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PH1137 | 407aa long hypothetical RNA methyltransferase; Catalyzes the formation of 5-methyl-uridine at position 54 (m5U54) in tRNA; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (407 aa) | ||||
PH1019 | 607aa long hypothetical aldehyde:ferredoxin oxidoreductase; Similar to owl:PFAOR1 percent identity: 80.629 in 606aa; owl:TLFORPKPF2 percent identity: 39.527 in 620aa; Belongs to the AOR/FOR family. (607 aa) | ||||
PH0819 | 459aa long hypothetical methyltransferase; Similar to Swiss_Prot:P26168 percent identity: 29.216 in 437aa; PIR:S75722 percent identity: 24.480 in 442aa. (459 aa) | ||||
PH0765 | 648aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (648 aa) | ||||
PH0685 | 334aa long hypothetical ferredoxin oxidoreductase beta subunit; Similar to owl:PFPORVOR11 percent identity: 92.145 in 331aa; PIR:C64333 percent identity: 62.821 in 252aa; owl:PFPORVOR8 percent identity: 55.187 in 257aa. motif=prokaryotic membrane lipoprotein lipid attachment site. (334 aa) | ||||
PH0682 | 108aa long hypothetical ferredoxin oxidoreductase delta subunit; Similar to owl:PFPORVOR9 percent identity: 95.238 in 105aa; owl:PFPORVOR6 percent identity: 62.667 in 75aa; PIR:E64333 percent identity: 58.824 in 85aa. motif=4Fe-4S ferredoxins, iron-sulfur binding region signature. (108 aa) | ||||
PH0679 | 105aa long hypothetical ferredoxin oxidoreductase delta subunit; Similar to owl:PFPORVOR6 percent identity: 86.667 in 105aa; owl:PFPORVOR9 percent identity: 65.333 in 75aa; PIR:E64333 percent identity: 61.333 in 75aa. motif=4Fe-4S ferredoxins, iron-sulfur binding region signature. (105 aa) | ||||
PH0635 | 254aa long hypothetical protein; Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7-carboxy-7- deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds. (254 aa) | ||||
PH1726 | 380aa long hypothetical isomerase; Catalyzes the isomerization between 2-isopropylmalate and 3- isopropylmalate, via the formation of 2-isopropylmaleate. (380 aa) | ||||
PH0300 | 310aa long hypothetical protein; Catalyzes the ATP-dependent 2-thiolation of 5-methyluridine residue at position 54 in the T loop of tRNAs, leading to 5-methyl-2- thiouridine (m(5)s(2)U or s(2)T). This modification allows thermal stabilization of tRNAs in thermophilic microorganisms, and is required for cell growth at high temperatures (By similarity). Can use free sulfide as sulfur source in vitro, which may be also the sulfur source in vivo ; Belongs to the TtcA family. TtuA subfamily. (310 aa) | ||||
PH0240 | 449aa long hypothetical amidophosphoribosyltransferase; Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine. (449 aa) | ||||
PH0196 | 397aa long hypothetical protein; Regulatory subunit of DNA primase, an RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication. Stabilizes and modulates the activity of the small subunit, increasing the rate of DNA synthesis, and conferring RNA synthesis capability. The DNA polymerase activity may enable DNA primase to also catalyze primer extension after primer synthesis. May also play a role in DNA repair. (397 aa) | ||||
PH0013 | 300aa long hypothetical quinolinate synthetase; Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate. (300 aa) | ||||
PH0114 | 316aa long hypothetical molybdenum cofactor biosynthesis protein; Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate; Belongs to the radical SAM superfamily. MoaA family. (316 aa) | ||||
PH1875 | 432aa long hypothetical protein; Catalyzes the methylthiolation of N6- threonylcarbamoyladenosine (t(6)A), leading to the formation of 2- methylthio-N6-threonylcarbamoyladenosine (ms(2)t(6)A) at position 37 in tRNAs that read codons beginning with adenine. (432 aa) | ||||
PH1498 | 222aa long hypothetical endonuclease III; DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N-glycosidic bond, leaving an AP (apurinic/apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'- phosphate. (222 aa) | ||||
PH1449 | 195aa long hypothetical NADH-ubiquinone oxidoreductase subunit; Similar to Swiss_Prot:P52766 percent identity:48.485 in 133aa; Swiss_Prot:P06410 percent identity:45.926 in 136aa; Swiss_Prot:P06409 percent identity:48.485 in 133aa; Belongs to the complex I 20 kDa subunit family. (195 aa) | ||||
PH1705 | 342aa long hypothetical protein; Component of the wyosine derivatives biosynthesis pathway that catalyzes the condensation of N-methylguanine with 2 carbon atoms from pyruvate to form the tricyclic 4-demethylwyosine (imG-14) on guanosine-37 of tRNA(Phe); Belongs to the TYW1 family. (342 aa) | ||||
PH1259 | 412aa long hypothetical protein; Catalyzes the formation of 5-methyl-uridine at position equivalent to 747 (m5U747) in 23S rRNA; Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family. (412 aa) | ||||
PH1138 | 618aa long hypothetical indolepyruvate ferredoxin oxidoreductase alpha subunit; Catalyzes the ferredoxin-dependent oxidative decarboxylation of arylpyruvates. (618 aa) | ||||
PH1105 | 342aa long hypothetical protein; Catalyzes the first step of diphthamide biosynthesis, i.e. the transfer of the 3-amino-3-carboxypropyl group from S-adenosyl-L- methionine (SAM) to the C2 position of the imidazole ring of the target histidine residue in translation elongation factor 2 (EF-2). (342 aa) |