Align Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)
to candidate 16751 b2661 succinate-semialdehyde dehydrogenase I, NADP-dependent (NCBI)
Query= reanno::pseudo13_GW456_L13:PfGW456L13_1974 (488 letters) >FitnessBrowser__Keio:16751 Length = 482 Score = 212 bits (539), Expect = 3e-59 Identities = 164/468 (35%), Positives = 229/468 (48%), Gaps = 24/468 (5%) Query: 6 IAGEWL-AGGGEAFESLNPVTQQVLWSGVGATAGQVESAVQAARQAFPDWARRTLEERIS 64 I GEWL A GEA + NP L S A + +A+ AA +A P W T +ER + Sbjct: 15 INGEWLDANNGEAIDVTNPANGDKLGSVPKMGADETRAAIDAANRALPAWRALTAKERAT 74 Query: 65 VLEAFAAALKNHADELAHTIGEETGKPLWEAATEVTSMVNKIAISVQSYRERTGEK-SGP 123 +L + + H D+LA + E GKPL EA E++ + I + + G+ G Sbjct: 75 ILRNWFNLMMEHQDDLARLMTLEQGKPLAEAKGEISYAASFIEWFAEEGKRIYGDTIPGH 134 Query: 124 LGDATAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNSVLFKPSELTPKVAELTVK 183 D ++ +P GV A P+NFP + PAL AG +++ KP+ TP A + Sbjct: 135 QADKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPFSALALAE 194 Query: 184 CWIEAGLPAGVLNLLQG-ARETGIALAANPGIDGLFFTGSSRTGNHLHQQFAGRPDKILA 242 I AG+PAGV N++ G A G L +NP + L FTGS+ G L +Q A + K ++ Sbjct: 195 LAIRAGVPAGVFNVVTGSAGAVGNELTSNPLVRKLSFTGSTEIGRQLMEQCA-KDIKKVS 253 Query: 243 LEMGGNNPLVVDQVADLDAAVYTIIQSAFISAGQRCTCARRLLVPQGAWGDSLLARLVAV 302 LE+GGN P +V ADLD AV + S F +AGQ C CA RL V G + D +L Sbjct: 254 LELGGNAPFIVFDDADLDKAVEGALASKFRNAGQTCVCANRLYVQDGVY-DRFAEKLQQA 312 Query: 303 SSTLSVGAFDQQPAPFMGSVVSLGA---AKALMDAQEHL---LANGAVALLEMTQPQAQS 356 S L +G + + V++G KA+ +EH+ L GA + + Sbjct: 313 VSKLHIG-------DGLDNGVTIGPLIDEKAVAKVEEHIADALEKGARVVCGGKAHERGG 365 Query: 357 ALLTPGIL-DVSAVADRPDEELFGPLLQVIRYADFEAAIAEANDTAYGLAAGLLSDSEAR 415 P IL DV A A EE FGPL + R+ D IA+ANDT +GLAA + +R Sbjct: 366 NFFQPTILVDVPANAKVSKEETFGPLAPLFRFKDEADVIAQANDTEFGLAAYFYARDLSR 425 Query: 416 YQQFWLESRAGIVNWNKQLTGAASS--APFGGVGASGNHRASAYYAAD 461 + GIV N TG S+ APFGG+ ASG R + Y + Sbjct: 426 VFRVGEALEYGIVGIN---TGIISNEVAPFGGIKASGLGREGSKYGIE 470 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: 527 Number of extensions: 31 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: 482 Length adjustment: 34 Effective length of query: 454 Effective length of database: 448 Effective search space: 203392 Effective search space used: 203392 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