Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_043532311.1 JH15_RS16505 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000759345.1:WP_043532311.1 Length = 487 Score = 315 bits (808), Expect = 2e-90 Identities = 173/464 (37%), Positives = 260/464 (56%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 YIDG +V IDV NPA VI R+P + +AI AA+ A P W A A ERA Sbjct: 15 YIDGSWVAADSGEQIDVFNPANGEVIGRVPRLGRAETERAITAADAAFPAWRAHTAQERA 74 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 L K + E E++ ++ E GK + A E+A+ A ++ + AE ARR GE I + Sbjct: 75 DILMKWHDLMHEHQEELATIMTLEQGKPLKEAAGEIAYAASFLRWFAEEARRMYGETIPA 134 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 +P + I++ K+ +GV I PWNFP +I RK+ AL G IV+KP+ TP +A A A Sbjct: 135 AKPNQRIVITKQPVGVVGAITPWNFPAAMITRKVGAALAAGCPIVVKPASQTPFSATALA 194 Query: 190 KIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVC 249 + + G+PRGVFN+V G + L +P+V ++ TGS G ++M+ A+++I K+ Sbjct: 195 LLAERAGVPRGVFNVVTGSAREIAAALTESPEVRKITFTGSTEVGRQLMSQASQHIQKIS 254 Query: 250 LELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAM 309 LELGG AP IV +DADL+ AV + ++ N GQ C C R VQ + + F +L AM Sbjct: 255 LELGGNAPFIVFEDADLDAAVDGAMAAKFRNGGQTCVCTNRFLVQSSVVNAFCEKLAVAM 314 Query: 310 QAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTL 369 + ++D+ +GPLI+A +E+V V AV++GA + GG G ++ PTL Sbjct: 315 NSELRVGDGLKDDVNIGPLIDADGVEKVSAHVHDAVDKGAELLLGGNPHPLGGNFFTPTL 374 Query: 370 LLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKG 429 + +M + EETFGP+ V FD EDA++MAND+ +GL S Y+++L + + Sbjct: 375 VNGANADMLVAQEETFGPLAAVFPFDDEEDAVAMANDTQFGLASYFYSRDLARVWRVAES 434 Query: 430 LKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQ 473 L++G IN G + SG+G G+ GL E+++T+ Sbjct: 435 LEYGMVGINTGLISNAAAPFGGVKASGLGREGGRQGLEEFVETK 478 Lambda K H 0.318 0.135 0.392 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: 519 Number of extensions: 18 Number of successful extensions: 1 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: 479 Length of database: 487 Length adjustment: 34 Effective length of query: 445 Effective length of database: 453 Effective search space: 201585 Effective search space used: 201585 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