Narcissus pseudonarcissus GN PDS1 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|178105
|
6 |
557 |
+ |
552 |
Gaps:15 |
97.89 |
569 |
79.89 |
0.0 |
PLN02487 PLN02487 zeta-carotene desaturase.
|
rpsblast_cdd |
gnl|CDD|131779
|
76 |
539 |
+ |
464 |
Gaps:10 |
100.00 |
474 |
72.57 |
0.0 |
TIGR02732 zeta_caro_desat 9 9'-di-cis-zeta-carotene desaturase. Carotene 7 8-desaturase also called zeta-carotene desaturase catalyzes multiple steps in the pathway from geranylgeranyl-PP to all-trans-lycopene in plants and cyanobacteria. A similar enzyme and pathway is found in the green sulfur bacterium Chlorobium tepidum.
|
rpsblast_cdd |
gnl|CDD|33157
|
76 |
541 |
+ |
466 |
Gaps:31 |
95.05 |
485 |
44.25 |
1e-111 |
COG3349 COG3349 Uncharacterized conserved protein [Function unknown].
|
rpsblast_cdd |
gnl|CDD|178222
|
57 |
548 |
+ |
492 |
Gaps:47 |
82.72 |
567 |
36.25 |
9e-73 |
PLN02612 PLN02612 phytoene desaturase.
|
rpsblast_cdd |
gnl|CDD|131778
|
76 |
539 |
+ |
464 |
Gaps:43 |
100.00 |
453 |
35.54 |
1e-72 |
TIGR02731 phytoene_desat phytoene desaturase. Plants and cyanobacteria (and supposedly Chlorobium tepidum) have a conserved pathway from two molecules geranylgeranyl-PP to one of all-trans-lycopene. Members of this family are the enzyme pytoene desaturase (also called phytoene dehydrogenase). This model does not include the region of the chloroplast transit peptide in plants. A closely related family excluded by this model is zeta-carotene desaturase another enzyme in the same pathway.
|
rpsblast_cdd |
gnl|CDD|201877
|
84 |
536 |
+ |
453 |
Gaps:40 |
99.32 |
444 |
23.13 |
4e-57 |
pfam01593 Amino_oxidase Flavin containing amine oxidoreductase. This family consists of various amine oxidases including maze polyamine oxidase (PAO) and various flavin containing monoamine oxidases (MAO). The aligned region includes the flavin binding site of these enzymes. The family also contains phytoene dehydrogenases and related enzymes. In vertebrates MAO plays an important role regulating the intracellular levels of amines via there oxidation these include various neurotransmitters neurotoxins and trace amines. In lower eukaryotes such as aspergillus and in bacteria the main role of amine oxidases is to provide a source of ammonium. PAOs in plants bacteria and protozoa oxidase spermidine and spermine to an aminobutyral diaminopropane and hydrogen peroxide and are involved in the catabolism of polyamines. Other members of this family include tryptophan 2-monooxygenase putrescine oxidase corticosteroid binding proteins and antibacterial glycoproteins.
|
rpsblast_cdd |
gnl|CDD|211821
|
77 |
538 |
+ |
462 |
Gaps:54 |
99.53 |
430 |
30.37 |
2e-46 |
TIGR03467 HpnE squalene-associated FAD-dependent desaturase. The sequences in this family are members of the pfam01593 superfamily of flavin-containing amine oxidases which include the phytoene desaturases. These sequences also include a FAD-dependent oxidoreductase domain pfam01266. The genes of the family modeled here are generally in the same locus with genes involved in the biosynthesis and elaboration of squalene the condensation product of the polyisoprenoid farnesyl pyrophosphate. This gene and its association with hopene biosynthesis in Zymomonas mobilis has been noted in the literature where the gene symbol hpnE was assigned. This gene is also found in contexts where the downstream conversion of squalene to hopenes is not evidence. The precise nature of the reaction catalyzed by this enzyme is unknown at this time.
|
rpsblast_cdd |
gnl|CDD|180899
|
76 |
538 |
+ |
463 |
Gaps:98 |
98.39 |
434 |
23.89 |
7e-17 |
PRK07233 PRK07233 hypothetical protein Provisional.
|
rpsblast_cdd |
gnl|CDD|205628
|
79 |
145 |
+ |
67 |
Gaps:1 |
100.00 |
66 |
36.36 |
4e-12 |
pfam13450 NAD_binding_8 NAD(P)-binding Rossmann-like domain.
|
rpsblast_cdd |
gnl|CDD|31425
|
76 |
309 |
+ |
234 |
Gaps:26 |
47.75 |
444 |
27.36 |
3e-11 |
COG1232 HemY Protoporphyrinogen oxidase [Coenzyme metabolism].
|