Align succinate-semialdehyde dehydrogenase [NAD(P)+] (EC 1.2.1.16) (characterized)
to candidate Dsui_0105 Dsui_0105 NAD-dependent aldehyde dehydrogenase
Query= BRENDA::Q0K2K1 (483 letters) >FitnessBrowser__PS:Dsui_0105 Length = 476 Score = 322 bits (826), Expect = 1e-92 Identities = 198/469 (42%), Positives = 255/469 (54%), Gaps = 8/469 (1%) Query: 11 SHCLIDGEWTGAQSGAELAVCNPATGERIGSVPLAGAAEAEQAVRAAERALPAWRAQTGK 70 S I G+W A + V NPAT I VP A +A++A RAA A PAW A +G Sbjct: 5 SRFYIGGQWVAPDGNAFIDVENPATETVIARVPEGTATDADRAARAAAAAFPAWAALSGA 64 Query: 71 ARAAVLRRWADLMLAHQEDLARLMTAEQGKPLPEARGEVAYAASFLEWFGEEAKRVDGEV 130 R A L++ AD + A Q++L RL+ +E G P+ A A F R+ E Sbjct: 65 ERGAFLQKIADGLKARQDELGRLIASEVGMPVKLATRVQAGNPIFTF---AACARIAAEG 121 Query: 131 LASPRSSQKMLVLREPVGVCAAITPWNFPAAMITRKVGPALAAGCTIIVKPAEQTPLTAL 190 A R Q LVL+ P G A ITPWNFP I KVG ALAAGCT+++KP+E PL A Sbjct: 122 FAEERIGQS-LVLKVPTGPVACITPWNFPLHQIAAKVGAALAAGCTVVLKPSEVAPLNAF 180 Query: 191 ALAVLGEQAGVPRGVLQVVTGDAVQIGGVLCASPVVRKLSFTGSTAIGKLLMAQCAGTVK 250 LA + E AG+P GV +VTG +G L A P + +SFTGSTA GK + A A TVK Sbjct: 181 LLAEVIEAAGLPAGVFNLVTGYGPVVGEALAAHPALAAVSFTGSTAAGKRVAAVAAATVK 240 Query: 251 KLSLELGGNAPLIIFDDADLDRAVEGILASKFRNSGQTCVCANRIYVHDRVYDEVARRLV 310 ++SLELGG + ++ DADL AV+G +A F NSGQ C R+ V Y E A V Sbjct: 241 RVSLELGGKSASVVLPDADLAAAVKGTVAGCFLNSGQACSALTRLLVPQERYAEAAALAV 300 Query: 311 SAVEQLRPGHGVDSGVTQGPLIDADAVAKVEAHIADALAQGATVLTGGQRHALG---GTF 367 A G + G GPL+ +V A I A+A GA +L GG G G + Sbjct: 301 QAAAAYTLGDPLAEGSRLGPLVSGLQRQRVRAMIEQAVADGAELLCGGSAAPEGLPTGYY 360 Query: 368 FAPTVLANATASMRVAREETFGPLAPLFRFTSEAEVVAMANDTESGLAAYFFSRDMAKIW 427 PTV +AREE FGP+ + + EAE A+AN T+ GLAA +S + A+ Sbjct: 361 VRPTVFGRVRPDAALAREEVFGPVLAILTYRDEAEAEAIANGTDYGLAAAVWSAEEARAL 420 Query: 428 RVAQGLEYGMVGINTGLISNEVAPFGGVKQSGLGREGSRHGIDEYLETK 476 A+ L G V IN G N +APFGG KQSG GRE RHG++++LET+ Sbjct: 421 AFARRLRAGQVDIN-GAFFNLLAPFGGFKQSGYGRELGRHGVEDFLETQ 468 Lambda K H 0.319 0.133 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: 600 Number of extensions: 25 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: 483 Length of database: 476 Length adjustment: 34 Effective length of query: 449 Effective length of database: 442 Effective search space: 198458 Effective search space used: 198458 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: 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