blastp_kegg |
lcl|fve:101314646
|
1 |
418 |
+ |
418 |
Gaps:3 |
100.00 |
415 |
87.95 |
0.0 |
mannose-1-phosphate guanyltransferase alpha-like
|
blastp_kegg |
lcl|tcc:TCM_017958
|
1 |
418 |
+ |
418 |
Gaps:5 |
100.00 |
417 |
87.29 |
0.0 |
ADP-glucose pyrophosphorylase family protein isoform 1
|
blastp_kegg |
lcl|cic:CICLE_v10015419mg
|
6 |
418 |
+ |
413 |
Gaps:3 |
99.76 |
411 |
88.78 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102615470
|
6 |
418 |
+ |
413 |
Gaps:4 |
99.76 |
412 |
89.05 |
0.0 |
mannose-1-phosphate guanyltransferase alpha-like
|
blastp_kegg |
lcl|vvi:100255999
|
1 |
418 |
+ |
418 |
Gaps:3 |
100.00 |
415 |
86.75 |
0.0 |
mannose-1-phosphate guanyltransferase alpha-like
|
blastp_kegg |
lcl|mtr:MTR_6g008840
|
4 |
418 |
+ |
415 |
Gaps:4 |
99.52 |
421 |
86.63 |
0.0 |
Mannose-1-phosphate guanyltransferase alpha-B
|
blastp_kegg |
lcl|pmum:103338287
|
1 |
418 |
+ |
418 |
Gaps:3 |
100.00 |
415 |
84.58 |
0.0 |
mannose-1-phosphate guanyltransferase alpha
|
blastp_kegg |
lcl|pper:PRUPE_ppa006436mg
|
5 |
418 |
+ |
414 |
Gaps:3 |
99.76 |
412 |
89.29 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cmo:103487048
|
1 |
418 |
+ |
418 |
Gaps:4 |
100.00 |
414 |
86.23 |
0.0 |
mannose-1-phosphate guanyltransferase alpha
|
blastp_kegg |
lcl|pmum:103329929
|
5 |
418 |
+ |
414 |
Gaps:3 |
99.76 |
412 |
89.29 |
0.0 |
mannose-1-phosphate guanyltransferase alpha
|
blastp_pdb |
4ecm_A
|
10 |
200 |
+ |
191 |
Gaps:10 |
67.29 |
269 |
24.31 |
5e-06 |
mol:protein length:269 Glucose-1-phosphate thymidylyltransferase
|
blastp_pdb |
3hl3_A
|
10 |
200 |
+ |
191 |
Gaps:10 |
67.29 |
269 |
24.31 |
5e-06 |
mol:protein length:269 Glucose-1-phosphate thymidylyltransferase
|
blastp_uniprot_sprot |
sp|Q86HG0|GMPPA_DICDI
|
1 |
418 |
+ |
418 |
Gaps:16 |
100.00 |
412 |
45.15 |
1e-122 |
Mannose-1-phosphate guanyltransferase alpha OS Dictyostelium discoideum GN gmppA PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7SXP8|GMPAB_DANRE
|
10 |
418 |
+ |
409 |
Gaps:28 |
99.29 |
422 |
45.11 |
2e-122 |
Mannose-1-phosphate guanyltransferase alpha-B OS Danio rerio GN gmppab PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6GMK8|GMPAA_DANRE
|
10 |
418 |
+ |
409 |
Gaps:36 |
99.29 |
422 |
44.87 |
3e-122 |
Mannose-1-phosphate guanyltransferase alpha-A OS Danio rerio GN gmppaa PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q0VFM6|GMPPA_XENTR
|
10 |
418 |
+ |
409 |
Gaps:33 |
99.29 |
421 |
45.22 |
1e-121 |
Mannose-1-phosphate guanyltransferase alpha OS Xenopus tropicalis GN gmppa PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6DKE9|GMPAA_XENLA
|
10 |
418 |
+ |
409 |
Gaps:33 |
99.29 |
421 |
44.98 |
8e-119 |
Mannose-1-phosphate guanyltransferase alpha-A OS Xenopus laevis GN gmppa-a PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q66KG5|GMPAB_XENLA
|
10 |
418 |
+ |
409 |
Gaps:28 |
99.30 |
426 |
44.44 |
1e-118 |
Mannose-1-phosphate guanyltransferase alpha-B OS Xenopus laevis GN gmppa-b PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q96IJ6|GMPPA_HUMAN
|
10 |
418 |
+ |
409 |
Gaps:34 |
99.29 |
420 |
44.84 |
9e-117 |
Mannose-1-phosphate guanyltransferase alpha OS Homo sapiens GN GMPPA PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q922H4|GMPPA_MOUSE
|
10 |
418 |
+ |
409 |
Gaps:28 |
99.29 |
420 |
44.12 |
1e-116 |
Mannose-1-phosphate guanyltransferase alpha OS Mus musculus GN Gmppa PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B0CM52|GMPPA_PAPAN
|
10 |
418 |
+ |
409 |
Gaps:26 |
99.29 |
420 |
44.36 |
2e-116 |
Mannose-1-phosphate guanyltransferase alpha OS Papio anubis GN GMPPA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|I3LUP1|GMPPA_PIG
|
10 |
418 |
+ |
409 |
Gaps:26 |
99.29 |
420 |
43.88 |
6e-115 |
Mannose-1-phosphate guanyltransferase alpha OS Sus scrofa GN GMPPA PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|133050
|
10 |
274 |
+ |
265 |
Gaps:8 |
100.00 |
257 |
54.09 |
1e-119 |
cd06428 M1P_guanylylT_A_like_N N-terminal domain of M1P_guanylyl_A_ like proteins are likely to be a isoform of GDP-mannose pyrophosphorylase. N-terminal domain of the M1P-guanylyltransferase A-isoform like proteins: The proteins of this family are likely to be a isoform of GDP-mannose pyrophosphorylase. Their sequences are highly conserved with mannose-1-phosphate guanyltransferase but generally about 40-60 bases longer. GDP-mannose pyrophosphorylase (GTP: alpha-d-mannose-1-phosphate guanyltransferase) catalyzes the formation of GDP-d-mannose from GTP and alpha-d-mannose-1-Phosphate. It contains an N-terminal catalytic domain that resembles a dinucleotide-binding Rossmann fold and a C-terminal LbH fold domain. GDP-d-mannose is the activated form of mannose for formation of cell wall lipoarabinomannan and various mannose-containing glycolipids and polysaccharides. The function of GDP-mannose pyrophosphorylase is essential for cell wall integrity morphogenesis and viability. Repression of GDP-mannose pyrophosphorylase in yeast leads to phenotypes including cell lysis defective cell wall and failure of polarized growth and cell separation.
|
rpsblast_cdd |
gnl|CDD|31401
|
10 |
397 |
+ |
388 |
Gaps:41 |
99.16 |
358 |
30.70 |
7e-49 |
COG1208 GCD1 Nucleoside-diphosphate-sugar pyrophosphorylase involved in lipopolysaccharide biosynthesis/translation initiation factor 2B gamma/epsilon subunits (eIF-2Bgamma/eIF-2Bepsilon) [Cell envelope biogenesis outer membrane / Translation ribosomal structure and biogenesis].
|
rpsblast_cdd |
gnl|CDD|133047
|
10 |
275 |
+ |
266 |
Gaps:35 |
99.14 |
233 |
36.80 |
2e-39 |
cd06425 M1P_guanylylT_B_like_N N-terminal domain of the M1P-guanylyltransferase B-isoform like proteins. GDP-mannose pyrophosphorylase (GTP: alpha-d-mannose-1-phosphate guanyltransferase) catalyzes the formation of GDP-d-mannose from GTP and alpha-d-mannose-1-Phosphate. It contains an N-terminal catalytic domain and a C-terminal Lefthanded-beta-Helix fold domain. GDP-d-mannose is the activated form of mannose for formation of cell wall lipoarabinomannan and various mannose-containing glycolipids and polysaccharides. The function of GDP-mannose pyrophosphorylase is essential for cell wall integrity morphogenesis and viability. Repression of GDP-mannose pyrophosphorylase in yeast leads to phenotypes such as cell lysis defective cell wall and failure of polarized growth and cell separation.
|
rpsblast_cdd |
gnl|CDD|133024
|
10 |
261 |
+ |
252 |
Gaps:36 |
99.54 |
217 |
31.94 |
1e-37 |
cd04181 NTP_transferase NTP_transferases catalyze the transfer of nucleotides onto phosphosugars. Nucleotidyltransferases transfer nucleotides onto phosphosugars. The enzyme family includes Alpha-D-Glucose-1-Phosphate Cytidylyltransferase Mannose-1-phosphate guanyltransferase and Glucose-1-phosphate thymidylyltransferase. The products are activated sugars that are precursors for synthesis of lipopolysaccharide glycolipids and polysaccharides.
|
rpsblast_cdd |
gnl|CDD|188507
|
10 |
362 |
+ |
353 |
Gaps:67 |
82.95 |
393 |
28.83 |
5e-26 |
TIGR03992 Arch_glmU UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase. The MJ_1101 protein from Methanococcus jannaschii has been characterized as the GlmU enzyme catalyzing the final two steps of UDP-GlcNAc biosynthesis. Many of the genes identified by this model are in proximity to the GlmS and GlmM genes and are also presumed to be GlmU. However some archaeal genomes contain multiple closely-related homologs from this family and it is not clear what the substrate specificity is for each of them.
|
rpsblast_cdd |
gnl|CDD|144176
|
10 |
196 |
+ |
187 |
Gaps:10 |
74.90 |
247 |
23.78 |
2e-22 |
pfam00483 NTP_transferase Nucleotidyl transferase. This family includes a wide range of enzymes which transfer nucleotides onto phosphosugars.
|
rpsblast_cdd |
gnl|CDD|133032
|
10 |
200 |
+ |
191 |
Gaps:11 |
76.27 |
236 |
29.44 |
6e-20 |
cd04189 G1P_TT_long G1P_TT_long represents the long form of glucose-1-phosphate thymidylyltransferase. This family is the long form of Glucose-1-phosphate thymidylyltransferase. Glucose-1-phosphate thymidylyltransferase catalyses the formation of dTDP-glucose from dTTP and glucose 1-phosphate. It is the first enzyme in the biosynthesis of dTDP-L-rhamnose a cell wall constituent and a feedback inhibitor of the enzyme.There are two forms of Glucose-1-phosphate thymidylyltransferase in bacteria and archeae short form and long form. The long form which has an extra 50 amino acids c-terminal is found in many species for which it serves as a sugar-activating enzyme for antibiotic biosynthesis and or other unknown pathways and in which dTDP-L-rhamnose is not necessarily produced.The long from enzymes also have a left-handed parallel helix domain at the c-terminus whereas th eshort form enzymes do not have this domain. The homotetrameric feedback inhibited short form is found in numerous bacterial species that produce dTDP-L-rhamnose.
|
rpsblast_cdd |
gnl|CDD|133065
|
10 |
254 |
+ |
245 |
Gaps:67 |
92.38 |
223 |
29.61 |
1e-19 |
cd06915 NTP_transferase_WcbM_like WcbM_like is a subfamily of nucleotidyl transferases. WcbM protein of Burkholderia mallei is involved in the biosynthesis export or translocation of capsule. It is a subfamily of nucleotidyl transferases that transfer nucleotides onto phosphosugars.
|