blastp_kegg |
lcl|pper:PRUPE_ppa011986mg
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
86.67 |
7e-114 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103961142
|
1 |
180 |
+ |
180 |
none |
97.30 |
185 |
85.56 |
3e-113 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_kegg |
lcl|pmum:103323991
|
1 |
180 |
+ |
180 |
none |
95.74 |
188 |
86.11 |
5e-113 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1
|
blastp_kegg |
lcl|fve:101296477
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
86.11 |
1e-112 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_kegg |
lcl|pxb:103964742
|
1 |
180 |
+ |
180 |
none |
97.30 |
185 |
85.00 |
2e-112 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_kegg |
lcl|cic:CICLE_v10006993mg
|
1 |
180 |
+ |
180 |
none |
82.95 |
217 |
84.44 |
2e-112 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102624829
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
84.44 |
8e-112 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_kegg |
lcl|sot:102599891
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
83.89 |
1e-111 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_kegg |
lcl|rcu:RCOM_0911100
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
85.00 |
9e-111 |
acireductone dioxygenase putative
|
blastp_kegg |
lcl|sly:101255136
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
82.22 |
5e-110 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1-like
|
blastp_pdb |
1vr3_A
|
1 |
169 |
+ |
169 |
none |
88.48 |
191 |
61.54 |
3e-72 |
mol:protein length:191 Acireductone dioxygenase
|
blastp_pdb |
2hji_A
|
53 |
154 |
+ |
102 |
Gaps:16 |
61.45 |
179 |
29.09 |
1e-06 |
mol:protein length:179 E-2/E-2' protein
|
blastp_pdb |
1zrr_A
|
53 |
154 |
+ |
102 |
Gaps:16 |
61.45 |
179 |
29.09 |
1e-06 |
mol:protein length:179 E-2/E-2' protein
|
blastp_uniprot_sprot |
sp|D7T737|MTND1_VITVI
|
1 |
180 |
+ |
180 |
none |
95.74 |
188 |
83.33 |
6e-112 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1 OS Vitis vinifera GN VIT_05s0020g04070 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8H185|MTND4_ARATH
|
1 |
180 |
+ |
180 |
none |
96.26 |
187 |
79.44 |
1e-104 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 4 OS Arabidopsis thaliana GN ARD4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|F6HDT7|MTND2_VITVI
|
1 |
172 |
+ |
172 |
none |
86.43 |
199 |
66.86 |
2e-88 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 2 OS Vitis vinifera GN VIT_05s0020g04080 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|C5X1F5|MTND1_SORBI
|
1 |
179 |
+ |
179 |
none |
99.44 |
180 |
65.36 |
2e-88 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1 OS Sorghum bicolor GN Sb01g021500 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q7XEJ5|MTND4_ORYSJ
|
15 |
180 |
+ |
166 |
none |
90.22 |
184 |
70.48 |
2e-87 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 4 OS Oryza sativa subsp. japonica GN ARD4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q10RE5|MTND2_ORYSJ
|
1 |
174 |
+ |
174 |
none |
87.88 |
198 |
66.09 |
3e-87 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 2 OS Oryza sativa subsp. japonica GN ARD2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A2XCT8|MTND2_ORYSI
|
1 |
174 |
+ |
174 |
none |
87.88 |
198 |
66.09 |
3e-87 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 2 OS Oryza sativa subsp. indica GN ARD2 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|C5WWY0|MTND2_SORBI
|
1 |
174 |
+ |
174 |
none |
96.13 |
181 |
66.09 |
5e-87 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase homolog 2 OS Sorghum bicolor GN Sb01g046360 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O48707|MTND1_ARATH
|
1 |
174 |
+ |
174 |
none |
87.44 |
199 |
65.52 |
4e-85 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1 OS Arabidopsis thaliana GN ARD1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A1L4T4|MTND1_ORYSJ
|
1 |
174 |
+ |
174 |
none |
87.44 |
199 |
64.94 |
1e-84 |
1 2-dihydroxy-3-keto-5-methylthiopentene dioxygenase 1 OS Oryza sativa subsp. japonica GN ARD1 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|111920
|
2 |
151 |
+ |
150 |
Gaps:1 |
96.18 |
157 |
56.95 |
2e-53 |
pfam03079 ARD ARD/ARD' family. The two acireductone dioxygenase enzymes (ARD and ARD' previously known as E-2 and E-2') from Klebsiella pneumoniae share the same amino acid sequence but bind different metal ions: ARD binds Ni2+ ARD' binds Fe2+. ARD and ARD' can be experimentally interconverted by removal of the bound metal ion and reconstitution with the appropriate metal ion. The two enzymes share the same substrate 1 2-dihydroxy-3-keto-5-(methylthio)pentene but yield different products. ARD' yields the alpha-keto precursor of methionine (and formate) thus forming part of the ubiquitous methionine salvage pathway that converts 5'-methylthioadenosine (MTA) to methionine. This pathway is responsible for the tight control of the concentration of MTA which is a powerful inhibitor of polyamine biosynthesis and transmethylation reactions. ARD yields methylthiopropanoate carbon monoxide and formate and thus prevents the conversion of MTA to methionine. The role of the ARD catalyzed reaction is unclear: methylthiopropanoate is cytotoxic and carbon monoxide can activate guanylyl cyclase leading to increased intracellular cGMP levels. This family also contains other members whose functions are not well characterized.
|
rpsblast_cdd |
gnl|CDD|31976
|
2 |
169 |
+ |
168 |
Gaps:7 |
92.27 |
181 |
31.74 |
5e-29 |
COG1791 COG1791 Uncharacterized conserved protein contains double-stranded beta-helix domain [Function unknown].
|
rpsblast_kog |
gnl|CDD|37318
|
2 |
172 |
+ |
171 |
none |
95.53 |
179 |
62.57 |
3e-68 |
KOG2107 KOG2107 KOG2107 Uncharacterized conserved protein contains double-stranded beta-helix domain [Function unknown].
|