Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB03280"

PredicateValue (sorted: default)
rdfs:label
"P1-(5'-Adenosyl)P5-(5'-Thymidyl)Pentaphosphate"
rdf:type
drugbank:description
" experimental This compound belongs to the pyrimidine 2'-deoxyribonucleoside polyphosphates. These are pyrimidine nucleotides with a polyphosphate (with 4 or more phosphate) group linked to the ribose moiety lacking an hydroxyl group at position 2. Pyrimidine 2'-deoxyribonucleoside Polyphosphates Organic Compounds Organooxygen Compounds Carbohydrates and Carbohydrate Conjugates Glycosyl Compounds Purine Nucleosides and Analogues Pentose Phosphates Organic Pyrophosphates Monosaccharide Phosphates Purines and Purine Derivatives Aminopyrimidines and Derivatives Pyrimidones Primary Aromatic Amines Organic Phosphoric Acids Organophosphate Esters N-substituted Imidazoles Hydropyrimidines Tetrahydrofurans Oxolanes 1,2-Diols Secondary Alcohols Ethers Polyamines pentose phosphate pentose-5-phosphate pentose monosaccharide monosaccharide phosphate organic pyrophosphate imidazopyrimidine purine aminopyrimidine pyrimidone hydropyrimidine primary aromatic amine phosphoric acid ester monosaccharide organic phosphate n-substituted imidazole pyrimidine tetrahydrofuran oxolane azole imidazole secondary alcohol 1,2-diol polyamine ether amine organonitrogen compound primary amine alcohol logP 0.44 ALOGPS logS -2.1 ALOGPS Water Solubility 6.30e+00 g/l ALOGPS logP -8.4 ChemAxon IUPAC Name [({[({[({[(2S,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)(hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl)oxy]({[(2S,3R,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy})phosphinic acid ChemAxon Traditional IUPAC Name {[({[(2S,3R,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy(hydroxy)phosphoryl]oxy(hydroxy)phosphoryl}oxy[(2S,3R,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3H-pyrimidin-1-yl)oxolan-2-yl]methoxyphosphinic acid ChemAxon Molecular Weight 891.3541 ChemAxon Monoisotopic Weight 891.008112861 ChemAxon SMILES CC1=CN([C@H]2C[C@@H](O)[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P@@](O)(=O)O[P@](O)(=O)O[P@@](O)(=O)OC[C@@H]3O[C@H]([C@H](O)[C@H]3O)N3C=NC4=C3N=CN=C4N)O2)C(=O)NC1=O ChemAxon Molecular Formula C20H30N7O23P5 ChemAxon InChI InChI=1S/C20H30N7O23P5/c1-8-3-26(20(32)25-18(8)31)12-2-9(28)10(45-12)4-43-51(33,34)47-53(37,38)49-55(41,42)50-54(39,40)48-52(35,36)44-5-11-14(29)15(30)19(46-11)27-7-24-13-16(21)22-6-23-17(13)27/h3,6-7,9-12,14-15,19,28-30H,2,4-5H2,1H3,(H,33,34)(H,35,36)(H,37,38)(H,39,40)(H,41,42)(H2,21,22,23)(H,25,31,32)/t9-,10+,11+,12-,14+,15-,19-/m1/s1 ChemAxon InChIKey InChIKey=JCFDSPQTEMXXLO-MZWJRZEOSA-N ChemAxon Polar Surface Area (PSA) 440.06 ChemAxon Refractivity 169.19 ChemAxon Polarizability 69.54 ChemAxon Rotatable Bond Count 16 ChemAxon H Bond Acceptor Count 21 ChemAxon H Bond Donor Count 10 ChemAxon pKa (strongest acidic) 0.42 ChemAxon pKa (strongest basic) 5 ChemAxon Physiological Charge -5 ChemAxon Number of Rings 5 ChemAxon Bioavailability 0 ChemAxon MDDR-Like Rule true ChemAxon PubChem Compound 46936628 PubChem Substance 46505960 PDB T5A BE0001221 Thymidylate kinase Human # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 # Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/10592235 unknown Thymidylate kinase Nucleotide transport and metabolism Catalyzes the conversion of dTMP to dTDP DTYMK 2q37.3 None 8.49 23820.0 Human HUGO Gene Nomenclature Committee (HGNC) HGNC:3061 GenAtlas DTYMK GeneCards DTYMK GenBank Gene Database X54729 GenBank Protein Database 37206 UniProtKB P23919 UniProt Accession KTHY_HUMAN dTMP kinase EC 2.7.4.9 >Thymidylate kinase MAARRGALIVLEGVDRAGKSTQSRKLVEALCAAGHRAELLRFPERSTEIGKLLSSYLQKK SDVEDHSVHLLFSANRWEQVPLIKEKLSQGVTLVVDRYAFSGVAFTGAKENFSLDWCKQP DVGLPKPDLVLFLQLQLADAAKRGAFGHERYENGAFQERALRCFHQLMKDTTLNWKMVDA SKSIEAVHEDIRVLSEDAIRTATEKPLGELWK >636 bp ATGGCGGCCCGGCGCGGGGCTCTCATAGTGCTGGAGGGCGTGGACCGCGCCGGGAAGAGC ACGCAGAGCCGCAAGCTGGTGGAAGCGCTGTCGCGCGGGCCACCGCCCGAACTGCTCCGG TTCCCGGAAAGATCAACTGAAATCGGCAAACTTCTGAGTTCCTACTTGCAAAAGAAAAGT GACGTGGAGGATCACTCGGTGCACCTGCTTTTTTCTGCAAATCGCTGGGAACAAGTGCCG TTAATTAAGGAAAAGTTGAGCCAGGGCGTGACCCTCGTCGTGGACAGATACGCATTTTCT GGTGTGGCCTTCACCGGTGCCAAGGAGAATTTTTCCCTAGACTGGTGTAAACAGCCAGAC GTGGGCCTTCCCAAACCCGACCTGGTCCTGTTCCTCCAGTTACAGCTGGCGGATGCTGCC AAGCGGGGAGCGTTTGGCCATGAGCGCTATGAGAACGGGGCTTTCCAGGAGCGGGCGCTC CGGTGTTTCCACCAGCTCATGAAAGACACGACTTTGAACTGGAAGATGGTGGATGCTTCC AAAAGACTCGAAGCTGTCCATGAGGAACTCCGCGTGCTCTCTGAGGACGCCATCCGCACT GCCACAGAGAAGCCGCTGGGGGAGCTATGGAAGTGA PF02223 Thymidylate_kin function catalytic activity function phosphotransferase activity, phosphate group as acceptor function nucleotide binding function thymidylate kinase activity function purine nucleotide binding function adenyl nucleotide binding function transferase activity function ATP binding function transferase activity, transferring phosphorus-containing groups function binding process nucleotide metabolism process pyrimidine nucleotide metabolism process metabolism process pyrimidine nucleotide biosynthesis process cellular metabolism process pyrimidine nucleoside triphosphate biosynthesis process pyrimidine deoxyribonucleoside triphosphate biosynthesis process dTTP biosynthesis process pyrimidine nucleoside diphosphate biosynthesis process pyrimidine deoxyribonucleoside diphosphate biosynthesis process nucleobase, nucleoside, nucleotide and nucleic acid metabolism process dTDP biosynthesis process physiological process BE0001932 Thymidylate kinase Shigella flexneri # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 unknown Thymidylate kinase Nucleotide transport and metabolism Catalyzes the reversible phosphorylation of deoxythymidine monophosphate (dTMP) to deoxythymidine diphosphate (dTDP), using ATP as its preferred phosphoryl donor. Situated at the junction of both de novo and salvage pathways of deoxythymidine triphosphate (dTTP) synthesis, is essential for DNA synthesis and cellular growth tmk None 5.16 23783.0 Shigella flexneri GenBank Gene Database AE005674 GenBank Protein Database 24051392 UniProtKB P0A721 UniProt Accession KTHY_SHIFL dTMP kinase EC 2.7.4.9 Thymidine monophosphate kinase TMPK >Thymidylate kinase MRSKYIVIEGLEGAGKTTARNVVVETLEQLGIRDMVFTREPGGTQLAEKLRSLVLDIKSV GDEVITDKAEVLMFYAARVQLVETVIKPALANGTWVIGDRHDLSTQAYQGGGRGIDQHML ATLRDAVLGDFRPDLTLYLDVTPEVGLKRARARGELDRIEQESFDFFNRTRARYLELAAQ DKSIHTIDATQPLEAVMDAIRTTVTHWVKELDA >642 bp ATGCGCAGTAAGTATATCGTCATTGAGGGGCTGGAAGGCGCAGGCAAAACTACCGCGCGT AATGTGGTGGTTGAGACGCTCGAGCAACTGGGTATCCGCGACATGGTTTTCACTCGGGAA CCTGGCGGTACGCAACTTGCCGAAAAGTTAAGAAGCCTGGTGCTGGATATCAAATCGGTA GGCGATGAAGTCATTACCGATAAAGCCGAAGTTCTGATGTTTTATGCCGCGCGCGTTCAA CTGGTAGAAACGGTCATCAAACCTGCGCTGGCTAACGGCACCTGGGTGATTGGCGATCGC CACGATCTTTCCACTCAGGCGTATCAGGGCGGAGGACGTGGTATTGACCAACATATGCTG GCAACACTGCGTGATGCTGTTCTCGGGGATTTTCGCCCAGACTTAACGCTCTATCTCGAT GTTACCCCGGAAGTTGGCTTAAAACGCGCGCGTGCGCGCGGCGAGCTGGATCGTATTGAG CAAGAGTCTTTCGATTTCTTTAATCGCACCCGCGCCCGCTATCTGGAACTGGCTGCACAA GATAAAAGTATTCATACCATTGATGCCACCCAGCCGCTGGAGGCCGTGATGGATGCAATC CGCACTACCGTGACCCACTGGGTGAAGGAGTTGGACGCATGA PF02223 Thymidylate_kin function purine nucleotide binding function adenyl nucleotide binding function transferase activity function ATP binding function transferase activity, transferring phosphorus-containing groups function binding function catalytic activity function phosphotransferase activity, phosphate group as acceptor function nucleotide binding function thymidylate kinase activity process pyrimidine nucleoside triphosphate biosynthesis process pyrimidine deoxyribonucleoside triphosphate biosynthesis process dTTP biosynthesis process pyrimidine nucleoside diphosphate biosynthesis process pyrimidine deoxyribonucleoside diphosphate biosynthesis process nucleobase, nucleoside, nucleotide and nucleic acid metabolism process dTDP biosynthesis process physiological process process nucleotide metabolism process pyrimidine nucleotide metabolism process metabolism process pyrimidine nucleotide biosynthesis process cellular metabolism BE0001929 Thymidine kinase EHV-4 # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 unknown Thymidine kinase Involved in thymidine kinase activity ATP + thymidine = ADP + thymidine 5'- phosphate TK None 7.19 38785.0 EHV-4 GenBank Gene Database D14486 GenBank Protein Database 221822 UniProtKB P24425 UniProt Accession KITH_EHV4 EC 2.7.1.21 >Thymidine kinase MAACVPPGEAPRSASGTPTRRQVTIVRIYLDGVYGIGKSTTGRVMASAASGGSPTLYFPE PMAYWRTLFETDVISGIYDTQNRKQQGNLAVDDAALITAHYQSRFTTPYLILHDHTCTLF GGNSLQRGTQPDLTLVFDRHPVASTVCFPAARYLLGDMSMCALMAMVATLPREPQGGNIV VTTLNVEEHIRRLRTRARIGEQIDITLIATLRNVYFMLVNTCHFLRSGRVWRDGWGELPT SCGAYKHRATQMDAFQERVSPELGDTLFALFKTQELLDDRGVILEVHAWALDALMLKLRN LNVFSADLSGTPRQCAAVVESLLPLMSSTLSDFDSASALERAARTFNAEMGV >1059 bp ATGGCTGCTTGCGTACCCCCGGGAGAAGCTCCACGAAGCGCCAGCGGAACGCCCACCCGG CGGCAAGTAACAATAGTTAGAATTTACCTCGATGGAGTTTATGGCATCGGTAAGAGCACG ACGGGACGAGTTATGGCATCGGCTGCTAGCGGAGGAAGTCCAACTCTATACTTTCCAGAG CCTATGGCGTACTGGCGGACTCTTTTTGAAACGGACGTAATTAGTGGTATTTACGACACC CAAAACCGGAAACAGCAGGGAAATTTGGCCGTTGATGACGCGGCATTAATAACTGCGCAT TACCAAAGCCGCTTTACCACGCCCTACCTGATACTCCACGATCACACTTGTACGTTGTTT GGGGGAAACAGCCTACAGCGTGGAACACAACCGGACCTGACCCTTGTGTTTGACCGCCAC CCGGTCGCCTCTACCGTATGCTTTCCAGCAGCCCGCTACCTACTCGGTGACATGTCAATG TGCGCGCTAATGGCTATGGTTGCTACTCTACCAAGAGAACCCCAGGGTGGTAACATTGTG GTTACCACCCTAAATGTAGAGGAGCATATACGGAGACTGCGTACGCGGGCTAGAATAGGA GAACAAATTGACATTACGCTGATTGCTACATTGCGAAATGTGTACTTTATGCTAGTTAAT ACATGTCACTTTTTGCGCTCTGGGCGAGTTTGGCGCGACGGTTGGGGTGAGCTACCCACT TCCTGTGGGGCTTATAAGCATCGCGCCACACAGATGGACGCCTTCCAAGAGCGCGTTTCA CCGGAGCTGGGCGACACTCTGTTTGCCCTGTTTAAAACTCAAGAACTGCTAGACGATCGC GGTGTAATATTGGAAGTTCACGCTTGGGCGTTGGACGCGCTTATGCTAAAACTGCGTAAC CTGAATGTTTTCAGTGCCGATTTAAGTGGTACACCGCGACAATGTGCAGCTGTTGTAGAG TCTTTGCTGCCACTTATGAGCAGCACCTTATCAGATTTTGATTCCGCCTCTGCTTTAGAG CGGGCGGCACGCACCTTTAACGCGGAGATGGGCGTCTGA PF00693 Herpes_TK function nucleotide binding function purine nucleotide binding function adenyl nucleotide binding function nucleobase, nucleoside, nucleotide kinase activity function transferase activity function nucleoside kinase activity function ATP binding function deoxynucleoside kinase activity function transferase activity, transferring phosphorus-containing groups function thymidine kinase activity function binding function kinase activity function catalytic activity process pyrimidine nucleoside monophosphate biosynthesis process pyrimidine ribonucleoside monophosphate biosynthesis process TMP biosynthesis process physiological process process nucleobase, nucleoside, nucleotide and nucleic acid metabolism process nucleotide metabolism process metabolism process pyrimidine nucleotide metabolism process cellular metabolism process pyrimidine nucleotide biosynthesis BE0001403 Thymidine kinase HHV-1 # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 unknown Thymidine kinase Involved in thymidine kinase activity In latent infection, may allow the virus to be reactivated and to grow in cells lacking a high concentration of phosphorylated nucleic acid precursors, such as nerve cells that do not replicate their genome TK - None 7.96 40973.0 HHV-1 GenBank Gene Database X14112 GenBank Protein Database 59524 UniProtKB P03176 UniProt Accession KITH_HHV11 EC 2.7.1.21 >Thymidine kinase MASYPCHQHASAFDQAARSRGHNNRRTALRPRRQQEATEVRPEQKMPTLLRVYIDGPHGM GKTTTTQLLVALGSRDDIVYVPEPMTYWRVLGASETIANIYTTQHRLDQGEISAGDAAVV MTSAQITMGMPYAVTDAVLAPHIGGEAGSSHAPPPALTLIFDRHPIAALLCYPAARYLMG SMTPQAVLAFVALIPPTLPGTNIVLGALPEDRHIDRLAKRQRPGERLDLAMLAAIRRVYG LLANTVRYLQCGGSWREDWGQLSGTAVPPQGAEPQSNAGPRPHIGDTLFTLFRAPELLAP NGDLYNVFAWALDVLAKRLRSMHVFILDYDQSPAGCRDALLQLTSGMVQTHVTTPGSIPT ICDLARTFAREMGEAN >1131 bp TCAGTTAGCCTCCCCCATCTCCCGGGCAAACGTGCGCGCCAGGTCGCAGATCGTCGGTAT GGAGCCTGGGGTGGTGACGTGGGTCTGGACCATCCCGGAGGTAAGTTGCAGCAGGGCGTC CCGGCAGCCGGCGGGCGATTGGTCGTAATCCAGGATAAAGACATGCATGGGACGGAGGCG TTTGGCCAAGACGTCCAAAGCCCAGGCAAACACGTTATACAGGTCGCCGTTGGGGGCCAG CAACTCGGGGGCCCGAAACAGGGTAAATAACGTGTCCCCGATATGGGGTCGTGGGCCCGC GTTGCTCTGGGGCTCGGCACCCTGGGGCGGCACGGCCGCCCCCGAAAGCTGTCCCCAATC CTCCCGCCACGACCCGCCGCCCTGCAGATACCGCACCGTATTGGCAAGCAGCCCATAAAC GCGGCGAATCGCGGCCAGCATAGCCAGGTCAAGCCGCTCGCCGGGGCGCTGGCGTTTGGC CAGGCGGTCGATGTGTCTGTCCTCCGGAAGGGCCCCCAACACGATGTTTGTGCCGGGCAA GGTCGGCGGGATGAGGGCCACGAACGCCAGCACGGCCTGGGGGGTCATGCTGCCCATAAG GTATCGCGCGGCCGGGTAGCACAGGAGGGCGGCGATGGGATGGCGGTCGAAGATGAGGGT GAGGGCCGGGGGCGGGGCATGTGAGCTCCCAGCCTCCCCCCCGATATGAGGAGCCAGAAC GGCGTCGGTCACGGCATAAGGCATGCCCATTGTTATCTGGGCGCTTGTCATTACCACCGC CGCGTCCCCGGCCGATATCTCACCCTGGTCGAGGCGGTGTTGTGTGGTGTAGATGTTCGC GATTGTCTCGGAAGCCCCCAACACCCGCCAGTAAGTCATCGGCTCGGGTACGTAGACGAT ATCGTCGCGCGAACCCAGGGCCACCAGCAGTTGCGTGGTGGTGGTTTTCCCCATCCCGTG GGGACCGTCTATATAAACCCGCAGTAGCGTGGGCATTTTCTGCTCCAGGCGGACTTCCGT GGCTTTTTGTTGCCGGCGAGGGCGCAACGCCGTACGTCGGTTGTTATGGCCGCGAGAACG CGCAGCCTGGTCGAACGCAGACGCGTGTTGATGGCAGGGGTACGAAGCCAT PF00693 Herpes_TK function catalytic activity function nucleotide binding function purine nucleotide binding function adenyl nucleotide binding function nucleobase, nucleoside, nucleotide kinase activity function transferase activity function nucleoside kinase activity function ATP binding function deoxynucleoside kinase activity function transferase activity, transferring phosphorus-containing groups function thymidine kinase activity function binding function kinase activity process nucleotide metabolism process metabolism process pyrimidine nucleotide metabolism process cellular metabolism process pyrimidine nucleotide biosynthesis process pyrimidine nucleoside monophosphate biosynthesis process pyrimidine ribonucleoside monophosphate biosynthesis process TMP biosynthesis process physiological process process nucleobase, nucleoside, nucleotide and nucleic acid metabolism BE0001218 Thymidylate kinase Mycobacterium tuberculosis # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 unknown Thymidylate kinase Nucleotide transport and metabolism Catalyzes the reversible phosphorylation of deoxythymidine monophosphate (dTMP) to deoxythymidine diphosphate (dTDP), using ATP as its preferred phosphoryl donor. Situated at the junction of both de novo and salvage pathways of deoxythymidine triphosphate (dTTP) synthesis, is essential for DNA synthesis and cellular growth. Has a broad specificity for nucleoside triphosphates, being highly active with ATP or dATP as phosphate donors, and less active with ITP, GTP, CTP and UTP tmk None 7.66 22635.0 Mycobacterium tuberculosis GenBank Gene Database BX842582 GenBank Protein Database 2072714 UniProtKB O05891 UniProt Accession KTHY_MYCTU dTMP kinase EC 2.7.4.9 Thymidine monophosphate kinase TMPK >Thymidylate kinase MLIAIEGVDGAGKRTLVEKLSGAFRAAGRSVATLAFPRYGQSVAADIAAEALHGEHGDLA SSVYAMATLFALDRAGAVHTIQGLCRGYDVVILDRYVASNAAYSAARLHENAAGKAAAWV QRIEFARLGLPKPDWQVLLAVSAELAGERSRGRAQRDPGRARDNYERDAELQQRTGAVYA ELAAQGWGGRWLVVGADVDPGRLAATLAPPDVPS >645 bp TCAACTTGGCACGTCTGGAGGCGCCAAAGTCGCCGCTAGTCGGCCCGGATCAACATCGGC GCCGACAACCAGCCACCGGCCGCCCCACCCTTGGGCCGCCAACTCGGCGTAGACCGCACC GGTGCGCTGCTGAAGTTCAGCGTCGCGTTCGTAATTGTCGCGCGCCCGACCGGGGTCACG CTGGGCACGGCCGCGGGATCGTTCCCCGGCGAGCTCGGCAGAGACCGCAAGGAGCACCTG CCAGTCGGGCTTGGGCAACCCGAGTCTTGCAAATTCGATCCGCTGAACCCAGGCCGCTGC CTTCCCGGCCGCGTTTTCATGTAGGCGCGCCGCGCTGTAGGCCGCGTTGGAGGCGACGTA GCGATCCAGGATCACCACGTCGTAGCCGCGACACAGCCCCTGGATCGTGTGGACCGCGCC AGCGCGGTCGAGCGCGAACAGCGTCGCCATCGCATACACCGACGATGCGAGGTCACCGTG CTCGCCGTGCAGCGCCTCCGCTGCGATGTCGGCGGCCACCGACTGTCCGTAGCGCGGGAA CGCCAGTGTGGCCACCGATCTCCCGGCTGCTCGAAAGGCCCCGGACAGCTTTTCCACCAA CGTCCGCTTGCCAGCGCCGTCAACGCCCTCAATCGCGATTAGCAC PF02223 Thymidylate_kin function purine nucleotide binding function adenyl nucleotide binding function transferase activity function ATP binding function transferase activity, transferring phosphorus-containing groups function binding function catalytic activity function phosphotransferase activity, phosphate group as acceptor function nucleotide binding function thymidylate kinase activity process pyrimidine nucleoside triphosphate biosynthesis process pyrimidine deoxyribonucleoside triphosphate biosynthesis process dTTP biosynthesis process pyrimidine nucleoside diphosphate biosynthesis process pyrimidine deoxyribonucleoside diphosphate biosynthesis process nucleobase, nucleoside, nucleotide and nucleic acid metabolism process dTDP biosynthesis process physiological process process nucleotide metabolism process pyrimidine nucleotide metabolism process metabolism process pyrimidine nucleotide biosynthesis process cellular metabolism "
owl:sameAs

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