Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_047093279.1 AAV99_RS06745 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_001013305.1:WP_047093279.1 Length = 472 Score = 427 bits (1098), Expect = e-124 Identities = 220/456 (48%), Positives = 304/456 (66%), Gaps = 5/456 (1%) Query: 18 VKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAERHAVVERFAALLESNKA 77 V P +G+ LW+G + V+ AR A+P+WA L A R ++ RF + + Sbjct: 8 VSFEPATGKELWRGAHGN---VDAIVARARRAWPKWAALPLANRIELMRRFVNEVRKDHD 64 Query: 78 ELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQRSEMP-DGAASLRHRPHG 136 E + +I+RETGKP WEA TEV A++ KI ISI+AY RTG+++ + G A+LRH+PHG Sbjct: 65 EFSELISRETGKPLWEARTEVEAVMAKIEISIRAYGERTGQRKLDSALQGIAALRHKPHG 124 Query: 137 VLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAVMRLWQQAGLPPGVLNL 196 V+AV GPYNFP HLPNGH++PAL+AGN +I KPSE TP G ++ L + G+P GV+ L Sbjct: 125 VMAVLGPYNFPAHLPNGHMIPALIAGNAVILKPSEKTPAVGAKLVELLNRCGIPEGVVQL 184 Query: 197 VQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKILALEMGGNNPLIIDEVA 256 + GG + G+AL A +D++G+LFTGSA G ++R+L+ P KILALEMGGNNP+I+ + Sbjct: 185 LIGGPDEGKALVAHDDVNGVLFTGSAQVGIAINRKLATDPGKILALEMGGNNPMIVWDTP 244 Query: 257 DIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVAVSQRLTPGNWDDEPQP 316 I A L +QSAF TAGQRCT ARRL++K+ + D +A ++ R G DEP P Sbjct: 245 KIADAAALIVQSAFTTAGQRCTAARRLIVKA-SMYDEVVAETKKLADRAIVGGPFDEPAP 303 Query: 317 FIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTPGIIEMTGVAGVPDEEV 376 F+G +I A Q+ ++ L + GG+ + R LQ ++P II+ T ++ PD E+ Sbjct: 304 FMGPVIDNATADQLTESFVYLLSNGGKAIKHMRRLQDDLPFVSPAIIDTTAMSDRPDVEL 363 Query: 377 FGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLLEARAGIVNWNKPLTGA 436 FGPLL+V + D FDEAI ANNTRFGLS LV +++++ RAGIVNWN+P GA Sbjct: 364 FGPLLQVIKVDDFDEAIAEANNTRFGLSASLVGGTPQQYNRFWANIRAGIVNWNRPTNGA 423 Query: 437 ASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESD 472 +S APFGG+G SGNHRP+A+YAADYCA+P+ S E + Sbjct: 424 SSAAPFGGVGYSGNHRPAAFYAADYCAYPVTSTEME 459 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: 646 Number of extensions: 25 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: 492 Length of database: 472 Length adjustment: 34 Effective length of query: 458 Effective length of database: 438 Effective search space: 200604 Effective search space used: 200604 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