Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate GFF4005 HP15_3945 aldehyde dehydrogenase family protein
Query= BRENDA::Q72IB9 (516 letters) >FitnessBrowser__Marino:GFF4005 Length = 471 Score = 238 bits (607), Expect = 4e-67 Identities = 161/477 (33%), Positives = 243/477 (50%), Gaps = 20/477 (4%) Query: 41 YIGGEWVDTKERMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKAFKTWKDWPQEDRSR 100 YI G+WV M+ ++ + +V+ AG E E A+ AA AF++W + E+R + Sbjct: 8 YINGQWVSWAGDMIDVHEAGTGDVIARVPAAGADEMEQAIAAADAAFESWSESTLEERIK 67 Query: 101 LLLKAAALMRRRKRELEATLVYEVGKNWVEASADVAEAIDFIEYYARAALRYRYPAVEVV 160 +L + A ++ R E+ T+ EVG ++ + + + + L +P E Sbjct: 68 VLEQLHAGLKERAPEIAETVCREVGMP-IKLATPIQAGMPAAVTKSYLKLLPDFPFTE-- 124 Query: 161 PYPGEDNESFYVPLGAGVVIAPWNFPVAIFTGMIMGPVAVGNTVIAKPAEDAVVVGAKVF 220 ++E Y P+G I PWN+P+ I+ +A G TV+ KP+E A + Sbjct: 125 --QSGNSEVQYAPVGVVGCITPWNYPLHQVILKIVPAIAAGCTVVLKPSEIAPQTAFILA 182 Query: 221 EIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGSLEVGLKIYEAAGRLAPGQT 280 EI P GV N + G G VG L++HP R ++FTGS G I AA Sbjct: 183 EILDGTDLPKGVFNMVCGYGHTVGDTLIKHPDVRMVSFTGSTRTGNLIAHAAA------D 236 Query: 281 WFKRAYVETGGKDAIIVDETADFDLAAEGVVVSAYGFQGQKCSAASRLILTQGAYEPVLE 340 FKR +E GGK A ++ AD A +G + + GQ C+A +R+++ ++ E Sbjct: 237 DFKRFALEMGGKSASVILPDADLAAAVKGTINNCLLNSGQTCTALTRMLVPADKHDEACE 296 Query: 341 RVLKRAERLSVG-PAEENPDLGPVVSAEQERKVLSYIEIGKNEG-QLVLGGKRL-EG--E 395 +++ G P EE LGP+ SA+Q KV+ YI++G EG +L+ GG EG + Sbjct: 297 LAAAAVAKMTPGNPLEETTRLGPLSSAQQRDKVIDYIKLGVQEGAKLIAGGPEAPEGCEK 356 Query: 396 GYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVANDTPYGLTGGVYSRKRE 455 GYF+ TVF V P +RIAQEEIFGPVL VI D AEA+++AN T YGL+G V+S Sbjct: 357 GYFVKATVFGNVKPDSRIAQEEIFGPVLCVIPYNDEAEAVKIANGTQYGLSGAVWSGDDA 416 Query: 456 HLEWARREFHVGNLYFNRKITGALVGVQPFGGFKLSGTNAKTGALDYLRLFLEMKAV 512 + + G ++ N GA + PFGGF SG + G L FLE++++ Sbjct: 417 KAKKIASKLRTGQVFVN---GGAFNPMAPFGGFGHSGIGREFGKWG-LEEFLEVRSL 469 Lambda K H 0.319 0.137 0.403 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: 526 Number of extensions: 33 Number of successful extensions: 6 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: 516 Length of database: 471 Length adjustment: 34 Effective length of query: 482 Effective length of database: 437 Effective search space: 210634 Effective search space used: 210634 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 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