Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_015887458.1 NGR_RS06520 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q1QTQ7 (489 letters) >NCBI__GCF_000018545.1:WP_015887458.1 Length = 491 Score = 200 bits (509), Expect = 8e-56 Identities = 152/468 (32%), Positives = 222/468 (47%), Gaps = 32/468 (6%) Query: 11 GAWVDGDAARFAKTDPVSGETLWTATAASATQVEHAVAAARQAFPDWARRSFAERQAVVE 70 GAW D A F +P +GE L T A+ AA +A P WA + +R A++ Sbjct: 28 GAW---DGATFDVFNPSTGELLATLPDMGIEDAHAAIEAAAKAQPIWAGKPAKDRSAILR 84 Query: 71 RFRECLETHREHLATAIAQETGKPLWEARTEVGAMIGKVAISITAYHERTGERARDI--- 127 + + + H + LA + E GKPL EA+ EV + +Y E E A+ I Sbjct: 85 CWHDLIVAHADDLAAILTAEMGKPLGEAKGEV--------LHAASYIEWYAEEAKRIYGE 136 Query: 128 ------GDARAVLRHRPHGVLAVYGPYNFPGHLPNGHIVPALLAGNAVVFKPSEQTPMTA 181 D R ++ +P GV+ P+NFP + I PAL AG A+V KP+EQTP+ A Sbjct: 137 TFPAPANDRRMLVIKQPVGVVGTITPWNFPASMVARKIAPALAAGCAIVLKPAEQTPLVA 196 Query: 182 DLTLQCWLEAGLPAGVINLVQGA--AEVGQALAGSADIDGLLFTGSAKVGGLLHRQFGGQ 239 +AG PAGV+NL+ + A +G+ L + + + FTGS +VG LL RQ Q Sbjct: 197 GAMFVLAEKAGFPAGVLNLLYASEGAPIGRELCSNPKVRKISFTGSTEVGRLLMRQCSDQ 256 Query: 240 VDKILALELGGNNPLVVKDVPDREAAVLSILQSAFASGGQRCTCARRLIVPHGAVGDDLI 299 + K+ +LELGGN P +V D D E AV +Q+ F + GQ C A R+ V AV D Sbjct: 257 IKKV-SLELGGNAPFIVFDDADIEEAVDGAIQAKFRNAGQTCVSANRIYV-QSAVHDAFA 314 Query: 300 DALTSAIAELRVAAPFSEPAPFYAGLTSVEAADGLLAAQDDLVARGGRPLSRMRRLQAGT 359 + + + ELRV FS P + A + + A D +A+G R+ Sbjct: 315 EKFVARVRELRVGDGFS-PDATIGPMIDGHAIEKIEAHVADALAKGAELRCGGGRIGTKG 373 Query: 360 SLLSPGLIDVTGCDV--PDEEHFGPLLKVHRYRDWDEAIALANDTRYGLSAGLIGGERAD 417 + P ++ D+ EE FGP+ + + ++ +A ANDT YGL+A Sbjct: 374 TFFEPTVLTGISHDMRAAQEETFGPIAPIIHFETAEQVVAEANDTIYGLAAYFYAENLKR 433 Query: 418 WDDFLLRIRAGIVNWNRQTTG--ASSDAPFGGIGDSGNHRPSAYYAAD 463 + G+V N TG +S APFGGI SG R + + + Sbjct: 434 VWHVAEALEYGMVGIN---TGRMSSEAAPFGGIKQSGIGREGSRHGLE 478 Lambda K H 0.319 0.135 0.409 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: 610 Number of extensions: 30 Number of successful extensions: 6 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: 489 Length of database: 491 Length adjustment: 34 Effective length of query: 455 Effective length of database: 457 Effective search space: 207935 Effective search space used: 207935 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