blastp_kegg |
lcl|pop:POPTR_0002s09570g
|
2 |
350 |
+ |
349 |
Gaps:3 |
99.14 |
349 |
71.10 |
7e-177 |
POPTRDRAFT_410213 hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa007824mg
|
1 |
350 |
+ |
350 |
Gaps:5 |
99.72 |
354 |
68.84 |
5e-174 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103319857
|
1 |
350 |
+ |
350 |
Gaps:5 |
99.72 |
354 |
67.71 |
3e-171 |
uncharacterized methyltransferase At1g78140 chloroplastic
|
blastp_kegg |
lcl|cit:102611456
|
13 |
350 |
+ |
338 |
Gaps:4 |
95.16 |
351 |
70.06 |
4e-168 |
uncharacterized LOC102611456
|
blastp_kegg |
lcl|vvi:100252381
|
1 |
350 |
+ |
350 |
Gaps:7 |
99.71 |
350 |
68.48 |
2e-163 |
uncharacterized LOC100252381
|
blastp_kegg |
lcl|gmx:100819297
|
32 |
350 |
+ |
319 |
Gaps:8 |
92.90 |
352 |
70.95 |
5e-162 |
uncharacterized LOC100819297
|
blastp_kegg |
lcl|mdm:103453319
|
1 |
350 |
+ |
350 |
Gaps:8 |
99.72 |
355 |
65.54 |
3e-159 |
uncharacterized methyltransferase At1g78140 chloroplastic-like
|
blastp_kegg |
lcl|pvu:PHAVU_009G030200g
|
32 |
350 |
+ |
319 |
Gaps:9 |
87.23 |
376 |
69.21 |
2e-158 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_034924
|
1 |
350 |
+ |
350 |
Gaps:23 |
99.73 |
366 |
64.93 |
2e-156 |
S-adenosylmethionine-dependent methyltransferase putative
|
blastp_kegg |
lcl|cam:101515568
|
39 |
350 |
+ |
312 |
Gaps:5 |
91.42 |
338 |
72.17 |
9e-156 |
uncharacterized LOC101515568
|
blastp_uniprot_sprot |
sp|Q8LBV4|Y1814_ARATH
|
70 |
350 |
+ |
281 |
Gaps:3 |
79.44 |
355 |
71.28 |
8e-145 |
Uncharacterized methyltransferase At1g78140 chloroplastic OS Arabidopsis thaliana GN At1g78140 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q0WPT7|Y2104_ARATH
|
1 |
350 |
+ |
350 |
Gaps:20 |
99.43 |
352 |
46.00 |
3e-92 |
Uncharacterized methyltransferase At2g41040 chloroplastic OS Arabidopsis thaliana GN At2g41040 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q4L6H3|UBIE_STAHJ
|
133 |
284 |
+ |
152 |
Gaps:23 |
55.65 |
239 |
34.59 |
5e-11 |
Demethylmenaquinone methyltransferase OS Staphylococcus haemolyticus (strain JCSC1435) GN ubiE PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6GGU0|UBIE_STAAR
|
133 |
284 |
+ |
152 |
Gaps:25 |
55.19 |
241 |
35.34 |
5e-11 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain MRSA252) GN ubiE PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P67063|UBIE_STAAW
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain MW2) GN ubiE PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A8Z450|UBIE_STAAT
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain USA300 / TCH1516) GN ubiE PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6G992|UBIE_STAAS
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain MSSA476) GN ubiE PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P67062|UBIE_STAAN
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain N315) GN ubiE PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P67061|UBIE_STAAM
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain Mu50 / ATCC 700699) GN ubiE PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A6QH20|UBIE_STAAE
|
184 |
284 |
+ |
101 |
Gaps:6 |
40.25 |
241 |
38.14 |
1e-10 |
Demethylmenaquinone methyltransferase OS Staphylococcus aureus (strain Newman) GN ubiE PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|203885
|
184 |
284 |
+ |
101 |
Gaps:10 |
98.91 |
92 |
36.26 |
4e-18 |
pfam08241 Methyltransf_11 Methyltransferase domain. Members of this family are SAM dependent methyltransferases.
|
rpsblast_cdd |
gnl|CDD|181382
|
165 |
345 |
+ |
181 |
Gaps:25 |
71.37 |
241 |
33.72 |
3e-16 |
PRK08317 PRK08317 hypothetical protein Provisional.
|
rpsblast_cdd |
gnl|CDD|211712
|
183 |
330 |
+ |
148 |
Gaps:16 |
55.00 |
240 |
32.58 |
3e-16 |
TIGR02072 BioC biotin biosynthesis protein BioC. This enzyme which is found in biotin biosynthetic gene clusters in proteobacteria firmicutes green-sulfur bacteria fusobacterium and bacteroides is believed to carry out an enzymatic step prior to the formation of pimeloyl-CoA (although attribution of this annotation is not traceable). The enzyme appears related to methyltransferases by homology.
|
rpsblast_cdd |
gnl|CDD|32408
|
141 |
284 |
+ |
144 |
Gaps:19 |
52.52 |
238 |
34.40 |
5e-15 |
COG2226 UbiE Methylase involved in ubiquinone/menaquinone biosynthesis [Coenzyme metabolism].
|
rpsblast_cdd |
gnl|CDD|200144
|
142 |
284 |
+ |
143 |
Gaps:22 |
55.16 |
223 |
31.71 |
4e-11 |
TIGR01934 MenG_MenH_UbiE ubiquinone/menaquinone biosynthesis methyltransferases. This model represents a family of methyltransferases involved in the biosynthesis of menaquinone and ubiqinone. Some members such as the UbiE enzyme from E. coli are believed to act in both pathways while others may act in only the menaquinone pathway. These methyltransferases are members of the UbiE/CoQ family of methyltransferases (pfam01209) which also contains ubiquinone methyltransferases and other methyltransferases. Members of this clade include a wide distribution of bacteria and eukaryotes but no archaea. An outgroup for this clade is provided by the phosphatidylethanolamine methyltransferase (EC 2.1.1.17) from Rhodobacter sphaeroides. Note that a number of non-orthologous genes which are members of pfam03737 have been erroneously annotated as MenG methyltransferases.
|
rpsblast_cdd |
gnl|CDD|182340
|
183 |
324 |
+ |
142 |
Gaps:14 |
51.00 |
251 |
35.16 |
5e-11 |
PRK10258 PRK10258 biotin biosynthesis protein BioC Provisional.
|
rpsblast_cdd |
gnl|CDD|178932
|
142 |
284 |
+ |
143 |
Gaps:25 |
52.72 |
239 |
34.92 |
1e-10 |
PRK00216 ubiE ubiquinone/menaquinone biosynthesis methyltransferase Reviewed.
|
rpsblast_cdd |
gnl|CDD|100107
|
183 |
290 |
+ |
108 |
Gaps:6 |
99.07 |
107 |
24.53 |
2e-10 |
cd02440 AdoMet_MTases S-adenosylmethionine-dependent methyltransferases (SAM or AdoMet-MTase) class I AdoMet-MTases are enzymes that use S-adenosyl-L-methionine (SAM or AdoMet) as a substrate for methyltransfer creating the product S-adenosyl-L-homocysteine (AdoHcy). There are at least five structurally distinct families of AdoMet-MTases class I being the largest and most diverse. Within this class enzymes can be classified by different substrate specificities (small molecules lipids nucleic acids etc.) and different target atoms for methylation (nitrogen oxygen carbon sulfur etc.)..
|
rpsblast_cdd |
gnl|CDD|203886
|
184 |
283 |
+ |
100 |
Gaps:2 |
100.00 |
98 |
24.49 |
3e-10 |
pfam08242 Methyltransf_12 Methyltransferase domain. Members of this family are SAM dependent methyltransferases.
|
rpsblast_cdd |
gnl|CDD|205104
|
183 |
288 |
+ |
106 |
Gaps:6 |
96.15 |
104 |
23.00 |
2e-09 |
pfam12847 Methyltransf_18 Methyltransferase domain. Protein in this family function as methyltransferases.
|