Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_090447414.1 BLS63_RS19270 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_900100495.1:WP_090447414.1 Length = 487 Score = 602 bits (1553), Expect = e-177 Identities = 302/483 (62%), Positives = 370/483 (76%) Query: 2 TLWINGDWITGQGASRVKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAER 61 T +I G+W GQG + NPVS +VLWQG A A QVE A +AARAAFP WA S R Sbjct: 3 THYIAGNWHLGQGEALESLNPVSQQVLWQGRGATAEQVEAAVQAARAAFPAWAAHSLDGR 62 Query: 62 HAVVERFAALLESNKAELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQRS 121 AV+ERFAA L+++ EL I ETGKP WE+ATEVT+M+NK+ ISI++Y RTGE+ Sbjct: 63 IAVLERFAASLKAHADELARAIGEETGKPLWESATEVTSMVNKVTISIQSYRERTGEKSG 122 Query: 122 EMPDGAASLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAVM 181 + D A LRH+PHGV+AVFGPYNFPGHLPNGHIVPALLAGN ++FKPSELTP E + Sbjct: 123 PLGDATAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNAVVFKPSELTPKVAELTV 182 Query: 182 RLWQQAGLPPGVLNLVQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKILA 241 + W +AGLP GVLNLVQG RETG AL+ +DGL FTGS+ TG LH Q +G+PEKILA Sbjct: 183 KCWIEAGLPAGVLNLVQGARETGVALAGNPGIDGLFFTGSSRTGNLLHNQFAGRPEKILA 242 Query: 242 LEMGGNNPLIIDEVADIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVAV 301 LEMGGNNPLI+D+VAD+DAAV+ +QSAF++AGQRCTCARRLL+ GA GDA LARLV V Sbjct: 243 LEMGGNNPLIVDQVADLDAAVYTIVQSAFISAGQRCTCARRLLVPQGAWGDALLARLVQV 302 Query: 302 SQRLTPGNWDDEPQPFIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTPG 361 + ++ G +D++P PF+G +IS AA+ ++ A QQL A G + LL Q G +LLTPG Sbjct: 303 AGQIRVGRYDEQPAPFMGSVISLGAAEHLLKAQQQLIAQGAQVLLEMTQPQPGAALLTPG 362 Query: 362 IIEMTGVAGVPDEEVFGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLLE 421 II++T V PDEE FGPLL+V RY FD AI ANNT+FGL+ GL+S + +++Q L Sbjct: 363 IIDVTAVGERPDEEFFGPLLQVIRYADFDAAILEANNTQFGLAAGLLSDSKARYEQFWLH 422 Query: 422 ARAGIVNWNKPLTGAASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESDSLTLPATLN 481 +RAGIVNWNK LTGAAS+APFGGIGASGNHR SA+YAADYCA+P+ASLES+SL+LPATL Sbjct: 423 SRAGIVNWNKQLTGAASSAPFGGIGASGNHRASAYYAADYCAYPVASLESESLSLPATLT 482 Query: 482 PGL 484 PG+ Sbjct: 483 PGV 485 Lambda K H 0.318 0.134 0.412 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: 847 Number of extensions: 40 Number of successful extensions: 1 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: 492 Length of database: 487 Length adjustment: 34 Effective length of query: 458 Effective length of database: 453 Effective search space: 207474 Effective search space used: 207474 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 (21.7 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