blastp_kegg |
lcl|cit:102613255
|
1 |
451 |
+ |
451 |
Gaps:1 |
94.14 |
478 |
84.00 |
0.0 |
homogentisate 1 2-dioxygenase-like
|
blastp_kegg |
lcl|sot:102579798
|
11 |
456 |
+ |
446 |
Gaps:1 |
90.45 |
492 |
84.72 |
0.0 |
homogentisate 1 2-dioxygenase-like
|
blastp_kegg |
lcl|sly:543605
|
11 |
456 |
+ |
446 |
Gaps:1 |
92.71 |
480 |
84.04 |
0.0 |
HGO homogentisate 1 2-dioxygenase
|
blastp_kegg |
lcl|pper:PRUPE_ppa005219mg
|
11 |
456 |
+ |
446 |
Gaps:1 |
94.28 |
472 |
83.82 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103928802
|
11 |
456 |
+ |
446 |
Gaps:1 |
94.28 |
472 |
82.92 |
0.0 |
homogentisate 1 2-dioxygenase
|
blastp_kegg |
lcl|tcc:TCM_031685
|
10 |
443 |
+ |
434 |
Gaps:1 |
96.01 |
451 |
86.37 |
0.0 |
Homogentisate 1 2-dioxygenase isoform 1
|
blastp_kegg |
lcl|pmum:103326022
|
11 |
456 |
+ |
446 |
Gaps:1 |
94.28 |
472 |
83.15 |
0.0 |
homogentisate 1 2-dioxygenase
|
blastp_kegg |
lcl|cam:101499118
|
1 |
456 |
+ |
456 |
Gaps:3 |
99.56 |
455 |
82.78 |
0.0 |
homogentisate 1 2-dioxygenase-like
|
blastp_kegg |
lcl|rcu:RCOM_1743950
|
2 |
454 |
+ |
453 |
Gaps:1 |
98.91 |
457 |
81.42 |
0.0 |
homogentisate 1 2-dioxygenase putative (EC:1.13.11.5)
|
blastp_kegg |
lcl|vvi:100264043
|
2 |
456 |
+ |
455 |
Gaps:1 |
98.06 |
463 |
81.50 |
0.0 |
homogentisate 1 2-dioxygenase-like
|
blastp_pdb |
1eyb_A
|
2 |
443 |
+ |
442 |
Gaps:16 |
93.84 |
471 |
57.01 |
1e-174 |
mol:protein length:471 HOMOGENTISATE 1 2-DIOXYGENASE
|
blastp_pdb |
1ey2_A
|
2 |
443 |
+ |
442 |
Gaps:16 |
93.84 |
471 |
57.01 |
1e-174 |
mol:protein length:471 HOMOGENTISATE 1 2-DIOXYGENASE
|
blastp_uniprot_sprot |
sp|Q9ZRA2|HGD_ARATH
|
14 |
453 |
+ |
440 |
Gaps:1 |
95.23 |
461 |
79.04 |
0.0 |
Homogentisate 1 2-dioxygenase OS Arabidopsis thaliana GN HGO PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q5VRH4|HGD_ORYSJ
|
2 |
443 |
+ |
442 |
Gaps:4 |
94.89 |
470 |
74.66 |
0.0 |
Homogentisate 1 2-dioxygenase OS Oryza sativa subsp. japonica GN HGO PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q54QI4|HGD_DICDI
|
6 |
441 |
+ |
436 |
Gaps:12 |
99.07 |
432 |
61.68 |
1e-180 |
Homogentisate 1 2-dioxygenase OS Dictyostelium discoideum GN hgd PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O09173|HGD_MOUSE
|
11 |
443 |
+ |
433 |
Gaps:16 |
97.30 |
445 |
58.66 |
2e-176 |
Homogentisate 1 2-dioxygenase OS Mus musculus GN Hgd PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q39J54|HGD_BURS3
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.44 |
4e-176 |
Homogentisate 1 2-dioxygenase OS Burkholderia sp. (strain 383) GN hmgA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A0K4Z6|HGD_BURCH
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.91 |
1e-175 |
Homogentisate 1 2-dioxygenase OS Burkholderia cenocepacia (strain HI2424) GN hmgA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q1BYQ6|HGD_BURCA
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.91 |
1e-175 |
Homogentisate 1 2-dioxygenase OS Burkholderia cenocepacia (strain AU 1054) GN hmgA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B1YTZ1|HGD_BURA4
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.67 |
9e-175 |
Homogentisate 1 2-dioxygenase OS Burkholderia ambifaria (strain MC40-6) GN hmgA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A9AFM6|HGD_BURM1
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.67 |
1e-174 |
Homogentisate 1 2-dioxygenase OS Burkholderia multivorans (strain ATCC 17616 / 249) GN hmgA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B1JWJ3|HGD_BURCC
|
14 |
445 |
+ |
432 |
Gaps:4 |
96.85 |
444 |
57.67 |
4e-174 |
Homogentisate 1 2-dioxygenase OS Burkholderia cenocepacia (strain MC0-3) GN hmgA PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|178264
|
14 |
448 |
+ |
435 |
none |
100.00 |
435 |
80.23 |
0.0 |
PLN02658 PLN02658 homogentisate 1 2-dioxygenase.
|
rpsblast_cdd |
gnl|CDD|180028
|
1 |
445 |
+ |
445 |
Gaps:9 |
99.54 |
438 |
60.55 |
0.0 |
PRK05341 PRK05341 homogentisate 1 2-dioxygenase Provisional.
|
rpsblast_cdd |
gnl|CDD|202933
|
13 |
442 |
+ |
430 |
Gaps:10 |
100.00 |
422 |
64.69 |
0.0 |
pfam04209 HgmA homogentisate 1 2-dioxygenase. Homogentisate dioxygenase cleaves the aromatic ring during the metabolic degradation of Phe and Tyr. Homogentisate dioxygenase deficiency causes alkaptonuria. The structure of homogentisate dioxygenase shows that the enzyme forms a hexamer arrangement comprised of a dimer of trimers. The active site iron ion is coordinated near the interface between the trimers.
|
rpsblast_cdd |
gnl|CDD|200065
|
11 |
442 |
+ |
432 |
Gaps:9 |
100.00 |
429 |
61.54 |
0.0 |
TIGR01015 hmgA homogentisate 1 2-dioxygenase. Missing in human disease alkaptonuria.
|
rpsblast_cdd |
gnl|CDD|33311
|
10 |
438 |
+ |
429 |
Gaps:8 |
98.59 |
427 |
57.01 |
1e-135 |
COG3508 HmgA Homogentisate 1 2-dioxygenase [Secondary metabolites biosynthesis transport and catabolism].
|
rpsblast_kog |
gnl|CDD|36631
|
7 |
443 |
+ |
437 |
Gaps:8 |
97.53 |
446 |
68.74 |
0.0 |
KOG1417 KOG1417 KOG1417 Homogentisate 1 2-dioxygenase [Amino acid transport and metabolism].
|