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| | atpB-2 | Hypothetical protein; Produces ATP from ADP in the presence of a proton gradient across the membrane. The V-type beta chain is a regulatory subunit. (493 aa) |
| | KALB_1021 | Hypothetical protein. (262 aa) |
| | KALB_1083 | Glutamine amidotransferase class-I/GMP synthase. (250 aa) |
| | KALB_1284 | Protein of unknown function UPF0157. (260 aa) |
| | KALB_134 | Phosphoglycerate mutase; Belongs to the phosphoglycerate mutase family. (208 aa) |
| | KALB_1369 | AMP-dependent synthetase and ligase. (563 aa) |
| | KALB_1550 | Flavoprotein. (181 aa) |
| | KALB_1552 | Hypothetical protein. (117 aa) |
| | ndk | Nucleoside diphosphate kinase; Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate; Belongs to the NDK family. (136 aa) |
| | KALB_1664 | Hypothetical protein. (151 aa) |
| | KALB_173 | GCN5-related N-acetyltransferase. (220 aa) |
| | KALB_1763 | Hypothetical protein. (417 aa) |
| | KALB_1819 | AMP-dependent synthetase and ligase. (515 aa) |
| | KALB_1850 | Pyruvate dehydrogenase E1 component; Component of the pyruvate dehydrogenase (PDH) complex, that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (925 aa) |
| | KALB_1940 | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components: 2- oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) (By similarity). (582 aa) |
| | pfp | Pyrophosphate--fructose 6-phosphate 1-phosphotransferase; Catalyzes the phosphorylation of D-fructose 6-phosphate, the first committing step of glycolysis. Uses inorganic phosphate (PPi) as phosphoryl donor instead of ATP like common ATP-dependent phosphofructokinases (ATP-PFKs), which renders the reaction reversible, and can thus function both in glycolysis and gluconeogenesis. Consistently, PPi-PFK can replace the enzymes of both the forward (ATP- PFK) and reverse (fructose-bisphosphatase (FBPase)) reactions. (341 aa) |
| | KALB_1997 | Putative ribose-phosphate pyrophosphokinase. (321 aa) |
| | coaA | Pantothenate kinase. (308 aa) |
| | KALB_2176 | LigA protein. (423 aa) |
| | KALB_2249 | 2-amino-4,5-dihydroxy-6-one-heptanoic acid-7-phosphate synthase; Catalyzes aldol condensation between L-aspartate-4- semialdehyde (ASA) and dihydroxyacetone phosphate (DHAP), to form 2-amino-4,5-dihydroxy-6-one-heptanoic acid-7-phosphate. (275 aa) |
| | KALB_240 | Hypothetical protein. (153 aa) |
| | KALB_2497 | Phosphoglycerate mutase family protein; Fructose-2,6-bisphosphatase. (218 aa) |
| | coaE | Dephospho-CoA kinase; Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A; Belongs to the CoaE family. (392 aa) |
| | KALB_2701 | Uridine kinase-like protein. (214 aa) |
| | KALB_2730 | ATP-binding protein. (422 aa) |
| | pyrB | Aspartate carbamoyltransferase; Belongs to the aspartate/ornithine carbamoyltransferase superfamily. ATCase family. (310 aa) |
| | pyrC | Dihydroorotase; Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate; Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily. (437 aa) |
| | KALB_2753 | Putative membrane protein. (173 aa) |
| | carA | Carbamoyl-phosphate synthase small chain; Belongs to the CarA family. (373 aa) |
| | carB | Carbamoyl-phosphate synthase large chain; Belongs to the CarB family. (1100 aa) |
| | pyrF | Orotidine 5'-phosphate decarboxylase; Belongs to the OMP decarboxylase family. Type 2 subfamily. (276 aa) |
| | KALB_2760 | Guanylate kinase; Essential for recycling GMP and indirectly, cGMP. (169 aa) |
| | KALB_2762 | Coenzyme A biosynthesis bifunctional protein CoaBC; Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4- phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine; In the C-terminal section; belongs to the PPC synthetase family. (417 aa) |
| | KALB_2801 | Glyceraldehyde-3-phosphate dehydrogenase; Belongs to the glyceraldehyde-3-phosphate dehydrogenase family. (334 aa) |
| | pgk | Phosphoglycerate kinase; Belongs to the phosphoglycerate kinase family. (412 aa) |
| | tpiA | Triosephosphate isomerase; Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D- glyceraldehyde-3-phosphate (G3P); Belongs to the triosephosphate isomerase family. (261 aa) |
| | KALB_2810 | Glucose-6-phosphate isomerase; Belongs to the GPI family. (539 aa) |
| | KALB_2929 | Hypothetical protein. (115 aa) |
| | KALB_2936 | Glyoxalase. (137 aa) |
| | KALB_3067 | Pyruvate dehydrogenase E1 protein subunit alpha. (365 aa) |
| | KALB_3069 | Branched-chain alpha-keto acid dehydrogenase subunit E2. (402 aa) |
| | acsA | Acetyl-coenzyme A synthetase; Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA; Belongs to the ATP-dependent AMP-binding enzyme family. (656 aa) |
| | KALB_3211 | Purine phosphoribosyltransferase. (173 aa) |
| | KALB_3349 | Hypothetical protein. (241 aa) |
| | KALB_3394 | Hypothetical protein. (126 aa) |
| | KALB_3448 | Acyl-coenzyme A synthetases/AMP-(fatty) acid ligases. (522 aa) |
| | KALB_3518 | Hypothetical protein. (187 aa) |
| | ackA | Acetate kinase; Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction; Belongs to the acetokinase family. (362 aa) |
| | KALB_360 | Hypoxanthine-guanine phosphoribosyltransferase; Belongs to the purine/pyrimidine phosphoribosyltransferase family. (182 aa) |
| | KALB_3637 | Glyceraldehyde-3-phosphate dehydrogenase; Belongs to the glyceraldehyde-3-phosphate dehydrogenase family. (335 aa) |
| | KALB_3655 | L-lactate dehydrogenase; Catalyzes the conversion of lactate to pyruvate. (318 aa) |
| | coaX | Type III pantothenate kinase; Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis. (257 aa) |
| | KALB_3789 | Hypothetical protein. (219 aa) |
| | atpB | ATP synthase A chain; Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. Belongs to the ATPase A chain family. (256 aa) |
| | KALB_3917 | Glyoxalase/bleomycin resistance protein/dioxygenase. (117 aa) |
| | KALB_3980 | Hypothetical protein. (118 aa) |
| | KALB_4030 | Hypothetical protein. (126 aa) |
| | KALB_4050 | Hypothetical protein. (114 aa) |
| | KALB_4090 | Hypothetical protein. (249 aa) |
| | KALB_4142 | Hypothetical protein. (141 aa) |
| | KALB_4144 | Hypothetical protein. (169 aa) |
| | KALB_4145 | Hypothetical protein. (572 aa) |
| | KALB_4147 | Hypothetical protein. (153 aa) |
| | KALB_4168 | Hypothetical protein. (305 aa) |
| | KALB_4169 | Hypothetical protein. (587 aa) |
| | pdhA | Hypothetical protein; The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). (331 aa) |
| | KALB_4172 | Hypothetical protein. (432 aa) |
| | KALB_4183 | Hypothetical protein. (598 aa) |
| | KALB_4339 | Hypothetical protein. (238 aa) |
| | KALB_4370 | Hypothetical protein. (229 aa) |
| | KALB_4387 | Hypothetical protein. (142 aa) |
| | KALB_4442 | Hypothetical protein. (423 aa) |
| | KALB_4446 | Hypothetical protein. (402 aa) |
| | KALB_4553 | Hypothetical protein. (140 aa) |
| | KALB_4640 | Hypothetical protein. (257 aa) |
| | KALB_4688 | Hypothetical protein. (174 aa) |
| | KALB_4997 | Hypothetical protein. (113 aa) |
| | KALB_5149 | Hypothetical protein. (449 aa) |
| | KALB_5456 | Hypothetical protein. (334 aa) |
| | KALB_5554 | Hypothetical protein; Catalyzes the conversion of dihydroorotate to orotate. (287 aa) |
| | coaD | Hypothetical protein; Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate. Belongs to the bacterial CoaD family. (136 aa) |
| | KALB_5668 | Hypothetical protein. (122 aa) |
| | KALB_5810 | Hypothetical protein. (324 aa) |
| | KALB_5995 | Hypothetical protein. (250 aa) |
| | KALB_6003 | Hypothetical protein. (238 aa) |
| | KALB_6415 | Hypothetical protein. (209 aa) |
| | KALB_6435 | Hypothetical protein. (211 aa) |
| | pyrG | Hypothetical protein; Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates. (565 aa) |
| | KALB_6456 | Hypothetical protein. (267 aa) |
| | KALB_6465 | Hypothetical protein. (129 aa) |
| | KALB_6512 | Hypothetical protein. (236 aa) |
| | KALB_6600 | Hypothetical protein; In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance. (766 aa) |
| | KALB_6601 | Hypothetical protein. (151 aa) |
| | KALB_67 | Pyruvate dehydrogenase E1 component. (781 aa) |
| | KALB_690 | Nucleoside diphosphate kinase; Belongs to the NDK family. (169 aa) |
| | KALB_7013 | Hypothetical protein. (314 aa) |
| | KALB_7014 | Hypothetical protein; Belongs to the pyruvate kinase family. (464 aa) |
| | pyrD | Hypothetical protein; Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor; Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily. (342 aa) |
| | KALB_719 | Hypothetical protein. (220 aa) |
| | KALB_7197 | Hypothetical protein; Belongs to the ribF family. (311 aa) |
| | KALB_7295 | Hypothetical protein. (263 aa) |
| | pyrH | Hypothetical protein; Catalyzes the reversible phosphorylation of UMP to UDP. (251 aa) |
| | coaD-2 | Hypothetical protein; Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate. Belongs to the bacterial CoaD family. (160 aa) |
| | KALB_7434 | Hypothetical protein. (217 aa) |
| | KALB_7494 | Hypothetical protein. (266 aa) |
| | KALB_7588 | Hypothetical protein. (260 aa) |
| | atpC | Hypothetical protein; Produces ATP from ADP in the presence of a proton gradient across the membrane. (121 aa) |
| | atpD | Hypothetical protein; Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits. (477 aa) |
| | atpG | Hypothetical protein; Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex. (308 aa) |
| | atpA | Hypothetical protein; Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit. (548 aa) |
| | atpH | Hypothetical protein; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. (277 aa) |
| | atpF | Hypothetical protein; Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0); Belongs to the ATPase B chain family. (180 aa) |
| | atpE | Hypothetical protein; F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. (73 aa) |
| | atpB-3 | Hypothetical protein; Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. Belongs to the ATPase A chain family. (260 aa) |
| | KALB_7721 | Hypothetical protein. (252 aa) |
| | prs | Ribose-phosphate pyrophosphokinase; Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib- 5-P); Belongs to the ribose-phosphate pyrophosphokinase family. Class I subfamily. (326 aa) |
| | KALB_7932 | Hypothetical protein. (237 aa) |
| | purE | Hypothetical protein; Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR). (163 aa) |
| | purK | Hypothetical protein; Catalyzes the ATP-dependent conversion of 5-aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5-carboxyaminoimidazole ribonucleotide (N5-CAIR). (386 aa) |
| | KALB_799 | Nucleoside-triphosphate pyrophosphatase. (321 aa) |
| | upp | Hypothetical protein; Catalyzes the conversion of uracil and 5-phospho-alpha-D- ribose 1-diphosphate (PRPP) to UMP and diphosphate. (207 aa) |
| | eno | Enolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. (428 aa) |
| | KALB_8077 | Hypothetical protein. (123 aa) |
| | purH | Hypothetical protein. (519 aa) |
| | KALB_8103 | Hypothetical protein. (185 aa) |
| | guaA | Hypothetical protein; Catalyzes the synthesis of GMP from XMP. (520 aa) |
| | guaB | Hypothetical protein; Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate-limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth. Belongs to the IMPDH/GMPR family. (503 aa) |
| | adk | Hypothetical protein; Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism; Belongs to the adenylate kinase family. (183 aa) |
| | KALB_8274 | Hypothetical protein. (476 aa) |
| | KALB_8368 | Hypothetical protein. (281 aa) |
| | gpmA | Hypothetical protein; Catalyzes the interconversion of 2-phosphoglycerate and 3- phosphoglycerate. (245 aa) |
| | purU | Hypothetical protein; Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4). (283 aa) |
| | KALB_8407 | Hypothetical protein. (119 aa) |
| | KALB_8484 | Hypothetical protein. (115 aa) |
| | KALB_8532 | Hypothetical protein. (296 aa) |
| | purM | Hypothetical protein. (359 aa) |
| | purF | Hypothetical protein; Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine. (511 aa) |
| | purL | Hypothetical protein; Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP- dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the am [...] (762 aa) |
| | purQ | Hypothetical protein; Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP- dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the am [...] (224 aa) |
| | purS | Hypothetical protein; Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP- dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the am [...] (79 aa) |
| | purC | Hypothetical protein; Belongs to the SAICAR synthetase family. (291 aa) |
| | KALB_8571 | Hypothetical protein; Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily. (477 aa) |
| | purD | Hypothetical protein; Belongs to the GARS family. (419 aa) |
| | purA | Hypothetical protein; Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP; Belongs to the adenylosuccinate synthetase family. (430 aa) |
| | KALB_8605 | Hypothetical protein; Catalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis; Belongs to the class II fructose-bisphosphate aldolase family. (343 aa) |
| | KALB_863 | Hypothetical protein. (202 aa) |
| | KALB_8633 | Hypothetical protein. (204 aa) |
| | pyrE | Hypothetical protein; Catalyzes the transfer of a ribosyl phosphate group from 5- phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP). (183 aa) |
| | KALB_8645 | Hypothetical protein. (219 aa) |
| | KALB_8661 | Hypothetical protein. (247 aa) |
| | KALB_8689 | Hypothetical protein. (447 aa) |
| | KALB_8691 | Hypothetical protein. (398 aa) |
