blastp_kegg |
lcl|pmum:103326752
|
1 |
1718 |
+ |
1718 |
Gaps:120 |
99.76 |
1678 |
61.23 |
0.0 |
uncharacterized LOC103326752
|
blastp_kegg |
lcl|pxb:103946970
|
1 |
1718 |
+ |
1718 |
Gaps:157 |
99.76 |
1665 |
59.90 |
0.0 |
uncharacterized LOC103946970
|
blastp_kegg |
lcl|pxb:103930870
|
1 |
1718 |
+ |
1718 |
Gaps:157 |
99.76 |
1665 |
59.84 |
0.0 |
uncharacterized LOC103930870
|
blastp_kegg |
lcl|mdm:103426921
|
1 |
1718 |
+ |
1718 |
Gaps:171 |
99.76 |
1657 |
60.31 |
0.0 |
uncharacterized LOC103426921
|
blastp_kegg |
lcl|mdm:103421895
|
1 |
1718 |
+ |
1718 |
Gaps:141 |
99.76 |
1671 |
59.27 |
0.0 |
uncharacterized LOC103421895
|
blastp_kegg |
lcl|pper:PRUPE_ppa000168mg
|
145 |
1718 |
+ |
1574 |
Gaps:103 |
99.74 |
1545 |
62.36 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103929546
|
1 |
1718 |
+ |
1718 |
Gaps:157 |
99.76 |
1657 |
59.35 |
0.0 |
uncharacterized LOC103929546
|
blastp_kegg |
lcl|tcc:TCM_040802
|
1 |
1714 |
+ |
1714 |
Gaps:110 |
87.52 |
1931 |
57.93 |
0.0 |
DNA binding zinc ion binding DNA binding putative isoform 1
|
blastp_kegg |
lcl|vvi:100260139
|
1 |
1705 |
+ |
1705 |
Gaps:222 |
85.68 |
1976 |
56.53 |
0.0 |
uncharacterized LOC100260139
|
blastp_kegg |
lcl|cic:CICLE_v10014020mg
|
1 |
1732 |
+ |
1732 |
Gaps:168 |
93.70 |
1761 |
57.94 |
0.0 |
hypothetical protein
|
blastp_pdb |
1mm3_A
|
679 |
731 |
+ |
53 |
none |
86.89 |
61 |
41.51 |
2e-08 |
mol:protein length:61 Mi2-beta(Chromodomain helicase-DNA-binding pr
|
blastp_pdb |
2l5u_A
|
678 |
731 |
+ |
54 |
Gaps:1 |
86.89 |
61 |
43.40 |
4e-07 |
mol:protein length:61 Chromodomain-helicase-DNA-binding protein 4
|
blastp_pdb |
2ke1_A
|
686 |
731 |
+ |
46 |
none |
69.70 |
66 |
47.83 |
9e-07 |
mol:protein length:66 Autoimmune regulator
|
blastp_pdb |
1xwh_A
|
686 |
731 |
+ |
46 |
none |
69.70 |
66 |
47.83 |
9e-07 |
mol:protein length:66 Autoimmune regulator
|
blastp_pdb |
2kft_A
|
686 |
731 |
+ |
46 |
none |
82.14 |
56 |
47.83 |
2e-06 |
mol:protein length:56 Autoimmune regulator
|
blastp_uniprot_sprot |
sp|Q12830|BPTF_HUMAN
|
479 |
784 |
+ |
306 |
Gaps:74 |
8.73 |
3046 |
29.32 |
3e-18 |
Nucleosome-remodeling factor subunit BPTF OS Homo sapiens GN BPTF PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9W0T1|NU301_DROME
|
480 |
784 |
+ |
305 |
Gaps:58 |
9.85 |
2669 |
29.66 |
7e-17 |
Nucleosome-remodeling factor subunit NURF301 OS Drosophila melanogaster GN E(bx) PE 1 SV 2
|
blastp_uniprot_sprot |
sp|O97159|CHDM_DROME
|
679 |
732 |
+ |
54 |
none |
4.84 |
1982 |
47.92 |
7e-09 |
Chromodomain-helicase-DNA-binding protein Mi-2 homolog OS Drosophila melanogaster GN Mi-2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q14839|CHD4_HUMAN
|
667 |
732 |
+ |
66 |
Gaps:3 |
6.01 |
1912 |
40.87 |
3e-08 |
Chromodomain-helicase-DNA-binding protein 4 OS Homo sapiens GN CHD4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q6PDQ2|CHD4_MOUSE
|
667 |
774 |
+ |
108 |
Gaps:15 |
6.58 |
1915 |
42.86 |
3e-08 |
Chromodomain-helicase-DNA-binding protein 4 OS Mus musculus GN Chd4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9ULU4|PKCB1_HUMAN
|
690 |
731 |
+ |
42 |
Gaps:2 |
3.37 |
1186 |
52.50 |
4e-08 |
Protein kinase C-binding protein 1 OS Homo sapiens GN ZMYND8 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|G5EBZ4|LE418_CAEEL
|
679 |
731 |
+ |
53 |
Gaps:2 |
2.79 |
1829 |
50.98 |
1e-07 |
Protein let-418 OS Caenorhabditis elegans GN let-418 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q96QT6|PHF12_HUMAN
|
686 |
737 |
+ |
52 |
Gaps:2 |
5.38 |
1004 |
44.44 |
2e-07 |
PHD finger protein 12 OS Homo sapiens GN PHF12 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q5SPL2|PHF12_MOUSE
|
686 |
737 |
+ |
52 |
Gaps:2 |
5.38 |
1003 |
44.44 |
2e-07 |
PHD finger protein 12 OS Mus musculus GN Phf12 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q22516|CHD3_CAEEL
|
661 |
738 |
+ |
78 |
Gaps:2 |
7.39 |
1787 |
36.36 |
3e-07 |
Chromodomain-helicase-DNA-binding protein 3 homolog OS Caenorhabditis elegans GN chd-3 PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|201356
|
690 |
731 |
+ |
42 |
Gaps:5 |
92.16 |
51 |
44.68 |
1e-08 |
pfam00628 PHD PHD-finger. PHD folds into an interleaved type of Zn-finger chelating 2 Zn ions in a similar manner to that of the RING and FYVE domains. Several PHD fingers have been identified as binding modules of methylated histone H3.
|
rpsblast_cdd |
gnl|CDD|197604
|
690 |
731 |
+ |
42 |
Gaps:4 |
97.87 |
47 |
41.30 |
2e-08 |
smart00249 PHD PHD zinc finger. The plant homeodomain (PHD) finger is a C4HC3 zinc-finger-like motif found in nuclear proteins thought to be involved in epigenetics and chromatin-mediated transcriptional regulation. The PHD finger binds two zinc ions using the so-called 'cross-brace' motif and is thus structurally related to the RING finger and the FYVE finger. It is not yet known if PHD fingers have a common molecular function. Several reports suggest that it can function as a protein-protein interacton domain and it was recently demonstrated that the PHD finger of p300 can cooperate with the adjacent BROMO domain in nucleosome binding in vitro. Other reports suggesting that the PHD finger is a ubiquitin ligase have been refuted as these domains were RING fingers misidentified as PHD fingers.
|
rpsblast_cdd |
gnl|CDD|202398
|
494 |
550 |
+ |
57 |
none |
93.44 |
61 |
33.33 |
4e-07 |
pfam02791 DDT DDT domain. This domain is approximately 60 residues in length and is predicted to be a DNA binding domain. The DDT domain is named after (DNA binding homeobox and Different Transcription factors). It is exclusively associated with nuclear domains and is thought to be arranged into three alpha helices.
|
rpsblast_kog |
gnl|CDD|36686
|
479 |
1282 |
+ |
804 |
Gaps:162 |
55.45 |
1414 |
27.30 |
2e-33 |
KOG1473 KOG1473 KOG1473 Nucleosome remodeling factor subunit NURF301/BPTF [Chromatin structure and dynamics Transcription].
|
rpsblast_kog |
gnl|CDD|35604
|
677 |
731 |
+ |
55 |
none |
7.90 |
696 |
34.55 |
4e-07 |
KOG0383 KOG0383 KOG0383 Predicted helicase [General function prediction only].
|