Align NAD+-dependent L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_092993135.1 BLP65_RS04695 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-16246 (477 letters) >NCBI__GCF_900102855.1:WP_092993135.1 Length = 481 Score = 268 bits (684), Expect = 4e-76 Identities = 168/471 (35%), Positives = 251/471 (53%), Gaps = 8/471 (1%) Query: 11 YIDGAFVESAAH-LEVFNPANGALLSRVPAASAEEVERALAAARAAQKDWARKPAIERAG 69 YI+G++ +V NPANG +L+ +PA AEE +A+ A R A + A R Sbjct: 13 YINGSWQRGVGEPFQVTNPANGEVLAEIPAMGAEETRQAIEAGRHALESSAGLET--RRA 70 Query: 70 HLRRIAAKIRADAGRIARTITLEQGKIASLAEVEVNFTADYLDYMAEWARRLEGEIIASD 129 L+ IA + + I R +T E GK EV++ A + Y E L+ + Sbjct: 71 WLQMIAEALTDNREEIGRILTHEHGKPWKEGIGEVDYAAGFFRYAGENIGLLKPYTLQEQ 130 Query: 130 RPGENIFLFRKPLGVVAGILPWNFPFFLIARKMAPALLTGNTIVVKPSEETPNNCFEFAR 189 G + ++ +P GVV + PWNFP +IA+K++ AL + VVKPS +TP Sbjct: 131 PRGLSWTVYHRPAGVVGLMTPWNFPIGMIAKKLSAALAADCSCVVKPSRKTPLTMIALFD 190 Query: 190 LVAET-DLPRGVFNVVCG-AGQVGGALSSHPGVDLISFTGSVETGARIMAAAAPNLTKLN 247 L+ T DLP G N+V G A + L HP V +ISFTGS G +++ +A + +L Sbjct: 191 LLDRTLDLPPGKVNLVMGGACPITDTLMEHPHVRVISFTGSTAVGRQLIRKSADGIKRLT 250 Query: 248 LELGGKAPAIVLADADLELAVKAIRDSRIINSGQVCNCAERVYVQRQVAEPFIERIAAAM 307 LELGG AP IV ADADL+ A + + ++ GQ C C+ R++V+R VA F E++A Sbjct: 251 LELGGNAPFIVFADADLDHAAEQLVSNKFRGGGQTCVCSNRIFVERPVAPEFAEKLAEKA 310 Query: 308 AATRYGDPLAEPEVEMGPLINRLGLEKIDAKVRTALAQGATLVTGGAIAE--RPGHHYQP 365 +A R G+ + + ++GPLI+R G EK+ + + AL +GA +V+GG E ++P Sbjct: 311 SALRVGNGM-DRVTDIGPLIDRSGYEKVRSHLTDALDKGAQMVSGGDPGEWSTARGFFRP 369 Query: 366 TVLTGCRADTRIMREEIFGPVLPIQIVDDLDEAIALANDCEYGLTSSVFTRDLNKAMHAL 425 TV+ G + REE FGP++PI D +E IA AND E+GL + +FT D +A H + Sbjct: 370 TVIRGVAPGMLVTREETFGPLVPIAEFDSEEEVIARANDTEFGLAAYLFTADPERAGHVV 429 Query: 426 RELDFGETYINREHFEAMQGFHAGVRKSGIGGADGKHGLYEYTHTHVVYLQ 476 L+F N + G+++SG G G+ GL E+ T V Q Sbjct: 430 SRLEFAHVGWNTGSGPTPEAPFGGMKQSGFGREGGREGLVEFVETQTVAQQ 480 Lambda K H 0.320 0.136 0.395 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: 559 Number of extensions: 25 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: 477 Length of database: 481 Length adjustment: 34 Effective length of query: 443 Effective length of database: 447 Effective search space: 198021 Effective search space used: 198021 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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