Protein Info for DDA3937_RS18415 in Dickeya dadantii 3937
Annotation: bifunctional aspartate kinase/homoserine dehydrogenase I
These analyses and tools can help you predict a protein's function, but be skeptical. For enzymes, over 10% of annotations from KEGG or SEED are probably incorrect. For other types of proteins, the error rates may be much higher. MetaCyc and Swiss-Prot have low error rates, but the best hits in these databases are often quite distant, so this protein's function may not be the same. TIGRFam has low error rates. Finally, many experimentally-characterized proteins are not in any of these databases. To find relevant papers, use PaperBLAST.
Protein Families and Features
Best Hits
Swiss-Prot: 84% identical to AK1H_SERMA: Bifunctional aspartokinase/homoserine dehydrogenase 1 (thrA) from Serratia marcescens
KEGG orthology group: K12524, bifunctional aspartokinase / homoserine dehydrogenase 1 [EC: 1.1.1.3 2.7.2.4] (inferred from 100% identity to ddd:Dda3937_00394)MetaCyc: 81% identical to fused aspartate kinase/homoserine dehydrogenase 1 (Escherichia coli K-12 substr. MG1655)
Aspartate kinase. [EC: 2.7.2.4]; Homoserine dehydrogenase. [EC: 2.7.2.4, 1.1.1.3]
Predicted SEED Role
"Aspartokinase (EC 2.7.2.4) / Homoserine dehydrogenase (EC 1.1.1.3)" in subsystem Lysine Biosynthesis DAP Pathway or Threonine and Homoserine Biosynthesis or Methionine Biosynthesis (EC 1.1.1.3, EC 2.7.2.4)
MetaCyc Pathways
- aspartate superpathway (24/25 steps found)
- superpathway of L-lysine, L-threonine and L-methionine biosynthesis I (18/18 steps found)
- superpathway of L-isoleucine biosynthesis I (13/13 steps found)
- L-lysine biosynthesis I (9/9 steps found)
- superpathway of S-adenosyl-L-methionine biosynthesis (9/9 steps found)
- superpathway of L-methionine biosynthesis (transsulfuration) (9/9 steps found)
- superpathway of L-methionine biosynthesis (by sulfhydrylation) (11/12 steps found)
- superpathway of L-homoserine and L-methionine biosynthesis (8/8 steps found)
- superpathway of L-lysine, L-threonine and L-methionine biosynthesis II (13/15 steps found)
- superpathway of L-threonine biosynthesis (6/6 steps found)
- L-lysine biosynthesis III (6/7 steps found)
- L-lysine biosynthesis VI (6/7 steps found)
- L-homoserine biosynthesis (3/3 steps found)
- L-lysine biosynthesis II (7/9 steps found)
- dipicolinate biosynthesis (3/4 steps found)
- ectoine biosynthesis (3/5 steps found)
- chorismate biosynthesis II (archaea) (8/12 steps found)
- L-methionine biosynthesis IV (2/4 steps found)
- spermidine biosynthesis II (2/4 steps found)
- norspermidine biosynthesis (3/6 steps found)
- 3-dehydroquinate biosynthesis II (archaea) (3/7 steps found)
- superpathway of polyamine biosynthesis III (3/8 steps found)
- cremeomycin biosynthesis (2/7 steps found)
- grixazone biosynthesis (2/8 steps found)
- platensimycin biosynthesis (6/26 steps found)
KEGG Metabolic Maps
- Biosynthesis of alkaloids derived from ornithine, lysine and nicotinic acid
- Biosynthesis of plant hormones
- Glycine, serine and threonine metabolism
- Lysine biosynthesis
Isozymes
Compare fitness of predicted isozymes for: 1.1.1.3, 2.7.2.4
Use Curated BLAST to search for 1.1.1.3 or 2.7.2.4
Sequence Analysis Tools
PaperBLAST (search for papers about homologs of this protein)
Search CDD (the Conserved Domains Database, which includes COG and superfam)
Predict protein localization: PSORTb (Gram-negative bacteria)
Predict transmembrane helices and signal peptides: Phobius
Check the current SEED with FIGfam search
Find homologs in fast.genomics or the ENIGMA genome browser
See E0SH30 at UniProt or InterPro
Protein Sequence (818 amino acids)
>DDA3937_RS18415 bifunctional aspartate kinase/homoserine dehydrogenase I (Dickeya dadantii 3937) MRVLKFGGTSVANAERFARVADIIESNARQGQVATVLSAPAKITNHLVAMIEKTVAKQDI QPNITEAEVIFADLLQGLAQSQPGFAYDRLKARVDEEFSQLKQVLHGIALLGQCPDSVNA AIICRGEKLSIAIMEAVFQARGYQVSVIDPVRSLLAQGHYLESTVDIAESTRRIDEQAIP ADHVILMAGFTAGNDKGELVVLGRNGSDYSAAVLAACLRADCCEIWTDVDGVYTCDPRQV PDARLLKSMSYQEAMELSYFGAKVLHPRTIAPIAQFQIPCLIKNTENPQAPGTLIGLESN DNQYPVKGITNLNNMAMINVSGPGMKGMVGMAARVFAAMSRAGISVVLITQSSSEYSISF CVSQSELPRARKTLEDEFYLELKEGVLEPLDVVQRLAIISVVGDGMRTLRGLSARLFTAL ASANINIVAIAQGSSERSISVVVNNDVATTGVRVAHQMLFNTNQALDVFVIGVGGVGGAL LEQIQRQQPWLKQKHIDVRVCGIANSKAMLTNVHGIPMDRWRDELARAREPFSPAALSRL VKEYHLLNPVIIDCTSSQAVADQYADFLADGFHVVTPNKKANTGTLRYYHQLRQAAAKSR RKFLYDTNVGAGLPVIENLQNLLNAGDELIRFNGILSGSLSFIFGKLDEGMSLSDATLLA KEKGFTEPDPRDDLSGMDVARKLLILAREAGYELELDDIQVDSVLPPEYSQGDVASFLAR LPELDAEFSRRVEAARSEGKVLRYVGKIDDGKCQVTISAVGGNDPLFKVKDGENALAFYS RYYQPLPLVLRGYGAGNDVTAAGVFADLLRTLSWKVGV