blastp_kegg |
lcl|pper:PRUPE_ppa000415mg
|
1 |
1198 |
+ |
1198 |
Gaps:33 |
99.92 |
1198 |
61.65 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103341418
|
1 |
1198 |
+ |
1198 |
Gaps:34 |
99.92 |
1197 |
61.37 |
0.0 |
putative nuclear matrix constituent protein 1-like protein
|
blastp_kegg |
lcl|mdm:103423761
|
1 |
1198 |
+ |
1198 |
Gaps:40 |
99.92 |
1217 |
59.05 |
0.0 |
putative nuclear matrix constituent protein 1-like protein
|
blastp_kegg |
lcl|pxb:103929210
|
1 |
1198 |
+ |
1198 |
Gaps:40 |
99.92 |
1217 |
58.96 |
0.0 |
putative nuclear matrix constituent protein 1-like protein
|
blastp_kegg |
lcl|cit:102617982
|
1 |
1198 |
+ |
1198 |
Gaps:72 |
100.00 |
1222 |
58.76 |
0.0 |
putative nuclear matrix constituent protein 1-like protein-like
|
blastp_kegg |
lcl|vvi:100242259
|
1 |
1198 |
+ |
1198 |
Gaps:71 |
100.00 |
1213 |
62.16 |
0.0 |
putative nuclear matrix constituent protein 1-like protein-like
|
blastp_kegg |
lcl|cic:CICLE_v10030538mg
|
1 |
1198 |
+ |
1198 |
Gaps:72 |
100.00 |
1222 |
58.67 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_011885
|
1 |
1198 |
+ |
1198 |
Gaps:64 |
100.00 |
1198 |
57.85 |
0.0 |
Nuclear matrix constituent protein-related putative isoform 1
|
blastp_kegg |
lcl|mdm:103402733
|
1 |
1198 |
+ |
1198 |
Gaps:45 |
100.00 |
1217 |
57.93 |
0.0 |
putative nuclear matrix constituent protein 1-like protein
|
blastp_kegg |
lcl|pop:POPTR_0008s11380g
|
19 |
1198 |
+ |
1180 |
Gaps:52 |
99.42 |
1205 |
56.51 |
0.0 |
POPTRDRAFT_766006 POPTRDRAFT_766007 hypothetical protein
|
blastp_uniprot_sprot |
sp|Q9FLH0|NMCP_ARATH
|
58 |
835 |
+ |
778 |
Gaps:58 |
78.69 |
1042 |
32.07 |
7e-80 |
Putative nuclear matrix constituent protein 1-like protein OS Arabidopsis thaliana GN At5g65770 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q21313|EPI1_CAEEL
|
160 |
646 |
+ |
487 |
Gaps:86 |
12.99 |
3672 |
23.48 |
4e-11 |
Laminin-like protein epi-1 OS Caenorhabditis elegans GN epi-1 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|173412
|
104 |
757 |
+ |
654 |
Gaps:229 |
37.52 |
2084 |
56.01 |
2e-16 |
PTZ00121 PTZ00121 MAEBL Provisional.
|
rpsblast_cdd |
gnl|CDD|31389
|
59 |
785 |
+ |
727 |
Gaps:328 |
74.89 |
1163 |
71.30 |
2e-15 |
COG1196 Smc Chromosome segregation ATPases [Cell division and chromosome partitioning].
|
rpsblast_cdd |
gnl|CDD|179675
|
195 |
740 |
+ |
546 |
Gaps:64 |
62.73 |
880 |
32.07 |
3e-15 |
PRK03918 PRK03918 chromosome segregation protein Provisional.
|
rpsblast_cdd |
gnl|CDD|162739
|
102 |
760 |
+ |
659 |
Gaps:196 |
74.98 |
1179 |
38.80 |
1e-13 |
TIGR02168 SMC_prok_B chromosome segregation protein SMC common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria archaea and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle.
|
rpsblast_cdd |
gnl|CDD|179385
|
103 |
703 |
+ |
601 |
Gaps:130 |
65.34 |
880 |
37.91 |
4e-12 |
PRK02224 PRK02224 chromosome segregation protein Provisional.
|
rpsblast_cdd |
gnl|CDD|30768
|
59 |
757 |
+ |
699 |
Gaps:155 |
67.62 |
908 |
62.21 |
9e-12 |
COG0419 SbcC ATPase involved in DNA repair [DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|162740
|
75 |
756 |
+ |
682 |
Gaps:338 |
60.74 |
1164 |
65.49 |
2e-11 |
TIGR02169 SMC_prok_A chromosome segregation protein SMC primarily archaeal type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria archaea and eukaryotes. It is found in a single copy and is homodimeric in prokaryotes but six paralogs (excluded from this family) are found in eukarotes where SMC proteins are heterodimeric. This family represents the SMC protein of archaea and a few bacteria (Aquifex Synechocystis etc) the SMC of other bacteria is described by TIGR02168. The N- and C-terminal domains of this protein are well conserved but the central hinge region is skewed in composition and highly divergent.
|
rpsblast_cdd |
gnl|CDD|202246
|
56 |
767 |
+ |
712 |
Gaps:38 |
74.61 |
1162 |
33.56 |
7e-11 |
pfam02463 SMC_N RecF/RecN/SMC N terminal domain. This domain is found at the N terminus of SMC proteins. The SMC (structural maintenance of chromosomes) superfamily proteins have ATP-binding domains at the N- and C-termini and two extended coiled-coil domains separated by a hinge in the middle. The eukaryotic SMC proteins form two kind of heterodimers: the SMC1/SMC3 and the SMC2/SMC4 types. These heterodimers constitute an essential part of higher order complexes which are involved in chromatin and DNA dynamics. This family also includes the RecF and RecN proteins that are involved in DNA metabolism and recombination.
|
rpsblast_cdd |
gnl|CDD|204830
|
53 |
751 |
+ |
699 |
Gaps:185 |
64.61 |
1198 |
27.00 |
1e-10 |
pfam12128 DUF3584 Protein of unknown function (DUF3584). This protein is found in bacteria and eukaryotes. Proteins in this family are typically between 943 to 1234 amino acids in length. This family contains a P-loop motif suggesting it is a nucleotide binding protein. It may be involved in replication.
|
rpsblast_cdd |
gnl|CDD|129705
|
108 |
734 |
+ |
627 |
Gaps:57 |
64.11 |
1042 |
14.82 |
2e-10 |
TIGR00618 sbcc exonuclease SbcC. All proteins in this family for which functions are known are part of an exonuclease complex with sbcD homologs. This complex is involved in the initiation of recombination to regulate the levels of palindromic sequences in DNA. This family is based on the phylogenomic analysis of JA Eisen (1999 Ph.D. Thesis Stanford University).
|
rpsblast_kog |
gnl|CDD|35383
|
73 |
751 |
+ |
679 |
Gaps:379 |
56.42 |
1930 |
59.32 |
3e-25 |
KOG0161 KOG0161 KOG0161 Myosin class II heavy chain [Cytoskeleton].
|
rpsblast_kog |
gnl|CDD|36180
|
54 |
769 |
+ |
716 |
Gaps:164 |
70.40 |
1294 |
34.03 |
3e-15 |
KOG0962 KOG0962 KOG0962 DNA repair protein RAD50 ABC-type ATPase/SMC superfamily [Replication recombination and repair].
|
rpsblast_kog |
gnl|CDD|36214
|
109 |
670 |
+ |
562 |
Gaps:81 |
55.22 |
1293 |
27.87 |
2e-12 |
KOG0996 KOG0996 KOG0996 Structural maintenance of chromosome protein 4 (chromosome condensation complex Condensin subunit C) [Chromatin structure and dynamics Cell cycle control cell division chromosome partitioning].
|
rpsblast_kog |
gnl|CDD|35832
|
104 |
740 |
+ |
637 |
Gaps:99 |
47.91 |
1317 |
31.54 |
3e-12 |
KOG0612 KOG0612 KOG0612 Rho-associated coiled-coil containing protein kinase [Signal transduction mechanisms].
|
rpsblast_kog |
gnl|CDD|36182
|
317 |
714 |
+ |
398 |
Gaps:32 |
28.83 |
1200 |
34.97 |
1e-11 |
KOG0964 KOG0964 KOG0964 Structural maintenance of chromosome protein 3 (sister chromatid cohesion complex Cohesin subunit SMC3) [Cell cycle control cell division chromosome partitioning].
|
rpsblast_kog |
gnl|CDD|36247
|
198 |
769 |
+ |
572 |
Gaps:149 |
34.08 |
1118 |
47.51 |
1e-11 |
KOG1029 KOG1029 KOG1029 Endocytic adaptor protein intersectin [Signal transduction mechanisms Intracellular trafficking secretion and vesicular transport].
|
rpsblast_kog |
gnl|CDD|35241
|
299 |
754 |
+ |
456 |
Gaps:58 |
48.99 |
1141 |
23.08 |
1e-11 |
KOG0018 KOG0018 KOG0018 Structural maintenance of chromosome protein 1 (sister chromatid cohesion complex Cohesin subunit SMC1) [Cell cycle control cell division chromosome partitioning].
|
rpsblast_kog |
gnl|CDD|36194
|
110 |
742 |
+ |
633 |
Gaps:80 |
55.57 |
1265 |
27.60 |
4e-11 |
KOG0976 KOG0976 KOG0976 Rho/Rac1-interacting serine/threonine kinase Citron [Signal transduction mechanisms].
|