blastp_kegg |
lcl|vvi:100258076
|
1 |
186 |
+ |
186 |
Gaps:4 |
38.85 |
489 |
74.21 |
4e-92 |
BTB/POZ and MATH domain-containing protein 2-like
|
blastp_kegg |
lcl|fve:101297795
|
1 |
186 |
+ |
186 |
Gaps:4 |
46.23 |
411 |
73.16 |
4e-90 |
BTB/POZ and MATH domain-containing protein 2-like
|
blastp_kegg |
lcl|cic:CICLE_v10020406mg
|
5 |
186 |
+ |
182 |
Gaps:4 |
45.70 |
407 |
73.12 |
4e-89 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102628741
|
5 |
186 |
+ |
182 |
Gaps:4 |
45.70 |
407 |
73.12 |
4e-89 |
BTB/POZ and MATH domain-containing protein 2-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa006488mg
|
3 |
186 |
+ |
184 |
Gaps:4 |
45.97 |
409 |
71.81 |
1e-87 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_004456
|
3 |
229 |
+ |
227 |
Gaps:9 |
47.87 |
493 |
60.59 |
2e-87 |
BTB-POZ and MATH domain 2
|
blastp_kegg |
lcl|cam:101497711
|
1 |
186 |
+ |
186 |
Gaps:4 |
38.23 |
497 |
71.05 |
2e-87 |
BTB/POZ and MATH domain-containing protein 2-like
|
blastp_kegg |
lcl|pda:103720364
|
1 |
186 |
+ |
186 |
Gaps:4 |
45.89 |
414 |
71.05 |
3e-87 |
BTB/POZ and MATH domain-containing protein 1-like
|
blastp_kegg |
lcl|rcu:RCOM_0648390
|
1 |
186 |
+ |
186 |
Gaps:4 |
38.00 |
500 |
71.58 |
9e-87 |
Speckle-type POZ protein putative
|
blastp_kegg |
lcl|vvi:100240933
|
5 |
186 |
+ |
182 |
Gaps:4 |
45.59 |
408 |
71.51 |
5e-86 |
BTB/POZ and MATH domain-containing protein 2-like
|
blastp_pdb |
3hu6_B
|
2 |
186 |
+ |
185 |
Gaps:13 |
60.26 |
312 |
27.13 |
8e-10 |
mol:protein length:312 Speckle-type POZ protein
|
blastp_pdb |
3hu6_A
|
2 |
186 |
+ |
185 |
Gaps:13 |
60.26 |
312 |
27.13 |
8e-10 |
mol:protein length:312 Speckle-type POZ protein
|
blastp_pdb |
3hqi_B
|
2 |
186 |
+ |
185 |
Gaps:13 |
60.26 |
312 |
27.13 |
8e-10 |
mol:protein length:312 Speckle-type POZ protein
|
blastp_pdb |
3hqi_A
|
2 |
186 |
+ |
185 |
Gaps:13 |
60.26 |
312 |
27.13 |
8e-10 |
mol:protein length:312 Speckle-type POZ protein
|
blastp_uniprot_sprot |
sp|Q9M8J9|BPM2_ARATH
|
2 |
235 |
+ |
234 |
Gaps:9 |
59.85 |
406 |
55.14 |
5e-80 |
BTB/POZ and MATH domain-containing protein 2 OS Arabidopsis thaliana GN BPM2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8L765|BPM1_ARATH
|
5 |
186 |
+ |
182 |
Gaps:4 |
45.70 |
407 |
65.05 |
7e-77 |
BTB/POZ and MATH domain-containing protein 1 OS Arabidopsis thaliana GN BPM1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SRV1|BPM4_ARATH
|
1 |
186 |
+ |
186 |
Gaps:4 |
40.86 |
465 |
61.05 |
2e-76 |
BTB/POZ and MATH domain-containing protein 4 OS Arabidopsis thaliana GN BPM4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A1L4W5|BPM6_ARATH
|
1 |
186 |
+ |
186 |
Gaps:4 |
45.78 |
415 |
58.42 |
2e-72 |
BTB/POZ and MATH domain-containing protein 6 OS Arabidopsis thaliana GN BPM6 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q1EBV6|BPM5_ARATH
|
1 |
186 |
+ |
186 |
Gaps:4 |
46.34 |
410 |
56.84 |
2e-71 |
BTB/POZ and MATH domain-containing protein 5 OS Arabidopsis thaliana GN BPM5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O22286|BPM3_ARATH
|
3 |
186 |
+ |
184 |
Gaps:4 |
46.08 |
408 |
57.45 |
1e-69 |
BTB/POZ and MATH domain-containing protein 3 OS Arabidopsis thaliana GN BPM3 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9VFP2|RDX_DROME
|
2 |
186 |
+ |
185 |
Gaps:13 |
22.68 |
829 |
27.66 |
1e-09 |
Protein roadkill OS Drosophila melanogaster GN rdx PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q6P8B3|SPOP_XENTR
|
3 |
186 |
+ |
184 |
Gaps:13 |
50.00 |
374 |
27.27 |
1e-09 |
Speckle-type POZ protein OS Xenopus tropicalis GN spop PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7ZX06|SPOPA_XENLA
|
3 |
186 |
+ |
184 |
Gaps:13 |
50.00 |
374 |
27.27 |
1e-09 |
Speckle-type POZ protein A OS Xenopus laevis GN spop-a PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q7T330|SPOP_DANRE
|
3 |
186 |
+ |
184 |
Gaps:13 |
50.00 |
374 |
27.27 |
1e-09 |
Speckle-type POZ protein OS Danio rerio GN spop PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|58100
|
7 |
136 |
+ |
130 |
Gaps:15 |
99.21 |
126 |
37.60 |
2e-18 |
cd00121 MATH MATH (meprin and TRAF-C homology) domain an independent folding unit with an eight-stranded beta-sandwich structure found in meprins TRAFs and other proteins. Meprins comprise a class of extracellular metalloproteases which are anchored to the membrane and are capable of cleaving growth factors extracellular matrix proteins and biologically active peptides. TRAF molecules serve as adapter proteins that link cell surface receptors of the Tumor Necrosis Factor and 1nterleukin-1/Toll-like families to downstream kinase cascades which results in the activation of transcription factors and the regulation of cell survival proliferation and stress responses in the immune and inflammatory systems. Other members include the ubiquitin ligases TRIM37 and SPOP and the ubiquitin-specific proteases HAUSP and Ubp21p. A large number of uncharacterized members mostly from lineage-specific expansions in C. elegans and rice contain MATH and BTB domains similar to SPOP. The MATH domain has been shown to bind peptide/protein substrates in TRAFs and HAUSP. It is possible that the MATH domain in other members of this superfamily also interacts with various protein substrates. The TRAF domain may also be involved in the trimerization of TRAFs. Based on homology it is postulated that the MATH domain in meprins may be involved in its tetramer assembly and that the MATH domain in general may take part in diverse modular arrangements defined by adjacent multimerization domains..
|