Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_111608297.1 DK187_RS15780 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q1QTQ7 (489 letters) >NCBI__GCF_003259225.1:WP_111608297.1 Length = 486 Score = 209 bits (533), Expect = 1e-58 Identities = 147/473 (31%), Positives = 235/473 (49%), Gaps = 33/473 (6%) Query: 8 LIDGAWVDGDAARFAKT-DPVSGETLWTATAASATQVEHAVAAARQAFPDWARRSFAERQ 66 LI+G WV+ +P +GE + T + + + A+AAA A W +++ ER Sbjct: 15 LINGEWVESSEGNTLDVFNPATGELVATVASVGPAETQQAIAAAEAAQKTWKKKTAKERA 74 Query: 67 AVVERFRECLETHREHLATAIAQETGKPLWEARTEVGAMIGKVAISITAYHERTGERARD 126 A++ R+ + L ++E LA + E GKPL E+R E+G A S + G+R Sbjct: 75 ALLRRWHDLLMANQEDLARLMTAEQGKPLAESRGEIG-----YAASFIEWFAEEGKRIYG 129 Query: 127 ------IGDARAVLRHRPHGVLAVYGPYNFPGHLPNGHIVPALLAGNAVVFKPSEQTPMT 180 D R ++ P GV A P+NFP + PAL AG ++ KP+ +TP++ Sbjct: 130 DMIPTYAPDRRILVMKEPVGVCAAITPWNFPAAMITRKAGPALAAGCTMIIKPASETPLS 189 Query: 181 ADLTLQCWLEAGLPAGVINLVQG-AAEVGQALAGSADIDGLLFTGSAKVGGLLHRQFGGQ 239 A +EAG+PAGVIN+V G A+ + + L S+ + L FTGS +G LL + Sbjct: 190 ALAMGVLAIEAGIPAGVINIVVGKASHIAKTLTDSSVVRKLTFTGSTPIGKLLMKDCADT 249 Query: 240 VDKILALELGGNNPLVVKDVPDREAAVLSILQSAFASGGQRCTCARRLIVPHGAVGDDLI 299 + K+ +LELGGN P VV D D + AV + S + + GQ C CA R+ V G V D + Sbjct: 250 MKKV-SLELGGNAPFVVFDDADIDEAVKGAMMSKYRNAGQTCVCANRIYVQAG-VYDTFV 307 Query: 300 DALTSAIAELRVAAPFSEPAPFYAGLTSVEAADGLLAAQDDLVARGGRPLSRMRRLQAGT 359 + + +A +++ +E L + A D + D +++GG+ ++ +R + G Sbjct: 308 EKFAAQVAAMKIGHG-TEDGVEQGPLINRAAVDKVDEHVQDAISKGGKIVTGGKRHELGD 366 Query: 360 SLLSPGLIDVTGCDV--PDEEHFGPLLKVHRYRDWDEAIALANDTRYGLSA-------GL 410 + P +I D+ EE FGPL + ++ D+ IA+ANDT YGL++ G Sbjct: 367 NFYHPTVIANATQDMLFAKEETFGPLAPIFKFETEDDVIAMANDTEYGLASYFYSRDIGR 426 Query: 411 IGGERADWDDFLLRIRAGIVNWNRQTTGASSDAPFGGIGDSGNHRPSAYYAAD 463 I + L+ + AG++ A+ APFGG +SG R + Y + Sbjct: 427 IFRVAEALETGLVGVNAGVI--------ATEVAPFGGYKESGLGREGSKYGIE 471 Lambda K H 0.319 0.135 0.409 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: 589 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: 489 Length of database: 486 Length adjustment: 34 Effective length of query: 455 Effective length of database: 452 Effective search space: 205660 Effective search space used: 205660 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