blastp_kegg |
lcl|vvi:100248785
|
1 |
162 |
+ |
162 |
Gaps:73 |
52.01 |
448 |
43.35 |
2e-46 |
4-hydroxyphenylpyruvate dioxygenase-like
|
blastp_kegg |
lcl|rcu:RCOM_1192240
|
1 |
162 |
+ |
162 |
Gaps:67 |
51.47 |
441 |
44.49 |
4e-46 |
4-hydroxyphenylpyruvate dioxygenase putative (EC:1.13.11.27)
|
blastp_kegg |
lcl|cic:CICLE_v10031587mg
|
2 |
162 |
+ |
161 |
Gaps:67 |
52.07 |
434 |
43.81 |
5e-46 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102618830
|
2 |
162 |
+ |
161 |
Gaps:67 |
52.07 |
434 |
43.81 |
5e-46 |
4-hydroxyphenylpyruvate dioxygenase-like
|
blastp_kegg |
lcl|tcc:TCM_001963
|
1 |
162 |
+ |
162 |
Gaps:68 |
51.94 |
439 |
42.98 |
2e-43 |
Phytoene desaturation 1 isoform 1
|
blastp_kegg |
lcl|csv:101215051
|
3 |
162 |
+ |
160 |
Gaps:75 |
51.21 |
455 |
43.35 |
4e-43 |
4-hydroxyphenylpyruvate dioxygenase-like
|
blastp_kegg |
lcl|cmo:103504117
|
2 |
162 |
+ |
161 |
Gaps:79 |
50.11 |
467 |
43.16 |
4e-43 |
4-hydroxyphenylpyruvate dioxygenase
|
blastp_kegg |
lcl|sot:102595018
|
3 |
162 |
+ |
160 |
Gaps:66 |
51.13 |
442 |
42.04 |
4e-43 |
4-hydroxyphenylpyruvate dioxygenase-like
|
blastp_kegg |
lcl|sly:101257377
|
1 |
162 |
+ |
162 |
Gaps:66 |
51.70 |
441 |
41.23 |
5e-43 |
4-hydroxyphenylpyruvate dioxygenase-like
|
blastp_kegg |
lcl|pop:POPTR_0002s05840g
|
1 |
162 |
+ |
162 |
Gaps:72 |
52.25 |
444 |
41.38 |
2e-42 |
POPTRDRAFT_798588 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE family protein
|
blastp_pdb |
1sp9_B
|
1 |
162 |
+ |
162 |
Gaps:70 |
51.24 |
445 |
39.47 |
8e-41 |
mol:protein length:445 4-hydroxyphenylpyruvate dioxygenase
|
blastp_pdb |
1sp9_A
|
1 |
162 |
+ |
162 |
Gaps:70 |
51.24 |
445 |
39.47 |
8e-41 |
mol:protein length:445 4-hydroxyphenylpyruvate dioxygenase
|
blastp_pdb |
1tg5_A
|
1 |
162 |
+ |
162 |
Gaps:70 |
53.77 |
424 |
39.47 |
1e-40 |
mol:protein length:424 4-hydroxyphenylpyruvate dioxygenase
|
blastp_pdb |
1tfz_A
|
1 |
162 |
+ |
162 |
Gaps:70 |
53.77 |
424 |
39.47 |
1e-40 |
mol:protein length:424 4-hydroxyphenylpyruvate dioxygenase
|
blastp_pdb |
1sqd_A
|
1 |
162 |
+ |
162 |
Gaps:70 |
53.77 |
424 |
39.47 |
1e-40 |
mol:protein length:424 4-hydroxyphenylpyruvate dioxygenase
|
blastp_pdb |
1sp8_D
|
1 |
162 |
+ |
162 |
Gaps:69 |
53.83 |
418 |
33.78 |
2e-28 |
mol:protein length:418 4-Hydroxyphenylpyruvate Dioxygenase
|
blastp_pdb |
1sp8_C
|
1 |
162 |
+ |
162 |
Gaps:69 |
53.83 |
418 |
33.78 |
2e-28 |
mol:protein length:418 4-Hydroxyphenylpyruvate Dioxygenase
|
blastp_pdb |
1sp8_B
|
1 |
162 |
+ |
162 |
Gaps:69 |
53.83 |
418 |
33.78 |
2e-28 |
mol:protein length:418 4-Hydroxyphenylpyruvate Dioxygenase
|
blastp_pdb |
1sp8_A
|
1 |
162 |
+ |
162 |
Gaps:69 |
53.83 |
418 |
33.78 |
2e-28 |
mol:protein length:418 4-Hydroxyphenylpyruvate Dioxygenase
|
blastp_uniprot_sprot |
sp|O23920|HPPD_DAUCA
|
1 |
162 |
+ |
162 |
Gaps:64 |
51.13 |
442 |
41.59 |
8e-43 |
4-hydroxyphenylpyruvate dioxygenase OS Daucus carota PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P93836|HPPD_ARATH
|
1 |
162 |
+ |
162 |
Gaps:70 |
51.24 |
445 |
39.47 |
3e-40 |
4-hydroxyphenylpyruvate dioxygenase OS Arabidopsis thaliana GN HPD PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9ARF9|HPPD_PLESU
|
26 |
162 |
+ |
137 |
Gaps:45 |
41.28 |
436 |
44.44 |
5e-35 |
4-hydroxyphenylpyruvate dioxygenase OS Plectranthus scutellarioides PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O48604|HPPD_HORVU
|
1 |
162 |
+ |
162 |
Gaps:70 |
51.61 |
434 |
33.93 |
1e-26 |
4-hydroxyphenylpyruvate dioxygenase OS Hordeum vulgare PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|178463
|
3 |
167 |
+ |
165 |
Gaps:75 |
59.80 |
398 |
39.08 |
2e-43 |
PLN02875 PLN02875 4-hydroxyphenylpyruvate dioxygenase.
|
rpsblast_cdd |
gnl|CDD|162275
|
3 |
161 |
+ |
159 |
Gaps:67 |
61.76 |
353 |
20.64 |
2e-12 |
TIGR01263 4HPPD 4-hydroxyphenylpyruvate dioxygenase. This protein oxidizes 4-hydroxyphenylpyruvate a tyrosine and phenylalanine catabolite to homogentisate. Homogentisate can undergo a further non-enzymatic oxidation and polymerization into brown pigments that protect some bacterial species from light. A similar process occurs spontaneously in blood and is hemolytic. In some bacterial species this enzyme has been studied as a hemolysin.
|
rpsblast_cdd |
gnl|CDD|176673
|
61 |
167 |
+ |
107 |
Gaps:47 |
77.49 |
191 |
27.03 |
2e-08 |
cd07250 HPPD_C_like C-terminal domain of 4-hydroxyphenylpyruvate dioxygenase (HppD) and hydroxymandelate Synthase (HmaS). HppD and HmaS are non-heme iron-dependent dioxygenases which modify a common substrate 4-hydroxyphenylpyruvate (HPP) but yield different products. HPPD catalyzes the second reaction in tyrosine catabolism the conversion of 4-hydroxyphenylpyruvate to homogentisate (2 5-dihydroxyphenylacetic acid HG). HmaS converts HPP to 4-hydroxymandelate a committed step in the formation of hydroxyphenylglycerine a structural component of nonproteinogenic macrocyclic peptide antibiotics such as vancomycin. If the emphasis is on catalytic chemistry HPPD and HmaS are classified as members of a large family of alpha-keto acid dependent mononuclear non-heme iron oxygenases most of which require Fe(II) molecular oxygen and an alpha-keto acid (typically alpha-ketoglutarate) to either oxygenate or oxidize a third substrate. Both enzymes are exceptions in that they require two instead of three substrates do not use alpha-ketoglutarate and incorporate both atoms of dioxygen into the aromatic product. Both HPPD and HmaS exhibit duplicate beta barrel topology in their N- and C-terminal domains which share sequence similarity suggestive of a gene duplication. Each protein has only one catalytic site located in at the C-terminal domain. This HPPD_C_like domain represents the C-terminal domain.
|
rpsblast_kog |
gnl|CDD|35857
|
3 |
161 |
+ |
159 |
Gaps:69 |
59.32 |
381 |
24.78 |
1e-18 |
KOG0638 KOG0638 KOG0638 4-hydroxyphenylpyruvate dioxygenase [Amino acid transport and metabolism].
|