Align Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized)
to candidate WP_244906035.1 B9O00_RS05420 NADP-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_900177295.1:WP_244906035.1 Length = 495 Score = 365 bits (937), Expect = e-105 Identities = 193/465 (41%), Positives = 271/465 (58%) Query: 10 QLLIDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAHE 69 Q IDG+W+DA SG T++V NPATG+ +G V G + RA+ AA + + AWR + E Sbjct: 24 QCYIDGQWLDADSGATLEVTNPATGETLGSVPKMGADETRRAIEAANAAWPAWRSLTGKE 83 Query: 70 RAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRIV 129 R+ +R+ L+ D + LMT EQGKPL EA+ E+ A +EWFA+E +RVYG ++ Sbjct: 84 RSNILRRWFELMMANQDDLGLLMTLEQGKPLPEAKGEIAYGASFVEWFAEEAKRVYGDVI 143 Query: 130 PPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPAA 189 P + V+K+PVG V A TPWNFP + RK ALA GC+ ++K TP S A Sbjct: 144 PGHQRDKRIVVLKQPVGVVGAITPWNFPNAMITRKAGPALAAGCTIVIKPATATPYSALA 203 Query: 190 LLRAFVDAGVPAGVIGLVYGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHMKR 249 L AG+P GV +V G + I L +P++RK++FTGST VGK L + +K+ Sbjct: 204 LCELAERAGIPKGVFNVVTGSSSAIGGELTGNPIVRKISFTGSTEVGKVLIKQSAETVKK 263 Query: 250 ATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRALVK 309 +MELGG+AP +V +DAD+ AV+ A +K+RNAGQ C+ R LV + + + F + L + Sbjct: 264 LSMELGGNAPFLVFDDADLDAAVEGAMASKYRNAGQTCVCANRLLVQDGVYEAFAQKLAE 323 Query: 310 HAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFAPT 369 + LKVGNGL+EG G L + + + I +A GA++ GG+R G+FF PT Sbjct: 324 KVKQLKVGNGLDEGVVQGPLIDMAAIEKVEEHIADAVAKGATVVVGGKRHALGGSFFEPT 383 Query: 370 VIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLLTQ 429 V+ V + V E FGPVA + F EE IA AN FGLA Y + R + V +++ Sbjct: 384 VLTGVTTEMKVTKEETFGPVAPLFRFGSDEEGIAMANDTEFGLASYFYARDMSRVWRVSE 443 Query: 430 RLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTK 474 LE G++ IN PFGGVK+SG G EG +E +L K Sbjct: 444 GLESGIVGINTGIISTEVAPFGGVKESGLGREGSKYGIEDFLEIK 488 Lambda K H 0.318 0.134 0.393 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: 657 Number of extensions: 26 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: 481 Length of database: 495 Length adjustment: 34 Effective length of query: 447 Effective length of database: 461 Effective search space: 206067 Effective search space used: 206067 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: 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