Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_090272859.1 BLU11_RS08070 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_900105005.1:WP_090272859.1 Length = 486 Score = 514 bits (1325), Expect = e-150 Identities = 261/478 (54%), Positives = 342/478 (71%), Gaps = 6/478 (1%) Query: 46 LLRGDSFVGGRWLPTPA--TFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 L R +V G+W + T V +PA+G LG V E AAV AA A W++ Sbjct: 11 LFRQQCYVNGQWQNASSGETLAVDNPANGDVLGHVPVLSAAEVGAAVDAASSALRQWRKR 70 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + +ER+ L W+DLM+++K++LA ++T E GKPL E+QGEI Y+A F+ WF+EEARR+Y Sbjct: 71 TAQERADCLLAWHDLMLEHKEDLATLMTLEQGKPLVESQGEIDYAASFIRWFAEEARRMY 130 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 G+ I + + +V +QPVGV + ITPWNFP+AMITRK GAALAAGCT++VKPA TP+ Sbjct: 131 GETIPGARIGQHIVVTRQPVGVCAAITPWNFPAAMITRKAGAALAAGCTIIVKPASATPF 190 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 SALALA LA +AGIP GV+NV+ KA E+ EVL P+V K+SFTGST G+ L+ Sbjct: 191 SALALAVLAEEAGIPHGVFNVV---TGKAGEISEVLTRSPVVRKLSFTGSTDVGRRLMAQ 247 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 + +++VS+ELGG APFIVFD A++ +AV GAM KFRN GQTCVC+NRFLVQ G+HD Sbjct: 248 CSEHIQKVSLELGGNAPFIVFDDADISRAVEGAMVCKFRNTGQTCVCANRFLVQSGVHDK 307 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 FV AEAM K LR+G+GFE G TQ LIN AVEKV +H +DA+AKGA V G Sbjct: 308 FVAALAEAMGK-LRIGDGFEPGVTQSALINGDAVEKVIEHFDDAMAKGAKRVCGPAPDAD 366 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GN+ +P LL+++ +M EETFGP+A V++FD EEEA+ +ANA GLA YFYS+D Sbjct: 367 RGNYVQPVLLTDINTNMTLCHEETFGPLAAVLRFDTEEEAIELANATPFGLAAYFYSRDI 426 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVCYG 521 ++WRVA+ LE G++G+NEGLIS+ PFGGVK+SGLGREGS++G+DEY E+KY+C G Sbjct: 427 HRVWRVADALEAGIIGINEGLISNPMAPFGGVKESGLGREGSRHGLDEYTELKYLCMG 484 Lambda K H 0.318 0.135 0.400 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: 633 Number of extensions: 20 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: 523 Length of database: 486 Length adjustment: 34 Effective length of query: 489 Effective length of database: 452 Effective search space: 221028 Effective search space used: 221028 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 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