Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_012536996.1 AFE_RS09825 aldehyde dehydrogenase family protein
Query= BRENDA::Q88RC0 (480 letters) >NCBI__GCF_000021485.1:WP_012536996.1 Length = 506 Score = 258 bits (659), Expect = 3e-73 Identities = 162/484 (33%), Positives = 252/484 (52%), Gaps = 18/484 (3%) Query: 10 RQQAYINGEWLDADNGQTIKVTNPATGEVIGTVPKMGTAETRRAIEAADKALPAWRALTA 69 R +I G W+ G+ +P G+ +P+ + A++AA A AW + Sbjct: 18 RYDNFIGGRWVAPVRGEYFDNISPINGKPFCQIPRSSAEDIELALDAAHAAKDAWGRTSV 77 Query: 70 KERSAKLRRWFELMIENQDDLARLMTTEQGKPLAEA-KGEIAYAASFIEWFAEEAKRIYG 128 RS L + + + N + LA T + GK + E ++ ++ +FA R Sbjct: 78 TARSNILLKIADRIDANLEMLAVAETWDNGKAVRETLNADVPLSSDHFRYFAG-CLRAQE 136 Query: 129 DTIPGHQPDKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPYS 188 TI + +P+GV I PWNFP M K PALAAG +VLKPA QTP S Sbjct: 137 GTIGEIDENTVAYHFHEPLGVVGQIIPWNFPLLMACWKLAPALAAGNCVVLKPAEQTPAS 196 Query: 189 ALALVELAHRAGIPAGVLSVVTGSAGEVGGELTGNSLVRKLSFTGSTEIGRQLMEECAKD 248 L ++EL +PAGVL+VV G E G L + + K++FTGST +G +M+ A++ Sbjct: 197 ILVMMELIADL-LPAGVLNVVNGYGVEAGKALATSKRIAKIAFTGSTPVGSLIMKYAAEN 255 Query: 249 IKKVSLELGGNAPFIVF------DDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDGVY 302 I ++ELGG +P I F +DA + KAVEGA+++ + N G+ C C +R+ +Q+ +Y Sbjct: 256 IIPSTVELGGKSPNIFFADVLDQEDAFVSKAVEGAVLAFF-NQGEVCTCPSRLLIQESIY 314 Query: 303 DAFAEKLAAAVAKLKIGNGLEEGTTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSGGKL-- 360 + F + A++K GN L+ G + K+ +I+ +GA+V++GG + Sbjct: 315 EKFIGMVVERSAQIKRGNPLDTEVMVGAQASQEQYDKILSYIQIGKDEGAEVITGGAVET 374 Query: 361 -----IEGNFFEPTILVDVPKTAAVAKEETFGPLAPLFRFKDEAEVIAMSNDTEFGLASY 415 EG + +PT+L V +EE FGP+ + FKDEAE +A++ND EFGL + Sbjct: 375 MSADYCEGYYIQPTLLKGT-NNMRVFQEEIFGPVVSVTTFKDEAEALAIANDIEFGLGAG 433 Query: 416 FYARDMSRVFRVAEALEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKY 475 + RDM+R +R+ ++ G V N + A FGG K SG+GRE K ++ Y + K Sbjct: 434 VWTRDMNRAYRMGRGIQAGRVWTNCYHMYPAHAAFGGYKKSGVGRETHKMMLDHYQQTKN 493 Query: 476 LCIS 479 L +S Sbjct: 494 LLVS 497 Lambda K H 0.317 0.134 0.384 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: 571 Number of extensions: 26 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: 480 Length of database: 506 Length adjustment: 34 Effective length of query: 446 Effective length of database: 472 Effective search space: 210512 Effective search space used: 210512 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 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