Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_101588603.1 BJEO58_RS06110 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_900169175.1:WP_101588603.1 Length = 488 Score = 327 bits (839), Expect = 4e-94 Identities = 180/473 (38%), Positives = 272/473 (57%), Gaps = 4/473 (0%) Query: 21 TGLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDP 80 TGLFIN ++ ++ +T +P+ IT + +A D DA+ AA A + W+ + P Sbjct: 12 TGLFINGQWRDAEGDRTLEVRNPANGSVITTIADASEADALDAINAARDA-QAGWAATAP 70 Query: 81 QVRMKVLYKLADLIDEHADTLAHIEALDNGKSLMCSKGDVALTAAYFRSCAGWTDKIKGS 140 + R ++L + DL+ E AD +A I + GK L SKG+VA A +FR + ++ G Sbjct: 71 RERAEILRRAFDLLHERADDIAAIMTAEMGKPLAESKGEVAYGAEFFRWFSEEAVRVGGD 130 Query: 141 VIETGDTHFNYT-RREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSA 199 +++ D +EP+G C I PWNFPL M + K+GP + GCT VLK A+ TPL++ Sbjct: 131 FVQSTDGKNRLMISKEPVGPCVLITPWNFPLAMGTRKIGPAIAAGCTMVLKPAQLTPLTS 190 Query: 200 LYLASLIKEAGAPPGVVNVV-SGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAES 258 L +++AG P GV+NVV S P +K++FTGST G ++MK AA+S Sbjct: 191 FMLVEALRDAGLPDGVLNVVTSSSARRVVTPWMESGIARKISFTGSTEVGVNLMKQAADS 250 Query: 259 NLKKVTLELGGKSPNIVFDDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKIVS 318 + K ++ELGG +P +V DDADV + ++ V N GE C A +RIYVQ+ + ++ Sbjct: 251 -VMKTSMELGGNAPFLVMDDADVDAAVEGAVLAKMRNNGEACTAANRIYVQKPVAEEFSR 309 Query: 319 EFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERFGNKGYF 378 + S+K+GD + T +G Q QLDK+ + +D GATV+TGG++ GYF Sbjct: 310 KLAERIGSMKVGDGLADGTQVGPLVDQDQLDKVAELVDQAVGAGATVLTGGQKVDGDGYF 369 Query: 379 IKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHTTNLSTAI 438 PT+ D+ E+ + +EIFGPV I F+T +E I LAN +EYGLA+ + T+L ++ Sbjct: 370 FAPTVLTDIPENATLRVEEIFGPVAPIVTFETDDEAIELANGTEYGLASYLFCTDLERSL 429 Query: 439 SVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRI 491 +S +I SG + +NT +P PFGG SG+GRE G +D Y + K V + Sbjct: 430 GLSERIESGMVGLNTGLVSNPAAPFGGVKHSGLGREGGTSGIDEYLETKYVAV 482 Lambda K H 0.316 0.133 0.389 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: 567 Number of extensions: 26 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: 495 Length of database: 488 Length adjustment: 34 Effective length of query: 461 Effective length of database: 454 Effective search space: 209294 Effective search space used: 209294 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 (21.6 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