Align N-succinylglutamate 5-semialdehyde dehydrogenase; Succinylglutamic semialdehyde dehydrogenase; SGSD; EC 1.2.1.71 (characterized)
to candidate WP_011938764.1 GURA_RS09480 L-glutamate gamma-semialdehyde dehydrogenase
Query= SwissProt::O50174 (487 letters) >NCBI__GCF_000016745.1:WP_011938764.1 Length = 1002 Score = 188 bits (478), Expect = 7e-52 Identities = 145/449 (32%), Positives = 217/449 (48%), Gaps = 22/449 (4%) Query: 16 ETLESLDPVGQG-VVWSGRGADATQVDAAVCAAREAFPAWARRPLEQRIELLERFAATLK 74 + L S++P G V+ A AT+V+ A+ AA AFPAW R L + A ++ Sbjct: 522 DLLPSINPAGPSEVIGLICQAGATEVEEAIAAAGAAFPAWRDTAPGSRAGYLIKAAQAVR 581 Query: 75 SRADELARVIGEETGKPLWESATEVTSMVNKVAISV-QAFRERTGEKSGPLADATAVLRH 133 R EL+ E GK ++ +VT ++ + + R ++ G T + Sbjct: 582 RRLFELSAWQVLEIGKQWDQAYADVTEAIDFLEYYAREMIRLGEPQRVGHAPGETNHYFY 641 Query: 134 KPHGVVAVFGPYNFPGHLPNGHIVPALLAGNCVVFKPSELTPKVAELTLKAWIQAGLPAG 193 + GV AV P+NFP + G + AL+ GNCVV+KPS LT + ++ + +AGLPAG Sbjct: 642 EAKGVAAVIAPWNFPLAISMGMVSAALVTGNCVVYKPSGLTSVIGRHLVEIFSEAGLPAG 701 Query: 194 VLNLVQGGRET-GVALAAHRGLDGLFFTGSSRTGNLLHSQF-----GGQPQKILALEMGG 247 V N + G G L H + + FTGS G + + G K + EMGG Sbjct: 702 VFNYIPGRSSVMGDFLVDHPHISLIAFTGSREVGLRIIERAAKVHPGQAKVKKIVCEMGG 761 Query: 248 NNPLVVEEVADLDAAVYTIIQSAFISAGQRCTCARRLLVPQGAWGDALLARLVAVSATLR 307 N +++++ ADLD AV ++ SAF GQ+C+ R +V G + D + RL++++ Sbjct: 762 KNGIIIDDDADLDEAVPHVLFSAFAFQGQKCSACSRAIVLDGVY-DKFVERLLSMARATS 820 Query: 308 VGRFDEQPAPFMGAVISLSAAEHLLKAQEHLIGKGAQPLLAMTQPIDGAALLTP-----G 362 VG E PA +MGAV A + +L E++ G + ++ P+ P G Sbjct: 821 VGP-AENPAFYMGAVADDKAMKRIL---EYIEIGGKEGVILYRSPVPSEGYFVPMTIIGG 876 Query: 363 ILDVSAVAERPDEEFFGPLLQVIRYSDFAAAIREANATQYGLAAGLLSDSRERFEQFLVE 422 I +A EE FGP+L V+R DF A+ AN+T Y L G+ S S E E Sbjct: 877 IRPEHRIAR---EEIFGPVLAVMRAKDFEQAVEWANSTSYALTGGVFSRSPEHLALARRE 933 Query: 423 SRAGIVNWNKQLTGA-ASSAPFGGIGASG 450 R G + +N+ TGA PFGG SG Sbjct: 934 FRVGNLYFNRNCTGALVERQPFGGSRMSG 962 Lambda K H 0.318 0.134 0.396 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: 1127 Number of extensions: 49 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: 1002 Length adjustment: 39 Effective length of query: 448 Effective length of database: 963 Effective search space: 431424 Effective search space used: 431424 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 (21.7 bits) S2: 54 (25.4 bits)
This GapMind analysis is from Apr 09 2024. 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