Align Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)
to candidate H281DRAFT_03178 H281DRAFT_03178 succinate semialdehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_1974 (488 letters) >FitnessBrowser__Burk376:H281DRAFT_03178 Length = 486 Score = 202 bits (514), Expect = 2e-56 Identities = 153/463 (33%), Positives = 220/463 (47%), Gaps = 12/463 (2%) Query: 5 YIAGEWL-AGGGEAFESLNPVTQQVLWSGVGATAGQVESAVQAARQAFPDWARRTLEERI 63 Y+AGEW A G FE +NP T +V+ + + A+ AA A+P W T ++R Sbjct: 17 YLAGEWQGADDGSTFEVVNPATGEVVATVPRMGTAETRRAIDAANAAWPAWRASTAKQRA 76 Query: 64 SVLEAFAAALKNHADELAHTIGEETGKPLWEAATEVTSMVNKIAISVQSYRERTGEK-SG 122 +L + + +AD+LA + E GKPL EA E+ + + + + G+ Sbjct: 77 VILRKWHDLMLENADDLALILTTEQGKPLAEAKGEIQYAASFLEWFAEEGKRLNGDTIPT 136 Query: 123 PLGDATAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNSVLFKPSELTPKVAELTV 182 P D V+ +P GV A P+NFP + + PAL AG ++ KP+E TP A Sbjct: 137 PANDKRIVVTKEPVGVCAAITPWNFPAAMITRKVGPALAAGCPIIVKPAEATPLSALALA 196 Query: 183 KCWIEAGLPAGVLNLLQG-ARETGIALAANPGIDGLFFTGSSRTGNHLHQQFAGRPDKIL 241 AG+P GV N++ G + G + NP + L FTGS+ G L Q A K+ Sbjct: 197 VLAERAGVPRGVFNVVTGEPKAIGAEMTGNPIVRKLSFTGSTPVGRLLMAQCAPTVKKV- 255 Query: 242 ALEMGGNNPLVVDQVADLDAAVYTIIQSAFISAGQRCTCARRLLVPQGAWGDSLLARLVA 301 +LE+GGN P +V ADLDAAV I S + ++GQ C C R V + D+ A+L A Sbjct: 256 SLELGGNAPFIVFDDADLDAAVAGAIASKYRNSGQTCVCTNRFYVHDKVY-DAFAAKLRA 314 Query: 302 VSSTLSVGAFDQQPAPFMGSVVSLGAAKALMDAQEHLLANGAVALLEMTQPQAQSALLTP 361 L+VG + G +++ A + E LA GA + + P Sbjct: 315 AVEQLTVGR-GTEAGVTQGPLINEAAVLKVESHIEDALAKGARVVTGGKRHALGHGFFEP 373 Query: 362 GIL-DVSAVADRPDEELFGPLLQVIRYADFEAAIAEANDTAYGLAAGLLSDSEARYQQFW 420 IL DV+ +E FGPL + R++ E IA ANDT +GLA+ S R + Sbjct: 374 TILADVTPDMKVARDETFGPLAPLFRFSSDEEVIALANDTEFGLASYFYSRDIGRVWRVA 433 Query: 421 LESRAGIVNWNKQLTGAASS--APFGGVGASGNHRASAYYAAD 461 G+V N TG S+ APFGGV SG R ++Y D Sbjct: 434 EALEYGMVGIN---TGLISNEVAPFGGVKQSGLGREGSHYGID 473 Lambda K H 0.316 0.132 0.388 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: 514 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: 488 Length of database: 486 Length adjustment: 34 Effective length of query: 454 Effective length of database: 452 Effective search space: 205208 Effective search space used: 205208 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