blastp_kegg |
lcl|rcu:RCOM_0679080
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
79.87 |
2e-85 |
Histidine-containing phosphotransfer protein putative (EC:1.3.1.74)
|
blastp_kegg |
lcl|pmum:103322898
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
81.82 |
7e-83 |
histidine-containing phosphotransfer protein 1
|
blastp_kegg |
lcl|tcc:TCM_021095
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
83.12 |
7e-83 |
Histidine-containing phosphotransfer protein 1 isoform 1
|
blastp_kegg |
lcl|cit:102625019
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
79.22 |
3e-82 |
histidine-containing phosphotransfer protein 1-like
|
blastp_kegg |
lcl|cic:CICLE_v10006135mg
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
78.57 |
2e-81 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100251055
|
1 |
150 |
+ |
150 |
none |
98.68 |
152 |
76.67 |
8e-81 |
HP3 histidine-containing phosphotransfer protein 1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa012790mg
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
79.87 |
1e-80 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103958531
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
77.27 |
2e-78 |
histidine-containing phosphotransfer protein 1-like
|
blastp_kegg |
lcl|mdm:103403806
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
77.27 |
2e-78 |
histidine-containing phosphotransfer protein 1-like
|
blastp_kegg |
lcl|gmx:100306648
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
77.92 |
1e-77 |
uncharacterized LOC100306648
|
blastp_pdb |
3us6_A
|
1 |
153 |
+ |
153 |
none |
100.00 |
153 |
75.16 |
8e-76 |
mol:protein length:153 Histidine-containing Phosphotransfer Protein
|
blastp_pdb |
2q4f_B
|
6 |
142 |
+ |
137 |
Gaps:1 |
92.62 |
149 |
49.28 |
1e-40 |
mol:protein length:149 Histidine-containing phosphotransfer protein
|
blastp_pdb |
2q4f_A
|
6 |
142 |
+ |
137 |
Gaps:1 |
92.62 |
149 |
49.28 |
1e-40 |
mol:protein length:149 Histidine-containing phosphotransfer protein
|
blastp_pdb |
1yvi_B
|
6 |
142 |
+ |
137 |
Gaps:1 |
92.62 |
149 |
49.28 |
1e-40 |
mol:protein length:149 histidine-containing phosphotransfer protein
|
blastp_pdb |
1yvi_A
|
6 |
142 |
+ |
137 |
Gaps:1 |
92.62 |
149 |
49.28 |
1e-40 |
mol:protein length:149 histidine-containing phosphotransfer protein
|
blastp_pdb |
1wn0_D
|
1 |
134 |
+ |
134 |
Gaps:1 |
93.10 |
145 |
45.93 |
5e-37 |
mol:protein length:145 histidine-containing phosphotransfer protein
|
blastp_pdb |
1wn0_C
|
1 |
134 |
+ |
134 |
Gaps:1 |
93.10 |
145 |
45.93 |
5e-37 |
mol:protein length:145 histidine-containing phosphotransfer protein
|
blastp_pdb |
1wn0_B
|
1 |
134 |
+ |
134 |
Gaps:1 |
93.10 |
145 |
45.93 |
5e-37 |
mol:protein length:145 histidine-containing phosphotransfer protein
|
blastp_pdb |
1wn0_A
|
1 |
134 |
+ |
134 |
Gaps:1 |
93.10 |
145 |
45.93 |
5e-37 |
mol:protein length:145 histidine-containing phosphotransfer protein
|
blastp_uniprot_sprot |
sp|Q9ZNV9|AHP1_ARATH
|
1 |
154 |
+ |
154 |
none |
100.00 |
154 |
70.13 |
2e-69 |
Histidine-containing phosphotransfer protein 1 OS Arabidopsis thaliana GN AHP1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SAZ5|AHP3_ARATH
|
3 |
152 |
+ |
150 |
Gaps:1 |
97.42 |
155 |
54.97 |
9e-55 |
Histidine-containing phosphotransfer protein 3 OS Arabidopsis thaliana GN AHP3 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9ZNV8|AHP2_ARATH
|
3 |
153 |
+ |
151 |
Gaps:1 |
97.44 |
156 |
52.63 |
6e-53 |
Histidine-containing phosphotransfer protein 2 OS Arabidopsis thaliana GN AHP2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8L9T7|AHP5_ARATH
|
3 |
153 |
+ |
151 |
Gaps:1 |
96.82 |
157 |
53.95 |
2e-52 |
Histidine-containing phosphotransfer protein 5 OS Arabidopsis thaliana GN AHP5 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q6VAK4|HP1_ORYSJ
|
1 |
142 |
+ |
142 |
Gaps:1 |
95.97 |
149 |
48.25 |
1e-40 |
Histidine-containing phosphotransfer protein 1 OS Oryza sativa subsp. japonica GN HP1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LU15|AHP4_ARATH
|
19 |
138 |
+ |
120 |
none |
94.49 |
127 |
46.67 |
1e-37 |
Histidine-containing phosphotransfer protein 4 OS Arabidopsis thaliana GN AHP4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9SSC9|AHP6_ARATH
|
1 |
149 |
+ |
149 |
Gaps:2 |
98.05 |
154 |
45.70 |
3e-26 |
Histidine-containing phosphotransfer protein 6 OS Arabidopsis thaliana GN AHP6 PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|201893
|
44 |
128 |
+ |
85 |
Gaps:2 |
100.00 |
87 |
22.99 |
3e-09 |
pfam01627 Hpt Hpt domain. The histidine-containing phosphotransfer (HPt) domain is a novel protein module with an active histidine residue that mediates phosphotransfer reactions in the two-component signaling systems. A multistep phosphorelay involving the HPt domain has been suggested for these signaling pathways. The crystal structure of the HPt domain of the anaerobic sensor kinase ArcB has been determined. The domain consists of six alpha helices containing a four-helix bundle-folding. The pattern of sequence similarity of the HPt domains of ArcB and components in other signaling systems can be interpreted in light of the three-dimensional structure and supports the conclusion that the HPt domains have a common structural motif both in prokaryotes and eukaryotes. In S. cerevisiae ypd1p this domain has been shown to contain a binding surface for Ssk1p (response regulator receiver domain containing protein pfam00072).
|
rpsblast_cdd |
gnl|CDD|28972
|
44 |
123 |
+ |
80 |
Gaps:11 |
96.81 |
94 |
28.57 |
1e-07 |
cd00088 HPT Histidine Phosphotransfer domain involved in signalling through a two part component systems in which an autophosphorylating histidine protein kinase serves as a phosphoryl donor to a response regulator protein the response regulator protein is modulated by phosphorylation and dephosphorylation of a conserved aspartic acid residue two-component proteins are abundant in most eubacteria In E. coli there are 62 two-component proteins involved in a variety of processes such as chemotaxis osmoregulation metabolism and transport 1 also present in both Gram positive and Gram negative pathogenic bacteria where they regulate basic housekeeping functions and control expression of toxins and other proteins important for pathogenesis in archaea and eukaryotes two-component pathways constitute a very small number of all signaling systems in fungi they mediate environmental stress responses and in pathogenic yeast hyphal development. In Dictyostelium and in plants they are involved in important processes such as osmoregulation cell growth and differentiation to date two-component proteins have not been identified in animals in most prokaryotic systems the output response is effected directly by the RR which functions as a transcription factor while in eukaryotic systems two-component proteins are found at the beginning of signaling pathways where they interface with more conventional eukaryotic signaling strategies such as MAP kinase and cyclic nucleotide cascades.
|
rpsblast_kog |
gnl|CDD|39944
|
3 |
148 |
+ |
146 |
Gaps:2 |
97.33 |
150 |
59.59 |
1e-39 |
KOG4747 KOG4747 KOG4747 Two-component phosphorelay intermediate involved in MAP kinase cascade regulation [Signal transduction mechanisms].
|