Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_012061606.1 SMED_RS23380 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q2SXN9 (487 letters) >NCBI__GCF_000017145.1:WP_012061606.1 Length = 491 Score = 204 bits (519), Expect = 6e-57 Identities = 152/463 (32%), Positives = 233/463 (50%), Gaps = 21/463 (4%) Query: 8 GAWVDGAGPVFASRNPGTNERVWEGASASADDVERAVASARRAFAAWSALDLDARCTIVK 67 G W AGP F NP T E + + + A+ +A A W+ R +++ Sbjct: 28 GEW---AGPTFDVFNPSTGELLAKLPDMGIKEARAAIDAAALAQPLWAGKPAKDRSIVLR 84 Query: 68 RFAALLVERKEALATMIGRETGKPLWEARTEVASMAAKVDISITAYHERTGEK-RAPMAD 126 R+ L+VE + LA ++ E GKP+ EA+ EV A+ ++ GE AP D Sbjct: 85 RWHDLIVEHVDDLAAILTAEMGKPVGEAKGEVLHAASYIEWYAEEAKRVYGETFPAPAND 144 Query: 127 GVAVLRHRPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSELAPGVARATVEIWR 186 ++ +P GVV P+NFP + I PAL AG T+V KP+E P VA A + Sbjct: 145 RRMLVIKQPVGVVGTITPWNFPASMVARKISPALAAGCTIVLKPAEQTPLVAGAMFALAE 204 Query: 187 DAGLPAGVLNLVQGEKDT--GVALANHRQIDGLFFTGSSDTGTLLHKQFGGRPEIVLALE 244 AG P GVLNL+ + G L ++ +I + FTGS++ G LL +Q + + V +LE Sbjct: 205 QAGFPEGVLNLLYASEGAPIGRELCSNPRIRKISFTGSTEVGRLLMRQCSDQIKKV-SLE 263 Query: 245 MGGNNPLVVAEVEDIDAAVHHAIQSAFLSAGQRCTCARRILVP---RGAFGDRFVARLAD 301 +GGN P +V + DID AV A+Q+ F +AGQ C A RI V AF ++FV R+ + Sbjct: 264 LGGNAPFIVFDDADIDEAVDGALQAKFRNAGQTCVSANRIYVQTAVHDAFAEKFVTRVRE 323 Query: 302 VASKITASVFDA-DPQPFMGAVISARAASRLVAAQARLVGLGASPIIEMKQRDPALGFVN 360 + +V D P +G +I A A ++ A + + GA + A F Sbjct: 324 L------TVGDGFAPGVTIGPMIDAHAIEKIEAHVSDAIAKGAEVRCGGNRIGTAGTFFE 377 Query: 361 AAIL-DVTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDTAFGLSAGLLADD-EQAWHT 418 +L +++ + EE FGP+A I+R+ + +A ANDT +GL+A A++ ++ WH Sbjct: 378 PTVLTGISHDMRVAQEETFGPIAPIIRFDSAEQVVAEANDTIYGLAAYFYAENLKRVWHV 437 Query: 419 FRRAIRAGIVNWNRPTNGASSAAPFGGAGRSGNHRPSAYYAAD 461 A+ G+V N +S AAPFGG +SG R + + + Sbjct: 438 -AEALEYGMVGIN-TGRMSSEAAPFGGIKQSGIGREGSRHGLE 478 Lambda K H 0.320 0.134 0.402 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: 516 Number of extensions: 26 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: 491 Length adjustment: 34 Effective length of query: 453 Effective length of database: 457 Effective search space: 207021 Effective search space used: 207021 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 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