blastp_kegg |
lcl|tcc:TCM_007667
|
1 |
309 |
+ |
309 |
Gaps:4 |
100.00 |
313 |
83.71 |
0.0 |
Translocase of the outer mitochondrial membrane 40
|
blastp_kegg |
lcl|cic:CICLE_v10032173mg
|
1 |
309 |
+ |
309 |
Gaps:2 |
100.00 |
311 |
83.92 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102616410
|
1 |
309 |
+ |
309 |
Gaps:2 |
100.00 |
311 |
83.92 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|sot:102587266
|
1 |
310 |
+ |
310 |
Gaps:2 |
100.00 |
312 |
82.37 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|pxb:103932065
|
1 |
310 |
+ |
310 |
Gaps:2 |
100.00 |
312 |
83.33 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|sly:101262530
|
1 |
310 |
+ |
310 |
Gaps:2 |
100.00 |
312 |
81.73 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|pmum:103322524
|
17 |
310 |
+ |
294 |
none |
94.23 |
312 |
86.39 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa008962mg
|
17 |
310 |
+ |
294 |
none |
94.23 |
312 |
86.39 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103449844
|
1 |
310 |
+ |
310 |
Gaps:2 |
100.00 |
312 |
83.01 |
0.0 |
mitochondrial import receptor subunit TOM40-1-like
|
blastp_kegg |
lcl|vvi:100268104
|
23 |
310 |
+ |
288 |
none |
93.20 |
309 |
88.54 |
0.0 |
mitochondrial import receptor subunit TOM40 homolog 1-like
|
blastp_uniprot_sprot |
sp|Q9LHE5|TO401_ARATH
|
1 |
309 |
+ |
309 |
Gaps:2 |
100.00 |
309 |
73.46 |
1e-165 |
Mitochondrial import receptor subunit TOM40-1 OS Arabidopsis thaliana GN TOM40-1 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9SX55|TO402_ARATH
|
1 |
306 |
+ |
306 |
Gaps:3 |
99.03 |
310 |
63.52 |
4e-141 |
Probable mitochondrial import receptor subunit TOM40-2 OS Arabidopsis thaliana GN TOM40-2 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q6P825|TOM40_XENTR
|
5 |
309 |
+ |
305 |
Gaps:52 |
92.56 |
336 |
31.51 |
7e-30 |
Mitochondrial import receptor subunit TOM40 homolog OS Xenopus tropicalis GN tomm40 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7ZTM6|TOM40_XENLA
|
5 |
309 |
+ |
305 |
Gaps:52 |
92.56 |
336 |
31.51 |
1e-29 |
Mitochondrial import receptor subunit TOM40 homolog OS Xenopus laevis GN tomm40 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O13656|TOM40_SCHPO
|
51 |
308 |
+ |
258 |
Gaps:47 |
79.36 |
344 |
32.60 |
4e-28 |
Probable mitochondrial import receptor subunit tom40 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN tom40 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|Q9CZR3|TM40L_MOUSE
|
3 |
309 |
+ |
307 |
Gaps:44 |
98.38 |
308 |
32.67 |
5e-27 |
Mitochondrial import receptor subunit TOM40B OS Mus musculus GN Tomm40l PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A4F267|TM40L_RAT
|
3 |
309 |
+ |
307 |
Gaps:44 |
98.38 |
308 |
32.67 |
7e-27 |
Mitochondrial import receptor subunit TOM40B OS Rattus norvegicus GN Tomm40l PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9QYA2|TOM40_MOUSE
|
29 |
309 |
+ |
281 |
Gaps:40 |
78.95 |
361 |
30.88 |
1e-25 |
Mitochondrial import receptor subunit TOM40 homolog OS Mus musculus GN Tomm40 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q75Q40|TOM40_RAT
|
29 |
309 |
+ |
281 |
Gaps:40 |
78.95 |
361 |
30.88 |
1e-25 |
Mitochondrial import receptor subunit TOM40 homolog OS Rattus norvegicus GN Tomm40 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O96008|TOM40_HUMAN
|
29 |
309 |
+ |
281 |
Gaps:40 |
78.95 |
361 |
30.88 |
2e-25 |
Mitochondrial import receptor subunit TOM40 homolog OS Homo sapiens GN TOMM40 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|132766
|
29 |
309 |
+ |
281 |
Gaps:22 |
100.00 |
279 |
41.22 |
6e-87 |
cd07305 Porin3_Tom40 Translocase of outer mitochondrial membrane 40 (Tom40). Tom40 forms a channel in the mitochondrial outer membrane with a pore about 1.5 to 2.5 nanometers wide. It functions as a transport channel for unfolded protein chains and forms a complex with Tom5 Tom6 Tom7 and Tom22. The primary receptors Tom20 and Tom70 recruit the unfolded precursor protein from the mitochondrial-import stimulating factor (MSF) or cytosolic Hsc70. The precursor passes through the Tom40 channel and through another channel in the inner membrane formed by Tim23 to be finally translocated into the mitochondrial matrix. The process depends on a proton motive force across the inner membrane and requires a contact site where the outer and inner membranes come close. Tom40 is also involved in inserting outer membrane proteins into the membrane most likely not via a lateral opening in the pore but by transfering precursor proteins to an outer membrane sorting and assembly machinery.
|
rpsblast_cdd |
gnl|CDD|201807
|
31 |
303 |
+ |
273 |
Gaps:37 |
100.00 |
272 |
30.88 |
2e-55 |
pfam01459 Porin_3 Eukaryotic porin.
|
rpsblast_cdd |
gnl|CDD|132765
|
35 |
309 |
+ |
275 |
Gaps:14 |
99.64 |
274 |
16.48 |
6e-20 |
cd07303 Porin3 Eukaryotic porin family that forms channels in the mitochondrial outer membrane. The porin family 3 contains two sub-families that play vital roles in the mitochondrial outer membrane a translocase for unfolded pre-proteins (Tom40) and the voltage-dependent anion channel (VDAC) that regulates the flux of mostly anionic metabolites through the outer mitochondrial membrane.
|
rpsblast_cdd |
gnl|CDD|130062
|
36 |
189 |
+ |
154 |
Gaps:27 |
92.55 |
161 |
32.89 |
8e-14 |
TIGR00989 3a0801s07tom40 mitochondrial import receptor subunit Tom40. The mitochondrial protein translocase (MPT) family which brings nuclearly encoded preproteins into mitochondria is very complex with 19 currently identified protein constituents.These proteins include several chaperone proteins four proteins of the outer membrane translocase (Tom) import receptor five proteins of the Tom channel complex five proteins of the inner membrane translocase (Tim) and three "motor" proteins. This family is specific for the Tom40 proteins.
|
rpsblast_cdd |
gnl|CDD|132767
|
152 |
306 |
+ |
155 |
Gaps:5 |
39.86 |
276 |
38.18 |
9e-08 |
cd07306 Porin3_VDAC Voltage-dependent anion channel of the outer mitochondrial membrane. The voltage-dependent anion channel (VDAC) regulates the flux of mostly anionic metabolites through the outer mitochondrial membrane which is highly permeable to small molecules. VDAC is the most abundant protein in the outer membrane and membrane potentials can toggle VDAC between open or high-conducting and closed or low-conducting forms. VDAC binds to and is regulated in part by hexokinase an interaction that renders mitochondria less susceptible to pro-apoptotic signals most likely by intefering with VDAC's capability to respond to Bcl-2 family proteins. While VDAC appears to play a key role in mitochondrially induced cell death a proposed involvement in forming the mitochondrial permeability transition pore which is characteristic for damaged mitochondria and apoptosis has been challenged by more recent studies.
|
rpsblast_kog |
gnl|CDD|38506
|
15 |
309 |
+ |
295 |
Gaps:13 |
98.70 |
308 |
33.88 |
2e-73 |
KOG3296 KOG3296 KOG3296 Translocase of outer mitochondrial membrane complex subunit TOM40 [Intracellular trafficking secretion and vesicular transport].
|