Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_110207793.1 DNK54_RS15005 aldehyde dehydrogenase
Query= BRENDA::C0P9J6 (505 letters) >NCBI__GCF_003194585.1:WP_110207793.1 Length = 501 Score = 352 bits (904), Expect = e-101 Identities = 201/485 (41%), Positives = 283/485 (58%), Gaps = 9/485 (1%) Query: 7 VPLRQLFVDGEWRPPAQGRRLPVVNPTTEAHIGEIPAGTAEDVDAAVAAARAALKRNRGR 66 VP Q F++G W G+ L V +P T + + G A ++DAAVAAA+AA + Sbjct: 3 VPHYQNFINGAWTD--NGQVLEVRSPATGELVATVAKGGAAEIDAAVAAAKAA---HAAG 57 Query: 67 DWARAPGAVRAKYLRAIAAKVIERKPELAKLEALDCGKPYD-EAAWDMDDVAGCFEYFAD 125 W P A RA + A+A + R ELA L++ + G A + ++ A Sbjct: 58 VWRNTPPAERAALINAVAGDLAGRLEELAALQSRENGATIRVTGALHVGLSIANMQFIAA 117 Query: 126 QAEALDKRQNSPVSLPMETFKCHLRREPIGVVGLITPWNYPLLMATWKIAPALAAGCTAV 185 QA + + P P+ + LRREP+GVVG I PWN PLL WK+ PALAAG T V Sbjct: 118 QAAEYEFEKAGPEIGPVPA-EGILRREPLGVVGAIVPWNIPLLTIVWKVTPALAAGNTVV 176 Query: 186 LKPSELASVTCLELADICKEVGLPSGVLNIVTGLGPDAGAPLSAHPDVDKVAFTGSFETG 245 LKP E A + LELA + GLP+GVLN+V G G DAGA LS HPDV K+ FTGS E G Sbjct: 177 LKPDEHAPLLALELAKAFEAAGLPAGVLNVVVGEGHDAGARLSQHPDVRKIGFTGSTEVG 236 Query: 246 KKIMASAAPMVKPVTLELGGKSPIVVFDDVDIDKAVEWTLFGCFWTNGQICSATSRLLIH 305 K I+ ++A +K VTLELGGK P ++ DD D+D A++ ++ C NG+ C A +RLL+ Sbjct: 237 KSILGASADNMKRVTLELGGKGPNILLDDADLDVAIDGAIYACMANNGEACEAGTRLLVP 296 Query: 306 TKIAKKFNERMVAWAKNIKVSDPLEEGCRLGPVVSEGQYEKIKKFISNAKSQGATILTGG 365 + ER+VA +K+ +PL+ +GP+++ Q +++ I+ A++QGA + GG Sbjct: 297 NSRKDEIVERLVARVGTMKIGNPLDPATDIGPLITADQRDRVLAHIAKAETQGAKVAIGG 356 Query: 366 VRPAHLE--KGFFIEPTIITDITTSMEIWREEVFGPVLCVKEFSTEDEAIELANDTQYGL 423 PA E G+F+EPT++TD+T SM + EEVFGPVL V + T DEAI +ANDT+YGL Sbjct: 357 SAPAGEEFANGYFVEPTVLTDVTPSMTVACEEVFGPVLSVLGYDTVDEAIAIANDTEYGL 416 Query: 424 AGAVISGDRERCQRLSEEIDAGCIWVNCSQPCFCQAPWGGNKRSGFGRELGEGGIDNYLS 483 + V D R ++ +++AG I+VN P+GG K+SG GRE G +D Y Sbjct: 417 SAGVWGTDETRVLDVARQLEAGMIYVNDWHVLHPAYPFGGYKQSGLGREGGPNALDAYTE 476 Query: 484 VKQVT 488 K ++ Sbjct: 477 QKYIS 481 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: 688 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: 505 Length of database: 501 Length adjustment: 34 Effective length of query: 471 Effective length of database: 467 Effective search space: 219957 Effective search space used: 219957 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