Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_055437407.1 ASC41_RS13180 aldehyde dehydrogenase
Query= curated2:Q87L22 (485 letters) >NCBI__GCF_001418085.1:WP_055437407.1 Length = 500 Score = 179 bits (454), Expect = 2e-49 Identities = 148/476 (31%), Positives = 231/476 (48%), Gaps = 27/476 (5%) Query: 3 HWIAGEWVQG-QGEEFVSLSPYNQEVIWRGNGATAEQVDQAVAAARAAFVEWKKRPFAER 61 ++I G++V +G+ F ++SP + +V + +T E +D A+ AA AF W ER Sbjct: 15 NFIGGKFVDPVKGQYFDNVSPVDGKVFTQAARSTQEDIDLALDAAHEAFPAWSTSSATER 74 Query: 62 EAIVLAFAEKVKENSEKIAEVIAKETGKPIWETRTEAAAMA----GKIAISIRAYHDRTG 117 ++L A+ +++N E +A + + GKPI E+R A IRA Sbjct: 75 SNMLLKIAQVMEDNFEYLATLETIDNGKPIRESRAADIPYCIDHFRYFAGVIRADEGSIS 134 Query: 118 EATREAAGNQIVLRHRPLGVMAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSEQTPWTG 177 E ++ ++ H P+GV+ P+NFP + I PAL AG T V KP+EQTP + Sbjct: 135 EHDKDTVS---IVLHEPVGVVGEIIPWNFPMLMLAWKIAPALAAGCTAVVKPAEQTPTSV 191 Query: 178 ELAMKLWEEAGLPKGVINLVQG-AKETGIALADAKGIDGILFTGSANTGH-ILHRQFAGQ 235 + M+L + LP GV+N+V G E G ALA +K I + FTGS TG +LH A + Sbjct: 192 IMLMELIGDI-LPAGVLNIVTGFGAEAGAALATSKRIAKLSFTGSTETGRKVLHN--AAE 248 Query: 236 PGKMLALEMGGNNPMVISDNYGDLDATVYT-IIQSAF---ISAGQRCTCARRLYVPFGEK 291 + +E+GG +P V + D D ++ I+ A ++ G+ CT R+ V + Sbjct: 249 NIIPVTMELGGKSPNVFFPSVADHDDDFFSKAIEGALMFSLNQGEICTAPSRILV-HEDI 307 Query: 292 GDALITKLVEATKNIRMDQPFAEPAPFMGPQISVAAAKFILD-------AQANLQSLGGE 344 D I K+ K I+ P +P +G Q+S ILD A + + G Sbjct: 308 ADLFIEKMKVRLKAIKTGNPL-DPETMIGSQVSKPQYDKILDYIKIGKDEGAEVVAGGDA 366 Query: 345 SLIEAKAGEAAFVSPGIIDVTNIAELPDEEYFGPLLQVVRYEGLDKAVELANDTRFGLSA 404 E + E ++ P ++ N + EE FGP++ + + ++A+ +ANDT +GL A Sbjct: 367 GNYEGELSEGYYIQPTVLKGNNKMRIFQEEIFGPVVALTTFSSTEEAIAIANDTPYGLGA 426 Query: 405 GLVSTDDQEWEYFVDHIRAGIVNRNRQLTGASGDAPFGGPGASGNLRPSAYYAADY 460 G+ S D E I+AG V N+ T APFGG SG R + A D+ Sbjct: 427 GVWSRDAHELYQVPRAIQAGRVWVNQYHT-YPAHAPFGGVKESGFGRENHKMALDH 481 Lambda K H 0.316 0.134 0.397 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: 547 Number of extensions: 32 Number of successful extensions: 4 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: 485 Length of database: 500 Length adjustment: 34 Effective length of query: 451 Effective length of database: 466 Effective search space: 210166 Effective search space used: 210166 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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