Align N-succinylglutamate 5-semialdehyde dehydrogenase; Succinylglutamic semialdehyde dehydrogenase; SGSD; EC 1.2.1.71 (characterized)
to candidate WP_011319687.1 AVA_RS14900 L-glutamate gamma-semialdehyde dehydrogenase
Query= SwissProt::O50174 (487 letters) >NCBI__GCF_000204075.1:WP_011319687.1 Length = 993 Score = 206 bits (525), Expect = 2e-57 Identities = 145/444 (32%), Positives = 225/444 (50%), Gaps = 13/444 (2%) Query: 16 ETLESLDPVGQGVVWSGRGA-DATQVDAAVCAAREAFPAWARRPLEQRIELLERFAATLK 74 E ++S++P G V G Q + A+ AA+ AFP W R P+++R +L R L+ Sbjct: 518 EVIDSVNPSNFGEVIGKVGLISVEQAEQAMQAAKAAFPGWRRTPVKERAAILRRAGDLLE 577 Query: 75 SRADELARVIGEETGKPLWESATEVTSMVNKVAISVQAFRERTGEKSGPLADATAVLRHK 134 R EL+ I E GKP+ E+ EV+ ++ + +A T ++ Sbjct: 578 ERRAELSAWIVLEVGKPVKEADAEVSEAIDFCRYYADEMERLYQGINYDVAGETNRYIYQ 637 Query: 135 PHGVVAVFGPYNFPGHLPNGHIVPALLAGNCVVFKPSELTPKVAELTLKAWIQAGLPAGV 194 P G+V V P+NFP + G V AL+ GNC + KP+E + + + ++AG+P GV Sbjct: 638 PRGIVVVISPWNFPLAIACGMTVAALVTGNCTLLKPAETSSVITAKLTEILLEAGIPKGV 697 Query: 195 LNLVQG-GRETGVALAAHRGLDGLFFTGSSRTGNLLHSQFGG-QPQ----KILALEMGGN 248 V G G + G L +H + FTGS G ++++ +PQ K + EMGG Sbjct: 698 FQYVPGKGSQVGAYLVSHPDTHLIAFTGSQEVGCRIYAEAATLKPQQRHMKRVIAEMGGK 757 Query: 249 NPLVVEEVADLDAAVYTIIQSAFISAGQRCTCARRLLVPQGAWGDALLARLVAVSATLRV 308 N ++V+E ADLD AV ++QSAF +GQ+C+ R++V + + DA + RLV + +L + Sbjct: 758 NAIIVDESADLDQAVIGVVQSAFGYSGQKCSACSRVIVVEAIY-DAFIHRLVEATKSLNI 816 Query: 309 GRFDEQPAPFMGAVISLSAAEHLLKAQEHLIGKG-AQPLLAMTQPIDGAALLTPGILDVS 367 G E P+ +G VI +A + + + E GK +Q L ++ P G + +V Sbjct: 817 GE-AELPSTQVGPVIDANARDRIREYIEK--GKAESQVALELSAPNHGYFVGPVIFGEVP 873 Query: 368 AVAERPDEEFFGPLLQVIRYSDFAAAIREANATQYGLAAGLLSDSRERFEQFLVESRAGI 427 +E FGP+L VI+ DFA A+ AN T Y L GL S + +Q E G Sbjct: 874 PHGTIAQQEIFGPVLAVIKAKDFAQALAIANDTDYALTGGLYSRTPSHIQQAQEEFEVGN 933 Query: 428 VNWNKQLTGA-ASSAPFGGIGASG 450 + N+ +TGA + PFGG SG Sbjct: 934 LYINRNITGAIVARQPFGGFKLSG 957 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: 936 Number of extensions: 48 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: 487 Length of database: 993 Length adjustment: 39 Effective length of query: 448 Effective length of database: 954 Effective search space: 427392 Effective search space used: 427392 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