Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_111605741.1 DK187_RS02405 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q2SXN9 (487 letters) >NCBI__GCF_003259225.1:WP_111605741.1 Length = 488 Score = 217 bits (552), Expect = 8e-61 Identities = 160/467 (34%), Positives = 232/467 (49%), Gaps = 12/467 (2%) Query: 2 TELFIDGAWVDG-AGPVFASRNPGTNERVWEGASASADDVERAVASARRAFAAWSALDLD 60 ++ +I G WV +G FA NP E + + A A++ AV +A +A W Sbjct: 13 SQSYIGGEWVAAKSGKTFAITNPANGEHIIDVADLGAEETTLAVEAAEKAQKEWQGRTAK 72 Query: 61 ARCTIVKRFAALLVERKEALATMIGRETGKPLWEARTEVASMAAKVDISITAYHERTGEK 120 R T+++R+ L+++ + LAT++ E GKP EA+ EVA A+ +D G+ Sbjct: 73 ERATLLRRWNQLILDNQNDLATLMTLEQGKPFAEAKGEVAYGASFIDWFADEARRLNGDV 132 Query: 121 RAPMADGVAVLRHRPH-GVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSELAPGVAR 179 A VL + GVVA P+NFP + PAL AG T+V KPS+ P A Sbjct: 133 IPTFAKDKRVLTIKQGIGVVAAITPWNFPIAMITRKAGPALAAGCTIVIKPSDETPLCAL 192 Query: 180 ATVEIWRDAGLPAGVLNLVQGE--KDTGVALANHRQIDGLFFTGSSDTGTLLHKQFGGRP 237 A E+ AG+PAGVLN+V G+ K G L +H + L FTGS+ G LL Q Sbjct: 193 ALAELAHQAGIPAGVLNVVVGKDAKAIGGVLTSHPTVRKLSFTGSTPVGKLLLSQCAQTV 252 Query: 238 EIVLALEMGGNNPLVVAEVEDIDAAVHHAIQSAFLSAGQRCTCARRILVPRGAFGDRFVA 297 + ++E+GGN P +V + D+DAAV AI S + +AGQ C CA RILV G + D F Sbjct: 253 KRT-SMELGGNAPFIVFDDADLDAAVEGAIASKYRNAGQTCVCANRILVQEGVY-DAFAE 310 Query: 298 RLAD-VASKITASVFDADPQPFMGAVISARAASRLVAAQARLVGLGASPII-EMKQRDPA 355 +LA VA+ T F +G +I+ A S++ + GA +I K Sbjct: 311 KLAKRVATFKTGDGFSEGVN--IGPLINPAAISKVEQLVGDAIAKGAKALIGGTKATHAG 368 Query: 356 LGFVNAAIL-DVTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDTAFGLSAGLLADDEQ 414 F IL VT ++ E FGP+A + ++ DDA+A AN+T FGL++ + + Sbjct: 369 AQFFEPTILTGVTEDMDIFSNEIFGPVAPLFKFKTEDDAVAMANNTPFGLASYFYSQNIA 428 Query: 415 AWHTFRRAIRAGIVNWNRPTNGASSAAPFGGAGRSGNHRPSAYYAAD 461 A+ G+V N +S APFGG SG+ R + Y D Sbjct: 429 RIWRVSEALEYGMVGINEGII-SSEVAPFGGVKESGSGREGSQYGID 474 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: 476 Number of extensions: 23 Number of successful extensions: 4 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: 488 Length adjustment: 34 Effective length of query: 453 Effective length of database: 454 Effective search space: 205662 Effective search space used: 205662 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