Align Alpha-aminoadipic semialdehyde dehydrogenase; Alpha-AASA dehydrogenase; Aldehyde dehydrogenase family 7 member A1; Antiquitin-1; Betaine aldehyde dehydrogenase; Delta1-piperideine-6-carboxylate dehydrogenase; P6c dehydrogenase; EC 1.2.1.31; EC 1.2.1.3; EC 1.2.1.8 (characterized)
to candidate WP_043531966.1 JH15_RS15380 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q9DBF1 (539 letters) >NCBI__GCF_000759345.1:WP_043531966.1 Length = 483 Score = 235 bits (599), Expect = 3e-66 Identities = 142/448 (31%), Positives = 234/448 (52%), Gaps = 8/448 (1%) Query: 71 PANNEPIARVRQASLKDYEETIGKAKKAWNIWADIPAPKRGEIVRKIGDAFREKIQLLGR 130 PA N+ + V + S + I A +A +W A +R I+R+ D E + L + Sbjct: 33 PATNDRLGTVPKLSKDEVSAAIDAADRALPLWKAKTAKERASILRRWFDLCMEHQEDLAQ 92 Query: 131 LVSLEMGKILVEGIGEVQEYVDVCDYAAGLSRMIGGPTLPSERPGHALIEMWNPLGLVGI 190 +++LE GK L E GE+ ++ ++ + G +P+ ++ P+G+V Sbjct: 93 ILTLEQGKPLQEARGEIAYGASFIEWFGEEAKRVYGDVIPAHAKDRRIVVTKEPVGVVAA 152 Query: 191 ITAFNFPVAVFGWNNAIALITGNVCLWKGAPTTSLVSVAVTKIIAQVLEDNLLPGAICSL 250 IT +NFP A+ A A+ G + K A +T ++A +A++ E +P + ++ Sbjct: 153 ITPWNFPNAMITRKAAAAMAAGCTVIVKPASSTPYSALA----LAELAERAGVPRGVLNV 208 Query: 251 VCGGADI-GTTMARDERVNLLSFTGSTQVGKEVALMVQERFGKSLLELGGNNAIIAFEDA 309 V G A + G + + RV LSFTGST+VGK + + K +ELGGN I FEDA Sbjct: 209 VTGSASVVGGELTANPRVRKLSFTGSTEVGKILLGECAKTVKKVSMELGGNAPFIIFEDA 268 Query: 310 DLSLVVPSVLFAAVGTAGQRCTTVRRLFLHESIHNEVVDRLRSAYSQIRVGNPWDPNILY 369 DL V V+ + GQ C R+F+H+ I+++ DRL +A S +VG+ + + Sbjct: 269 DLDQAVAGVMASKFRNTGQTCVCANRIFVHDKIYDDFTDRLATAVSAQKVGSGLEDGVSL 328 Query: 370 GPLHTKQAVSMFVRAVEEAKKQGGTVVYGGKVMDHPGNYVEPTIVTGLAHDAPIVHQETF 429 GPL AV + +E+A +G +V GGK + GN+ +PTI+T ++ D+ ++H ETF Sbjct: 329 GPLINPAAVEKVEQHIEDAIAKGASVYLGGKRHELQGNFFQPTILTNVSSDSMLMHDETF 388 Query: 430 APILYVFKFQDEEEVFEWNNEVKQGLSSSIFTKDLGRIFRWLGPKGSDCGIVNVNIPTSG 489 P+ + +F DE++V N+ GL+S +T+D+GR+ W + +CGIV +N Sbjct: 389 GPVAPLLRFTDEDDVIRQANDTTLGLASYFYTRDVGRV--WRVAEALECGIVGINEGIIS 446 Query: 490 AEIGGAFGGEKHTGGGRESGSDAWKQYM 517 +E+ FGG K +G GRE Y+ Sbjct: 447 SEL-APFGGVKESGIGREGSKYGIDDYI 473 Lambda K H 0.319 0.137 0.421 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: 671 Number of extensions: 34 Number of successful extensions: 3 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: 539 Length of database: 483 Length adjustment: 34 Effective length of query: 505 Effective length of database: 449 Effective search space: 226745 Effective search space used: 226745 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 (21.7 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