Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_043529624.1 JH15_RS09245 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_000759345.1:WP_043529624.1 Length = 489 Score = 555 bits (1429), Expect = e-162 Identities = 280/482 (58%), Positives = 345/482 (71%), Gaps = 1/482 (0%) Query: 3 LWINGDWITGQGASRVKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAERH 62 L I+G WI GQ K +PVSGE LW A A QVE A AAR AFP WAR +F+ R Sbjct: 7 LLIDGRWIDGQDEQFAKADPVSGEPLWTAAAASAEQVETAVAAARRAFPAWARSAFSGRQ 66 Query: 63 AVVERFAALLESNKAELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQRSE 122 A+VERF LE ++ L IA ETGKP WEA TEV AMI K+AIS +AYH RTG E Sbjct: 67 ALVERFRETLERHRENLAEAIAHETGKPLWEARTEVGAMIGKVAISTRAYHERTGTHERE 126 Query: 123 MPDGAASLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAVMR 182 D A LRHRPHGV+AVFGPYNFPGHLPNGHIVPALLAGNT++FKPSE TP + + M+ Sbjct: 127 AGDAKAVLRHRPHGVMAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSEQTPLTADLTMQ 186 Query: 183 LWQQAGLPPGVLNLVQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKILAL 242 W +AGLP GV+NLVQG GQALS +D+DGLLFTGSA G LH QL+GQ +KILAL Sbjct: 187 CWVEAGLPEGVINLVQGAAPVGQALSQAKDIDGLLFTGSAKVGGILHTQLAGQFDKILAL 246 Query: 243 EMGGNNPLIIDEVADIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVAVS 302 EMGGNN L++ +V D DAAV +QSAF++ GQRCTCARRL++ G GD + LV+ Sbjct: 247 EMGGNNALVVKDVPDEDAAVLTILQSAFLSGGQRCTCARRLMVPEGEVGDRLIDALVSAI 306 Query: 303 QRLTPGNWDDEPQPFIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTPGI 362 +RL DEP PF GGL+ +A ++ A LEA+GG L + L+ GT+LL+P + Sbjct: 307 ERLRIAPQFDEPAPFYGGLVGAASADGLLKAQADLEALGGTVLTRMQRLKEGTTLLSPAL 366 Query: 363 IEMTGVAGVPDEEVFGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLLEA 422 I++TG+ +PDEE FGPLL++ RY +DEAI +AN+TR+GLS GL+ ER +D LL Sbjct: 367 IDVTGLE-IPDEEHFGPLLKLQRYRDWDEAITLANDTRYGLSAGLIGGERGDWDDFLLRI 425 Query: 423 RAGIVNWNKPLTGAASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESDSLTLPATLNP 482 RAGIVNWN+ TGA+ APFGG+G SGNHRPSA+YAADYCA+P+AS+E+++L LP L P Sbjct: 426 RAGIVNWNRQTTGASGDAPFGGVGDSGNHRPSAYYAADYCAYPVASMEAEALVLPDNLPP 485 Query: 483 GL 484 G+ Sbjct: 486 GV 487 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: 783 Number of extensions: 38 Number of successful extensions: 2 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