blastp_kegg |
lcl|pmum:103330833
|
15 |
531 |
+ |
517 |
Gaps:16 |
87.43 |
573 |
78.44 |
0.0 |
uncharacterized LOC103330833
|
blastp_kegg |
lcl|vvi:100244583
|
23 |
531 |
+ |
509 |
Gaps:11 |
86.51 |
578 |
78.80 |
0.0 |
putative amidohydrolase ytcJ-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa003990mg
|
53 |
531 |
+ |
479 |
none |
89.37 |
536 |
79.96 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_1452470
|
1 |
531 |
+ |
531 |
Gaps:16 |
90.07 |
574 |
74.85 |
0.0 |
Exoenzymes regulatory protein aepA precursor putative
|
blastp_kegg |
lcl|pxb:103952132
|
1 |
531 |
+ |
531 |
Gaps:20 |
99.04 |
520 |
75.15 |
0.0 |
uncharacterized LOC103952132
|
blastp_kegg |
lcl|mdm:103438564
|
51 |
531 |
+ |
481 |
none |
84.39 |
570 |
77.55 |
0.0 |
uncharacterized LOC103438564
|
blastp_kegg |
lcl|cit:102606925
|
1 |
531 |
+ |
531 |
Gaps:13 |
90.09 |
575 |
74.71 |
0.0 |
uncharacterized LOC102606925
|
blastp_kegg |
lcl|cam:101501162
|
1 |
531 |
+ |
531 |
Gaps:11 |
90.16 |
579 |
70.50 |
0.0 |
putative amidohydrolase YtcJ-like
|
blastp_kegg |
lcl|fve:101307247
|
15 |
531 |
+ |
517 |
Gaps:19 |
87.83 |
567 |
74.30 |
0.0 |
putative amidohydrolase YtcJ-like
|
blastp_kegg |
lcl|tcc:TCM_045119
|
1 |
531 |
+ |
531 |
Gaps:11 |
90.12 |
577 |
72.69 |
0.0 |
Amidohydrolase family ISF2 isoform 1
|
blastp_pdb |
3igh_X
|
60 |
508 |
+ |
449 |
Gaps:44 |
84.57 |
486 |
33.58 |
9e-41 |
mol:protein length:486 UNCHARACTERIZED METAL-DEPENDENT HYDROLASE
|
blastp_pdb |
3icj_A
|
20 |
512 |
+ |
493 |
Gaps:61 |
85.02 |
534 |
33.48 |
4e-38 |
mol:protein length:534 uncharacterized metal-dependent hydrolase
|
blastp_pdb |
3ggm_D
|
53 |
122 |
+ |
70 |
Gaps:1 |
85.19 |
81 |
36.23 |
6e-06 |
mol:protein length:81 uncharacterized protein BT9727_2919
|
blastp_pdb |
3ggm_C
|
53 |
122 |
+ |
70 |
Gaps:1 |
85.19 |
81 |
36.23 |
6e-06 |
mol:protein length:81 uncharacterized protein BT9727_2919
|
blastp_pdb |
3ggm_B
|
53 |
122 |
+ |
70 |
Gaps:1 |
85.19 |
81 |
36.23 |
6e-06 |
mol:protein length:81 uncharacterized protein BT9727_2919
|
blastp_pdb |
3ggm_A
|
53 |
122 |
+ |
70 |
Gaps:1 |
85.19 |
81 |
36.23 |
6e-06 |
mol:protein length:81 uncharacterized protein BT9727_2919
|
blastp_uniprot_sprot |
sp|O34355|YTCJ_BACSU
|
61 |
530 |
+ |
470 |
Gaps:39 |
87.15 |
529 |
35.36 |
2e-67 |
Putative amidohydrolase YtcJ OS Bacillus subtilis (strain 168) GN ytcJ PE 4 SV 1
|
blastp_uniprot_sprot |
sp|Q68AP4|NFDA_ARTPS
|
55 |
530 |
+ |
476 |
Gaps:38 |
87.45 |
542 |
29.54 |
1e-35 |
N-substituted formamide deformylase OS Arthrobacter pascens GN nfdA PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q06555|AEPA_PECCC
|
47 |
439 |
+ |
393 |
Gaps:34 |
84.09 |
465 |
27.11 |
5e-25 |
Exoenzymes regulatory protein AepA OS Pectobacterium carotovorum subsp. carotovorum GN aepA PE 4 SV 1
|
blastp_uniprot_sprot |
sp|A9BIU9|ADEC_PETMO
|
54 |
121 |
+ |
68 |
Gaps:8 |
10.53 |
570 |
46.67 |
1e-05 |
Adenine deaminase OS Petrotoga mobilis (strain DSM 10674 / SJ95) GN ade PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|30043
|
75 |
531 |
+ |
457 |
Gaps:12 |
94.15 |
479 |
44.12 |
1e-120 |
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
|
50 |
531 |
+ |
482 |
Gaps:13 |
88.79 |
535 |
39.58 |
1e-102 |
COG1574 COG1574 Predicted metal-dependent hydrolase with the TIM-barrel fold [General function prediction only].
|
rpsblast_cdd |
gnl|CDD|116579
|
109 |
531 |
+ |
423 |
Gaps:91 |
92.86 |
392 |
32.69 |
2e-37 |
pfam07969 Amidohydro_3 Amidohydrolase family.
|
rpsblast_cdd |
gnl|CDD|30035
|
247 |
528 |
+ |
282 |
Gaps:40 |
90.18 |
275 |
23.39 |
3e-12 |
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
|
77 |
149 |
+ |
73 |
Gaps:11 |
16.71 |
371 |
38.71 |
3e-10 |
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
|
54 |
147 |
+ |
94 |
Gaps:19 |
21.43 |
406 |
34.48 |
6e-10 |
PRK09356 PRK09356 imidazolonepropionase Validated.
|
rpsblast_cdd |
gnl|CDD|73255
|
55 |
120 |
+ |
66 |
Gaps:5 |
14.70 |
415 |
42.62 |
1e-09 |
cd01297 D-aminoacylase D-aminoacylases (N-acyl-D-Amino acid amidohydrolases) catalyze the hydrolysis of N-acyl-D-amino acids to produce the corresponding D-amino acids which are used as intermediates in the synthesis of pesticides bioactive peptides and antibiotics..
|
rpsblast_cdd |
gnl|CDD|181388
|
55 |
121 |
+ |
67 |
Gaps:10 |
12.42 |
459 |
40.35 |
3e-09 |
PRK08323 PRK08323 phenylhydantoinase Validated.
|
rpsblast_cdd |
gnl|CDD|181711
|
76 |
120 |
+ |
45 |
none |
10.39 |
433 |
33.33 |
4e-08 |
PRK09228 PRK09228 guanine deaminase Provisional.
|
rpsblast_cdd |
gnl|CDD|184033
|
55 |
129 |
+ |
75 |
Gaps:11 |
14.68 |
477 |
40.00 |
1e-07 |
PRK13404 PRK13404 dihydropyrimidinase Provisional.
|