Align NAD+-dependent L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_012066669.1 SMED_RS12210 aldehyde dehydrogenase
Query= metacyc::MONOMER-16246 (477 letters) >NCBI__GCF_000017145.1:WP_012066669.1 Length = 478 Score = 588 bits (1515), Expect = e-172 Identities = 298/471 (63%), Positives = 358/471 (76%), Gaps = 4/471 (0%) Query: 10 NYIDGAFVES--AAHLEVFNPANGALLSRVPAASAEEVERALAAARAAQKDWARKPAIER 67 +YIDG FVE + + V+NPA+ ++ +P AE V+ A+ AAR AQ W+ P IER Sbjct: 6 HYIDGRFVEDRISGRIAVYNPASEEQIAEIPDGPAEVVDAAVDAARKAQPAWSELPPIER 65 Query: 68 AGHLRRIAAKIRADAGRIARTITLEQGKIASLAEVEVNFTADYLDYMAEWARRLEGEIIA 127 AG+++ IA KIRA +A TI+ EQGK+ SLA EV A +DYMAEWARR+EGEIIA Sbjct: 66 AGYVKAIAEKIRAKVDILAETISREQGKVVSLARGEVLGMAGLMDYMAEWARRIEGEIIA 125 Query: 128 SDRPGENIFLFRKPLGVVAGILPWNFPFFLIARKMAPALLTGNTIVVKPSEETPNNCFEF 187 SDR GE I+L R P+GVVAGILPWNFPF+LI RK+APAL+ GNTIV+KPSEETP N F F Sbjct: 126 SDRKGETIYLNRVPIGVVAGILPWNFPFYLIGRKLAPALVAGNTIVIKPSEETPLNAFLF 185 Query: 188 ARLVAETDLPRGVFNVVCGAGQ-VGGALSSHPGVDLISFTGSVETGARIMAAAAPNLTKL 246 A L E LP+GVFN+V G G+ G ALS HPG+DL+SFTGSV TG IM AAA NLT++ Sbjct: 186 AELADEVGLPKGVFNMVSGRGRTTGAALSGHPGIDLVSFTGSVPTGVAIMEAAAKNLTRV 245 Query: 247 NLELGGKAPAIVLADADLELAVKAIRDSRIINSGQVCNCAERVYVQRQVAEPFIERIAAA 306 NLELGGKAPAIVL DADL+LAV+AI SR+IN+GQVCNCAER++V+RQVA+ F +R Sbjct: 246 NLELGGKAPAIVLKDADLDLAVEAITASRVINTGQVCNCAERIFVERQVADEFTDRFVKR 305 Query: 307 MAATRYGDPLAEPEVEMGPLINRLGLEKIDAKVRTALAQGATLVTGGAIAERP-GHHYQP 365 MAA YGDP+AEP V+MGPL+N L L+K++A V A GA++ GG AER GHHY+P Sbjct: 306 MAAVTYGDPIAEPTVDMGPLVNALQLDKVEAMVERAREAGASVALGGKRAERNCGHHYEP 365 Query: 366 TVLTGCRADTRIMREEIFGPVLPIQIVDDLDEAIALANDCEYGLTSSVFTRDLNKAMHAL 425 TVLTGC D IMR+EIFGPV PI +V+D DEA+ AND EYGLTSS++T+DLNKAM Sbjct: 366 TVLTGCTPDMEIMRKEIFGPVAPIAVVEDADEAVHYANDTEYGLTSSLYTQDLNKAMRVT 425 Query: 426 RELDFGETYINREHFEAMQGFHAGVRKSGIGGADGKHGLYEYTHTHVVYLQ 476 R L FGETYINRE+ EA QGFHAG +KSGIGGADGKHG YEY T VY+Q Sbjct: 426 RRLQFGETYINRENGEAYQGFHAGRKKSGIGGADGKHGFYEYMETQAVYIQ 476 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: 652 Number of extensions: 26 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: 477 Length of database: 478 Length adjustment: 34 Effective length of query: 443 Effective length of database: 444 Effective search space: 196692 Effective search space used: 196692 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