Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_010891011.1 SARO_RS17045 aldehyde dehydrogenase family protein
Query= BRENDA::Q402C7 (499 letters) >NCBI__GCF_000013325.1:WP_010891011.1 Length = 501 Score = 909 bits (2349), Expect = 0.0 Identities = 449/501 (89%), Positives = 479/501 (95%), Gaps = 2/501 (0%) Query: 1 MATQLKSAENEYGIKPEYGHFIGGEWVSGDSGKTIDLINPATGAVLTKIQAGNAKDIQRA 60 MATQL+SAENEYGIK EYGH+IGGEW++GDSGKTIDL+NP+TG VLTKIQAGNAKDI+RA Sbjct: 1 MATQLRSAENEYGIKSEYGHYIGGEWIAGDSGKTIDLLNPSTGKVLTKIQAGNAKDIERA 60 Query: 61 VAAAKAAFPKWSESSPAERQEILIEVARRLKARHQHYATLETLNNGKPIRESMYFDMPQA 120 +AAAKAAFPKWS+S P ERQEILIEVARRLKARH HYATLETLNNGKP+RESMYFDMPQ Sbjct: 61 IAAAKAAFPKWSQSLPGERQEILIEVARRLKARHSHYATLETLNNGKPMRESMYFDMPQT 120 Query: 121 ISQFEVFAGAAYGLHGQTLDYPDAIGIVHREPLGVCAQIIPWNVPILMMACKIAPALASG 180 I QFE+FAGAAYGLHGQTLDYPDAIGIVHREPLGVCAQIIPWNVP+LMMACKIAPALASG Sbjct: 121 IGQFELFAGAAYGLHGQTLDYPDAIGIVHREPLGVCAQIIPWNVPMLMMACKIAPALASG 180 Query: 181 NTVVLKPAETVCLSVIEFFVEMADLLPPGVINVVTGYGADVGEALVTHEDVRKVAFTGSV 240 NTVVLKPAETVCLSVIEFFVEMADLLPPGVINVVTGYGADVGEALVT DV KVAFTGS+ Sbjct: 181 NTVVLKPAETVCLSVIEFFVEMADLLPPGVINVVTGYGADVGEALVTSPDVAKVAFTGSI 240 Query: 241 ATARRIIQYASSNIIPQTLELGGKSAHIVCADADIDAAVESATMSTVFNKGEVCLAGSRL 300 ATARRIIQYAS+NIIPQTLELGGKSAHIVC DADIDAAVESATMSTV NKGEVCLAGSRL Sbjct: 241 ATARRIIQYASANIIPQTLELGGKSAHIVCGDADIDAAVESATMSTVLNKGEVCLAGSRL 300 Query: 301 FLHQSIQDEFLAKFKVALEGIRQGDPLDFATQLGAQASQMQMDKVQSYLQLATEEGATVL 360 FLHQSIQDEFLAKFK ALEGIRQGDPLD ATQLGAQAS+MQ DKVQSYL+LATEEGA VL Sbjct: 301 FLHQSIQDEFLAKFKTALEGIRQGDPLDMATQLGAQASKMQFDKVQSYLRLATEEGAEVL 360 Query: 361 TGGSRNES--LADGHFIKPTVFTNVSNSMRIAREEIFGPVTSVLTWNDEDDMMALANDTT 418 TGGSR+++ LADG+FIKPTVFTNV+NSMRIA+EEIFGPVTSV+TW+DEDDMM AN+TT Sbjct: 361 TGGSRSDAADLADGNFIKPTVFTNVNNSMRIAQEEIFGPVTSVITWSDEDDMMKQANNTT 420 Query: 419 YGLAGGVWTRDISRAHRIARKLETGTVWVNRYYNLKPNMPLGGYKQSGFGREFSHEVLHH 478 YGLAGGVWT+DI+RAHRIARKLETGTVW+NRYYNLK NMPLGGYKQSGFGREFSHEVL+H Sbjct: 421 YGLAGGVWTKDIARAHRIARKLETGTVWINRYYNLKANMPLGGYKQSGFGREFSHEVLNH 480 Query: 479 YTQTKSVVINLQEGRVGMFDQ 499 YTQTKSVV+NLQEGR GMFDQ Sbjct: 481 YTQTKSVVVNLQEGRTGMFDQ 501 Lambda K H 0.318 0.133 0.390 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: 901 Number of extensions: 25 Number of successful extensions: 2 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: 499 Length of database: 501 Length adjustment: 34 Effective length of query: 465 Effective length of database: 467 Effective search space: 217155 Effective search space used: 217155 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