blastp_kegg |
lcl|mdm:103409089
|
2 |
167 |
+ |
166 |
Gaps:2 |
33.33 |
498 |
71.08 |
7e-71 |
molybdenum cofactor sulfurase-like
|
blastp_kegg |
lcl|mdm:103435418
|
2 |
167 |
+ |
166 |
Gaps:2 |
20.34 |
816 |
71.08 |
4e-69 |
molybdenum cofactor sulfurase
|
blastp_kegg |
lcl|pxb:103952011
|
2 |
167 |
+ |
166 |
Gaps:2 |
20.32 |
817 |
71.08 |
1e-68 |
molybdenum cofactor sulfurase
|
blastp_kegg |
lcl|pmum:103325694
|
2 |
167 |
+ |
166 |
Gaps:3 |
20.27 |
824 |
68.86 |
5e-68 |
molybdenum cofactor sulfurase
|
blastp_kegg |
lcl|vvi:100247369
|
2 |
167 |
+ |
166 |
Gaps:2 |
20.07 |
827 |
71.69 |
1e-67 |
molybdenum cofactor sulfurase-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa001477mg
|
2 |
167 |
+ |
166 |
Gaps:3 |
20.44 |
817 |
68.86 |
1e-67 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0007s08330g
|
2 |
167 |
+ |
166 |
Gaps:2 |
20.00 |
830 |
68.67 |
7e-67 |
POPTRDRAFT_719124 ABA deficient 3 family protein
|
blastp_kegg |
lcl|fve:101310007
|
6 |
167 |
+ |
162 |
Gaps:4 |
20.24 |
820 |
66.87 |
9e-66 |
molybdenum cofactor sulfurase-like
|
blastp_kegg |
lcl|rcu:RCOM_1575730
|
2 |
167 |
+ |
166 |
Gaps:3 |
20.62 |
810 |
66.47 |
1e-65 |
molybdopterin cofactor sulfurase putative (EC:2.8.1.7)
|
blastp_kegg |
lcl|cic:CICLE_v10004324mg
|
6 |
168 |
+ |
163 |
Gaps:6 |
19.47 |
827 |
70.19 |
1e-65 |
hypothetical protein
|
blastp_uniprot_sprot |
sp|Q8LGM7|MOCOS_SOLLC
|
2 |
167 |
+ |
166 |
Gaps:3 |
19.98 |
816 |
59.51 |
5e-58 |
Molybdenum cofactor sulfurase OS Solanum lycopersicum GN FLACCA PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9C5X8|MOCOS_ARATH
|
8 |
167 |
+ |
160 |
Gaps:10 |
18.80 |
819 |
63.64 |
8e-57 |
Molybdenum cofactor sulfurase OS Arabidopsis thaliana GN ABA3 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q655R6|MOCOS_ORYSJ
|
11 |
167 |
+ |
157 |
Gaps:9 |
19.42 |
824 |
60.00 |
2e-52 |
Molybdenum cofactor sulfurase OS Oryza sativa subsp. japonica GN MCSU3 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q559G8|MOCOS_DICDI
|
17 |
146 |
+ |
130 |
Gaps:21 |
14.00 |
1007 |
40.43 |
4e-22 |
Molybdenum cofactor sulfurase OS Dictyostelium discoideum GN mocos PE 3 SV 2
|
blastp_uniprot_sprot |
sp|A4RK48|MOCOS_MAGO7
|
19 |
139 |
+ |
121 |
Gaps:16 |
14.85 |
842 |
40.80 |
3e-18 |
Molybdenum cofactor sulfurase OS Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN hxB PE 3 SV 2
|
blastp_uniprot_sprot |
sp|A2VD33|MOCOS_DANRE
|
24 |
166 |
+ |
143 |
Gaps:10 |
16.49 |
831 |
40.15 |
6e-18 |
Molybdenum cofactor sulfurase OS Danio rerio GN mocos PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q5VT66|MOSC1_HUMAN
|
21 |
130 |
+ |
110 |
Gaps:12 |
29.08 |
337 |
39.80 |
7e-16 |
MOSC domain-containing protein 1 mitochondrial OS Homo sapiens GN MARC1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A2QIK9|MOCOS_ASPNC
|
24 |
167 |
+ |
144 |
Gaps:30 |
18.47 |
823 |
39.47 |
1e-15 |
Molybdenum cofactor sulfurase OS Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN hxB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A1CX75|MOCOS_NEOFI
|
24 |
167 |
+ |
144 |
Gaps:15 |
18.21 |
851 |
33.55 |
3e-15 |
Molybdenum cofactor sulfurase OS Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN hxB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A1CHL0|MOCOS_ASPCL
|
24 |
167 |
+ |
144 |
Gaps:19 |
18.82 |
845 |
33.96 |
8e-15 |
Molybdenum cofactor sulfurase OS Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN hxB PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|178325
|
2 |
167 |
+ |
166 |
Gaps:9 |
19.50 |
805 |
57.32 |
3e-62 |
PLN02724 PLN02724 Molybdenum cofactor sulfurase.
|
rpsblast_cdd |
gnl|CDD|33030
|
23 |
143 |
+ |
121 |
Gaps:13 |
41.48 |
270 |
36.61 |
2e-16 |
COG3217 COG3217 Uncharacterized Fe-S protein [General function prediction only].
|
rpsblast_cdd |
gnl|CDD|202655
|
22 |
114 |
+ |
93 |
Gaps:16 |
66.94 |
124 |
40.96 |
3e-13 |
pfam03473 MOSC MOSC domain. The MOSC (MOCO sulfurase C-terminal) domain is a superfamily of beta-strand-rich domains identified in the molybdenum cofactor sulfurase and several other proteins from both prokaryotes and eukaryotes. These MOSC domains contain an absolutely conserved cysteine and occur either as stand-alone forms or fused to other domains such as NifS-like catalytic domain in Molybdenum cofactor sulfurase. The MOSC domain is predicted to be a sulfur-carrier domain that receives sulfur abstracted by the pyridoxal phosphate-dependent NifS-like enzymes on its conserved cysteine and delivers it for the formation of diverse sulfur-metal clusters.
|
rpsblast_kog |
gnl|CDD|37573
|
25 |
139 |
+ |
115 |
Gaps:20 |
33.04 |
336 |
36.04 |
6e-17 |
KOG2362 KOG2362 KOG2362 Uncharacterized Fe-S protein [General function prediction only].
|