Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_068106355.1 I601_RS03205 aldehyde dehydrogenase family protein
Query= BRENDA::C0P9J6 (505 letters) >NCBI__GCF_001653335.1:WP_068106355.1 Length = 472 Score = 301 bits (772), Expect = 3e-86 Identities = 191/485 (39%), Positives = 254/485 (52%), Gaps = 18/485 (3%) Query: 6 MVPLRQLFVDGEWRPPAQGRRLPVVNPTTEAHIGEIPAGTAEDVDAAVAAARAALKRNRG 65 M ++ +VDG W P + V + + + AEDV A AAA A Sbjct: 1 MRTVQATYVDGAWAPGTGSTEVEVSSAADGSVLTRFQGAGAEDVARACAAAGRAWP---- 56 Query: 66 RDWARAPGAVRAKYLRAIAAKVIERKPELAKLEALDCGKPYDEAAWDMDD-VAGCFEYFA 124 WA P RA LR A V +R EL A + G P A VA A Sbjct: 57 -GWAATPVTDRADLLRTAAELVEKRADELGATAAQEVGTPIRMAPIVHGHMVAATMRDVA 115 Query: 125 DQAEALDKRQNSPVSLPMETFKCHLRREPIGVVGLITPWNYPLLMATWKIAPALAAGCTA 184 D+ E+ + SL + RE +GV IT WNYPL K+ PALA GCT Sbjct: 116 DKVESHTFEERVGSSLVL--------RESVGVAAAITAWNYPLYQLATKLVPALAVGCTV 167 Query: 185 VLKPSELASVTCLELADICKEVGLPSGVLNIVTGLGPDAGAPLSAHPDVDKVAFTGSFET 244 VLKPSE+A +T + + E GLP GV N+V G G +AG PL P V V+FTGS T Sbjct: 168 VLKPSEIAPLTTIGFFEALAEAGLPGGVANLVVGTGAEAGEPLVTDPRVGAVSFTGSTRT 227 Query: 245 GKKIMASAAPMVKPVTLELGGKSPIVVFDDVDIDKAVEWTLFGCFWTNGQICSATSRLLI 304 G +I AA V VTLELGGKS V+ DD D+ AV TL GC NGQ C+A +RL++ Sbjct: 228 GVRIAELAAAGVTRVTLELGGKSASVLLDDADLATAVPATLNGCLLNNGQTCAALTRLIV 287 Query: 305 HTKIAKKFNERMVAWAKNIKVSDPLEEGCRLGPVVSEGQYEKIKKFISNAKSQGATILTG 364 + E + A ++V DP + +GPV S Q+ ++ + + A GAT+++G Sbjct: 288 PRARLAEVEEILAAAVAQLRVGDPRDPDTAVGPVASAAQHHRVLQHLRGALDDGATVVSG 347 Query: 365 GV-RPAHLEK-GFFIEPTIITDITTSMEIWREEVFGPVLCVKEFSTEDEAIELANDTQYG 422 G+ P + G+++ PT++ + SM I REEVFGPVLCV +EDEA+ +ANDT YG Sbjct: 348 GLDAPEGVPAGGYYVRPTVLR-VEPSMRIAREEVFGPVLCVIAVDSEDEAVAVANDTDYG 406 Query: 423 LAGAVISGDRERCQRLSEEIDAGCIWVNCSQPCFCQAPWGGNKRSGFGRELGEGGIDNYL 482 L+GAV S D +R ++ + G + VN AP+GG KRSG+GRE G G+D YL Sbjct: 407 LSGAVWSADPDRALAVARRLRTGQVAVN-GGAFNISAPFGGYKRSGYGREGGRFGLDEYL 465 Query: 483 SVKQV 487 K V Sbjct: 466 ETKAV 470 Lambda K H 0.318 0.135 0.422 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: 599 Number of extensions: 27 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: 505 Length of database: 472 Length adjustment: 34 Effective length of query: 471 Effective length of database: 438 Effective search space: 206298 Effective search space used: 206298 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 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