Align N-succinylglutamate 5-semialdehyde dehydrogenase 1; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase 1; SGSD 1 (uncharacterized)
to candidate WP_057687530.1 ABB28_RS16890 betaine-aldehyde dehydrogenase
Query= curated2:Q12QD2 (498 letters) >NCBI__GCF_001431535.1:WP_057687530.1 Length = 490 Score = 201 bits (511), Expect = 5e-56 Identities = 146/459 (31%), Positives = 229/459 (49%), Gaps = 15/459 (3%) Query: 12 QTQFIAGQWL-AGKGPSFSSVNPANGEVIWQGLGADAGQVDAAITSARAAFYTWSAMSLT 70 Q +I G+ + A G +F S+NPA G+VI + A+ V+ A+ SA W+AM+ Sbjct: 7 QQLYIHGKLVDATSGKTFQSINPATGKVIAEVQIANQADVERAVASAAEGQKVWAAMTAM 66 Query: 71 ERLVIVEAFAEQLKEHAELFARTIALETGKALWESRTEVGAMTGKIAISIKANAERTGTV 130 ER I+ + L+E + A+ L+TGKAL E+ T V +TG + A T Sbjct: 67 ERSRILRRAVDLLRERNDALAQLETLDTGKALSETTT-VDIVTGADVLEYYAGLA-TAIE 124 Query: 131 ENPMPGAKA---FIRHKPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVLFKPSELTPKV 187 N +P ++ + R +P GVVA G +N+P + PAL AGN ++FKPSE+TP Sbjct: 125 GNQVPLRESSFFYTRREPLGVVAGIGAWNYPVQIALWKSAPALAAGNAMVFKPSEVTPLT 184 Query: 188 AELTMQLWQQAGLPNGVLNLLQGE-IATGKALASHKGIDGLFFTGSSNTGHLLHQQYAGQ 246 +++ +AG+P+GV N++QG G+ L H I+ + FTG TG + A Sbjct: 185 VIELAKIYTEAGVPDGVFNVVQGPGREVGQWLTEHPVIEKISFTGGVETGKKVMASAASS 244 Query: 247 PGKILALEMGGNNPLIITEVANVDAAVHDIIQSAFISSGQRCTCARRLFIPKTANGDAIL 306 K + +E+GG +PL+I + A ++ A + + F SSGQ CT R+F+P+ A Sbjct: 245 SLKEVTMELGGKSPLVICDDAQLERAADIAVMANFFSSGQVCTNGTRVFVPRPMLA-AFE 303 Query: 307 AKLLTSTAKIALGDPFAETQPFFGAMISDKAAAGMVKAQADIQAAGGVSLIELTQVTPGL 366 A ++ +I +GDP + Q FG M S +++ + G L + T G Sbjct: 304 AAVVERVKRIRIGDP-QDAQTNFGPMTSFAHMDNVLRLIETGKREGARLLTGGGRATDGA 362 Query: 367 ----GFVTPGII-DVTDASPLADEEHFGPLLKVYRYTDFDAAIDEANNTSFGLSAGLLAD 421 +V P + D D + EE FGP++ + Y D + I AN+T FGL+AG++++ Sbjct: 363 LAKGAYVLPTVFSDCRDDMTIVREEIFGPVMSILAYDDEEEVIARANDTHFGLAAGVVSN 422 Query: 422 SETDYQHFYRRIRAGIVNWNKPITGASSAAPFGGIGASG 460 R+ AGI W + + P GG SG Sbjct: 423 DIARAHRIIHRLEAGIC-WINTWGESPAEMPVGGYKQSG 460 Lambda K H 0.317 0.133 0.390 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: 574 Number of extensions: 24 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: 498 Length of database: 490 Length adjustment: 34 Effective length of query: 464 Effective length of database: 456 Effective search space: 211584 Effective search space used: 211584 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: 52 (24.6 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