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_052591776.1 VV02_RS12055 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q9DBF1 (539 letters) >NCBI__GCF_001190945.1:WP_052591776.1 Length = 486 Score = 204 bits (520), Expect = 5e-57 Identities = 139/451 (30%), Positives = 218/451 (48%), Gaps = 13/451 (2%) Query: 71 PANNEPIARVRQASLKDYEETIGKAKKAWNIWADIPAPKRGEIVRKIGDAFREKIQLLGR 130 PA E + V S+KD + + A A WA P RGE++R + E+ + L Sbjct: 36 PATGEALTHVADGSVKDGDAALAAAAAAQADWAKTPPRDRGELLRSAYEMLVERTEDLAT 95 Query: 131 LVSLEMGKILVEGIGEVQEYVDVCDYAAGLSRMIGGPTLPSERPGHALIEMWNPLGLVGI 190 L++LEMGK L E GEV + + + + I G + L+ M P+G + Sbjct: 96 LMTLEMGKPLAESRGEVAYGSEFFRWFSEEAVRISGRWSTAPNGATRLVTMKQPVGPTLM 155 Query: 191 ITAFNFPVAVFGWNNAIALITGNVCLWKGAPTTSLVSVAVTKIIAQVLEDNLLPGAICSL 250 IT +NFP+A+ A+ G + K A T L + ++AQ+LE+ LP + ++ Sbjct: 156 ITPWNFPLAMGTRKIGPAIAAGCTMVVKPAAETPLTML----LLAQILEEVGLPKGVLNV 211 Query: 251 VCGGAD--IGTTMARDERVNLLSFTGSTQVGKEVALMVQERFGKSLLELGGNNAIIAFED 308 + + + RD R L+FTGST +G+++ E+ + +ELGGN + FED Sbjct: 212 ITTSTSGQVMEPLIRDPRSRKLTFTGSTPIGQKLIEQSAEQLLRVSMELGGNAPFLVFED 271 Query: 309 ADLSLVVPSVLFAAVGTAGQRCTTVRRLFLHESIHNEVVDRLRSAYSQIRVGNPWDPNIL 368 ADL V + A + G+ CT R +H + +E RL + VG+ D + Sbjct: 272 ADLDAAVEGAMLAKMRNIGEACTAANRFLVHADVADEFSRRLAERMGALTVGDGMDDDTK 331 Query: 369 YGPLHTKQAVSMFVRAVEEAKKQGGTVVYGGKVMDHPGNYVEPTIVTGLAHDAPIVHQET 428 GPL +AV VE+AK +G VV GG+ + G + PT++T + +A + +E Sbjct: 332 VGPLINAKAVDKVKALVEDAKGRGARVVTGGETVGDRGFFYAPTVLTDVTGEADMAREEI 391 Query: 429 FAPILYVFKFQDEEEVFEWNNEVKQGLSSSIFTKDLGRIFRWLGPKGSDCGIVNVN--IP 486 F P+ + F DE + E N + GL + FTKD R R + + G+V VN I Sbjct: 392 FGPVAGIQTFTDEADAIERANSTEYGLVAYFFTKDFSRAIR--VSEALEYGMVGVNQGIV 449 Query: 487 TSGAEIGGAFGGEKHTGGGRESGSDAWKQYM 517 ++ A FGG K +G GRE G + +Y+ Sbjct: 450 SNPA---APFGGVKASGFGREGGFEGIDEYL 477 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: 654 Number of extensions: 31 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: 539 Length of database: 486 Length adjustment: 35 Effective length of query: 504 Effective length of database: 451 Effective search space: 227304 Effective search space used: 227304 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