blastp_kegg |
lcl|pxb:103933610
|
46 |
385 |
+ |
340 |
Gaps:6 |
92.52 |
361 |
70.36 |
1e-178 |
apoptosis-inducing factor 2-like
|
blastp_kegg |
lcl|csv:101207218
|
43 |
385 |
+ |
343 |
Gaps:6 |
91.83 |
367 |
68.84 |
3e-174 |
apoptosis-inducing factor homolog A-like
|
blastp_kegg |
lcl|cmo:103489371
|
46 |
385 |
+ |
340 |
Gaps:6 |
91.01 |
367 |
69.16 |
9e-174 |
apoptosis-inducing factor 2-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa007651mg
|
46 |
385 |
+ |
340 |
Gaps:6 |
92.78 |
360 |
71.26 |
2e-173 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103330980
|
46 |
385 |
+ |
340 |
Gaps:6 |
91.26 |
366 |
70.96 |
6e-173 |
apoptosis-inducing factor 2-like
|
blastp_kegg |
lcl|vvi:100263525
|
32 |
387 |
+ |
356 |
Gaps:6 |
95.89 |
365 |
66.29 |
7e-172 |
apoptosis-inducing factor homolog A-like
|
blastp_kegg |
lcl|cic:CICLE_v10018036mg
|
43 |
385 |
+ |
343 |
Gaps:7 |
92.05 |
365 |
66.67 |
7e-164 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_041271
|
29 |
385 |
+ |
357 |
Gaps:8 |
91.93 |
384 |
60.62 |
8e-156 |
FAD/NAD(P)-binding oxidoreductase family protein
|
blastp_kegg |
lcl|pmum:103329195
|
43 |
386 |
+ |
344 |
Gaps:8 |
93.15 |
365 |
62.94 |
8e-154 |
apoptosis-inducing factor homolog B
|
blastp_kegg |
lcl|cic:CICLE_v10028687mg
|
43 |
385 |
+ |
343 |
Gaps:8 |
91.87 |
369 |
64.01 |
9e-154 |
hypothetical protein
|
blastp_pdb |
1zx9_A
|
98 |
298 |
+ |
201 |
Gaps:12 |
43.90 |
467 |
23.90 |
6e-06 |
mol:protein length:467 Mercuric reductase
|
blastp_pdb |
1zk7_A
|
98 |
298 |
+ |
201 |
Gaps:12 |
43.90 |
467 |
23.90 |
6e-06 |
mol:protein length:467 Mercuric reductase
|
blastp_uniprot_sprot |
sp|Q54NS9|AIFA_DICDI
|
3 |
385 |
+ |
383 |
Gaps:52 |
95.83 |
408 |
31.71 |
1e-42 |
Apoptosis-inducing factor homolog A OS Dictyostelium discoideum GN aifA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q54NS8|AIFB_DICDI
|
29 |
385 |
+ |
357 |
Gaps:44 |
97.93 |
387 |
32.19 |
8e-42 |
Apoptosis-inducing factor homolog B OS Dictyostelium discoideum GN aifB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B5FXE5|AIFM2_TAEGU
|
64 |
382 |
+ |
319 |
Gaps:42 |
88.20 |
373 |
30.09 |
6e-33 |
Apoptosis-inducing factor 2 OS Taeniopygia guttata GN AIFM2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|B4F6I3|AIFM2_XENTR
|
75 |
382 |
+ |
308 |
Gaps:20 |
85.56 |
374 |
30.94 |
1e-28 |
Apoptosis-inducing factor 2 OS Xenopus tropicalis GN aifm2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6GLW8|AIFM2_XENLA
|
75 |
382 |
+ |
308 |
Gaps:20 |
85.56 |
374 |
29.69 |
2e-28 |
Apoptosis-inducing factor 2 OS Xenopus laevis GN aifm2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9BRQ8|AIFM2_HUMAN
|
75 |
385 |
+ |
311 |
Gaps:19 |
86.33 |
373 |
26.71 |
2e-25 |
Apoptosis-inducing factor 2 OS Homo sapiens GN AIFM2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A5PJM4|AIFM2_BOVIN
|
75 |
385 |
+ |
311 |
Gaps:19 |
86.33 |
373 |
27.64 |
3e-25 |
Apoptosis-inducing factor 2 OS Bos taurus GN AIFM2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8BUE4|AIFM2_MOUSE
|
75 |
385 |
+ |
311 |
Gaps:25 |
86.33 |
373 |
28.57 |
2e-24 |
Apoptosis-inducing factor 2 OS Mus musculus GN Aifm2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O32117|YUTJ_BACSU
|
32 |
369 |
+ |
338 |
Gaps:40 |
96.34 |
355 |
26.32 |
2e-14 |
NADH dehydrogenase-like protein YutJ OS Bacillus subtilis (strain 168) GN yutJ PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q8GXR9|DHNA_ARATH
|
24 |
301 |
+ |
278 |
Gaps:51 |
63.39 |
519 |
27.36 |
7e-13 |
Alternative NAD(P)H-ubiquinone oxidoreductase C1 chloroplastic/mitochondrial OS Arabidopsis thaliana GN NDC1 PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|31444
|
29 |
361 |
+ |
333 |
Gaps:58 |
90.12 |
405 |
27.95 |
1e-36 |
COG1252 Ndh NADH dehydrogenase FAD-containing subunit [Energy production and conversion].
|
rpsblast_cdd |
gnl|CDD|163170
|
100 |
368 |
+ |
269 |
Gaps:34 |
78.30 |
364 |
22.81 |
9e-22 |
TIGR03169 Nterm_to_SelD pyridine nucleotide-disulfide oxidoreductase family protein. Members of this protein family include N-terminal sequence regions of (probable) bifunctional proteins whose C-terminal sequences are SelD or selenide water dikinase the selenium donor protein necessary for selenium incorporation into protein (as selenocysteine) tRNA (as 2-selenouridine) or both. However some members of this family occur in species that do not show selenium incorporation and the function of this protein family is unknown.
|
rpsblast_cdd |
gnl|CDD|203833
|
32 |
300 |
+ |
269 |
Gaps:47 |
99.65 |
283 |
22.70 |
4e-19 |
pfam07992 Pyr_redox_2 Pyridine nucleotide-disulphide oxidoreductase. This family includes both class I and class II oxidoreductases and also NADH oxidases and peroxidases. This domain is actually a small NADH binding domain within a larger FAD binding domain.
|
rpsblast_cdd |
gnl|CDD|30795
|
33 |
338 |
+ |
306 |
Gaps:42 |
78.55 |
415 |
22.70 |
6e-17 |
COG0446 HcaD Uncharacterized NAD(FAD)-dependent dehydrogenases [General function prediction only].
|
rpsblast_cdd |
gnl|CDD|31441
|
27 |
319 |
+ |
293 |
Gaps:53 |
73.13 |
454 |
21.99 |
6e-16 |
COG1249 Lpd Pyruvate/2-oxoglutarate dehydrogenase complex dihydrolipoamide dehydrogenase (E3) component and related enzymes [Energy production and conversion].
|
rpsblast_cdd |
gnl|CDD|162675
|
31 |
331 |
+ |
301 |
Gaps:57 |
72.14 |
463 |
21.26 |
2e-12 |
TIGR02053 MerA mercuric reductase. This model represents the mercuric reductase found in the mer operon for the detoxification of mercury compounds. MerA is a FAD-containing flavoprotein which reduces Hg(II) to Hg(0) utilizing NADPH.
|
rpsblast_cdd |
gnl|CDD|185553
|
21 |
363 |
+ |
343 |
Gaps:80 |
90.80 |
424 |
22.08 |
3e-12 |
PTZ00318 PTZ00318 NADH dehydrogenase-like protein Provisional.
|
rpsblast_cdd |
gnl|CDD|179902
|
85 |
319 |
+ |
235 |
Gaps:52 |
61.80 |
377 |
30.47 |
4e-11 |
PRK04965 PRK04965 NADH:flavorubredoxin oxidoreductase Provisional.
|