Align N-succinylglutamate 5-semialdehyde dehydrogenase 1; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase 1; SGSD 1 (uncharacterized)
to candidate WP_036260778.1 DL86_RS09925 aldehyde dehydrogenase family protein
Query= curated2:Q9AAL5 (472 letters) >NCBI__GCF_000746085.1:WP_036260778.1 Length = 500 Score = 184 bits (467), Expect = 6e-51 Identities = 150/452 (33%), Positives = 210/452 (46%), Gaps = 17/452 (3%) Query: 2 SASRLISRDPYTGEAIADFAVNDARSIDAACHSARAAFAEWAMTPLAERRAIALRFAETV 61 S L SR P G + + AA A AF W P R + F + + Sbjct: 17 SVGALASRCPIDGSELGRAGEYSPPDVSAAIGRAHEAFLRWRSVPGPRRGQLIRGFGDVL 76 Query: 62 RARREEIATLIARETGKPMWEALTEADSVA--AKVAISIRAQDERAGERSEPMADATARL 119 RA +E++ L+ ETGK + E L E + A+ + Q +E A Sbjct: 77 RAHKEDLGLLVTCETGKIIEEGLGEVQEMIDICDYAVGLSRQLYGLTIAAERPGHAMRET 136 Query: 120 AHRPHGVLAVIGPFNFPMHLANGHIVPALLAGNAVVFKPSEKTPACGQLMGELWRAAG-- 177 H P GV+ +I FNFP+ + + V AL+ G+A V+KPSEKTP C L+ A Sbjct: 137 WH-PLGVVGIITAFNFPVAVWAWNAVIALVCGDACVWKPSEKTPLCALAAQALFDKAADA 195 Query: 178 ---LPDHVLTIVIGGGEAGEALVRHEALDGVLFTGGVQAGRAIHRALADAPHKILALELG 234 +P ++ +V GG GEALV + V TG + GR I LA + + LELG Sbjct: 196 LDFVPPNLSQLVTGGQRTGEALVGDPRVPLVSATGSTRMGREIAPQLAKRFARCI-LELG 254 Query: 235 GNAPLVVWDVADIEAAAHLIVQSAYVTAGQRCTCARRLILPEGARGDALLEALTMLMDRL 294 GN ++V AD+ A IV +A TAGQRCT RRLI+ + R AL+E L + + Sbjct: 255 GNNAMIVAPSADLSLATRAIVFAAVGTAGQRCTSLRRLIVHDSLR-PALIERLKLAYGQA 313 Query: 295 VIGGPFQSPAPFMGPVIDAHAAAQVLAAQDRMTADGGR---PLRLAAVREARSALLSPGL 351 IG P + +GP+ID A + A A GGR R+ R + + P L Sbjct: 314 TIGDP-RDRRHLIGPLIDKAAFDSMQRALKEAAAAGGRVHGGERILIERWPDAYYVRPAL 372 Query: 352 IELTD-APLRDEEIFGPLLQVRRAADFDAALALANATRFGLAAGLISDDEALYRRFWTSV 410 +E+ D AP+ E F P+L V D+D A+ L N GLA+ + + D RF ++ Sbjct: 373 VEMPDQAPIVHRETFAPILYVLGYRDWDEAIRLHNGVPQGLASSIFTTDLREAERFLSAS 432 Query: 411 RA--GIVNWNRPTTGASSAAPFGGVGGSGNHR 440 + GI N N +GA FGG SG R Sbjct: 433 GSDCGIANVNIGPSGAEIGGAFGGEKESGGGR 464 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: 613 Number of extensions: 30 Number of successful extensions: 5 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: 500 Length adjustment: 34 Effective length of query: 438 Effective length of database: 466 Effective search space: 204108 Effective search space used: 204108 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 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