blastp_kegg |
lcl|mdm:103420733
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.70 |
460 |
76.52 |
2e-127 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic-like
|
blastp_kegg |
lcl|rcu:RCOM_0938310
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.00 |
466 |
76.92 |
2e-127 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase putative (EC:1.17.1.2)
|
blastp_kegg |
lcl|gmx:100818067
|
2 |
230 |
+ |
229 |
Gaps:19 |
53.68 |
462 |
74.60 |
3e-127 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic-like
|
blastp_kegg |
lcl|sly:100316901
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.58 |
461 |
75.71 |
6e-127 |
ISPH protein
|
blastp_kegg |
lcl|pop:POPTR_0009s11480g
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.70 |
460 |
76.52 |
8e-127 |
POPTRDRAFT_557296 chloroplast biogenesis family protein
|
blastp_kegg |
lcl|pxb:103964132
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.70 |
460 |
76.11 |
8e-127 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic
|
blastp_kegg |
lcl|pxb:103962553
|
2 |
229 |
+ |
228 |
Gaps:19 |
64.66 |
382 |
75.71 |
1e-126 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic-like
|
blastp_kegg |
lcl|mus:103993826
|
2 |
229 |
+ |
228 |
Gaps:19 |
54.29 |
455 |
74.90 |
2e-126 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic-like
|
blastp_kegg |
lcl|gmx:100805941
|
2 |
230 |
+ |
229 |
Gaps:19 |
53.68 |
462 |
74.19 |
2e-126 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic-like
|
blastp_kegg |
lcl|pmum:103335515
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.58 |
461 |
75.30 |
4e-126 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic
|
blastp_uniprot_sprot |
sp|Q94B35|ISPH_ARATH
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.00 |
466 |
72.87 |
3e-123 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic OS Arabidopsis thaliana GN ISPH PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6AVG6|ISPH_ORYSJ
|
2 |
228 |
+ |
227 |
Gaps:19 |
53.59 |
459 |
73.98 |
2e-122 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase chloroplastic OS Oryza sativa subsp. japonica GN ISPH PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B8HWD3|ISPH_CYAP4
|
2 |
222 |
+ |
221 |
Gaps:27 |
57.78 |
405 |
59.40 |
2e-86 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Cyanothece sp. (strain PCC 7425 / ATCC 29141) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5N249|ISPH_SYNP6
|
2 |
222 |
+ |
221 |
Gaps:27 |
58.79 |
398 |
55.98 |
7e-83 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Synechococcus sp. (strain ATCC 27144 / PCC 6301 / SAUG 1402/1) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q31S64|ISPH_SYNE7
|
2 |
222 |
+ |
221 |
Gaps:27 |
58.79 |
398 |
55.98 |
7e-83 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Synechococcus elongatus (strain PCC 7942) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P58674|ISPH_NOSS1
|
2 |
227 |
+ |
226 |
Gaps:25 |
59.45 |
402 |
56.07 |
2e-82 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Nostoc sp. (strain PCC 7120 / UTEX 2576) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q3M8X6|ISPH_ANAVT
|
2 |
227 |
+ |
226 |
Gaps:25 |
59.45 |
402 |
55.65 |
4e-82 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Anabaena variabilis (strain ATCC 29413 / PCC 7937) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B0C4N8|ISPH_ACAM1
|
2 |
226 |
+ |
225 |
Gaps:21 |
59.28 |
415 |
53.25 |
7e-81 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Acaryochloris marina (strain MBIC 11017) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B2IZV5|ISPH_NOSP7
|
2 |
227 |
+ |
226 |
Gaps:25 |
59.45 |
402 |
54.81 |
7e-80 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Nostoc punctiforme (strain ATCC 29133 / PCC 73102) GN ispH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8DK29|ISPH_THEEB
|
2 |
227 |
+ |
226 |
Gaps:27 |
59.45 |
402 |
57.32 |
2e-79 |
4-hydroxy-3-methylbut-2-enyl diphosphate reductase OS Thermosynechococcus elongatus (strain BP-1) GN ispH PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|178416
|
2 |
229 |
+ |
228 |
Gaps:19 |
53.70 |
460 |
75.30 |
1e-119 |
PLN02821 PLN02821 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase.
|
rpsblast_cdd |
gnl|CDD|184010
|
2 |
226 |
+ |
225 |
Gaps:25 |
61.50 |
387 |
58.82 |
8e-95 |
PRK13371 PRK13371 4-hydroxy-3-methylbut-2-enyl diphosphate reductase Provisional.
|
rpsblast_cdd |
gnl|CDD|190300
|
2 |
221 |
+ |
220 |
Gaps:61 |
64.64 |
280 |
34.81 |
8e-27 |
pfam02401 LYTB LytB protein. The mevalonate-independent 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway for isoprenoid biosynthesis is essential in many eubacteria plants and the malaria parasite. The LytB gene is involved in the trunk line of the MEP pathway.
|
rpsblast_cdd |
gnl|CDD|161769
|
2 |
221 |
+ |
220 |
Gaps:63 |
63.93 |
280 |
37.99 |
1e-22 |
TIGR00216 ispH_lytB (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate reductase (IPP and DMAPP forming). The IspH protein (previously designated LytB) has now been recognized as the last enzyme in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Escherichia coli LytB protein had been found to regulate the activity of RelA (guanosine 3' 5'-bispyrophosphate synthetase I) which in turn controls the level of a regulatory metabolite. It is involved in penicillin tolerance and the stringent response.
|
rpsblast_cdd |
gnl|CDD|31104
|
2 |
222 |
+ |
221 |
Gaps:60 |
62.24 |
294 |
33.33 |
8e-22 |
COG0761 LytB Penicillin tolerance protein [Lipid metabolism / Cell envelope biogenesis outer membrane].
|
rpsblast_cdd |
gnl|CDD|179212
|
88 |
227 |
+ |
140 |
Gaps:32 |
44.97 |
298 |
32.84 |
6e-12 |
PRK01045 ispH 4-hydroxy-3-methylbut-2-enyl diphosphate reductase Reviewed.
|
rpsblast_cdd |
gnl|CDD|178853
|
88 |
222 |
+ |
135 |
Gaps:32 |
19.32 |
647 |
34.40 |
1e-10 |
PRK00087 PRK00087 4-hydroxy-3-methylbut-2-enyl diphosphate reductase/S1 RNA-binding domain protein Reviewed.
|
rpsblast_cdd |
gnl|CDD|183472
|
86 |
221 |
+ |
136 |
Gaps:28 |
44.84 |
281 |
27.78 |
9e-07 |
PRK12360 PRK12360 4-hydroxy-3-methylbut-2-enyl diphosphate reductase Provisional.
|