Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_055437407.1 ASC41_RS13180 aldehyde dehydrogenase
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_001418085.1:WP_055437407.1 Length = 500 Score = 348 bits (892), Expect = e-100 Identities = 201/496 (40%), Positives = 298/496 (60%), Gaps = 20/496 (4%) Query: 11 FIDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDWSAAS 70 FI G++ P+ + N++P + +T+ED+DLA+DAA A WS +S Sbjct: 16 FIGGKFVDPVKGQYFDNVSPVDGKVFTQAARSTQEDIDLALDAAHEAFPA-----WSTSS 70 Query: 71 GSLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEA-LADLDDVVACFEYYAGLAEELD 129 + R+ L IA +++ + L LE+ID GKP+ E+ AD+ + F Y+AG+ Sbjct: 71 ATERSNMLLKIAQVMEDNFEYLATLETIDNGKPIRESRAADIPYCIDHFRYFAGVIRA-- 128 Query: 130 SKQKAPISLPMDTFKSYILKEPIGVVALITPWNYPFLMATWKIAPALAAGCAAILKPSEL 189 + IS S +L EP+GVV I PWN+P LM WKIAPALAAGC A++KP+E Sbjct: 129 --DEGSISEHDKDTVSIVLHEPVGVVGEIIPWNFPMLMLAWKIAPALAAGCTAVVKPAEQ 186 Query: 190 ASVTCLELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGSKIMTT 249 + + L E+ ++ LP GVLNIVTG G EAGA+LA+ + K+SFTGS+ TG K++ Sbjct: 187 TPTSVIMLMELIGDI-LPAGVLNIVTGFGAEAGAALATSKRIAKLSFTGSTETGRKVLHN 245 Query: 250 AAQLVKPVSLELGGKSPIVVFEDV---DLDKVAEWTVFGCFFT--NGQICSATSRLIVHE 304 AA+ + PV++ELGGKSP V F V D D ++ F+ G+IC+A SR++VHE Sbjct: 246 AAENIIPVTMELGGKSPNVFFPSVADHDDDFFSKAIEGALMFSLNQGEICTAPSRILVHE 305 Query: 305 SIAVEFVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGGR 364 IA F++K+ + IK +PL+ +G VS+ QY K+L+ I K EGA ++ GG Sbjct: 306 DIADLFIEKMKVRLKAIKTGNPLDPETMIGSQVSKPQYDKILDYIKIGKDEGAEVVAGGD 365 Query: 365 RPEH---LKKGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTEEEAINLANDTHYGL 421 + L +GY+++PT++ M+I++EE+FGPV+A+ TFS+ EEAI +ANDT YGL Sbjct: 366 AGNYEGELSEGYYIQPTVLKG-NNKMRIFQEEIFGPVVALTTFSSTEEAIAIANDTPYGL 424 Query: 422 GSAVMSNDLERCERLSKALQAGIVWINCAQPSFIQAPWGGIKRSGFGRELGEWGLENYLS 481 G+ V S D ++ +A+QAG VW+N AP+GG+K SGFGRE + L++Y Sbjct: 425 GAGVWSRDAHELYQVPRAIQAGRVWVNQYHTYPAHAPFGGVKESGFGRENHKMALDHYRV 484 Query: 482 VKQVTRYTSDEPWGWY 497 VK + +P G++ Sbjct: 485 VKNMLISYDKKPMGFF 500 Lambda K H 0.317 0.134 0.402 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: 597 Number of extensions: 27 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: 503 Length of database: 500 Length adjustment: 34 Effective length of query: 469 Effective length of database: 466 Effective search space: 218554 Effective search space used: 218554 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