Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_068863622.1 I603_RS07320 aldehyde dehydrogenase family protein
Query= curated2:Q2SXN9 (487 letters) >NCBI__GCF_001677335.1:WP_068863622.1 Length = 506 Score = 168 bits (425), Expect = 5e-46 Identities = 151/477 (31%), Positives = 229/477 (48%), Gaps = 44/477 (9%) Query: 5 FIDGAWVDGAGPV----FASRNPGTNERVWEGASASADDVERAVASARRAFAAWSALDLD 60 FI G WV PV F + +P +RV + A SA+D+E A+ +A +A AAW Sbjct: 22 FIGGQWV---APVKCQYFDNISPVNGKRVCQVARGSAEDIELALDAAHKARAAWGRTSTT 78 Query: 61 ARCTIVKRFAALLVERKEALATMIGRETGKPLWEARTEVASMAAKVDISITAYHERTGEK 120 R I+ R A + + + LA + + GKP+ E + AA + +++ + G Sbjct: 79 ERSNILNRIAQRIEDNLDLLALVETIDNGKPIRE------TTAADLPLAVDHFRYFAGAL 132 Query: 121 RAPMA-------DGVAVLRHRPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSEL 173 RA D +A H P GVV P+NFP + + PAL AGN VV KP+E Sbjct: 133 RAQEGGISEIDHDTIAYHFHEPLGVVGQIIPWNFPLLMAVWKLAPALAAGNCVVLKPAEQ 192 Query: 174 APGVARATVEIWRDAGLPAGVLNLVQGEK-DTGVALANHRQIDGLFFTGSSDTGTLLHKQ 232 P +E+ D LP GV+N+V G + G LA +I + FTG + TG L+ Q Sbjct: 193 TPMSIMVLMEVIGDL-LPEGVVNVVNGFGIEAGKPLATSPRIAKIAFTGETTTGRLI-MQ 250 Query: 233 FGGRPEIVLALEMGGNNPL-----VVAEVED-IDAAVHHAIQSAFLSAGQRCTCARRILV 286 + I LE+GG +P V+ E +D +D A+ A L+ G+ CTC R L+ Sbjct: 251 YASENLIPCTLELGGKSPNIFFADVMREDDDYLDKALEGFAMFA-LNQGEVCTCPSRALI 309 Query: 287 PRGAFGDRFVAR-LADVASKITASVFDADPQPFMGAVISARAASRLVAAQARLVGLGASP 345 + DRF+ + +A V + S DA +GA S ++++ G GA Sbjct: 310 HESIY-DRFMEKAIARVNAIKLGSPLDA--ATMIGAQASNDQLEKILSYIEIGKGEGAKV 366 Query: 346 II----EMKQRDPALGF-VNAAILDVTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDT 400 + + + + A G+ V +L+ N + EE FGP+ + + D D+A++ ANDT Sbjct: 367 LTGGGRHIHEGELAEGYYVKPTVLEGHNKMRIFQEEIFGPVLSVTTFKDNDEALSIANDT 426 Query: 401 AFGLSAGLLADDEQAWHTFRRAIRAGIVNWNRPTNGASSAAPFGGAGRSG----NHR 453 +GL AG+ + D + F RAI AG V W + + A FGG +SG NH+ Sbjct: 427 LYGLGAGVWSRDANTCYRFGRAIEAGRV-WTNCYHAYPAHAAFGGYKQSGIGRENHK 482 Lambda K H 0.320 0.134 0.402 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: 463 Number of extensions: 22 Number of successful extensions: 2 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: 487 Length of database: 506 Length adjustment: 34 Effective length of query: 453 Effective length of database: 472 Effective search space: 213816 Effective search space used: 213816 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 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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