Align Putative aldehyde dehydrogenase AldA; EC 1.2.1.3 (uncharacterized)
to candidate WP_095511359.1 BSZ37_RS15140 aldehyde dehydrogenase family protein
Query= curated2:Q2YV11 (495 letters) >NCBI__GCF_002283365.1:WP_095511359.1 Length = 497 Score = 329 bits (844), Expect = 1e-94 Identities = 192/482 (39%), Positives = 282/482 (58%), Gaps = 7/482 (1%) Query: 16 FINGEFVKGSSDETIEVTNPA-TGETLSHITRAKDKDVDHAVEVAQEAFESWSLTSKSER 74 FI GE+V +S +T E NPA T + + + DV AVE A+EAF++W L +R Sbjct: 9 FIGGEWVAAASGDTFESRNPADTTDVIGSFPSSTADDVARAVEAAKEAFKTWRLVPAPKR 68 Query: 75 AQMLRDIGDKLMAQKDKIAMIETLNNGKPIRETTAIDIPFAARHFHYFASVIETEEG-TV 133 ++L+ +GD + +K +IA T GKP ET D+ A +Y ++ G TV Sbjct: 69 GEILKRVGDLMTERKSEIARAMTREMGKPFFETKG-DVQEAIDTAYYAMTMGRQLFGHTV 127 Query: 134 NDIDKDTMSIVRHEPIGVVGAVVAWNFPMLLAAWKIAPAIAAGNTIVIQPSSSTPLSLLE 193 + ++ PIGV G + AWNFP+ + WK+ PAI +GNT+V +PS P S Sbjct: 128 PSEMNNKFNMTVRRPIGVCGLITAWNFPVAVPTWKMFPAILSGNTVVFKPSEDAPHSGAL 187 Query: 194 VAKIFQEV-LPKGVVNILTGKGSESGNAIFNHDGVDKLSFTGSTDVGYQVAEAAAKHLVP 252 + ++ ++ +P GVVN++ G G E+G AI +H+ V +SFTGS++ G +A +AAK Sbjct: 188 LVQVLEDAGVPAGVVNLVQGAG-ETGQAIVDHEDVAAISFTGSSETGAGIASSAAKRHAR 246 Query: 253 ATLELGGKSANIILDDANLDLAVEGIQLGILFNQGEVCSAGSRLLVHEKIYDQLVPRLQE 312 +LE+GGK+ I+++DA+LDLA+EG+ G G+ C+A SRL+VHE ++D+LV R++ Sbjct: 247 VSLEMGGKNPAIVMEDADLDLAMEGMIWGAYGTTGQRCTATSRLIVHEDVHDELVERVKA 306 Query: 313 AFSNIKVGDPQDEATQMGSQTGKDQLDKIQSYIDVAKESDAQILAGGHRLTENGLDKGFF 372 S +++G D+ T MG + LDK+ SY+DVA+E A I GG R T +GLD GFF Sbjct: 307 KASELRLGYGNDDDTDMGPLINQKALDKVTSYMDVAREDGATIAMGGERATGDGLDDGFF 366 Query: 373 FEPTLIAVPDNHHKLAQEEIFGPVLTVIKVKDDQEAIDIANDSKYGLAGGVFSQNITRAL 432 F+PTL ++A+EEIFGPVL+VIKV EAI++AND YGL+ V++ +I RA Sbjct: 367 FQPTLFTGVTRDMRVAREEIFGPVLSVIKVTSFDEAIEVANDVAYGLSSAVYTSDIARAF 426 Query: 433 NIAKAVRTGRIWINTYNQVPEG-APFGGYKKSGIG-RETYKGALSNYQQVKNIYIDTSNA 490 + + G +IN E FGG K +G G RE Y + K YID S Sbjct: 427 RALRDIDAGITYINGPTIGAEAHMSFGGVKATGNGHREGGWEVYDFYTETKTCYIDFSGG 486 Query: 491 LK 492 L+ Sbjct: 487 LQ 488 Lambda K H 0.315 0.133 0.377 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: 586 Number of extensions: 27 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: 495 Length of database: 497 Length adjustment: 34 Effective length of query: 461 Effective length of database: 463 Effective search space: 213443 Effective search space used: 213443 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: 42 (22.0 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