Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_040474635.1 MDG893_RS14400 aldehyde dehydrogenase
Query= curated2:Q2SXN9 (487 letters) >NCBI__GCF_000170835.1:WP_040474635.1 Length = 509 Score = 189 bits (481), Expect = 1e-52 Identities = 152/477 (31%), Positives = 229/477 (48%), Gaps = 26/477 (5%) Query: 4 LFIDG-AWVDGA------GPVFASRNPGTNERVWEGASASADDVERAVASARRAFAA--W 54 L I+G A+V G+ G F S +P + + AS D ++AVA AR+ F W Sbjct: 27 LAIEGRAYVKGSYRWAVNGETFPSISPVNGRELAQVASCDKADADKAVAIARKVFERGDW 86 Query: 55 SALDLDARCTIVKRFAALLVERKEALATMIGRETGKPLWEART-EVASMAAKVDISITAY 113 L R ++ RFA L+ + LA + + GKP+ ART +V + A + + A Sbjct: 87 RELAPIKRKAVLIRFAELIEAHGDELALLDTLDMGKPISHARTVDVPATARAIRWTAEAI 146 Query: 114 HERTGEKRAPMADGVAVLRHRPHGVVAVFGPYNFPGHLPNGHIVPALIAGNTVVFKPSEL 173 + GE + + ++ P GVVA P+NFP + I PAL GN+V+ KPSE Sbjct: 147 DKVYGELAPTPHNQIGMISREPMGVVAAIVPWNFPMIMAAWKIAPALATGNSVILKPSEK 206 Query: 174 APGVARATVEIWRDAGLPAGVLNLVQGEKDT-GVALANHRQIDGLFFTGSSDTGTLLHKQ 232 +P A + +AG+P GV N++ G T G ALA H +D L FTGS++ L Sbjct: 207 SPLTAIRLAALATEAGIPDGVFNVLPGFGHTVGKALALHMDVDCLVFTGSTNVAKQLMVY 266 Query: 233 FGGRPEIVLALEMGGNNP-LVVAEVEDIDAAVHHAIQSAFLSAGQRCTCARRILVPRGAF 291 G + LE GG +P +V A+ D+ A A + + G+ CT R+LV + Sbjct: 267 AGQSNMKRVWLEAGGKSPNIVFADAPDLKKAAAEAASAIAFNQGEVCTAGSRLLVEE-SV 325 Query: 292 GDRFVARLADVASKITASVFDADPQPFMGAVISARAASRLVAAQARLVGLGAS---PIIE 348 FV + + A K DP GA++ R++ +G+G S ++E Sbjct: 326 RTEFVGLIRE-ALKTWRPGHPLDPATTCGAIVDQAQLDRII----DYIGIGQSEGAKLVE 380 Query: 349 MKQRDPALG---FVNAAILD-VTNVRELPDEEHFGPLAQIVRYTDLDDAIARANDTAFGL 404 QR A FV + D V N + EE FGP+ ++ +T ++AI AND+ +GL Sbjct: 381 GGQRVMAETGGLFVQPTVFDGVNNRMRIASEEIFGPVLSVIGFTTAEEAIEIANDSIYGL 440 Query: 405 SAGLLADDEQAWHTFRRAIRAGIVNWNRPTNGASSAAPFGGAGRSGNHRPSAYYAAD 461 +A + + H +A+RAG V W +G APFGG +SGN R + +A D Sbjct: 441 AAAVWTSNINTAHKVAKALRAGSV-WINHYDGGDMTAPFGGFKQSGNGRDKSLHAFD 496 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: 550 Number of extensions: 31 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: 509 Length adjustment: 34 Effective length of query: 453 Effective length of database: 475 Effective search space: 215175 Effective search space used: 215175 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 Sep 24 2021. 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