Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_028999950.1 H537_RS0124485 aldehyde dehydrogenase family protein
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_000430725.1:WP_028999950.1 Length = 503 Score = 365 bits (937), Expect = e-105 Identities = 195/483 (40%), Positives = 296/483 (61%), Gaps = 13/483 (2%) Query: 7 SRQLFIDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDW 66 S +L+IDG W P ++P+T I + +DVD AV AA++A +G +W Sbjct: 25 SHRLYIDGRWVDASSGATRPVLDPATGQQISVMAEGNVQDVDAAVRAARKAF---DGGEW 81 Query: 67 SAASGSLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEALADLDDVVAC--FEYYAGL 124 S + R+R + I I EL +LE +D G P + D +A F YYAG Sbjct: 82 RRLSTNERSRIVWKIGELIDVHAQELAELEVLDEGAPFA-VVKDFWVRLAADHFRYYAGW 140 Query: 125 AEELDSKQKAPISLPMDTFKSYILKEPIGVVALITPWNYPFLMATWKIAPALAAGCAAIL 184 +L+ P+++P + + +Y ++EP+GVV I PWN PFLMA WK+APALAAGC +L Sbjct: 141 PNKLNG-DTIPVNMPGE-WHAYTVREPVGVVGQIIPWNVPFLMAAWKLAPALAAGCTVVL 198 Query: 185 KPSELASVTCLELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGS 244 KP+E +T L L E+C+E G+P GV+N++TG G +AGA+L +HPD+DKI+FTGS+ TG Sbjct: 199 KPAEDTPLTALRLAELCREAGVPDGVVNVITG-GGDAGAALVAHPDIDKIAFTGSTETGK 257 Query: 245 KIMTTAAQLVKPVSLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRLIVHE 304 I+ AAQ +K VSLELGGKSP+ VF D DL V GQ C+A SRL +HE Sbjct: 258 AIVRAAAQNLKRVSLELGGKSPVFVFPDADLANVIPGVAQAVLLNAGQACTAGSRLYIHE 317 Query: 305 SIAVEFVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGGR 364 + +D + ++A ++K+ L+ +LGP++S Q+ +V + + EGA ++ GG+ Sbjct: 318 DVYDRVIDGVAQYASSLKLGHGLDPASQLGPLISARQFSRVSRMLQTGLDEGAQLVVGGQ 377 Query: 365 RPEHLKKGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTE--EEAINLANDTHYGLG 422 +H +GYF++PT++T V M ++R+E+FGPV+A S E + AN+T YGLG Sbjct: 378 --QHGDRGYFMQPTLLTGVRPGMSVYRDEIFGPVIAAMKISGENLDALAREANNTTYGLG 435 Query: 423 SAVMSNDLERCERLSKALQAGIVWINCAQPSFIQAPWGGIKRSGFGRELGEWGLENYLSV 482 +++ +ND++R +L+ ++AG++WIN P+GG K+SG+GRE+G+ G+E Y + Sbjct: 436 ASIWTNDVKRAHQLAARIRAGVIWINAHHSIDAAFPFGGFKQSGWGREMGKPGIELYTEL 495 Query: 483 KQV 485 K V Sbjct: 496 KSV 498 Lambda K H 0.317 0.134 0.402 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: 595 Number of extensions: 34 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: 503 Length of database: 503 Length adjustment: 34 Effective length of query: 469 Effective length of database: 469 Effective search space: 219961 Effective search space used: 219961 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 (21.6 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