Align N-succinylglutamate 5-semialdehyde dehydrogenase 1; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase 1; SGSD 1 (uncharacterized)
to candidate WP_057506719.1 ABB28_RS00370 aldehyde dehydrogenase family protein
Query= curated2:Q9AAL5 (472 letters) >NCBI__GCF_001431535.1:WP_057506719.1 Length = 510 Score = 162 bits (409), Expect = 3e-44 Identities = 138/456 (30%), Positives = 207/456 (45%), Gaps = 38/456 (8%) Query: 10 DPYTGEAIADFAVNDARSIDAACHSARAAFAEWAMTPLAERRAIALRFA-ETVRARREEI 68 +P TGEAIA A + A+ AF W TP A RR A+R E +RA ++ + Sbjct: 38 NPTTGEAIAQVRATTADEYETVIARAQEAFKIWRTTP-APRRGEAVRLCGEALRANKDAL 96 Query: 69 ATLIARETGKPMWEALTEADSVA---------AKVAISIRAQDERAGERSEPMADATARL 119 +L+A E GK E E + +++ ER G R Sbjct: 97 GSLVALEMGKSKPEGDGEVQEMIDIADFAVGQSRMLYGYTMHSERPGHRMYEQ------- 149 Query: 120 AHRPHGVLAVIGPFNFPMHLANGHIVPALLAGNAVVFKPSEKTP----ACGQLMGELWRA 175 ++P G++ +I FNFP+ + + A + G+ ++KPS KTP A ++ E R Sbjct: 150 -YQPLGLVGIISAFNFPVAVWAWNAFLATVCGDICLWKPSNKTPLTAIASMRICNEALRD 208 Query: 176 AGLPDHVLTIVIGGGEAGEALVRHEALDGVLFTGGVQAGRAIHRALADAPHKILALELGG 235 AG PD I G E +V + + + FTG Q GR + +A + L LELGG Sbjct: 209 AGFPDLFFLINDAGTALSETMVADKRVPLISFTGSTQVGRTVAEKVAHRLGRCL-LELGG 267 Query: 236 NAPLVVWDVADIEAAAHLIVQSAYVTAGQRCTCARRLILPEGARGD---ALLEALTMLMD 292 N +++ + AD++ A IV A TAGQRCT RRLI+ E D L++A + Sbjct: 268 NNAIILDETADLKLAIPGIVFGAVGTAGQRCTTTRRLIVHESIHDDVLATLVKAYKQVEG 327 Query: 293 RLVIGGPFQSPAPFMGPVIDAHAAAQVLAAQDRMTADGGRPLRLAAVREARSALLSPGLI 352 + IG P PA MGP+ A Q LA+ ++ A GG + + P ++ Sbjct: 328 K--IGDP-TDPANLMGPLNSDGAVQQFLASIEKAKASGGTVQTGGTRIDRAGNFVLPAIV 384 Query: 353 ELTDAPLRDE----EIFGPLLQVRRAADFDAALALANATRFGLAAGLISDDEALYRRFWT 408 T DE E F P+L V + + D A+ + N GL++ + + + RF + Sbjct: 385 --TGLKNSDEVVQHETFAPILYVMKYSTLDEAIDMQNGVPQGLSSSIFTTNLKTAERFLS 442 Query: 409 SVRA--GIVNWNRPTTGASSAAPFGGVGGSGNHRPS 442 + + GI N N T+GA FGG +G R S Sbjct: 443 AAGSDCGIANVNIGTSGAEIGGAFGGEKDTGGGRES 478 Lambda K H 0.320 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: 606 Number of extensions: 25 Number of successful extensions: 7 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: 472 Length of database: 510 Length adjustment: 34 Effective length of query: 438 Effective length of database: 476 Effective search space: 208488 Effective search space used: 208488 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 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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