Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate CA265_RS19780 CA265_RS19780 aldehyde dehydrogenase family protein
Query= curated2:Q87L22 (485 letters) >FitnessBrowser__Pedo557:CA265_RS19780 Length = 513 Score = 187 bits (476), Expect = 6e-52 Identities = 136/448 (30%), Positives = 224/448 (50%), Gaps = 17/448 (3%) Query: 19 SLSPYNQEVIWRGNGATAEQVDQAVAAARAAFVEWKKRPFAEREAIVLAFAEKVKENSEK 78 S SP + ++I ATA+ D V A+ AF W+ P +R IV F + ++EN + Sbjct: 38 SFSPVDGKLIASAKIATADDYDAVVLKAQEAFTAWRSVPAPKRGEIVRQFGDALRENKDA 97 Query: 79 IAEVIAKETGKPIWETRTEAAAMAGKIAISIRAYHDRTGEATR-EAAGNQIVLRHRPLGV 137 + +++ E GK + E E M ++ G E +++ + PLG+ Sbjct: 98 LGTLVSYEMGKSLQEGFGEVQEMIDICDFAVGLSRQLYGLTMHSERPSHRMYEQWHPLGI 157 Query: 138 MAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSEQTPWTG----ELAMKLWEEAGLPKGV 193 + + +NFP + + + AL+ GN ++KPSE+TP T + K++++ + +GV Sbjct: 158 VGIISAFNFPVAVWSWNTALALVCGNVCIWKPSEKTPLTAIACQHIIAKVFKDNDIAEGV 217 Query: 194 INLVQGAKETGIALADAKGIDGILFTGSANTGHILHRQFAGQPGKMLALEMGGNNPMVIS 253 NL+ G +E G + + I I TGS G + + GK L LE+GGNN ++IS Sbjct: 218 CNLILGDREVGERMTNDGRIPLISATGSTRMGKAVGAAVGARLGKSL-LELGGNNAIIIS 276 Query: 254 DNYGDLDATVYTIIQSAFISAGQRCTCARRLYVPFGEKGDALITKLVEATKNIRMDQPFA 313 + + DLD ++ + A +AGQRCT RRL + DA KLV+A +R+ P Sbjct: 277 E-HADLDMSLIGAVFGAVGTAGQRCTSTRRLII-HESVYDAFTAKLVKAYGQLRIGDPL- 333 Query: 314 EPAPFMGPQISVAAAKFILDAQANLQSLGGESLIE--AKAGEA----AFVSPGIIDVTNI 367 + +GP I A LD+ A ++ GG ++E +G+A +V P I +V N Sbjct: 334 DQNNHVGPLIDTDAVAAYLDSIAKCKAEGGNFVVEGGVLSGDAYTSGCYVKPCIAEVQND 393 Query: 368 AELPDEEYFGPLLQVVRYEGLDKAVELANDTRFGLSAGLVSTDDQEWEYFVD--HIRAGI 425 ++ E F P+L +++Y+ LD+A+ L N GLS+ +++ + +E E F+ GI Sbjct: 394 FKIVQHETFAPILYLIKYKTLDEAIALQNGVPQGLSSAIMTLNLREAEQFLSAKGSDCGI 453 Query: 426 VNRNRQLTGASGDAPFGGPGASGNLRPS 453 N N +GA FGG +G R S Sbjct: 454 ANVNIGTSGAEIGGAFGGEKETGGGRES 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: 545 Number of extensions: 35 Number of successful extensions: 8 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: 513 Length adjustment: 34 Effective length of query: 451 Effective length of database: 479 Effective search space: 216029 Effective search space used: 216029 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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