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_057507192.1 ABB28_RS02945 aldehyde dehydrogenase family protein
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_001431535.1:WP_057507192.1 Length = 460 Score = 228 bits (580), Expect = 4e-64 Identities = 153/449 (34%), Positives = 227/449 (50%), Gaps = 17/449 (3%) Query: 26 IDVVNPATGKPIGRVAHAGIADLDRALAAAQSGF---EAWRKVPAHERAATMRKAAALVR 82 + VV PI + A L++ L+AA+ F + W +P HER A +R+ AAL+ Sbjct: 2 LTVVQAFDRAPITEIGFDTAAALEQKLSAAERVFKDRDGW--LPPHERIAILRRLAALMD 59 Query: 83 ERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRIVP----PRNLGAQQ 138 + D +A + +E GKPL +A +E A D + ADE R GR +P +G Sbjct: 60 AKRDHLALQIAREGGKPLPDAIIETTRAIDGVHNAADELRNFGGREIPMGLSAAAVGRWA 119 Query: 139 TVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPAALLRAFVDAG 198 +EP+G VAA + +N P+N +V +++ A+A GC ++K TP S L+ +AG Sbjct: 120 FTTREPIGIVAAISAFNHPLNLIVHQVAPAIAVGCPVIIKPASATPLSCLDLVAMVHEAG 179 Query: 199 VPAGVIGLVYGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHMKRATMELGGHA 258 +P + +++ L + ++F GS VG L S H R+ +E GG A Sbjct: 180 LPEPWCQSFMPEGNDLAEALATDKRVAFLSFIGSARVGWSLHSKLA-HGARSALEHGGVA 238 Query: 259 PVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRALVKHAEGLKVGN 318 P IV +AD++ ++ + +AGQVC+S R VH+ I D+FT ALV E L+ G+ Sbjct: 239 PAIVDRNADLSRIIEPIVKGGYYHAGQVCVSTQRIFVHDDIADDFTEALVARVERLRTGD 298 Query: 319 GLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFAPTVIANVPLDA 378 + T +G L PR +A ID A K GA + TGG+R+ PTV+ + DA Sbjct: 299 PTLKDTDVGPLIQPREADRVAEWIDEAVKGGAKLATGGKRLSE--TTLQPTVLLDPASDA 356 Query: 379 DVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLLTQRLEVGMLWI 438 V E FGPV A+ + L+EAI+ AN LP FT+ RL+ + I Sbjct: 357 RVTTQEVFGPVVAVYRYADLDEAISRANSLPTAFQASIFTQDIDIALRAANRLDASAVMI 416 Query: 439 NQPA---TPWPEMPFGGVKDSGYGSEGGP 464 N T W MPF G ++SGYG+ G P Sbjct: 417 NDATAFRTDW--MPFAGRRESGYGTGGIP 443 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: 589 Number of extensions: 32 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: 481 Length of database: 460 Length adjustment: 33 Effective length of query: 448 Effective length of database: 427 Effective search space: 191296 Effective search space used: 191296 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: 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