Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_043527627.1 JH15_RS05155 aldehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000759345.1:WP_043527627.1 Length = 506 Score = 343 bits (879), Expect = 1e-98 Identities = 197/485 (40%), Positives = 285/485 (58%), Gaps = 19/485 (3%) Query: 16 TYEQPTGLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSW 75 ++E+ G +I EFV + F VSP E ++ + +EDID A++AA A +W Sbjct: 14 SFEKRYGNYIGGEFVAPVKGQYFDNVSPVNGEVFCEIPRSTAEDIDMALDAAHKAA-PAW 72 Query: 76 STSDPQVRMKVLYKLADLIDEHADTLAHIEALDNGKSLMCS-KGDVALTAAYFRSCAGWT 134 + R VL ++AD I+++ + LA E DNGK++ + D+ L +FR AG Sbjct: 73 GKTSAAERSNVLLRIADRIEQNLEMLAVAETWDNGKAVRETLNADLPLAVDHFRYFAGCI 132 Query: 135 DKIKGSVIETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAES 194 +G+ + Y EP+GV GQIIPWNFPLLMA+WKL P L G VLK AE Sbjct: 133 RAQEGTAADIDANTVAYHFHEPLGVVGQIIPWNFPLLMATWKLAPALAAGNCVVLKPAEQ 192 Query: 195 TPLSALYLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKA 254 TP S L L LI + P GVVNVV+G+G AG +++ +I K+AFTGST G HI+K Sbjct: 193 TPASILVLMQLIGDL-LPSGVVNVVNGYGVEAGQALATSKRIAKIAFTGSTPVGAHILKC 251 Query: 255 AAESNLKKVTLELGGKSPNIVFDDADVKST----IQHLVTGI---FYNTGEVCCAGSRIY 307 AAE N+ T+ELGGKSPNI F AD+ + I G+ F+N GEVC SR Sbjct: 252 AAE-NIIPSTVELGGKSPNIYF--ADIMNAEPEFIDKAAEGLVLAFFNQGEVCTCPSRAL 308 Query: 308 VQEGIYDKIVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVIT 367 +QE +YD ++ + ++K G+P D +GAQ SQ Q DKI+ Y+ I + EGA +T Sbjct: 309 IQESMYDAFMARVMDRVGTIKRGNPLDTDVQVGAQASQEQYDKIMSYMQIARDEGAEFLT 368 Query: 368 GGERFG-----NKGYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSE 422 GG++ +KG++I+PT+ + ++ ++EIFGPVV +T FK E +A+AND+E Sbjct: 369 GGDKESFDPAYDKGFYIQPTLLKGHNK-MRVFQEEIFGPVVAVTTFKDEAEALAIANDTE 427 Query: 423 YGLAAGVHTTNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDN 482 +GL AGV + +++ A + I +G +W N Y+ + FGGY +SG+GRE + AL++ Sbjct: 428 FGLGAGVWSRDINVAFRMGRGIQAGRVWTNCYHQYPAHAAFGGYKKSGVGRETHKVALEH 487 Query: 483 YTQVK 487 Y Q K Sbjct: 488 YQQTK 492 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: 620 Number of extensions: 29 Number of successful extensions: 7 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: 506 Length adjustment: 34 Effective length of query: 461 Effective length of database: 472 Effective search space: 217592 Effective search space used: 217592 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