319435166
|
8 |
glutamyl-tRNA synthetase |
58% |
5 |
55,23 |
5,25 |
56 |
Dietzia cinnamea
|
Catalyze a binding of an amino acid to the tRNA molecule (Farah et al. 2014FARAH C, LEVICÁN G, IBBA M & ORELLANA O. 2014. Effect of hydrogen peroxide on the biosynthesis of heme and proteins: Potential implications for the partitioning of Glu-tRNAGlu between these pathways. Int J Mol Sci 15: 23011-23023.) |
630028390
|
14 |
Hypothetical protein PFICI_09699 |
45% |
6,18 |
9,52 |
7,12 |
39 |
Pestalotiopsis fici
|
Unknown |
697511537
|
32 |
Proteasome subunit aloha type-1 |
48% |
6,08 |
30,353 |
6,05 |
31 |
Fulmarus glacilis
|
It participates in cell cycle regulation, differentiation, inflammatory responses, signal transduction pathways, apoptosis (Huang & Chen 2009HUANG L & CHEN C. 2009. Proteasome Regulators: Activators and Inhibitors. Curr Med Chem 16: 931-939.) |
464316105
|
33 |
PAS domain S-box protein, parcial |
48% |
4,9 |
30,069 |
5,68 |
29 |
Leptospira interrogans serovar
|
Works as sensors to light stimuli (Zhulin et al. 1997ZHULIN IB, TAYLOR BL & DIXON R. 1997. PAS domain S-boxes in Archaea, Bacteria and sensors for oxygen and redox. Trends Biochem Sci 22: 331-333.); Has function in signal detection and transduction (Pellequer et al. 1998PELLEQUER JL, WAGER-SMITH KA, KAY SA & GETZOFF ED. 1998. Photoactive yellow protein: A structural prototype for the three-dimensional fold of the PAS domain superfamily. Proc Natl Acad Sci 95: 5884-5890.) |
768927828
|
34 |
Uroporphyrinogen-III sythase |
47% |
5,33 |
30,087 |
5,92 |
29 |
Bacillus subtilis
|
It is involved in the conversion of hydroxymethyl to bilane uroporphyrinogen III. Its deficiency causes Congenital Erythropoietic Porphyria (PEC) ) (Bishop et al. 2010BISHOP DF, XIAOYE SY, CLAVERO S, YOO HW, MINDER EI & DESNICK RJ. 2010. Congenital erythropoietic porphyria: A novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcripts. Blood 115: 1062-1069.) |
637279932
|
56 |
Deleted in malignant brain tumors 1 protein-like |
81% |
5,16 |
15,122 |
5,97 |
17 |
Anolis carolinensis
|
Tumor supressor (Mollenhauer et al. 2001MOLLENHAUER J ET AL. 2001. Deleted in malignant brain tumors 1 is a versatile mucin-like molecule likely to play a differential role in digestive tract cancer. Cancer Res 61: 8880-8886.) |
LIN-51_TETNG
|
60 |
protein lin-52 homolog |
35% |
4,53 |
12,637 |
4,77 |
12 |
tetraodon nigroviridis
|
It participates in a large protein complex with important transcriptional regulators of cell proliferation and death (Bhaskar et al. 2012BHASKAR PK, MUKHERJEE A & MUTSUDDI M. 2012. Dynamic pattern of expression of dlin52, a member of the Myb/MuvB complex, during Drosophila development. Gene Expr Patterns 12: 77-84.) |
B2MG-CHICK
|
61 |
Beta-2-microglobulin |
27% |
5,84 |
13,148 |
4,96 |
13 |
Gallus gallus
|
It is associated with inflammatory and hematological diseases (Skare et al. 2014SKARE TL, FERRI K & SANTOS MA. 2014. Systemic lupus erythematosus activity and beta two microglobulin levels. Sao Paulo Med J 132: 239-242.) |
VM3B4-BOTSA
|
65 |
Zinc metalloproteinase-disintegrin-like bothrojarin-4 (fragment) |
28% |
5,36 |
11,436 |
5,65 |
10 |
Bothrops jararaca
|
Participates in fabric remodeling (Oliveira et al. 2013OLIVEIRA CP, RODRIGUES LMR, FREGNI MVVD, GOTFRYD A, MADE AM & PINHAL MAS. 2013. Extracellular matrix remodeling in experimental intervertebral disc degeneration. Acta Ortop Bras 21: 144-149.) |
659870098
|
66 |
Killer protein |
85% |
6.73 |
10,8 |
5,83 |
10 |
Caulobacter sp.
|
Causes cell death by blocking calcium channels (Schmitt & Breinig 2006SCHMITT MJ & BREINIG F. 2006. Yeast viral killer toxins: lethality and self-protection. Nat Rev Microbiol 4: 212-221.); Check resistance to fungal infections (Magliani et al. 2008MAGLIANI W, CONTI S, TRAVASSOS LR & POLONELLI L. 2008. From yeast killer toxins to antibiobodies and beyond. FEMS Microbiol Lett 288: 1-8.) |
543371659
|
70 |
mitochondrial import inner membrane translocase subunit Tim10 |
54% |
5,9 |
10,638 |
6,97 |
10 |
Pseud
opodoces humilis
|
It participates in the import and insertion of transmembrane proteins in the inner membrane of mitochondria. It acts as a chaperone-like protein that protects the hydrophobic precursors and guides them through the mitochondrial intermembrane space (Muehlenbein et al. 2004MUEHLENBEIN N, HOFMANN S, ROTHBAUER U & BAUER MF. 2004. Organization and Function of the Small Tim Complexes Acting along the Import Pathway of Metabolite Carriers into Mammalian Mitochondria. Int J Biol Chem 279: 13540-13546.) |
831563256
|
71 |
Zinc finger protein 654 |
13% |
7,12 |
15,05 |
7,16 |
14 |
Fundulus heteroditus
|
Regulates programmed cell death (Wang et al. 2005WANG L, PEI Z, TIAN Y & HE C. 2005. OsLSD1, a rice zinc finger protein, regulates programmed cell death and callus differentiation. Mol Plant Microbe Interact 18: 375-384.) |
657576201
|
73 |
deoxynucleoside triphosphate triphosphohydrolase SAMHD1-LIKE isoform X2 |
60% |
7,71 |
14,995 |
8,27 |
13 |
Stegastes partitus
|
Blocks early replication of the virus. And it is still highly expressed in dendritic cells (Goldstone et al. 2011GOLDSTONE DC ET AL. 2011. HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase. Nature 480: 379-382.) |
915245772
|
76 |
Hypothetical protein NECAME_18605 |
78% |
9,91 |
11,658 |
8,37 |
11 |
Necator americanos
|
Unknown |