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_058929629.1 AU252_RS04095 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_001484605.1:WP_058929629.1 Length = 499 Score = 337 bits (864), Expect = 6e-97 Identities = 189/471 (40%), Positives = 264/471 (56%), Gaps = 1/471 (0%) Query: 9 TQLLIDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAH 68 T LLI+GEW AASGKT DV +PATGK + +A AG D AL AA + E+W KVPA Sbjct: 23 TGLLINGEWRPAASGKTFDVEDPATGKVLLSIADAGAEDGKAALDAAAAAQESWAKVPAR 82 Query: 69 ERAATMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRI 128 ER +R+A +V RA+ A LMT E GKPL EAR EV A+ + WF++E R +GR Sbjct: 83 ERGEILRRAFEMVTARAEDFALLMTMEMGKPLAEARGEVAYGAEFLRWFSEEAVRAFGRY 142 Query: 129 VPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPA 188 + ++ V K+PVGP TPWNFP+ RK++ A+A GC+ ++K+ TP + Sbjct: 143 SVSPDGKSRLLVTKKPVGPCLLITPWNFPLAMATRKIAPAVAAGCTMVLKSANLTPLTSQ 202 Query: 189 ALLRAFVDAGVPAGVIGLVYGDPAEISSY-LIPHPVIRKVTFTGSTPVGKQLASLAGLHM 247 +AG+PAGV+ ++ A ++ LI +RK++FTGST VG++L + A + Sbjct: 203 LFAAVMQEAGLPAGVLNVIPTSTAGATTGPLIKDQRLRKLSFTGSTEVGRRLLADASETV 262 Query: 248 KRATMELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRAL 307 R +MELGG+AP +V EDAD+ AV A AK RN G+ C + RF+VH S+ DEF + Sbjct: 263 LRTSMELGGNAPFVVFEDADLDAAVAGAMLAKLRNMGEACTAANRFIVHESVADEFAQKF 322 Query: 308 VKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFA 367 + G E + +G L + + + ++ +A GA GG G F+ Sbjct: 323 AAKMGEMTTARGTEPESKVGPLIDAKSRDKVHELVSDAVASGAKAVLGGAPAEGPGYFYP 382 Query: 368 PTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLL 427 PT++ V + + E FGPVA I F +EA+ AN +GL Y FTR + Sbjct: 383 PTILTGVTEGTRILSEEIFGPVAPIITFGTEDEAVRLANNTEYGLVAYVFTRDLNRGIRM 442 Query: 428 TQRLEVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKSVTV 478 +RLE GML +N PFGGVK SG G EGG E +E YL T+ + + Sbjct: 443 GERLETGMLGLNAGVISNAAAPFGGVKQSGLGREGGLEGIEEYLYTQYIGI 493 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: 678 Number of extensions: 22 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: 499 Length adjustment: 34 Effective length of query: 447 Effective length of database: 465 Effective search space: 207855 Effective search space used: 207855 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