blastp_kegg |
lcl|tcc:TCM_046722
|
56 |
259 |
+ |
204 |
Gaps:6 |
37.97 |
532 |
80.69 |
3e-112 |
Bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 2 putative
|
blastp_kegg |
lcl|vvi:100247253
|
56 |
259 |
+ |
204 |
Gaps:2 |
38.04 |
531 |
77.72 |
3e-111 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 2-like
|
blastp_kegg |
lcl|atr:s00068p00163030
|
46 |
259 |
+ |
214 |
Gaps:4 |
40.15 |
523 |
74.29 |
1e-107 |
AMTR_s00068p00163030 hypothetical protein
|
blastp_kegg |
lcl|cmo:103493479
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.45 |
512 |
74.75 |
5e-106 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1
|
blastp_kegg |
lcl|mus:103989253
|
56 |
259 |
+ |
204 |
Gaps:2 |
38.48 |
525 |
73.27 |
7e-106 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1 {ECO:0000255|HAMAP-Rule:MF_03118}
|
blastp_kegg |
lcl|csv:101205098
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.45 |
512 |
73.76 |
6e-105 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1-like
|
blastp_kegg |
lcl|sly:101257584
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.76 |
508 |
73.27 |
2e-104 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1-like
|
blastp_kegg |
lcl|sot:102592458
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.22 |
515 |
72.28 |
2e-104 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1-like
|
blastp_kegg |
lcl|brp:103852010
|
56 |
259 |
+ |
204 |
Gaps:2 |
40.32 |
501 |
73.27 |
1e-103 |
probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1
|
blastp_kegg |
lcl|pper:PRUPE_ppa004202mg
|
56 |
259 |
+ |
204 |
Gaps:2 |
38.62 |
523 |
75.25 |
1e-102 |
hypothetical protein
|
blastp_uniprot_sprot |
sp|E0CTF3|MTBC2_VITVI
|
56 |
259 |
+ |
204 |
Gaps:2 |
38.04 |
531 |
77.72 |
1e-112 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 2 OS Vitis vinifera GN VIT_12s0028g03470 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|B9SQI7|MTBC_RICCO
|
56 |
259 |
+ |
204 |
Gaps:2 |
38.33 |
527 |
73.76 |
3e-102 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Ricinus communis GN RCOM_0591060 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B9N1F9|MTBC_POPTR
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.00 |
518 |
72.77 |
5e-100 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Populus trichocarpa GN POPTR_0001s40980g PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9FN41|MTBC_ARATH
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.84 |
507 |
73.27 |
9e-100 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Arabidopsis thaliana GN At5g53850 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|E0CSI1|MTBC1_VITVI
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.07 |
517 |
74.26 |
1e-99 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 1 OS Vitis vinifera GN VIT_19s0014g02480 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|A9RBS1|MTBC_PHYPA
|
56 |
259 |
+ |
204 |
Gaps:2 |
40.00 |
505 |
68.81 |
1e-96 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Physcomitrella patens subsp. patens GN PHYPADRAFT_111231 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q2R483|MTBC_ORYSJ
|
51 |
259 |
+ |
209 |
Gaps:4 |
39.58 |
518 |
68.29 |
5e-95 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Oryza sativa subsp. japonica GN Os11g0484000 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|C6JS30|MTBC_SORBI
|
51 |
259 |
+ |
209 |
Gaps:4 |
39.65 |
517 |
66.83 |
9e-95 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Sorghum bicolor GN SORBIDRAFT_0019s002010 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B4G0F3|MTBC_MAIZE
|
56 |
259 |
+ |
204 |
Gaps:2 |
39.07 |
517 |
65.35 |
5e-92 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Zea mays PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B8BKI7|MTBC_ORYSI
|
51 |
259 |
+ |
209 |
Gaps:4 |
39.58 |
518 |
67.32 |
9e-92 |
Probable bifunctional methylthioribulose-1-phosphate dehydratase/enolase-phosphatase E1 OS Oryza sativa subsp. indica GN OsI_36120 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|163216
|
69 |
268 |
+ |
200 |
Gaps:28 |
99.48 |
193 |
32.29 |
8e-55 |
TIGR03328 salvage_mtnB methylthioribulose-1-phosphate dehydratase. Members of this family are the methylthioribulose-1-phosphate dehydratase of the methionine salvage pathway. This pathway allows methylthioadenosine left over from polyamine biosynthesis to be recycled to methionine.
|
rpsblast_cdd |
gnl|CDD|198075
|
69 |
257 |
+ |
189 |
Gaps:23 |
91.89 |
185 |
30.00 |
9e-24 |
smart01007 Aldolase_II Class II Aldolase and Adducin N-terminal domain. This family includes class II aldolases and adducins which have not been ascribed any enzymatic function.
|
rpsblast_cdd |
gnl|CDD|201333
|
69 |
257 |
+ |
189 |
Gaps:29 |
90.61 |
181 |
28.05 |
4e-22 |
pfam00596 Aldolase_II Class II Aldolase and Adducin N-terminal domain. This family includes class II aldolases and adducins which have not been ascribed any enzymatic function.
|
rpsblast_cdd |
gnl|CDD|180679
|
70 |
260 |
+ |
191 |
Gaps:23 |
83.65 |
208 |
30.46 |
4e-18 |
PRK06754 mtnB methylthioribulose-1-phosphate dehydratase Reviewed.
|
rpsblast_cdd |
gnl|CDD|30584
|
58 |
257 |
+ |
200 |
Gaps:28 |
79.45 |
219 |
24.71 |
6e-17 |
COG0235 AraD Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases [Carbohydrate transport and metabolism].
|
rpsblast_cdd |
gnl|CDD|29521
|
70 |
252 |
+ |
183 |
Gaps:28 |
75.12 |
209 |
26.11 |
6e-11 |
cd00398 Aldolase_II Class II Aldolase and Adducin head (N-terminal) domain. Aldolases are ubiquitous enzymes catalyzing central steps of carbohydrate metabolism. Based on enzymatic mechanisms this superfamily has been divided into two distinct classes (Class I and II). Class II enzymes are further divided into two sub-classes A and B. This family includes class II A aldolases and adducins which has not been ascribed any enzymatic function. Members of this class are primarily bacterial and eukaryotic in origin and include L-fuculose-1-phosphate L-rhamnulose-1-phosphate aldolases and L-ribulose-5-phosphate 4-epimerases. They all share the ability to promote carbon-carbon bond cleavage and stabilize enolate intermediates using divalent cations..
|
rpsblast_kog |
gnl|CDD|37842
|
56 |
259 |
+ |
204 |
Gaps:21 |
81.93 |
238 |
49.23 |
6e-64 |
KOG2631 KOG2631 KOG2631 Class II aldolase/adducin N-terminal domain protein [Carbohydrate transport and metabolism].
|