Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_108401521.1 B9Z44_RS01610 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A0E3T3B5 (503 letters) >NCBI__GCF_003063475.1:WP_108401521.1 Length = 487 Score = 274 bits (701), Expect = 5e-78 Identities = 163/486 (33%), Positives = 264/486 (54%), Gaps = 17/486 (3%) Query: 11 FIDGEWREPVLKKRIPIINPATEQIIGDIPAATAEDVEIAVEAARKALARNKGRD-WALA 69 FI+G WR + +INPATE +G++ A AE V A+ AA +A + W Sbjct: 13 FINGTWRAGSESASV-MINPATEISLGEMKPAGAEQVTEAIAAAYEARTSMRALTAWN-- 69 Query: 70 PGAVRAKYLRAIAAKIAERKSEIAKLEAIDCGKPLDEAAWDIDDVSGCFEYYADLAE--- 126 R+ LR A I ER + L A++ GKP+ +A + + +++AD A Sbjct: 70 ----RSALLRRAATFINERAEMLGHLVALETGKPIRQAVGEAKASAESVDWFADEARRVF 125 Query: 127 GLDAQQKTPISLPMEQFKSHVLKEPIGVVGLITPWNYPLLMATWKVAPALAAGCAAILKP 186 G+ + + + +++ H+ EP+GVV PWN+PLL+ K+APALAAG +++P Sbjct: 126 GMSYESR----VKSDRYLVHM--EPLGVVAAFVPWNFPLLLLARKMAPALAAGNTLVIRP 179 Query: 187 SELASVTCLELADVCREVGLPPGVLNILTGLGHEAGAPLASHPHVDKIAFTGSTMTGSKI 246 S A+ + + L + G P GV+N++ G E + + V K++FTGS G +I Sbjct: 180 SSEAAGSTMALIKCFEDAGFPKGVVNLVIGRPAEITPTIMNDSRVAKVSFTGSVPIGRQI 239 Query: 247 MTAAAQLVKPVSLELGGKSPIVVFDDVDIDKAAEWTAFGIFWTNGQICSATSRLIIHENI 306 + +A +K VS+ELGG +P++V D DID A A G F GQ+C++ +R +HE+I Sbjct: 240 VEQSAITLKRVSMELGGHAPVIVHSDADIDAFAAMAAPGKFRNAGQVCASPTRFYVHESI 299 Query: 307 AAKFLDRLVQWCKNIKIADPLEEGCRLGPVVSGGQYEKILKFIATAKSEGARVLSGGARP 366 A + ++L+ + +++ PL++ LGP+ + + + I + + A S GARVLSGG RP Sbjct: 300 AKEVEEKLITATRALRVGSPLDDATDLGPLATRRRRDAIEQLVDNAVSGGARVLSGGMRP 359 Query: 367 EHLKKGFFIEPTIITDVTTSMQIWREEVFGPVLCVKTFSSEDEALELANDSHYGLGAAVI 426 + +G+F EPT +T + + +E FGP+ + TFS+ D+ + AN + L A V Sbjct: 360 RRMDRGYFYEPTWLTQLQPDALVLNDEPFGPIGTLATFSTLDQVIAEANRLPFALAAYVF 419 Query: 427 SKDLERCERVSKALQAGIVWINCSQPCFCQAPWGGNKRSGFGRELGKWGLDNYLTVKQVT 486 ++ L + LQAG++ +N + P+GG+K SGFGRE G + +YL K V Sbjct: 420 TRSLTKTHATVDRLQAGVIGVNTFVAATAETPFGGSKDSGFGREGGPHAIRDYLDTKFVN 479 Query: 487 EYVSDD 492 + D Sbjct: 480 VSMPTD 485 Lambda K H 0.319 0.136 0.419 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: 24 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: 503 Length of database: 487 Length adjustment: 34 Effective length of query: 469 Effective length of database: 453 Effective search space: 212457 Effective search space used: 212457 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