Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_090272859.1 BLU11_RS08070 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q87L22 (485 letters) >NCBI__GCF_900105005.1:WP_090272859.1 Length = 486 Score = 189 bits (481), Expect = 1e-52 Identities = 146/464 (31%), Positives = 228/464 (49%), Gaps = 15/464 (3%) Query: 4 WIAGEWVQGQGEEFVSL-SPYNQEVIWRGNGATAEQVDQAVAAARAAFVEWKKRPFAERE 62 ++ G+W E +++ +P N +V+ +A +V AV AA +A +W+KR ER Sbjct: 17 YVNGQWQNASSGETLAVDNPANGDVLGHVPVLSAAEVGAAVDAASSALRQWRKRTAQERA 76 Query: 63 AIVLAFAEKVKENSEKIAEVIAKETGKPIWETRTE---AAAMAGKIAISIRAYHDRTGEA 119 +LA+ + + E+ E +A ++ E GKP+ E++ E AA+ A R + T Sbjct: 77 DCLLAWHDLMLEHKEDLATLMTLEQGKPLVESQGEIDYAASFIRWFAEEARRMYGETIPG 136 Query: 120 TREAAGNQIVLRHRPLGVMAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSEQTPWTGEL 179 R G IV+ +P+GV A P+NFP + AL AG T++ KP+ TP++ Sbjct: 137 AR--IGQHIVVTRQPVGVCAAITPWNFPAAMITRKAGAALAAGCTIIVKPASATPFSALA 194 Query: 180 AMKLWEEAGLPKGVINLVQG-AKETGIALADAKGIDGILFTGSANTGHILHRQFAGQPGK 238 L EEAG+P GV N+V G A E L + + + FTGS + G L Q + K Sbjct: 195 LAVLAEEAGIPHGVFNVVTGKAGEISEVLTRSPVVRKLSFTGSTDVGRRLMAQCSEHIQK 254 Query: 239 MLALEMGGNNPMVISDNYGDLDATVYTIIQSAFISAGQRCTCARRLYVPFGEKGDALITK 298 ++LE+GGN P ++ D+ D+ V + F + GQ C CA R V G D + Sbjct: 255 -VSLELGGNAPFIVFDD-ADISRAVEGAMVCKFRNTGQTCVCANRFLVQSGVH-DKFVAA 311 Query: 299 LVEATKNIRMDQPFAEPAPFMGPQISVAAAKFILDAQANLQSLGGESLI--EAKAGEAAF 356 L EA +R+ F EP I+ A + +++ + + G + + A + Sbjct: 312 LAEAMGKLRIGDGF-EPGVTQSALINGDAVEKVIEHFDDAMAKGAKRVCGPAPDADRGNY 370 Query: 357 VSPGII-DVTNIAELPDEEYFGPLLQVVRYEGLDKAVELANDTRFGLSAGLVSTDDQEWE 415 V P ++ D+ L EE FGPL V+R++ ++A+ELAN T FGL+A S D Sbjct: 371 VQPVLLTDINTNMTLCHEETFGPLAAVLRFDTEEEAIELANATPFGLAAYFYSRDIHRVW 430 Query: 416 YFVDHIRAGIVNRNRQLTGASGDAPFGGPGASGNLRPSAYYAAD 459 D + AGI+ N L ++ APFGG SG R + + D Sbjct: 431 RVADALEAGIIGINEGLI-SNPMAPFGGVKESGLGREGSRHGLD 473 Lambda K H 0.316 0.134 0.397 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: 605 Number of extensions: 28 Number of successful extensions: 5 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: 485 Length of database: 486 Length adjustment: 34 Effective length of query: 451 Effective length of database: 452 Effective search space: 203852 Effective search space used: 203852 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 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