Protein : Qrob_P0280830.2 Q. robur
Protein Identifier  ? Qrob_P0280830.2 Organism . Name  Quercus robur
Score  100.0 Score Type  egn
Protein Description  (M=4) K13248 - pyridoxal phosphate phosphatase PHOSPHO2 [EC:3.1.3.74] Code Enzyme  EC:3.6.1.1
Gene Prediction Quality  validated Protein length 

Sequence

Length: 206  
Kegg Orthology  K13248
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0 Synonyms

2 GO Terms

Identifier Name Description
GO:0008152 metabolic process The chemical reactions and pathways, including anabolism and catabolism, by which living organisms transform chemical substances. Metabolic processes typically transform small molecules, but also include macromolecular processes such as DNA repair and replication, and protein synthesis and degradation.
GO:0016791 phosphatase activity Catalysis of the hydrolysis of phosphoric monoesters, releasing inorganic phosphate.

24 Blast

Analysis Hit Start End Strand Length Note Hit Coverage Hit Length Hit Pident E Val Hit Description
blastp_kegg lcl|cic:CICLE_v10009204mg 1 205 + 205 Gaps:1 76.98 265 63.73 1e-94 hypothetical protein
blastp_kegg lcl|cit:102621280 1 205 + 205 Gaps:1 76.98 265 63.73 1e-94 inorganic pyrophosphatase 3-like
blastp_kegg lcl|rcu:RCOM_1047850 1 205 + 205 none 81.03 253 63.90 1e-94 Pyridoxal phosphate phosphatase PHOSPHO2 putative (EC:3.1.3.75)
blastp_kegg lcl|pda:103699233 1 190 + 190 none 69.85 272 67.89 3e-94 inorganic pyrophosphatase 2-like
blastp_kegg lcl|pda:103711193 1 201 + 201 none 73.09 275 63.68 3e-93 inorganic pyrophosphatase 2
blastp_kegg lcl|vvi:100247400 1 195 + 195 none 72.49 269 66.67 3e-93 inorganic pyrophosphatase 2-like
blastp_kegg lcl|cic:CICLE_v10026096mg 1 190 + 190 none 59.19 321 67.89 2e-92 hypothetical protein
blastp_kegg lcl|cit:102617018 1 190 + 190 none 69.09 275 67.37 9e-92 inorganic pyrophosphatase 1-like
blastp_kegg lcl|tcc:TCM_037696 1 196 + 196 none 70.50 278 64.29 4e-91 Pyridoxal phosphate phosphatase-related protein
blastp_kegg lcl|pop:POPTR_0008s20130g 1 199 + 199 none 71.84 277 61.81 2e-89 POPTRDRAFT_657611 hypothetical protein
blastp_uniprot_sprot sp|Q9SU92|PPSP3_ARATH 1 190 + 190 Gaps:1 77.96 245 58.64 2e-77 Inorganic pyrophosphatase 3 OS Arabidopsis thaliana GN At4g29530 PE 2 SV 1
blastp_uniprot_sprot sp|Q9FZ62|PPSP2_ARATH 1 190 + 190 Gaps:1 68.46 279 54.45 1e-75 Inorganic pyrophosphatase 2 OS Arabidopsis thaliana GN At1g17710 PE 2 SV 1
blastp_uniprot_sprot sp|Q67YC0|PPSP1_ARATH 1 184 + 184 Gaps:2 63.05 295 54.84 7e-75 Inorganic pyrophosphatase 1 OS Arabidopsis thaliana GN PS2 PE 1 SV 1
blastp_uniprot_sprot sp|Q6DBV4|PHOP1_DANRE 11 188 + 178 Gaps:17 63.44 279 36.16 1e-27 Probable phosphatase phospho1 OS Danio rerio GN phospho1 PE 2 SV 1
blastp_uniprot_sprot sp|Q66KD6|PHOP2_XENTR 44 186 + 143 Gaps:10 57.56 238 40.15 4e-23 Probable phosphatase phospho2 OS Xenopus tropicalis GN phospho2 PE 2 SV 1
blastp_uniprot_sprot sp|O73884|PHOP1_CHICK 1 187 + 187 Gaps:15 70.90 268 30.00 1e-21 Phosphoethanolamine/phosphocholine phosphatase OS Gallus gallus GN PHOSPHO1 PE 2 SV 1
blastp_uniprot_sprot sp|Q8TCT1|PHOP1_HUMAN 1 186 + 186 Gaps:16 69.66 267 32.80 5e-21 Phosphoethanolamine/phosphocholine phosphatase OS Homo sapiens GN PHOSPHO1 PE 1 SV 1
blastp_uniprot_sprot sp|Q8R2H9|PHOP1_MOUSE 1 187 + 187 Gaps:13 71.16 267 30.53 3e-20 Phosphoethanolamine/phosphocholine phosphatase OS Mus musculus GN Phospho1 PE 2 SV 1
blastp_uniprot_sprot sp|Q9D9M5|PHOP2_MOUSE 44 187 + 144 Gaps:16 59.75 241 34.72 7e-18 Pyridoxal phosphate phosphatase PHOSPHO2 OS Mus musculus GN Phospho2 PE 2 SV 1
blastp_uniprot_sprot sp|Q66HC4|PHOP2_RAT 44 187 + 144 Gaps:16 59.75 241 34.72 4e-17 Pyridoxal phosphate phosphatase PHOSPHO2 OS Rattus norvegicus GN Phospho2 PE 2 SV 1
rpsblast_cdd gnl|CDD|203542 1 187 + 187 Gaps:9 79.49 234 52.15 9e-70 pfam06888 Put_Phosphatase Putative Phosphatase. This family contains a number of putative eukaryotic acid phosphatases. Some family members represent the products of the PSI14 phosphatase family in Lycopersicon esculentum (Tomato).
rpsblast_cdd gnl|CDD|211659 1 151 + 151 Gaps:16 74.21 190 31.91 2e-34 TIGR01489 DKMTPPase-SF 2 3-diketo-5-methylthio-1-phosphopentane phosphatase. This phosphatase is a member of the IB subfamily (TIGR01488) of the haloacid dehalogenase (HAD) superfamily of aspartate-nucleophile hydrolases. With the exception of OMNI|NTL01BS01361 from B. subtilis and GP|15024582 from Clostridium acetabutylicum the members of this group are all eukaryotic spanning metazoa plants and fungi. The B. subtilus gene (YkrX renamed MtnX) is part of an operon for the conversion of methylthioribose (MTR) to methionine. It works with the enolase MtnW a RuBisCO homolog. The combination of MtnW and MtnX achieves the same overall reaction as the enolase-phosphatase MtnC. The function of MtnX was shown by Ashida et al. (2003) to be 2 3-diketo-5-methylthio-1-phosphopentane phosphatase rather than 2 3-diketo-5-methylthio-1-phosphopentane phosphatase as proposed earlier. See the Genome Property for methionine salvage for more details. In eukaryotes methionine salvage from methylthioadenosine also occurs. It seems reasonable that members of this family in eukaryotes fulfill a similar role as in Bacillus. A more specific equivalog-level model is TIGR03333. Note that a member of this family from S. cerevisiae is annotated as a "probable membrane protein" due to a predicted transmembrane helix. The region in question contains the second of the three conserved HAD superfamily catalytic motifs and thus considering the fold of the HAD catalytic domain is unlikely to be a transmembrane region in fact.
rpsblast_cdd gnl|CDD|162386 22 141 + 120 Gaps:14 59.89 177 22.64 2e-12 TIGR01488 HAD-SF-IB Haloacid Dehalogenase superfamily subfamily IB phosphoserine phosphatase-like. This model represents a subfamily of the Haloacid Dehalogenase superfamily of aspartate-nucleophile hydrolases. Subfamily IA B C and D are distinguished from the rest of the superfamily by the presence of a variable domain between the first and second conserved catalytic motifs. In subfamilies IA and IB this domain consists of an alpha-helical bundle. It was necessary to model these two subfamilies separately breaking them at a an apparent phylogenetic bifurcation so that the resulting model(s) are not so broadly defined that members of subfamily III (which lack the variable domain) are included. Subfamily IA includes the enzyme phosphoserine phosphatase (TIGR00338) as well as three hypothetical equivalogs. Many members of these hypothetical equivalogs have been annotated as PSPase-like or PSPase-family proteins. In particular the hypothetical equivalog which appears to be most closely related to PSPase contains only Archaea (while TIGR00338 contains only eukaryotes and bacteria) of which some are annotated as PSPases. Although this is a reasonable conjecture none of these sequences has sufficient evidence for this assignment. If such should be found this model should be retired while the PSPase model should be broadened to include these sequences.
rpsblast_kog gnl|CDD|38330 1 194 + 194 Gaps:7 75.39 256 49.22 3e-62 KOG3120 KOG3120 KOG3120 Predicted haloacid dehalogenase-like hydrolase [General function prediction only].

7 Domain Motifs

Analysis Begin End Length Domain Identifier Cross Ref Description Inter Pro
PANTHER 1 187 187 PTHR20889:SF0 none none none
PANTHER 1 187 187 PTHR20889 none none none
SUPERFAMILY 2 153 152 SSF56784 none none IPR023214
PIRSF 1 191 191 PIRSF031051 none none IPR016965
Pfam 1 187 187 PF06888 none Putative Phosphatase IPR016965
TIGRFAM 2 151 150 TIGR01489 none DKMTPPase-SF: 2,3-diketo-5-methylthio-1-phosphopentane phosphatase IPR006384
TIGRFAM 3 139 137 TIGR01488 none HAD-SF-IB: HAD phosphoserine phosphatase-like hydrolase, family IB IPR006383

0 Localization

9 Qtllist

Qtl Name Chromosome Name Linkage Group Prox Marker Dist Marker Position QTL Pos One Pos Two Test Type Test Value R 2
Bourran1_2003_QTL2_peak_Bud_burst_A4 Qrob_Chr02 2 s_1B0H8U_259 s_1CB1VL_554 17 0 87 lod 3,3 8,7
Bourran2_2004_QTL9_peak_Bud_burst_3P Qrob_Chr02 2 s_1C34E9_788 v_12238_322 50 25 75 lod 4,4 10,1
NancyGreenhouseCO2_2001_ambient_elevated_leaf_cellulose_QTL2_d13Cf Qrob_Chr02 2 s_1AQA4Z_1644 s_1AK5QX_947 53.67 14,01 79,68 lod 5.6594 0.03
Bourran1_2004_QTL2_peak_Bud_burst_3P Qrob_Chr02 2 s_1AW12F_382 s_1A77MR_223 42 6 64 lod 3,6 9,6
Bourran_2000_2002_QTL2_Delta.F Qrob_Chr02 2 s_1CSO13_1244 s_1AVEUF_1540 55.44 46,71 63,68 lod 7.3232 0.058
Bourran2_2002_QTL9_peak_Bud_burst_A4 Qrob_Chr02 2 s_1BFNDA_375 s_1A3VA1_2139 32,5 17 62 lod 3,1 4,2
Bourran2_2003_QTL8_peak_Bud_burst_3P Qrob_Chr02 2 s_1ANG6_1446 v_11270_161 40 0 72 lod 4,4 9,9
Bourran2_2014_nP_A4 Qrob_Chr11 11 s_1B58GB_1413 s_1A5BYY_1671 11,15 0 42,38 lod 1,8913 4,5
NancyGreenhouseCO2_2001_ambient_elevated_leaf_cellulose_QTL6_d13Cf Qrob_Chr02 2 s_1AEP21_172 v_6048_204 46.33 22,5 65,23 lod 4.972 0.03

0 Targeting