Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_022669887.1 G415_RS0101870 aldehyde dehydrogenase family protein
Query= BRENDA::Q9K9B2 (515 letters) >NCBI__GCF_000420385.1:WP_022669887.1 Length = 474 Score = 265 bits (676), Expect = 4e-75 Identities = 158/463 (34%), Positives = 251/463 (54%), Gaps = 20/463 (4%) Query: 35 KEYPLIINGERVTTEDKIQSWNPARKDQLVGSVSKANQDLAEKAIQSADEAFQTWRNVNP 94 KE+ I GE V+T I + +++ V KA++ L +KA+ +A EAF+ ++ + Sbjct: 2 KEFKTYIGGEWVSTNKTIDVIDKY-SGEVIAKVPKADKKLVDKAVDAAAEAFEEFKKMPA 60 Query: 95 EERANILVKAAAIIRRRKHEFSAWLVHEAGKPWKEADADTAEAIDFLEYYARQMIELNRG 154 +R+ IL KAA +I+ R E + + EAGK WK + + + ++ + + ++ G Sbjct: 61 YQRSEILEKAADLIKERSDEIAETICREAGKAWKYSVGEVNRGFETFKFASEEAKRIH-G 119 Query: 155 KEI-----LSRPGEQNRYFYTPMGVTVTISPWNFALAIMVGTAVAPIVTGNTVVLKPAST 209 + + G Y PMGV I+P+NF L ++ I +GNT+VLKPAS+ Sbjct: 120 ETVPMDASAGGVGRVGYYIRVPMGVLGAITPFNFPLNLVAHKVAPAIASGNTIVLKPASS 179 Query: 210 TPVVAAKFVEVLEDAGLPKGVINYVPGSGAEVGDYLVDHPKTSLITFTGSKDVGVRLYER 269 TP+ A E+LE+AGLPKGV N V G G EVG+ LV + K ITFTGS VG RL + Sbjct: 180 TPITALILAEILEEAGLPKGVFNVVIGPGGEVGESLVTNDKVRKITFTGSAKVGHRLTQI 239 Query: 270 AAVVRPGQNHLKRVIVEMGGKDTVVVDRDADLDLAAESILVSAFGFSGQKCSAGSRAVIH 329 A + KR+ +E+G ++++DAD+D A + SAF SGQ C + R +H Sbjct: 240 AGI--------KRITLELGNNSATIIEKDADIDKAIPRCVDSAFANSGQVCISLQRIYVH 291 Query: 330 KDVYDEVLEKTVALAKNLTVGDPTNRDNYMGPVIDEKAFEKIMSYIEIGKKEG-RLMTGG 388 KD+ DE EK K L VG+P +D +GP+IDE ++ +I+ G L+ GG Sbjct: 292 KDIADEFTEKFAEATKKLKVGNPVEKDTDLGPMIDENEAKRAEEWIKEAVNMGAELVVGG 351 Query: 389 EGDSSTGFFIQPTIIADLDPEAVIMQEEIFGPVVAFSKANDFDHALEIANNTEYGLTGAV 448 + + G +QPT++ + + +M E+F P+V+ + + F+ A++ N+++YGL + Sbjct: 352 KRE---GRVLQPTVLRNTTKDMRVMCMEVFAPIVSIVEYDTFEDAIQHVNDSDYGLQAGI 408 Query: 449 ITRNRAHIEQAKREFHVGNLYFNRNCTGAIVGYHPFGGFKMSG 491 T + I A VG + N + + V + P+GG KMSG Sbjct: 409 YTNDIRKIHYAIDNLDVGGVMIN-DTSIFRVDHMPYGGNKMSG 450 Lambda K H 0.316 0.134 0.388 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: 601 Number of extensions: 39 Number of successful extensions: 5 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: 515 Length of database: 474 Length adjustment: 34 Effective length of query: 481 Effective length of database: 440 Effective search space: 211640 Effective search space used: 211640 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 (21.6 bits) S2: 52 (24.6 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