Align Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate Dsui_1464 Dsui_1464 NAD-dependent aldehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_495 (480 letters) >FitnessBrowser__PS:Dsui_1464 Length = 506 Score = 251 bits (640), Expect = 5e-71 Identities = 161/483 (33%), Positives = 240/483 (49%), Gaps = 22/483 (4%) Query: 10 RQQAFIDGAWVDADNGQTIKVNNPATGEILGTVPKMGAAETRRAIEAADKALPAWRALTA 69 R FI G WV GQ V P TG+ + GA + A++AA A W +A Sbjct: 18 RYDNFIGGKWVAPVKGQYFDVITPITGKPYTQAAQSGAEDIELALDAAHAAADKWGKTSA 77 Query: 70 KERATKLRRWYELIIENQDDLARLMTLEQGKPLAEA-KGEIVYAASFIEWFAEEAKRIYG 128 ER+ L + + I N + LA + T++ GK + E +I AA +FA + G Sbjct: 78 TERSNILLKIADRIEANLEMLAYVETVDNGKAIRETLNADIPLAADHFRYFAGCLRSQEG 137 Query: 129 DVIPGHQPDKRLIV--IKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTP 186 + + D+ I +P+GV I PWNFP M K PAL AG +VLKPA TP Sbjct: 138 SI---SEIDENTIAYHFHEPLGVVGQIIPWNFPILMAAWKLAPALGAGNCVVLKPAESTP 194 Query: 187 FSAFALAELAQRAGIPAGVFSVVSGSAGDIGSELTSNPIVRKLSFTGSTEIGRQLMSECA 246 S LAEL +P GV ++V+G D G L S+ + K++FTGST GR + A Sbjct: 195 ISILVLAELIADL-LPPGVLNIVNGYGRDAGMALASSKRIAKIAFTGSTATGRVIAQAAA 253 Query: 247 KDIKKVSLELGGNAPFIVF------DDADLDKAVEGAIISKYRNNGQTCVCANRLYIQDG 300 + +LELGG +P I F DD DKA+EG ++ + N G+ C C +R I + Sbjct: 254 NSLIPATLELGGKSPNIFFADVAAADDDFFDKAIEGLVLFAF-NQGEVCTCPSRALIHES 312 Query: 301 VYDAFAEKLKVAVAKLKIGNGLEAGTTTGPLIDEKAVAKVQEHIADALSKGATVLA---- 356 +YD F E++ V +K G+ L+ + G + + K+ ++A +GA L Sbjct: 313 IYDHFMERVLARVKAIKQGSPLDTDSMMGAQASQMQMDKIMSYLAIGKEEGAQCLVGGDR 372 Query: 357 ---GGKPMEGNFFEPTILTNVPNNAAVAKEETFGPLAPLFRFKDEADVIAMSNDTEFGLA 413 GG+ EG + +PT+ N + +EE FGP+ + FK EA+ + ++NDT +GL Sbjct: 373 ARLGGELAEGYYIQPTLFKG-HNKMRIFQEEIFGPVLAVTTFKTEAEALEIANDTPYGLG 431 Query: 414 SYFYARDLGRVFRVAEALEYGMVGVNTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEI 473 + ++RD +R+ ++ G V N A FGG K SG+GRE K ++ Y + Sbjct: 432 AGVWSRDGNTAYRMGRGIKAGRVWTNCYHAYPAHATFGGYKESGIGRETHKMMLDHYQQT 491 Query: 474 KYL 476 K L Sbjct: 492 KNL 494 Lambda K H 0.317 0.135 0.390 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: 535 Number of extensions: 32 Number of successful extensions: 7 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 (21.7 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