Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_058931030.1 AU252_RS12650 aldehyde dehydrogenase family protein
Query= BRENDA::Q4F895 (507 letters) >NCBI__GCF_001484605.1:WP_058931030.1 Length = 507 Score = 779 bits (2012), Expect = 0.0 Identities = 375/507 (73%), Positives = 427/507 (84%) Query: 1 MTVYARPGTADAIMSFQSRYDNWIGNEWVAPVKGQYFENPTPVTGQNFCDVARSTAEDIE 60 MTVY +PG + + + F+ RY+NWIG EWVAP GQY EN +PV G+ F +VAR A D+E Sbjct: 1 MTVYVQPGQSGSKVQFKDRYENWIGGEWVAPTTGQYIENVSPVNGKQFTEVARGAAADVE 60 Query: 61 LALDAAHAAAPAWGKTSVAERAIILNKIADRMEENLESIALAESWDNGKPIRETLNADIP 120 LALDAAH AAPAWGK S ERA +LNKIADR++ NLE +A+AESWDNGKPIRETLNADIP Sbjct: 61 LALDAAHKAAPAWGKASATERAAVLNKIADRIDANLEMLAVAESWDNGKPIRETLNADIP 120 Query: 121 LAIDHFRYFAGAIRAQEGSLSEINSDTVAYHFHEPLGVVGQIIPWNFPILMAVWKLAPAL 180 LA DHFRYFA AIRAQEG LS+++ DT AYHFHEPLGVVGQIIPWNFPILMAVWK+APAL Sbjct: 121 LAADHFRYFASAIRAQEGRLSQLDDDTTAYHFHEPLGVVGQIIPWNFPILMAVWKMAPAL 180 Query: 181 AAGNAIVLKPAEQTPVSILHLIGIIGDLLPAGVLNIVNGFGVEAGKPLASSPRIKKIAFT 240 AAGNA+VLKPA TP SIL L +I DLLPAG+LNIVNGFG E GKPLASSPRI+KIAFT Sbjct: 181 AAGNAVVLKPASNTPASILVLAELIADLLPAGLLNIVNGFGAEVGKPLASSPRIRKIAFT 240 Query: 241 GETTTGRLIMQYASQNLIPVTLELGGKSPNIFFSDVLASNDDYQDKALEGFTMFALNQGE 300 GET+TGRLI QYASQNLIPVTLELGGKSPNIFF+DV SND + DKALEGFT++A NQGE Sbjct: 241 GETSTGRLISQYASQNLIPVTLELGGKSPNIFFNDVAESNDAFYDKALEGFTLYAFNQGE 300 Query: 301 VCTCPSRSLIQEDIFDEFLAMAAIRTKAVRQGDPLDTDTMIGAQASNDQLEKILSYIEIG 360 VC+ PSR+L+Q+ I+D F+A A RT+ + QG+PLDT+T IGAQAS Q+EKILSYI+IG Sbjct: 301 VCSSPSRALVQDGIYDSFMADAVARTEQIIQGNPLDTNTQIGAQASVGQMEKILSYIDIG 360 Query: 361 KAEGAKVITGGERAELGGDLSGGYYVQPTVFTGNNKMRIFQEEIFGPVVSVTSFKDYDEA 420 EGA +++GG R EL GDL+GGYYVQPT+F G N MRIFQEEIFGPVVSV F DY +A Sbjct: 361 LEEGATILSGGARTELDGDLAGGYYVQPTIFEGQNSMRIFQEEIFGPVVSVARFGDYKDA 420 Query: 421 IEIANDTLYGLGAGVWSRDGGVAYRAGRDIQAGRVWTNTYHQYPAHAAFGGYKQSGIGRE 480 + IANDTLYGLGAGVWSR+G VAYRAGR+IQAGRVW N YH YPA AAFGGYK SGIGRE Sbjct: 421 VSIANDTLYGLGAGVWSRNGNVAYRAGREIQAGRVWVNNYHAYPAGAAFGGYKSSGIGRE 480 Query: 481 NHLMMLSHYQQTKNLLVSYAQKAQGFF 507 NH MML HYQQTKNLLVS+++ GFF Sbjct: 481 NHSMMLDHYQQTKNLLVSHSENKLGFF 507 Lambda K H 0.318 0.135 0.401 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: 838 Number of extensions: 20 Number of successful extensions: 1 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: 507 Length of database: 507 Length adjustment: 34 Effective length of query: 473 Effective length of database: 473 Effective search space: 223729 Effective search space used: 223729 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 (21.7 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