Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_058858411.1 AS188_RS07995 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_001482365.1:WP_058858411.1 Length = 515 Score = 351 bits (900), Expect = e-101 Identities = 206/482 (42%), Positives = 278/482 (57%), Gaps = 18/482 (3%) Query: 40 FINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDAS 99 +I +W V + F ++P G+ +VA G ED+D A+ AA AA W + + Sbjct: 31 WIGGQWVPPVQGRYFENISPVNGKPFTEVARGTAEDIDAALDAAWAA---APAWGKTPVA 87 Query: 100 HRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHGK 159 R +L+R+AD +E++ LA ET DNGKP + D+ + + RY+AG G Sbjct: 88 ERALVLHRVADRMEQNLEMLAVAETWDNGKPVRETINADIALAIDHFRYFAGAIRAQEGT 147 Query: 160 TIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTAL 219 +D + SY HEP+GV GQIIPWNFP+LM WKL PALA GN VV+K AEQTP + + Sbjct: 148 LSQLDDNTTSYHFHEPLGVVGQIIPWNFPILMGVWKLAPALAAGNAVVLKPAEQTPASIM 207 Query: 220 YVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSSNL 279 + L+ + PPGVVN+V GFG AG +AS + K+AFTG T GR+I A S N+ Sbjct: 208 VLMELLADI-LPPGVVNVVNGFGVEAGKPLASSPRIRKIAFTGETTTGRLIMQYA-SQNI 265 Query: 280 KRVTLELGGKSPNIIMSD--ADMDWAVEQA--HFALF-FNQGQCCCAGSRTFVQEDIYDE 334 VTLELGGKSPNI D A D ++A FA F NQG+ C SR +Q IYD Sbjct: 266 IPVTLELGGKSPNIFFEDVAAAQDSFYDKALEGFAFFALNQGEVCTCPSRALIQGSIYDR 325 Query: 335 FVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGG------ 388 + V R K V GNP D T+ G Q Q +KIL YI+ G+QEGAK+L GG Sbjct: 326 LLADGVERVKGMVQGNPLDLDTQVGAQASNDQLQKILSYIDIGRQEGAKVLVGGERNVLD 385 Query: 389 GIAADRGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAV 448 G A+ G+++ PTVF + ++ M I +EEIFGPV+ + +F + + AN++ YGL A V Sbjct: 386 GDLAE-GFYVSPTVF-EGENSMRIFQEEIFGPVLSVTRFTDYADAMATANDTLYGLGAGV 443 Query: 449 FTKDLDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTV 508 + ++ + A + +QAG VWVN Y + A S FGGYK SG GRE L Y + K + Sbjct: 444 WARNGNLAYRAGRDIQAGRVWVNQYHNYPAHSAFGGYKSSGIGRENHLMMLDHYQQTKNL 503 Query: 509 TV 510 V Sbjct: 504 LV 505 Lambda K H 0.319 0.136 0.409 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: 641 Number of extensions: 29 Number of successful extensions: 6 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: 517 Length of database: 515 Length adjustment: 35 Effective length of query: 482 Effective length of database: 480 Effective search space: 231360 Effective search space used: 231360 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: 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