Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate BWI76_RS12820 BWI76_RS12820 NAD-dependent phenylacetaldehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >FitnessBrowser__Koxy:BWI76_RS12820 Length = 499 Score = 365 bits (937), Expect = e-105 Identities = 190/476 (39%), Positives = 298/476 (62%), Gaps = 9/476 (1%) Query: 22 GLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHS-SWSTSDP 80 GL+++ ++S++ +P+T + I +A + D+D AV +A AF S SW+ P Sbjct: 21 GLYLDGTQQAAESEQRLTVWNPATGQAIASTADANAADVDRAVMSAWRAFVSRSWAGRTP 80 Query: 81 QVRMKVLYKLADLIDEHADTLAHIEALDNGKSLMCSKG-DVALTAAYFRSCAGWTDKIKG 139 R ++L + ADL+++H + LA +E L+ GKS+ S+ +V T + R AG T KI G Sbjct: 81 ADRERILLRFADLVEQHGEELAQLETLEQGKSINISRAFEVGCTLNWMRYTAGLTTKISG 140 Query: 140 SVIET------GDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAE 193 ++ G + +T++EP+GV I+PWNFPL++ WK+ P L GC+ V+K +E Sbjct: 141 RTLDVSIPFPAGGRYQAWTKKEPVGVVAGIVPWNFPLMIGMWKVMPALAAGCSIVIKPSE 200 Query: 194 STPLSALYLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMK 253 +TPL+ L +A L EAG P GV NVV+G G GA ++SHP + KV+FTGSTATG+ I + Sbjct: 201 TTPLTLLRVAELATEAGVPDGVFNVVTGSGAGCGAALTSHPLVAKVSFTGSTATGKQIAR 260 Query: 254 AAAESNLKKVTLELGGKSPNIVFDDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIY 313 AA+ L +VTLELGGK+P IV DAD + I+ L+TG F N G+VC A SRIY++ ++ Sbjct: 261 VAAD-RLTRVTLELGGKNPAIVLKDADPQWVIEGLMTGSFLNQGQVCAASSRIYIEAPLF 319 Query: 314 DKIVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERFG 373 D +VS F+ A +SL++G E + + SQ K+ Y+D +++ A +I+G Sbjct: 320 DTLVSGFEQAVKSLQVGPGMLESSQINPVVSQAHCAKVAAYLDEARQQKAELISGHAGPD 379 Query: 374 NKGYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHTTN 433 +GY+I PT+ + ++ R+E+FGPVV + + EE + LANDS++GL A V T + Sbjct: 380 AQGYYIAPTLVINPDAGLRLCREEVFGPVVNLVRVADGEEALLLANDSDFGLTASVWTRD 439 Query: 434 LSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAV 489 L+ A+S ++++ +GT+WVN++ +PFGG QSG GR+ G + LD++ + K+V Sbjct: 440 LTQALSYTDRLQAGTVWVNSHTLIDANLPFGGMKQSGTGRDFGPDWLDDWCETKSV 495 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: 564 Number of extensions: 25 Number of successful extensions: 4 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: 499 Length adjustment: 34 Effective length of query: 461 Effective length of database: 465 Effective search space: 214365 Effective search space used: 214365 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 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