Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_054343560.1 Nant_RS20560 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_001305295.1:WP_054343560.1 Length = 489 Score = 581 bits (1498), Expect = e-170 Identities = 292/483 (60%), Positives = 357/483 (73%) Query: 2 TLWINGDWITGQGASRVKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAER 61 +L+ING W+ GQGA+ NP +GE +W G A+ AQV A +AAR+A WA +SF +R Sbjct: 4 SLFINGQWLAGQGAAFNSVNPATGEAIWSGQAANQAQVAAAVKAARSASADWANVSFEQR 63 Query: 62 HAVVERFAALLESNKAELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQRS 121 A V R+A L NK L IA ETGKP WE TE A+I KI ISIKA RTGE+ S Sbjct: 64 CAQVRRYAEQLSENKILLARTIAEETGKPFWETQTEAAAVIGKIEISIKAAIERTGERCS 123 Query: 122 EMPDGAASLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAVM 181 +MP A LRH+PHGV+A+FGPYNFP HLPNGHIVPA+LAGN++IFKPSELTP E ++ Sbjct: 124 DMPGAKAVLRHKPHGVVAIFGPYNFPAHLPNGHIVPAVLAGNSVIFKPSELTPKVAELMI 183 Query: 182 RLWQQAGLPPGVLNLVQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKILA 241 LW++AGLP GV+NLVQG +ETG AL+A D+DGL FTGS+ TG+ LH Q +G P KILA Sbjct: 184 SLWEKAGLPAGVINLVQGEKETGIALAANPDIDGLFFTGSSRTGHLLHEQFAGHPGKILA 243 Query: 242 LEMGGNNPLIIDEVADIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVAV 301 LEMGGNNPLIIDE++DI AAVH TIQSA++T+GQRCTCARRL + A GDAFL +L A Sbjct: 244 LEMGGNNPLIIDEISDIKAAVHETIQSAYITSGQRCTCARRLFVPLNATGDAFLEQLKAA 303 Query: 302 SQRLTPGNWDDEPQPFIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTPG 361 + ++ G DEP PF+G LISE AA +VT QQL MG LL L+AGT L++PG Sbjct: 304 ASQIQVGGQFDEPAPFMGSLISEAAADGMVTVQQQLLDMGATSLLRLEKLKAGTGLVSPG 363 Query: 362 IIEMTGVAGVPDEEVFGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLLE 421 +I++T V +PD+E FGPLL+V RY FD+AIR AN T+FGLS GL S E F+ Sbjct: 364 LIDVTAVKDMPDDEHFGPLLKVIRYSDFDDAIRQANATQFGLSAGLFSDNAEHFEHFYRH 423 Query: 422 ARAGIVNWNKPLTGAASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESDSLTLPATLN 481 RAGIVNWNK LTGA+S APFGGIGASGNHR SA+YAADYCA+P+A +E++ L+LP TL+ Sbjct: 424 IRAGIVNWNKQLTGASSAAPFGGIGASGNHRASAYYAADYCAYPVAGIEAEHLSLPDTLS 483 Query: 482 PGL 484 PGL Sbjct: 484 PGL 486 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: 790 Number of extensions: 27 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: 489 Length adjustment: 34 Effective length of query: 458 Effective length of database: 455 Effective search space: 208390 Effective search space used: 208390 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