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_043532311.1 JH15_RS16505 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_000759345.1:WP_043532311.1 Length = 487 Score = 378 bits (970), Expect = e-109 Identities = 207/467 (44%), Positives = 276/467 (59%), Gaps = 1/467 (0%) Query: 13 IDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEAWRKVPAHERAA 72 IDG WV A SG+ IDV NPA G+ IGRV G A+ +RA+ AA + F AWR A ERA Sbjct: 16 IDGSWVAADSGEQIDVFNPANGEVIGRVPRLGRAETERAITAADAAFPAWRAHTAQERAD 75 Query: 73 TMRKAAALVRERADAIAQLMTQEQGKPLTEARVEVLSAADIIEWFADEGRRVYGRIVPPR 132 + K L+ E + +A +MT EQGKPL EA E+ AA + WFA+E RR+YG +P Sbjct: 76 ILMKWHDLMHEHQEELATIMTLEQGKPLKEAAGEIAYAASFLRWFAEEARRMYGETIPAA 135 Query: 133 NLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPAALLR 192 + + K+PVG V A TPWNFP + RK+ AALA GC +VK +TP S AL Sbjct: 136 KPNQRIVITKQPVGVVGAITPWNFPAAMITRKVGAALAAGCPIVVKPASQTPFSATALAL 195 Query: 193 AFVDAGVPAGVIGLVYGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGLHMKRATM 252 AGVP GV +V G EI++ L P +RK+TFTGST VG+QL S A H+++ ++ Sbjct: 196 LAERAGVPRGVFNVVTGSAREIAAALTESPEVRKITFTGSTEVGRQLMSQASQHIQKISL 255 Query: 253 ELGGHAPVIVAEDADVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFTRAL-VKHA 311 ELGG+AP IV EDAD+ AV A AKFRN GQ C+ RFLV +S+ + F L V Sbjct: 256 ELGGNAPFIVFEDADLDAAVDGAMAAKFRNGGQTCVCTNRFLVQSSVVNAFCEKLAVAMN 315 Query: 312 EGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGNFFAPTVI 371 L+VG+GL++ +G L + + +++ + +A GA + GG GNFF PT++ Sbjct: 316 SELRVGDGLKDDVNIGPLIDADGVEKVSAHVHDAVDKGAELLLGGNPHPLGGNFFTPTLV 375 Query: 372 ANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFANVHLLTQRL 431 D V E FGP+AA+ FD E+A+A AN FGLA Y ++R A V + + L Sbjct: 376 NGANADMLVAQEETFGPLAAVFPFDDEEDAVAMANDTQFGLASYFYSRDLARVWRVAESL 435 Query: 432 EVGMLWINQPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKSVTV 478 E GM+ IN PFGGVK SG G EGG + LE ++ TK + + Sbjct: 436 EYGMVGINTGLISNAAAPFGGVKASGLGREGGRQGLEEFVETKYLCI 482 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: 648 Number of extensions: 27 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: 487 Length adjustment: 34 Effective length of query: 447 Effective length of database: 453 Effective search space: 202491 Effective search space used: 202491 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 Sep 24 2021. 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