Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_011976387.1 SMED_RS11280 aldehyde dehydrogenase
Query= BRENDA::C6KEM4 (506 letters) >NCBI__GCF_000017145.1:WP_011976387.1 Length = 502 Score = 349 bits (896), Expect = e-100 Identities = 205/500 (41%), Positives = 286/500 (57%), Gaps = 23/500 (4%) Query: 11 GLFIGGAWREPCLGRRLPVVNPATEATIGDIPAGTAEDVEIAVAAARDAFSRDGGRQWSR 70 G FIGG WREP GR P T T+ + A D+E+A+ AA A + W R Sbjct: 16 GNFIGGEWREPVAGRYFDNTTPITGGTLCQVARSDAADIELALDAAHAAREK-----WGR 70 Query: 71 APGAVRANFLRAIAAKIKDRKSELALLETLDSGKPLDEA-SGDMDDVAACFEYYADLAEA 129 P A R+N L IA +++D LA ET D+GKP+ E + D+ F Y+A A Sbjct: 71 TPAAERSNILMKIATRMEDNLELLARAETWDNGKPIRETMAADIPLAIDHFRYFASCIRA 130 Query: 130 LDGKQRSPISLPMENFKSYVLKEPIGVVGLITPWNYPLLMATWKVAPALAAGCTTILKPS 189 +G I + +Y EP+GVVG I PWN+P+LMA+WK+APALAAG +LKP+ Sbjct: 131 QEGS----IGEIDHDTVAYHFHEPLGVVGQIIPWNFPILMASWKLAPALAAGNCVVLKPA 186 Query: 190 ELASVSCLELGAICMEIGLPPGVLNIITGLGPEAGAPLSSHSHVDKVAFTGSTETGKRIM 249 E S L + ++ LPPGVLNI+ G G EAG PL++ + K+AFTG T TG+ IM Sbjct: 187 EQTPGSILVWADLVGDL-LPPGVLNIVNGFGLEAGKPLATSPRIAKIAFTGETTTGRLIM 245 Query: 250 TSAAQMVKPVSLELGGKSPLIVFDDIGD-----IDKAVEWTMFGIFA-NAGQVCSATSRL 303 A+Q + PV+LELGGKSP I F D+ DKA+E F +FA N G+VC+ SR Sbjct: 246 QYASQNLIPVTLELGGKSPNIFFADVASEDDDFFDKALEG--FAMFALNQGEVCTCPSRA 303 Query: 304 LLHEKIAKKFLDRLVAWAKNIKVSDPLEEGCRLGSVISEGQYEKIKKFISTARSEGATIL 363 L+ E I +F++R V + I+ +PL+ +G+ S Q EKI +I + EGA +L Sbjct: 304 LVQESIYDRFMERAVKRVEAIRQGNPLDAATMIGAQASSEQLEKILAYIEIGKEEGADVL 363 Query: 364 YGGGR---PQHLRRGFFLEPTIITDVSTSMQIWQEEVFGPVICVKEFRTDSEAVELANDT 420 GGGR L G++++PT+ M+I+QEE+FGPV+ V F+T++EA+E+ANDT Sbjct: 364 TGGGRNVLEGDLSGGYYVKPTVFHG-HNKMRIFQEEIFGPVVSVTTFKTEAEALEIANDT 422 Query: 421 HYGLAGAVISNDQERCERISKALHSGIIWINCSQPCFVQAPWGGNKRSGFGRELGEWGLD 480 YGL V S D RC R + + +G +W NC A +GG K+SG GRE + LD Sbjct: 423 LYGLGAGVWSRDANRCYRFGREIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRETHKMMLD 482 Query: 481 NYLTVKQVTKYCSDEPWGWY 500 +Y K + S + G++ Sbjct: 483 HYQQTKNMLVSYSPKALGFF 502 Lambda K H 0.318 0.136 0.418 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: 701 Number of extensions: 40 Number of successful extensions: 6 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: 506 Length of database: 502 Length adjustment: 34 Effective length of query: 472 Effective length of database: 468 Effective search space: 220896 Effective search space used: 220896 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