Align Succinate-semialdehyde dehydrogenase, mitochondrial; At-SSADH1; Aldehyde dehydrogenase family 5 member F1; NAD(+)-dependent succinic semialdehyde dehydrogenase; Protein ENLARGED FIL EXPRESSING DOMAIN 1; EC 1.2.1.24 (characterized)
to candidate WP_022669887.1 G415_RS0101870 aldehyde dehydrogenase family protein
Query= SwissProt::Q9SAK4 (528 letters) >NCBI__GCF_000420385.1:WP_022669887.1 Length = 474 Score = 344 bits (883), Expect = 4e-99 Identities = 182/471 (38%), Positives = 298/471 (63%), Gaps = 12/471 (2%) Query: 57 IGGKWLDSYDNKTIKVNNPATGEIIADVACMGTKETNDAIASSYEAFTSWSRLTAGERSK 116 IGG+W+ + NKTI V + +GE+IA V K + A+ ++ EAF + ++ A +RS+ Sbjct: 8 IGGEWVST--NKTIDVIDKYSGEVIAKVPKADKKLVDKAVDAAAEAFEEFKKMPAYQRSE 65 Query: 117 VLRRWYDLLIAHKEELGQLITLEQGKPLKEAIGEVAYGASFIEYYAEEAKRVYGDIIPPN 176 +L + DL+ +E+ + I E GK K ++GEV G ++ +EEAKR++G+ +P + Sbjct: 66 ILEKAADLIKERSDEIAETICREAGKAWKYSVGEVNRGFETFKFASEEAKRIHGETVPMD 125 Query: 177 LS----DRRLLVLKQPVGVVGAITPWNFPLAMITRKVGPALASGCTVVVKPSELTPLTAL 232 S R ++ P+GV+GAITP+NFPL ++ KV PA+ASG T+V+KP+ TP+TAL Sbjct: 126 ASAGGVGRVGYYIRVPMGVLGAITPFNFPLNLVAHKVAPAIASGNTIVLKPASSTPITAL 185 Query: 233 AAAELALQAGVPPGALNVVMGNAPEIGDALLTSPQVRKITFTGSTAVGKKLMAAAAPTVK 292 AE+ +AG+P G NVV+G E+G++L+T+ +VRKITFTGS VG +L A +K Sbjct: 186 ILAEILEEAGLPKGVFNVVIGPGGEVGESLVTNDKVRKITFTGSAKVGHRLTQIAG--IK 243 Query: 293 KVSLELGGNAPSIVFDDADLDVAVKGTLAAKFRNSGQTCVCANRVLVQDGIYDKFAEAFS 352 +++LELG N+ +I+ DAD+D A+ + + F NSGQ C+ R+ V I D+F E F+ Sbjct: 244 RITLELGNNSATIIEKDADIDKAIPRCVDSAFANSGQVCISLQRIYVHKDIADEFTEKFA 303 Query: 353 EAVQKLEVGDGFRDGTTQGPLINDAAVQKVETFVQDAVSKGAKIIIGGKRHSLGMTFYEP 412 EA +KL+VG+ T GP+I++ ++ E ++++AV+ GA++++GGKR +P Sbjct: 304 EATKKLKVGNPVEKDTDLGPMIDENEAKRAEEWIKEAVNMGAELVVGGKREG---RVLQP 360 Query: 413 TVIRDVSDNMIMSKEEIFGPVAPLIRFKTEEDAIRIANDTIAGLAAYIFTNSVQRSWRVF 472 TV+R+ + +M + E+F P+ ++ + T EDAI+ ND+ GL A I+TN +++ Sbjct: 361 TVLRNTTKDMRVMCMEVFAPIVSIVEYDTFEDAIQHVNDSDYGLQAGIYTNDIRKIHYAI 420 Query: 473 EALEYGLVGVNE-GLISTEVAPFGGVKQSGLGREGSKYGMDEYLEIKYVCL 522 + L+ G V +N+ + + P+GG K SG+GREG ++ ++E IK V + Sbjct: 421 DNLDVGGVMINDTSIFRVDHMPYGGNKMSGIGREGVRFAIEEMTNIKMVMI 471 Lambda K H 0.317 0.134 0.383 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: 605 Number of extensions: 32 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: 528 Length of database: 474 Length adjustment: 34 Effective length of query: 494 Effective length of database: 440 Effective search space: 217360 Effective search space used: 217360 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