Amino Acids and Derivatives
|
Agmatine utilization
|
1 (3) |
0 (0) |
1 (1) |
15 |
Allantoin utilization
|
6 (18) |
0 (0) |
6 (6) |
42 |
Amino acid efflux
|
1 (4) |
0 (0) |
1 (1) |
8 |
Amino acid metabolism
|
8 (49) |
92 (873) |
100 (100) |
137 |
Amino acid transport
|
2 (8) |
0 (0) |
2 (2) |
10 |
Amino acid utilization
|
2 (18) |
0 (0) |
2 (2) |
21 |
Arginine biosynthesis
|
27 (230) |
0 (0) |
27 (27) |
249 |
Arginine degradation
|
11 (109) |
0 (0) |
11 (11) |
101 |
Aromatic amino acid metabolism
|
9 (69) |
0 (0) |
9 (9) |
78 |
Asparagine degradation
|
7 (18) |
0 (0) |
7 (7) |
72 |
Aspartate utilization
|
7 (19) |
0 (0) |
7 (7) |
72 |
Betaine utilization
|
2 (4) |
0 (0) |
2 (2) |
30 |
Branched-chain amino acid biosynthesis
|
2 (28) |
4 (42) |
6 (6) |
47 |
Branched-chain amino acid degradation
|
19 (127) |
0 (0) |
19 (19) |
159 |
Creatinine utilization
|
1 (4) |
0 (0) |
1 (1) |
5 |
Cysteine metabolism
|
5 (48) |
0 (0) |
5 (5) |
41 |
Ectoine utilization
|
6 (22) |
0 (0) |
6 (6) |
69 |
Gamma-aminobutyrate utilization
|
15 (50) |
0 (0) |
15 (15) |
96 |
Glutamate metabolism
|
3 (15) |
0 (0) |
3 (3) |
18 |
Glutamine utilization
|
1 (6) |
0 (0) |
1 (1) |
11 |
Glycine betaine synthesis
|
2 (12) |
0 (0) |
2 (2) |
23 |
Glycine metabolism
|
3 (35) |
18 (145) |
21 (21) |
188 |
Histidine biosynthesis
|
6 (46) |
5 (46) |
11 (11) |
105 |
Histidine utilization
|
20 (122) |
0 (0) |
20 (20) |
179 |
L-cystine transporter
|
1 (2) |
0 (0) |
1 (1) |
11 |
Leucine biosynthesis
|
7 (50) |
0 (0) |
7 (7) |
58 |
Lysine biosynthesis
|
2 (15) |
10 (102) |
12 (12) |
136 |
Methionine biosynthesis
|
23 (191) |
13 (96) |
36 (36) |
273 |
Methionine metabolism
|
19 (152) |
11 (91) |
30 (30) |
246 |
Ornithine degradation
|
1 (8) |
1 (12) |
2 (2) |
26 |
Proline and 4-hydrohyproline utilization
|
13 (46) |
0 (0) |
13 (13) |
126 |
Proline utilization
|
1 (4) |
0 (0) |
1 (1) |
11 |
Serine biosynthesis
|
0 (0) |
3 (32) |
3 (3) |
34 |
Spermidine biosynthesis
|
1 (9) |
0 (0) |
1 (1) |
11 |
Threonine biosynthesis
|
0 (0) |
4 (45) |
4 (4) |
47 |
Tryptophan biosynthesis
|
10 (51) |
6 (48) |
16 (16) |
117 |
Tyrosine degradation
|
6 (30) |
0 (0) |
6 (6) |
38 |
Carbohydrates
|
1,5-Anhydro-d-Fructose utilization
|
2 (7) |
0 (0) |
2 (2) |
30 |
2-ketogluconate utilization
|
4 (19) |
0 (0) |
4 (4) |
34 |
Acetoin production
|
1 (4) |
0 (0) |
1 (1) |
11 |
Acetoin utilization
|
1 (6) |
0 (0) |
1 (1) |
11 |
Alginate utilization
|
1 (1) |
0 (0) |
1 (1) |
16 |
Allose utilization
|
3 (5) |
0 (0) |
3 (3) |
31 |
Alpha-galactosides utilization
|
3 (10) |
0 (0) |
3 (3) |
26 |
Alpha-glucosides utilization
|
2 (12) |
0 (0) |
2 (2) |
30 |
Alpha-mannans utilization
|
3 (6) |
0 (0) |
3 (3) |
11 |
Amino sugar metabolism
|
0 (0) |
6 (44) |
6 (6) |
63 |
Arabinan utilization
|
2 (12) |
0 (0) |
2 (2) |
11 |
Arabinogalactan utilization
|
1 (1) |
0 (0) |
1 (1) |
11 |
Arabinose oligosaccharide utilization
|
3 (15) |
0 (0) |
3 (3) |
10 |
Arabinose utilization
|
8 (57) |
0 (0) |
8 (8) |
94 |
Ascorbate utilization
|
8 (41) |
0 (0) |
8 (8) |
62 |
Beta-glucosides utilization
|
26 (91) |
0 (0) |
26 (26) |
121 |
C4-dicarboxylate transport
|
1 (4) |
0 (0) |
1 (1) |
11 |
Carbohydrate metabolism
|
21 (62) |
0 (0) |
21 (21) |
43 |
Carbon catabolism
|
6 (64) |
0 (0) |
6 (6) |
64 |
Carbon dioxide fixation
|
1 (11) |
0 (0) |
1 (1) |
14 |
Carbon fixation
|
1 (12) |
0 (0) |
1 (1) |
14 |
Carbon monoxide utilization
|
1 (8) |
0 (0) |
1 (1) |
10 |
Cellobiose utilization
|
13 (53) |
0 (0) |
13 (13) |
91 |
Cellodextrin utilization
|
1 (1) |
0 (0) |
1 (1) |
10 |
Central carbohydrate metabolism
|
17 (140) |
0 (0) |
17 (17) |
150 |
Chitobiose utilization
|
1 (8) |
0 (0) |
1 (1) |
11 |
Chondroitin sulphate utilization
|
1 (7) |
0 (0) |
1 (1) |
11 |
Citrate metabolism
|
2 (10) |
0 (0) |
2 (2) |
11 |
Citrate utilization
|
2 (10) |
0 (0) |
2 (2) |
19 |
D-threitol utilization
|
2 (4) |
0 (0) |
2 (2) |
9 |
Erythritol utilization
|
1 (2) |
0 (0) |
1 (1) |
9 |
Ethanolamine utilization
|
5 (21) |
0 (0) |
5 (5) |
59 |
Formate metabolism
|
3 (21) |
0 (0) |
3 (3) |
46 |
Fructooligosaccharides utilization
|
4 (10) |
0 (0) |
4 (4) |
45 |
Fructose utilization
|
20 (108) |
0 (0) |
20 (20) |
204 |
Fructoselysine utilization
|
1 (2) |
0 (0) |
1 (1) |
11 |
Fructosides utilization
|
1 (10) |
0 (0) |
1 (1) |
11 |
Fucose utilization
|
5 (16) |
0 (0) |
5 (5) |
63 |
Fucose-glucose oligosaccharide utilization
|
1 (5) |
0 (0) |
1 (1) |
11 |
Galactan utilization
|
2 (11) |
0 (0) |
2 (2) |
21 |
Galactarate utilization
|
13 (53) |
0 (0) |
13 (13) |
75 |
Galacto-N-biose utilization
|
1 (4) |
0 (0) |
1 (1) |
10 |
Galactonate utilization
|
2 (7) |
0 (0) |
2 (2) |
24 |
Galactooligosaccharide utilization
|
3 (16) |
0 (0) |
3 (3) |
10 |
Galactose utilization
|
12 (74) |
0 (0) |
12 (12) |
117 |
Galactosides utilization
|
14 (55) |
0 (0) |
14 (14) |
82 |
Galacturonate utilization
|
18 (79) |
0 (0) |
18 (18) |
134 |
Global catabolite repression
|
1 (15) |
0 (0) |
1 (1) |
15 |
Glucarate utilization
|
13 (55) |
0 (0) |
13 (13) |
75 |
Glucomannan utilization
|
2 (10) |
0 (0) |
2 (2) |
15 |
Gluconate utilization
|
21 (87) |
0 (0) |
21 (21) |
203 |
Gluconeogenesis
|
3 (19) |
0 (0) |
3 (3) |
41 |
Glucosamine utilization
|
1 (5) |
0 (0) |
1 (1) |
11 |
Glucose utilization
|
2 (11) |
0 (0) |
2 (2) |
21 |
Glucuronate utilization
|
30 (110) |
0 (0) |
30 (30) |
177 |
Glycerate utilization
|
9 (42) |
0 (0) |
9 (9) |
82 |
Glycerol utilization
|
2 (16) |
0 (0) |
2 (2) |
22 |
Glycolate utilization
|
15 (45) |
0 (0) |
15 (15) |
102 |
Glycolysis
|
3 (29) |
0 (0) |
3 (3) |
33 |
Glyoxylate bypass
|
1 (10) |
0 (0) |
1 (1) |
12 |
Heparin utilization
|
1 (4) |
0 (0) |
1 (1) |
11 |
Hexulose metabolism
|
2 (4) |
0 (0) |
2 (2) |
25 |
Hyaluronan utilization
|
1 (7) |
0 (0) |
1 (1) |
11 |
Hyaluronate utilization
|
1 (6) |
0 (0) |
1 (1) |
15 |
Idonate utilization
|
2 (11) |
0 (0) |
2 (2) |
27 |
Inositol utilization
|
18 (55) |
0 (0) |
18 (18) |
134 |
Kojibiose utilization
|
3 (9) |
0 (0) |
3 (3) |
23 |
L-galactose utilization
|
1 (6) |
0 (0) |
1 (1) |
11 |
L-gulonate utilization
|
3 (10) |
0 (0) |
3 (3) |
39 |
L-lyxose utilization
|
1 (4) |
0 (0) |
1 (1) |
12 |
L-talarate utilization
|
3 (5) |
0 (0) |
3 (3) |
29 |
L-xylulose utilization
|
1 (1) |
0 (0) |
1 (1) |
10 |
Lactate utilization
|
30 (126) |
0 (0) |
30 (30) |
213 |
Lacto-N-biose utilization
|
1 (4) |
0 (0) |
1 (1) |
10 |
Lactose utilization
|
6 (39) |
0 (0) |
6 (6) |
59 |
Levan utilization
|
1 (2) |
0 (0) |
1 (1) |
11 |
Malate utilization
|
3 (22) |
0 (0) |
3 (3) |
41 |
Maltodextrin utilization
|
19 (106) |
0 (0) |
19 (19) |
106 |
Maltose utilization
|
26 (124) |
0 (0) |
26 (26) |
130 |
Mannan and beta-mannosides utilization
|
1 (5) |
0 (0) |
1 (1) |
11 |
Mannitol utilization
|
7 (36) |
0 (0) |
7 (7) |
94 |
Mannose utilization
|
10 (25) |
0 (0) |
10 (10) |
68 |
Mannosides utilization
|
7 (17) |
0 (0) |
7 (7) |
44 |
Methylcitrate utilization
|
10 (60) |
0 (0) |
10 (10) |
88 |
N-acetylgalactosamine utilization
|
13 (42) |
0 (0) |
13 (13) |
100 |
N-acetylglucosamine utilization
|
33 (174) |
0 (0) |
33 (33) |
267 |
Neotrehalosadiamine biosynthesis
|
1 (3) |
0 (0) |
1 (1) |
11 |
Nigerose utilization
|
2 (3) |
0 (0) |
2 (2) |
30 |
O-glycans utilization
|
2 (2) |
0 (0) |
2 (2) |
11 |
Oligoglucoside utilization
|
1 (1) |
0 (0) |
1 (1) |
15 |
Pectic galactan utilization
|
1 (3) |
0 (0) |
1 (1) |
11 |
Pectin and polygalacturonate utlization
|
3 (15) |
0 (0) |
3 (3) |
31 |
Pectin utilization
|
1 (5) |
0 (0) |
1 (1) |
11 |
Pentose utilization
|
1 (2) |
0 (0) |
1 (1) |
15 |
Polysaccharides utilization
|
2 (4) |
0 (0) |
2 (2) |
11 |
Possibly alpha-mannosides utilization
|
1 (7) |
0 (0) |
1 (1) |
11 |
Psicose utilization
|
1 (4) |
0 (0) |
1 (1) |
15 |
Pyruvate metabolism
|
8 (63) |
0 (0) |
8 (8) |
75 |
Raffinose utilization
|
2 (11) |
0 (0) |
2 (2) |
22 |
Rhamnogalacturonides utilization
|
6 (28) |
0 (0) |
6 (6) |
49 |
Rhamnose oligosaccharides utilization
|
2 (5) |
0 (0) |
2 (2) |
16 |
Rhamnose utilization
|
16 (61) |
0 (0) |
16 (16) |
136 |
Rhizopine catabolism
|
1 (5) |
0 (0) |
1 (1) |
15 |
Ribitol utilization
|
2 (3) |
0 (0) |
2 (2) |
25 |
Ribose utilization
|
23 (113) |
0 (0) |
23 (23) |
222 |
Ribulose monophosphate pathway
|
1 (6) |
0 (0) |
1 (1) |
11 |
Santhopine utilization
|
2 (4) |
0 (0) |
2 (2) |
30 |
Sialic acid utilization
|
12 (56) |
0 (0) |
12 (12) |
88 |
Sorbitol utilization
|
5 (20) |
0 (0) |
5 (5) |
71 |
Sorbitol utilization
|
1 (5) |
0 (0) |
1 (1) |
12 |
Sorbose utilization
|
1 (1) |
0 (0) |
1 (1) |
12 |
Starch utilization
|
2 (11) |
0 (0) |
2 (2) |
11 |
Sucrose utilization
|
21 (88) |
0 (0) |
21 (21) |
164 |
Sugar utilization
|
71 (215) |
0 (0) |
71 (71) |
217 |
Tagatose utilization
|
2 (5) |
0 (0) |
2 (2) |
30 |
Trehalose utilization
|
21 (94) |
0 (0) |
21 (21) |
185 |
Tricarboxylic acid cycle
|
11 (78) |
2 (14) |
13 (13) |
89 |
Xylitol utilization
|
4 (7) |
0 (0) |
4 (4) |
50 |
Xylooligosacharides utilization
|
1 (4) |
0 (0) |
1 (1) |
10 |
Xylose utilization
|
10 (57) |
0 (0) |
10 (10) |
86 |
Cell Wall and Capsule
|
Biofilm formation
|
3 (18) |
0 (0) |
3 (3) |
33 |
Cell wall metabolism
|
3 (19) |
6 (37) |
9 (9) |
87 |
Intercellular adhesion
|
2 (12) |
0 (0) |
2 (2) |
17 |
Lipopolysaccharide biosynthesis
|
1 (16) |
0 (0) |
1 (1) |
16 |
N-acetylmuramate utilization
|
5 (18) |
0 (0) |
5 (5) |
60 |
Cofactors, Vitamins, Prosthetic Groups, Pigments
|
Biotin biosynthesis
|
30 (235) |
0 (0) |
30 (30) |
282 |
Cobalamin biosynthesis
|
4 (27) |
21 (197) |
25 (25) |
252 |
Folate metabolism
|
0 (0) |
3 (22) |
3 (3) |
50 |
Heme efflux
|
1 (7) |
0 (0) |
1 (1) |
7 |
Iron-sulfur cluster biogenesis
|
26 (216) |
0 (0) |
26 (26) |
223 |
Molybdopterin biosynthesis
|
12 (54) |
16 (81) |
28 (28) |
243 |
NAD biosynthesis
|
42 (199) |
0 (0) |
42 (42) |
315 |
Pyridoxine biosynthesis
|
18 (71) |
0 (0) |
18 (18) |
150 |
Pyridoxine/pyridoxal homeostasis
|
79 (164) |
0 (0) |
79 (79) |
256 |
Riboflavin biosynthesis
|
8 (44) |
37 (251) |
45 (45) |
386 |
Thiamine biosynthesis
|
4 (28) |
39 (361) |
43 (43) |
399 |
Thiamine transport
|
4 (28) |
1 (3) |
5 (5) |
36 |
Dormancy and Sporulation
|
Dormancy
|
1 (12) |
0 (0) |
1 (1) |
12 |
Sporulation
|
1 (7) |
0 (0) |
1 (1) |
11 |
Drug resistance
|
Antibiotic resistance
|
9 (43) |
0 (0) |
9 (9) |
98 |
Bacitracin resistance
|
2 (11) |
0 (0) |
2 (2) |
11 |
Beta-lactam resistance
|
1 (4) |
0 (0) |
1 (1) |
7 |
Drug resistance
|
5 (27) |
0 (0) |
5 (5) |
65 |
Macrolides efflux
|
1 (2) |
0 (0) |
1 (1) |
8 |
Multidrug efflux
|
44 (176) |
0 (0) |
44 (44) |
182 |
Multidrug resistance
|
55 (297) |
23 (107) |
78 (78) |
308 |
Penicillin and methicillin resistance
|
1 (1) |
0 (0) |
1 (1) |
7 |
Penicillin resistance
|
1 (5) |
0 (0) |
1 (1) |
11 |
Ramoplanin resistance
|
1 (7) |
0 (0) |
1 (1) |
11 |
Salicylic acid resistance
|
1 (3) |
0 (0) |
1 (1) |
11 |
Fatty Acids, Lipids, and Isoprenoids
|
Acyclic terpenes degradation
|
1 (1) |
0 (0) |
1 (1) |
11 |
Fatty acid biosynthesis
|
17 (125) |
0 (0) |
17 (17) |
146 |
Fatty acid degradation
|
22 (172) |
0 (0) |
22 (22) |
153 |
Fatty acid metabolism
|
4 (20) |
0 (0) |
4 (4) |
38 |
Lipoprotein export
|
1 (3) |
0 (0) |
1 (1) |
8 |
Membrane Transport
|
Hypothetical ABC transporter
|
6 (39) |
0 (0) |
6 (6) |
71 |
Metabolite transport
|
74 (219) |
0 (0) |
74 (74) |
304 |
Metabolism of Aromatic Compounds
|
3-hydroxybenzoate degradation
|
1 (2) |
0 (0) |
1 (1) |
8 |
Benzoate degradation
|
1 (2) |
0 (0) |
1 (1) |
8 |
p-aminobenzoyl-glutamate utilization
|
1 (4) |
0 (0) |
1 (1) |
12 |
Phenylacetic acid degradation
|
17 (80) |
0 (0) |
17 (17) |
138 |
Protocatechuate degradation
|
2 (4) |
0 (0) |
2 (2) |
8 |
Utilization of aromatic compounds
|
3 (24) |
0 (0) |
3 (3) |
32 |
Vanillate utilization
|
10 (28) |
0 (0) |
10 (10) |
83 |
Metal homeostasis
|
Copper homeostasis
|
4 (39) |
0 (0) |
4 (4) |
51 |
Iron homeostasis
|
36 (303) |
0 (0) |
36 (36) |
268 |
Lead resistance
|
18 (96) |
0 (0) |
18 (18) |
170 |
Magnesium homeostasis
|
0 (0) |
9 (44) |
9 (9) |
100 |
Manganese homeostasis
|
21 (155) |
0 (0) |
21 (21) |
157 |
Mercury resistance
|
13 (32) |
0 (0) |
13 (13) |
129 |
Metal homeostasis
|
2 (9) |
0 (0) |
2 (2) |
25 |
Molybdenum homeostasis
|
22 (107) |
13 (63) |
35 (35) |
251 |
Nickel homeostasis
|
16 (57) |
0 (0) |
16 (16) |
171 |
Potassium homeostasis
|
1 (2) |
0 (0) |
1 (1) |
10 |
Tungsten homeostasis
|
4 (23) |
1 (7) |
5 (5) |
39 |
Zinc homeostasis
|
47 (360) |
0 (0) |
47 (47) |
332 |
Miscellaneous
|
Anaerobic metabolism
|
3 (39) |
0 (0) |
3 (3) |
39 |
Competence
|
1 (4) |
0 (0) |
1 (1) |
11 |
Flavonoids response
|
1 (2) |
0 (0) |
1 (1) |
11 |
Malonate metabolism
|
10 (27) |
0 (0) |
10 (10) |
79 |
NULL
|
1 (2) |
0 (0) |
1 (1) |
8 |
Phage infection protein
|
1 (15) |
0 (0) |
1 (1) |
15 |
Polyamine homeostasis
|
1 (7) |
0 (0) |
1 (1) |
11 |
Toxin-antitoxin system
|
1 (8) |
0 (0) |
1 (1) |
11 |
Transport
|
5 (37) |
0 (0) |
5 (5) |
30 |
unknown
|
4 (19) |
0 (0) |
4 (4) |
41 |
Motility and Chemotaxis
|
Motility
|
4 (38) |
0 (0) |
4 (4) |
10 |
Nitrogen Metabolism
|
Denitrification
|
7 (25) |
0 (0) |
7 (7) |
72 |
Nitrate and nitrite respiration
|
8 (64) |
0 (0) |
8 (8) |
81 |
Nitrogen assimilation
|
27 (254) |
1 (9) |
28 (28) |
249 |
Nitrogen fixation
|
12 (75) |
0 (0) |
12 (12) |
60 |
Nitrogen metabolism
|
9 (35) |
0 (0) |
9 (9) |
64 |
Nucleosides and Nucleotides
|
Adenosine utilization
|
1 (4) |
0 (0) |
1 (1) |
15 |
Deoxynucleoside utilization
|
2 (10) |
0 (0) |
2 (2) |
26 |
Deoxyribonucleoside utilization
|
1 (11) |
0 (0) |
1 (1) |
12 |
Deoxyribonucleotide biosynthesis
|
42 (351) |
0 (0) |
42 (42) |
366 |
Nucleoside utilization
|
4 (19) |
0 (0) |
4 (4) |
26 |
Purine metabolism
|
8 (95) |
8 (69) |
16 (16) |
126 |
Pyrimidine metabolism
|
0 (0) |
9 (79) |
9 (9) |
95 |
Pyrimidine utilization
|
20 (97) |
0 (0) |
20 (20) |
126 |
Queuosine biosynthesis
|
0 (0) |
9 (68) |
9 (9) |
92 |
Ribonucleoside utilization
|
2 (8) |
0 (0) |
2 (2) |
10 |
Ribonucleotide reductases
|
1 (12) |
0 (0) |
1 (1) |
12 |
Uridine utilization
|
1 (2) |
0 (0) |
1 (1) |
8 |
Xanthine utilization
|
3 (12) |
0 (0) |
3 (3) |
24 |
Xanthosine utilization
|
1 (4) |
0 (0) |
1 (1) |
12 |
Phosphorus Metabolism
|
2-aminoethylphosphonate utilization
|
15 (46) |
0 (0) |
15 (15) |
98 |
Phosphate metabolism
|
3 (32) |
0 (0) |
3 (3) |
35 |
Phosphonate utilization
|
24 (85) |
0 (0) |
24 (24) |
167 |
Phosphonoacetate utilization
|
1 (2) |
0 (0) |
1 (1) |
11 |
Photosynthesis
|
Photosynthesis
|
2 (16) |
0 (0) |
2 (2) |
29 |
Protein Metabolism
|
Proteolysis
|
1 (8) |
0 (0) |
1 (1) |
8 |
Ribosome biogenesis
|
0 (0) |
46 (451) |
46 (46) |
190 |
Regulation and Cell signaling
|
Quorum sensing
|
2 (12) |
0 (0) |
2 (2) |
19 |
Second messenger response
|
0 (0) |
9 (50) |
9 (9) |
104 |
Respiration
|
Energy metabolism
|
32 (233) |
0 (0) |
32 (32) |
168 |
Formate oxydation
|
6 (19) |
0 (0) |
6 (6) |
48 |
Tetrathionate reduction
|
4 (14) |
0 (0) |
4 (4) |
47 |
Thiosulfate reduction
|
3 (29) |
0 (0) |
3 (3) |
26 |
Stress Response
|
2-Methylhydroquinone and catechol resistance
|
1 (10) |
0 (0) |
1 (1) |
11 |
Alkaline stress response
|
1 (1) |
0 (0) |
1 (1) |
10 |
Carbonyl stress response
|
12 (33) |
0 (0) |
12 (12) |
123 |
Cell wall-active antibiotics stress response
|
1 (11) |
0 (0) |
1 (1) |
11 |
Cold shock response
|
1 (6) |
0 (0) |
1 (1) |
11 |
DNA alkylation response
|
1 (6) |
0 (0) |
1 (1) |
11 |
Glutathione metabolism
|
1 (8) |
0 (0) |
1 (1) |
16 |
Heat shock response
|
49 (392) |
0 (0) |
49 (49) |
355 |
Light-dependent DNA repair
|
4 (23) |
0 (0) |
4 (4) |
40 |
Nitrosative stress response
|
39 (210) |
0 (0) |
39 (39) |
239 |
Osmotic stress response
|
4 (38) |
5 (34) |
9 (9) |
92 |
Oxidative stress response
|
14 (121) |
0 (0) |
14 (14) |
109 |
Peroxide stress response
|
6 (52) |
0 (0) |
6 (6) |
54 |
Phage shock response
|
1 (5) |
0 (0) |
1 (1) |
10 |
Phenolic acid stress response
|
3 (10) |
0 (0) |
3 (3) |
41 |
Protein secretion stress response
|
1 (5) |
0 (0) |
1 (1) |
11 |
Salt stress response
|
1 (3) |
0 (0) |
1 (1) |
14 |
SOS response
|
40 (319) |
0 (0) |
40 (40) |
339 |
Superoxide stress response
|
18 (85) |
0 (0) |
18 (18) |
164 |
Toxic fatty acid stress response
|
2 (8) |
0 (0) |
2 (2) |
26 |
Sulfur Metabolism
|
Alkanesulfonates utilization
|
5 (10) |
0 (0) |
5 (5) |
38 |
Sulfite reduction
|
1 (8) |
0 (0) |
1 (1) |
11 |
Sulfur metabolism
|
4 (12) |
1 (8) |
5 (5) |
31 |
Taurine utilization
|
9 (26) |
0 (0) |
9 (9) |
89 |
Toxic metal resistance
|
Arsenic resistance
|
10 (59) |
0 (0) |
10 (10) |
63 |
Cadmium resistance
|
26 (157) |
0 (0) |
26 (26) |
230 |
Cobalt resistance
|
7 (42) |
0 (0) |
7 (7) |
64 |
Copper resistance
|
29 (179) |
0 (0) |
29 (29) |
240 |
Heavy metal resistance
|
4 (22) |
0 (0) |
4 (4) |
40 |
Metal efflux
|
1 (6) |
0 (0) |
1 (1) |
11 |
Nickel resistance
|
5 (36) |
0 (0) |
5 (5) |
49 |
Uranium reduction
|
1 (3) |
0 (0) |
1 (1) |
10 |
Zinc resistance
|
17 (107) |
0 (0) |
17 (17) |
159 |
Virulence
|
Virulence
|
2 (10) |
0 (0) |
2 (2) |
7 |