blastp_kegg |
lcl|pmum:103342727
|
3 |
342 |
+ |
340 |
Gaps:51 |
98.90 |
363 |
57.94 |
7e-133 |
mitochondrial import inner membrane translocase subunit TIM50
|
blastp_kegg |
lcl|pvu:PHAVU_008G278100g
|
73 |
324 |
+ |
252 |
Gaps:33 |
85.59 |
333 |
65.61 |
1e-132 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa007559mg
|
3 |
342 |
+ |
340 |
Gaps:49 |
98.90 |
363 |
57.10 |
2e-131 |
hypothetical protein
|
blastp_kegg |
lcl|gmx:100775411
|
83 |
324 |
+ |
242 |
Gaps:33 |
82.09 |
335 |
67.27 |
8e-131 |
mitochondrial import inner membrane translocase subunit TIM50-like
|
blastp_kegg |
lcl|gmx:100803155
|
83 |
324 |
+ |
242 |
Gaps:33 |
82.58 |
333 |
67.27 |
1e-130 |
mitochondrial import inner membrane translocase subunit TIM50-like
|
blastp_kegg |
lcl|cam:101509691
|
83 |
324 |
+ |
242 |
Gaps:33 |
82.09 |
335 |
66.55 |
8e-129 |
mitochondrial import inner membrane translocase subunit TIM50-like
|
blastp_kegg |
lcl|mtr:MTR_5g095530
|
83 |
324 |
+ |
242 |
Gaps:33 |
73.53 |
374 |
66.55 |
3e-128 |
Mitochondrial import inner membrane translocase subunit TIM50
|
blastp_kegg |
lcl|cmo:103501237
|
3 |
342 |
+ |
340 |
Gaps:69 |
98.89 |
359 |
57.18 |
1e-127 |
mitochondrial import inner membrane translocase subunit TIM50
|
blastp_kegg |
lcl|cic:CICLE_v10010336mg
|
3 |
324 |
+ |
322 |
Gaps:56 |
98.31 |
354 |
57.18 |
3e-125 |
hypothetical protein
|
blastp_kegg |
lcl|sot:102600826
|
1 |
342 |
+ |
342 |
Gaps:52 |
99.16 |
359 |
55.90 |
3e-124 |
mitochondrial import inner membrane translocase subunit TIM50-like
|
blastp_pdb |
3qle_A
|
192 |
324 |
+ |
133 |
Gaps:37 |
81.37 |
204 |
33.73 |
6e-23 |
mol:protein length:204 Tim50p
|
blastp_uniprot_sprot |
sp|Q8VYE2|TIM50_ARATH
|
3 |
324 |
+ |
322 |
Gaps:49 |
94.41 |
376 |
50.14 |
5e-103 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Arabidopsis thaliana GN TIM50 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q4I099|TIM50_GIBZE
|
166 |
326 |
+ |
161 |
Gaps:34 |
36.76 |
525 |
37.31 |
5e-34 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN TIM50 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q874C1|TIM50_NEUCR
|
168 |
329 |
+ |
162 |
Gaps:34 |
35.93 |
540 |
36.08 |
3e-32 |
Mitochondrial import inner membrane translocase subunit tim-50 OS Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN tim-50 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q5B4P0|TIM50_EMENI
|
171 |
329 |
+ |
159 |
Gaps:34 |
35.90 |
532 |
36.13 |
1e-30 |
Mitochondrial import inner membrane translocase subunit tim50 OS Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN tim50 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q4WI16|TIM50_ASPFU
|
171 |
325 |
+ |
155 |
Gaps:34 |
37.33 |
501 |
35.83 |
4e-30 |
Mitochondrial import inner membrane translocase subunit tim50 OS Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN tim50 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|O13636|TIM50_SCHPO
|
171 |
337 |
+ |
167 |
Gaps:36 |
44.47 |
452 |
34.83 |
4e-29 |
Mitochondrial import inner membrane translocase subunit tim50 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN tim50 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6CDV7|TIM50_YARLI
|
156 |
329 |
+ |
174 |
Gaps:40 |
44.64 |
466 |
33.65 |
2e-28 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Yarrowia lipolytica (strain CLIB 122 / E 150) GN TIM50 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5S7T7|TIM50_PHYIN
|
155 |
313 |
+ |
159 |
Gaps:37 |
47.92 |
409 |
35.71 |
3e-28 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Phytophthora infestans GN TIM50 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q4PEW9|TIM50_USTMA
|
171 |
329 |
+ |
159 |
Gaps:36 |
39.15 |
493 |
32.12 |
3e-27 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Ustilago maydis (strain 521 / FGSC 9021) GN TIM50 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6BVY9|TIM50_DEBHA
|
23 |
329 |
+ |
307 |
Gaps:73 |
66.67 |
471 |
30.57 |
3e-26 |
Mitochondrial import inner membrane translocase subunit TIM50 OS Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN TIM50 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|202514
|
191 |
306 |
+ |
116 |
Gaps:43 |
100.00 |
153 |
29.41 |
5e-25 |
pfam03031 NIF NLI interacting factor-like phosphatase. This family contains a number of NLI interacting factor isoforms and also an N-terminal regions of RNA polymerase II CTC phosphatase and FCP1 serine phosphatase. This region has been identified as the minimal phosphatase domain.
|
rpsblast_cdd |
gnl|CDD|162785
|
191 |
295 |
+ |
105 |
Gaps:51 |
95.06 |
162 |
29.22 |
4e-15 |
TIGR02251 HIF-SF_euk Dullard-like phosphatase domain. This model represents the putative phosphatase domain of a family of eukaryotic proteins including "Dullard" and the NLI interacting factor (NIF)-like phosphatases. This domain is a member of the haloacid dehalogenase (HAD) superfamily by virtue of a conserved set of three catalytic motifs and a conserved fold as predicted by PSIPRED. The third motif in this family is distinctive (hhhhDNxPxxa) and aparrently lacking the last aspartate. This domain is classified as a "Class III" HAD since there is no large "cap" domain found between motifs 1 and 2 or motifs 2 and 3. This domain is related to domains found in FCP1-like phosphatases (TIGR02250) and together both are detected by the Pfam model pfam03031.
|
rpsblast_cdd |
gnl|CDD|197796
|
191 |
285 |
+ |
95 |
Gaps:59 |
98.65 |
148 |
30.82 |
6e-15 |
smart00577 CPDc catalytic domain of ctd-like phosphatases.
|
rpsblast_kog |
gnl|CDD|38043
|
68 |
327 |
+ |
260 |
Gaps:48 |
77.86 |
393 |
33.33 |
2e-45 |
KOG2832 KOG2832 KOG2832 TFIIF-interacting CTD phosphatase including NLI-interacting factor (involved in RNA polymerase II regulation) [Transcription].
|