Align Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_012968598.1 KVAR_RS16685 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_495 (480 letters) >NCBI__GCF_000025465.1:WP_012968598.1 Length = 482 Score = 624 bits (1610), Expect = 0.0 Identities = 307/482 (63%), Positives = 383/482 (79%), Gaps = 2/482 (0%) Query: 1 MQLKDTQLFRQQAFIDGAWVDADNGQTIKVNNPATGEILGTVPKMGAAETRRAIEAADKA 60 M + + LFRQQA I G+W DA +G T+ V+NP+TG LG +P MG AE ++A+EAA A Sbjct: 1 MSVFHSDLFRQQALIAGSWRDAADGTTLAVSNPSTGAALGQIPNMGRAEAQQAVEAAAAA 60 Query: 61 LPAWRALTAKERATKLRRWYELIIENQDDLARLMTLEQGKPLAEAKGEIVYAASFIEWFA 120 LPAWRALTA +RAT L+ W+ LI+EN+ LA++MT EQGKPLAEA+GEI YAASFIEWFA Sbjct: 61 LPAWRALTAAQRATLLKNWHRLILENKTALAQIMTAEQGKPLAEAEGEIAYAASFIEWFA 120 Query: 121 EEAKRIYGDVIPGHQPDKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLK 180 E+ KR G++IP DKRL+VI+Q +GV AAITPWNFPAAMITRKAGPALAAGCTMV+K Sbjct: 121 EQGKRTNGEIIPSPGADKRLMVIRQGVGVCAAITPWNFPAAMITRKAGPALAAGCTMVIK 180 Query: 181 PASQTPFSAFALAELAQRAGIPAGVFSVVSGSAGDIGSELTSNPIVRKLSFTGSTEIGRQ 240 PA++TPF+A A+AELA +AGIP GV +VV+G + +IG+ T + VRKLSFTGSTE+GR Sbjct: 181 PANETPFTALAMAELANQAGIPQGVINVVTGQSREIGAVFTGDERVRKLSFTGSTEVGRV 240 Query: 241 LMSECAKDIKKVSLELGGNAPFIVFDDADLDKAVEGAIISKYRNNGQTCVCANRLYIQDG 300 LM +CA+ IKK+SLELGGNAPFIVFDDAD+DKAVEGA+I+K+RN GQTCVC NR YI Sbjct: 241 LMRQCAESIKKLSLELGGNAPFIVFDDADIDKAVEGALIAKFRNAGQTCVCVNRFYIHRA 300 Query: 301 VYDAFAEKLKVAVAKLKIGNGLEAGTTTGPLIDEKAVAKVQEHIADALSKGATVLAGGK- 359 VYD F +K VA LK+G+G E+G GPLI+ A KVQ + DAL++GAT+L GGK Sbjct: 301 VYDQFCDKFVARVAALKVGDGNESGVQIGPLINADAGRKVQSLLDDALTRGATLLTGGKA 360 Query: 360 -PMEGNFFEPTILTNVPNNAAVAKEETFGPLAPLFRFKDEADVIAMSNDTEFGLASYFYA 418 P+ GNFF PT++ +V + + +EE FGP+A L +F DE VI +N+T +GLASYFY+ Sbjct: 361 HPLGGNFFTPTVIGDVQPGSLLLQEEIFGPVAALVKFDDEQQVIEQANNTIYGLASYFYS 420 Query: 419 RDLGRVFRVAEALEYGMVGVNTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCL 478 D R++RV+E LEYGMVG+NTGLISNEVAPFGG+K SGLGREGS++GIEDYLE+KYLC Sbjct: 421 NDAARIWRVSEQLEYGMVGINTGLISNEVAPFGGVKQSGLGREGSEHGIEDYLEMKYLCQ 480 Query: 479 GI 480 G+ Sbjct: 481 GL 482 Lambda K H 0.317 0.135 0.390 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 669 Number of extensions: 21 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 480 Length of database: 482 Length adjustment: 34 Effective length of query: 446 Effective length of database: 448 Effective search space: 199808 Effective search space used: 199808 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory