Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate BPHYT_RS29875 BPHYT_RS29875 betaine-aldehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >FitnessBrowser__BFirm:BPHYT_RS29875 Length = 483 Score = 390 bits (1003), Expect = e-113 Identities = 190/456 (41%), Positives = 287/456 (62%), Gaps = 3/456 (0%) Query: 41 VSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQVRMKVLYKLADLIDEHADT 100 ++P+TEE I V + + D+D AV AA AA W+ R ++L +LA L+ + + Sbjct: 30 INPATEEPIALVAQGSAADVDTAVRAARAAL-KVWNGIRTAERARILMRLAGLMRANLEE 88 Query: 101 LAHIEALDNGKSLMC-SKGDVALTAAYFRSCAGWTDKIKGSVIETGDTHFNYTRREPIGV 159 LA +E+LD GK + + D+ AGW DKI G V+ YT REP+GV Sbjct: 89 LAALESLDAGKPIAAVMRQDIPAAIDTLEYYAGWCDKINGQVVPVRPDALTYTLREPVGV 148 Query: 160 CGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSALYLASLIKEAGAPPGVVNVV 219 I+PWNFPL++ WK+ P L GCT ++K AE TPL+AL + L EAG PPGV+N+V Sbjct: 149 VAAIVPWNFPLMIGMWKIAPALACGCTLIVKPAEITPLTALRIGELALEAGVPPGVLNIV 208 Query: 220 SGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNLKKVTLELGGKSPNIVFDDA 279 +G G G + +HP + KV FTGS + GR I++ AA N K+VTLELGGKS N++F DA Sbjct: 209 TGKGRVVGDALVAHPGVDKVTFTGSPSVGRGILQGAA-GNFKRVTLELGGKSANLIFPDA 267 Query: 280 DVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKIVSEFKNAAESLKIGDPFKEDTFM 339 ++ + ++ +GIF+NTG+VC AGSRI +YD++V A+S+K+GDP +T M Sbjct: 268 NLDNAVRAAASGIFFNTGQVCSAGSRILAHRDVYDEVVERLAARAKSIKVGDPSSRETSM 327 Query: 340 GAQTSQLQLDKILKYIDIGKKEGATVITGGERFGNKGYFIKPTIFGDVKEDHQIVRDEIF 399 G S Q+ +L Y++ G+ EGA+++TGG R G +G+F++PT+F +V+ + +I ++EIF Sbjct: 328 GPLISAAQMKTVLGYVETGRAEGASLVTGGARVGERGFFVEPTVFANVEHEMRISQEEIF 387 Query: 400 GPVVTITKFKTVEEVIALANDSEYGLAAGVHTTNLSTAISVSNKINSGTIWVNTYNDFHP 459 GPV ++ +F + I +AN + Y LAAGV + ++ V+ + +GT+W+NTY Sbjct: 388 GPVASVIRFNDEADAIRIANGTLYSLAAGVWSADIGRVHRVARDLRAGTVWINTYGYTDV 447 Query: 460 MVPFGGYSQSGIGREMGEEALDNYTQVKAVRIGLSQ 495 +P+GG SG GRE G+ A++N+T+ KAV + + Q Sbjct: 448 RLPWGGSGDSGFGREHGDVAIENFTEPKAVWLAIDQ 483 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: 595 Number of extensions: 24 Number of successful extensions: 3 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: 483 Length adjustment: 34 Effective length of query: 461 Effective length of database: 449 Effective search space: 206989 Effective search space used: 206989 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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