Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate 7025944 Shewana3_3092 succinate semialdehyde dehydrogenase (RefSeq)
Query= curated2:Q2SXN9 (487 letters) >FitnessBrowser__ANA3:7025944 Length = 482 Score = 189 bits (480), Expect = 2e-52 Identities = 142/463 (30%), Positives = 219/463 (47%), Gaps = 8/463 (1%) Query: 3 ELFIDGAWVDGAGP-VFASRNPGTNERVWEGASASADDVERAVASARRAFAAWSALDLDA 61 + +I+G W D A NP T + + + A+A+A A AW AL Sbjct: 12 QCYINGQWCDAQSKETVAIANPATGAVIASVPVMGQAETQAAIAAAEAALPAWRALTAKE 71 Query: 62 RCTIVKRFAALLVERKEALATMIGRETGKPLWEARTEVASMAAKVDISITAYHERTGEK- 120 R ++R+ LL E + LA M+ E GKPL EA+ EV A+ ++ G+ Sbjct: 72 RGVKLRRWFELLNENSDDLALMMTSEQGKPLAEAKGEVTYAASFIEWFAEEAKRVYGDTI 131 Query: 121 RAPMADGVAVLRHRPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSELAPGVARA 180 D ++ +P GV A P+NFP + PAL AG T+V KP+ P A A Sbjct: 132 PGHQGDKRIMVIKQPVGVTAAITPWNFPAAMITRKAAPALAAGCTMVVKPAPQTPFTALA 191 Query: 181 TVEIWRDAGLPAGVLNLVQGEK-DTGVALANHRQIDGLFFTGSSDTGTLLHKQFGGRPEI 239 + AG+PAGV +++ G+ G + ++ + L FTGS+ G L +Q + Sbjct: 192 LAVLAERAGIPAGVFSVITGDAIGIGNEMCSNPVVRKLSFTGSTQVGIKLMEQCAPTLK- 250 Query: 240 VLALEMGGNNPLVVAEVEDIDAAVHHAIQSAFLSAGQRCTCARRILVPRGAFGDRFVARL 299 L+LE+GGN P +V + +IDAAV A+ + + +AGQ C CA RI V G + D F +L Sbjct: 251 KLSLELGGNAPFIVFDDANIDAAVEGAMIAKYRNAGQTCVCANRIYVQAGVY-DEFARKL 309 Query: 300 ADVASKITASVFDADPQPFMGAVISARAASRLVAAQARLVGLGASPIIEMKQRDPALGFV 359 + K+ + G +I+ A ++ + + GA+ + K F Sbjct: 310 SIAVGKLKVGEGIGEGVT-TGPLINCAAVEKVQSHLEDALSKGATVVAGGKPHSLGGNFF 368 Query: 360 NAAIL-DVTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDTAFGLSAGLLADDEQAWHT 418 +L +V + + EE FGPLA + ++TD+DD I +ANDT FGL+A D Sbjct: 369 EPTVLTNVDSSMRVAREETFGPLAPLFKFTDVDDVIKQANDTEFGLAAYFYGRDISLVWK 428 Query: 419 FRRAIRAGIVNWNRPTNGASSAAPFGGAGRSGNHRPSAYYAAD 461 A+ G+V N ++ APFGG SG R + + + Sbjct: 429 VTEALEYGMVGVNTGLI-STEVAPFGGMKSSGLGREGSKFGIE 470 Lambda K H 0.320 0.134 0.402 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: 488 Number of extensions: 20 Number of successful extensions: 4 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: 487 Length of database: 482 Length adjustment: 34 Effective length of query: 453 Effective length of database: 448 Effective search space: 202944 Effective search space used: 202944 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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