blastp_kegg |
lcl|csv:101224375
|
3 |
257 |
+ |
255 |
Gaps:3 |
98.44 |
256 |
80.16 |
5e-143 |
hemK methyltransferase family member 2-like
|
blastp_kegg |
lcl|csv:101206675
|
3 |
257 |
+ |
255 |
Gaps:3 |
98.44 |
256 |
80.16 |
5e-143 |
hemK methyltransferase family member 2-like
|
blastp_kegg |
lcl|cic:CICLE_v10016345mg
|
1 |
258 |
+ |
258 |
Gaps:2 |
100.00 |
256 |
77.73 |
2e-142 |
hypothetical protein
|
blastp_kegg |
lcl|cmo:103495363
|
3 |
255 |
+ |
253 |
Gaps:3 |
97.66 |
256 |
80.40 |
4e-142 |
hemK methyltransferase family member 2
|
blastp_kegg |
lcl|pmum:103325545
|
1 |
256 |
+ |
256 |
Gaps:5 |
99.60 |
252 |
80.08 |
1e-141 |
hemK methyltransferase family member 2
|
blastp_kegg |
lcl|cit:102617336
|
1 |
258 |
+ |
258 |
Gaps:2 |
100.00 |
256 |
77.34 |
3e-141 |
hemK methyltransferase family member 2-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa018312mg
|
1 |
256 |
+ |
256 |
Gaps:5 |
99.60 |
252 |
79.68 |
2e-140 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101294148
|
1 |
258 |
+ |
258 |
Gaps:5 |
100.00 |
253 |
78.26 |
9e-140 |
hemK methyltransferase family member 2-like
|
blastp_kegg |
lcl|rcu:RCOM_0096960
|
1 |
257 |
+ |
257 |
Gaps:1 |
100.00 |
256 |
78.12 |
8e-139 |
n6-DNA-methyltransferase putative
|
blastp_kegg |
lcl|tcc:TCM_021198
|
1 |
258 |
+ |
258 |
Gaps:1 |
98.47 |
261 |
75.10 |
2e-138 |
S-adenosyl-L-methionine-dependent methyltransferases superfamily protein
|
blastp_pdb |
3q87_B
|
18 |
210 |
+ |
193 |
Gaps:36 |
92.35 |
170 |
37.58 |
5e-16 |
mol:protein length:170 N6 adenine specific DNA methylase
|
blastp_uniprot_sprot |
sp|Q9Y5N5|HEMK2_HUMAN
|
16 |
213 |
+ |
198 |
Gaps:5 |
90.19 |
214 |
45.08 |
3e-44 |
HemK methyltransferase family member 2 OS Homo sapiens GN N6AMT1 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9UT94|MTQ2_SCHPO
|
6 |
213 |
+ |
208 |
Gaps:16 |
93.51 |
231 |
33.33 |
7e-27 |
eRF1 methyltransferase catalytic subunit mtq2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN mtq2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q58338|Y928_METJA
|
1 |
213 |
+ |
213 |
Gaps:17 |
99.49 |
197 |
32.65 |
6e-23 |
Putative protein methyltransferase MJ0928 OS Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN MJ0928 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q03920|MTQ2_YEAST
|
14 |
213 |
+ |
200 |
Gaps:21 |
95.48 |
221 |
29.38 |
1e-15 |
eRF1 methyltransferase catalytic subunit MTQ2 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN MTQ2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q748B2|PRMC_GEOSL
|
42 |
198 |
+ |
157 |
Gaps:17 |
54.23 |
284 |
27.92 |
2e-07 |
Release factor glutamine methyltransferase OS Geobacter sulfurreducens (strain ATCC 51573 / DSM 12127 / PCA) GN prmC PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O28490|Y1784_ARCFU
|
47 |
213 |
+ |
167 |
Gaps:19 |
84.75 |
177 |
32.67 |
6e-07 |
Putative protein methyltransferase AF_1784 OS Archaeoglobus fulgidus (strain ATCC 49558 / VC-16 / DSM 4304 / JCM 9628 / NBRC 100126) GN AF_1784 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9Y5R4|HEMK1_HUMAN
|
45 |
199 |
+ |
155 |
Gaps:16 |
47.63 |
338 |
31.68 |
1e-06 |
HemK methyltransferase family member 1 OS Homo sapiens GN HEMK1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O66506|PRMC_AQUAE
|
47 |
169 |
+ |
123 |
Gaps:17 |
43.42 |
281 |
35.25 |
4e-06 |
Release factor glutamine methyltransferase OS Aquifex aeolicus (strain VF5) GN prmC PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A0R213|PRMC_MYCS2
|
59 |
167 |
+ |
109 |
Gaps:6 |
39.50 |
281 |
35.14 |
8e-06 |
Release factor glutamine methyltransferase OS Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN prmC PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|184932
|
14 |
213 |
+ |
200 |
Gaps:23 |
99.47 |
188 |
29.95 |
6e-29 |
PRK14968 PRK14968 putative methyltransferase Provisional.
|
rpsblast_cdd |
gnl|CDD|129628
|
17 |
212 |
+ |
196 |
Gaps:17 |
100.00 |
179 |
32.96 |
2e-23 |
TIGR00537 hemK_rel_arch HemK-related putative methylase. The gene hemK from E. coli was found to contribute to heme biosynthesis and originally suggested to be protoporphyrinogen oxidase. Functional analysis of the nearest homolog in Saccharomyces cerevisiae YNL063w finds it is not protoporphyrinogen oxidase and sequence analysis suggests that HemK homologs have S-adenosyl-methionine-dependent methyltransferase activity. Homologs are found usually in a single copy in nearly all completed genomes but varying somewhat in apparent domain architecture. This model represents an archaeal and eukaryotic protein family that lacks an N-terminal domain found in HemK and its eubacterial homologs. It is found in a single copy in the first six completed archaeal and eukaryotic genomes.
|
rpsblast_cdd |
gnl|CDD|32715
|
15 |
171 |
+ |
157 |
Gaps:17 |
53.57 |
280 |
32.67 |
6e-22 |
COG2890 HemK Methylase of polypeptide chain release factors [Translation ribosomal structure and biogenesis].
|
rpsblast_cdd |
gnl|CDD|184931
|
15 |
200 |
+ |
186 |
Gaps:12 |
78.03 |
223 |
32.76 |
8e-19 |
PRK14967 PRK14967 putative methyltransferase Provisional.
|
rpsblast_cdd |
gnl|CDD|200288
|
15 |
171 |
+ |
157 |
Gaps:21 |
60.56 |
251 |
32.89 |
2e-14 |
TIGR03534 RF_mod_PrmC protein-(glutamine-N5) methyltransferase release factor-specific. Members of this protein family are HemK (PrmC) a protein once thought to be involved in heme biosynthesis but now recognized to be a protein-glutamine methyltransferase that modifies the peptide chain release factors. All members of the seed alignment are encoded next to the release factor 1 gene (prfA) and confirmed by phylogenetic analysis. SIMBAL analysis (manuscript in prep.) shows the motif [LIV]PRx[DE]TE (in Escherichia coli IPRPDTE) confers specificity for the release factors rather than for ribosomal protein L3.
|
rpsblast_cdd |
gnl|CDD|181780
|
27 |
171 |
+ |
145 |
Gaps:18 |
51.27 |
275 |
30.50 |
3e-13 |
PRK09328 PRK09328 N5-glutamine S-adenosyl-L-methionine-dependent methyltransferase Provisional.
|
rpsblast_cdd |
gnl|CDD|205836
|
43 |
173 |
+ |
131 |
Gaps:20 |
98.29 |
117 |
27.83 |
7e-10 |
pfam13659 Methyltransf_26 Methyltransferase domain. This family contains methyltransferase domains.
|
rpsblast_cdd |
gnl|CDD|203189
|
13 |
173 |
+ |
161 |
Gaps:34 |
79.41 |
170 |
27.41 |
3e-09 |
pfam05175 MTS Methyltransferase small domain. This domain is found in ribosomal RNA small subunit methyltransferase C as well as other methyltransferases .
|
rpsblast_cdd |
gnl|CDD|129627
|
26 |
169 |
+ |
144 |
Gaps:17 |
49.65 |
284 |
31.21 |
3e-08 |
TIGR00536 hemK_fam HemK family putative methylases. The gene hemK from E. coli was found to contribute to heme biosynthesis and originally suggested to be protoporphyrinogen oxidase. Functional analysis of the nearest homolog in Saccharomyces cerevisiae YNL063w finds it is not protoporphyrinogen oxidase and sequence analysis suggests that HemK homologs have S-adenosyl-methionine-dependent methyltransferase activity. Homologs are found usually in a single copy in nearly all completed genomes but varying somewhat in apparent domain architecture. Both E. coli and H. influenzae have two members rather than one. The members from the Mycoplasmas have an additional C-terminal domain.
|
rpsblast_cdd |
gnl|CDD|163416
|
11 |
209 |
+ |
199 |
Gaps:25 |
76.49 |
251 |
27.60 |
3e-07 |
TIGR03704 PrmC_rel_meth putative protein-(glutamine-N5) methyltransferase unknown substrate-specific. This protein family is closely related to two different families of protein-(glutamine-N5) methyltransferase. The first is PrmB which modifies ribosomal protein L3 in some bacteria. The second is PrmC (HemK) which modifies peptide chain release factors 1 and 2 in most bacteria and also in eukaryotes. The glutamine side chain-binding motif NPPY shared by PrmB and PrmC is N[VAT]PY in this family. The protein substrate is unknown.
|