blastp_kegg |
lcl|cmo:103489516
|
1 |
482 |
+ |
482 |
Gaps:60 |
90.79 |
597 |
63.84 |
0.0 |
uncharacterized LOC103489516
|
blastp_kegg |
lcl|gmx:100786364
|
7 |
482 |
+ |
476 |
Gaps:60 |
92.73 |
578 |
64.37 |
0.0 |
uncharacterized LOC100786364
|
blastp_kegg |
lcl|vvi:100244583
|
5 |
482 |
+ |
478 |
Gaps:5 |
86.16 |
578 |
77.31 |
0.0 |
putative amidohydrolase ytcJ-like
|
blastp_kegg |
lcl|pop:POPTR_0003s19570g
|
1 |
482 |
+ |
482 |
Gaps:52 |
93.91 |
558 |
65.65 |
0.0 |
POPTRDRAFT_414750 LAF1 ISOFORM 1 family protein
|
blastp_kegg |
lcl|rcu:RCOM_1452470
|
2 |
482 |
+ |
481 |
none |
83.97 |
574 |
76.56 |
0.0 |
Exoenzymes regulatory protein aepA precursor putative
|
blastp_kegg |
lcl|csv:101220362
|
1 |
482 |
+ |
482 |
Gaps:60 |
99.45 |
545 |
62.73 |
0.0 |
putative amidohydrolase YtcJ-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa003990mg
|
8 |
482 |
+ |
475 |
none |
88.81 |
536 |
77.31 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103330833
|
1 |
482 |
+ |
482 |
none |
84.29 |
573 |
76.60 |
0.0 |
uncharacterized LOC103330833
|
blastp_kegg |
lcl|mdm:103438564
|
5 |
482 |
+ |
478 |
none |
84.04 |
570 |
76.62 |
0.0 |
uncharacterized LOC103438564
|
blastp_kegg |
lcl|cit:102606925
|
2 |
482 |
+ |
481 |
none |
85.04 |
575 |
75.26 |
0.0 |
uncharacterized LOC102606925
|
blastp_pdb |
3igh_X
|
14 |
457 |
+ |
444 |
Gaps:52 |
95.88 |
486 |
29.18 |
1e-31 |
mol:protein length:486 UNCHARACTERIZED METAL-DEPENDENT HYDROLASE
|
blastp_pdb |
3icj_A
|
14 |
457 |
+ |
444 |
Gaps:69 |
85.96 |
534 |
30.50 |
2e-29 |
mol:protein length:534 uncharacterized metal-dependent hydrolase
|
blastp_uniprot_sprot |
sp|O34355|YTCJ_BACSU
|
65 |
481 |
+ |
417 |
Gaps:37 |
77.13 |
529 |
33.82 |
1e-48 |
Putative amidohydrolase YtcJ OS Bacillus subtilis (strain 168) GN ytcJ PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q68AP4|NFDA_ARTPS
|
9 |
481 |
+ |
473 |
Gaps:38 |
84.87 |
542 |
31.52 |
3e-22 |
N-substituted formamide deformylase OS Arthrobacter pascens GN nfdA PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q06555|AEPA_PECCC
|
8 |
371 |
+ |
364 |
Gaps:36 |
75.91 |
465 |
29.18 |
6e-10 |
Exoenzymes regulatory protein AepA OS Pectobacterium carotovorum subsp. carotovorum GN aepA PE 4 SV 1
|
blastp_uniprot_sprot |
sp|A7GQZ8|HUTI_BACCN
|
22 |
191 |
+ |
170 |
Gaps:43 |
32.86 |
423 |
38.13 |
5e-08 |
Imidazolonepropionase OS Bacillus cereus subsp. cytotoxis (strain NVH 391-98) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B8JBF9|HUTI_ANAD2
|
7 |
119 |
+ |
113 |
Gaps:20 |
25.42 |
421 |
38.32 |
9e-07 |
Imidazolonepropionase OS Anaeromyxobacter dehalogenans (strain 2CP-1 / ATCC BAA-258) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|B4UEL6|HUTI_ANASK
|
7 |
119 |
+ |
113 |
Gaps:20 |
25.42 |
421 |
37.38 |
3e-06 |
Imidazolonepropionase OS Anaeromyxobacter sp. (strain K) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q733I0|HUTI_BACC1
|
23 |
191 |
+ |
169 |
Gaps:43 |
32.62 |
423 |
35.51 |
4e-06 |
Imidazolonepropionase OS Bacillus cereus (strain ATCC 10987) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|C1EN91|HUTI_BACC3
|
23 |
191 |
+ |
169 |
Gaps:43 |
32.62 |
423 |
35.51 |
5e-06 |
Imidazolonepropionase OS Bacillus cereus (strain 03BB102) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A0RH37|HUTI_BACAH
|
23 |
191 |
+ |
169 |
Gaps:43 |
32.62 |
423 |
35.51 |
5e-06 |
Imidazolonepropionase OS Bacillus thuringiensis (strain Al Hakam) GN hutI PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8RFG1|HUTI_FUSNN
|
30 |
120 |
+ |
91 |
Gaps:12 |
19.13 |
413 |
36.71 |
5e-06 |
Imidazolonepropionase OS Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / CIP 101130 / JCM 8532 / LMG 13131) GN hutI PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|30043
|
29 |
453 |
+ |
425 |
Gaps:11 |
88.94 |
479 |
44.84 |
5e-96 |
cd01300 YtcJ_like YtcJ_like metal dependent amidohydrolases. YtcJ is a Bacillus subtilis ORF of unknown function. The Arabidopsis homolog LAF3 has been identified as a factor required for photochrome A signalling..
|
rpsblast_cdd |
gnl|CDD|31762
|
5 |
481 |
+ |
477 |
Gaps:13 |
94.21 |
535 |
37.70 |
1e-74 |
COG1574 COG1574 Predicted metal-dependent hydrolase with the TIM-barrel fold [General function prediction only].
|
rpsblast_cdd |
gnl|CDD|116579
|
78 |
453 |
+ |
376 |
Gaps:77 |
81.89 |
392 |
33.33 |
8e-33 |
pfam07969 Amidohydro_3 Amidohydrolase family.
|
rpsblast_cdd |
gnl|CDD|31421
|
8 |
482 |
+ |
475 |
Gaps:90 |
96.80 |
406 |
27.99 |
5e-18 |
COG1228 HutI Imidazolonepropionase and related amidohydrolases [Secondary metabolites biosynthesis transport and catabolism].
|
rpsblast_cdd |
gnl|CDD|30035
|
126 |
433 |
+ |
308 |
Gaps:47 |
96.36 |
275 |
24.15 |
2e-14 |
cd01292 metallo-dependent_hydrolases Superfamily of metallo-dependent hydrolases (also called amidohydrolase superfamily) is a large group of proteins that show conservation in their 3-dimensional fold (TIM barrel) and in details of their active site. The vast majority of the members have a conserved metal binding site involving four histidines and one aspartic acid residue. In the common reaction mechanism the metal ion (or ions) deprotonate a water molecule for a nucleophilic attack on the substrate. The family includes urease alpha adenosine deaminase phosphotriesterase dihydroorotases allantoinases hydantoinases AMP- adenine and cytosine deaminases imidazolonepropionase aryldialkylphosphatase chlorohydrolases formylmethanofuran dehydrogenases and others..
|
rpsblast_cdd |
gnl|CDD|30039
|
31 |
477 |
+ |
447 |
Gaps:57 |
72.24 |
371 |
32.09 |
4e-14 |
cd01296 Imidazolone-5PH Imidazolonepropionase/imidazolone-5-propionate hydrolase (Imidazolone-5PH) catalyzes the third step in the histidine degradation pathway the hydrolysis of (S)-3-(5-oxo-4 5-dihydro-3H-imidazol-4-yl)propanoate to N-formimidoyl-L-glutamate. In bacteria the enzyme is part of histidine utilization (hut) operon..
|
rpsblast_cdd |
gnl|CDD|181795
|
7 |
167 |
+ |
161 |
Gaps:45 |
33.50 |
406 |
35.29 |
1e-12 |
PRK09356 PRK09356 imidazolonepropionase Validated.
|
rpsblast_cdd |
gnl|CDD|162260
|
29 |
121 |
+ |
93 |
Gaps:14 |
20.95 |
377 |
37.97 |
7e-10 |
TIGR01224 hutI imidazolonepropionase. This enzyme catalyzes the third step in histidine degradation.
|