Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_034269899.1 AMYHA_RS08895 aldehyde dehydrogenase
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_000504245.1:WP_034269899.1 Length = 492 Score = 375 bits (962), Expect = e-108 Identities = 211/485 (43%), Positives = 281/485 (57%), Gaps = 8/485 (1%) Query: 1 MAITVSSRQLFIDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISR 60 M T+ +L I G + NP T +P DVD AV AA+ A Sbjct: 1 MTATLERTKLLIGGHTVDATSGATFESRNPYTGQSWAVLPDGGVADVDAAVAAARDAFES 60 Query: 61 KNGRDWSAASGSLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEALADLDDVVACFEY 120 +W + +G RA +R +A I E + L +LE D GK E L + + Y Sbjct: 61 ----EWGSTTGQRRAALMRRLADLIDENAERLARLEVNDSGKLYREMQGQLGALGGWYHY 116 Query: 121 YAGLAEELDSKQKAPISLPMDTFKSYILKEPIGVVALITPWNYPFLMATWKIAPALAAGC 180 YAGLA++L+ +Q I P + Y KEPIGVVA ITPWN P L+ +WK+APALAAGC Sbjct: 117 YAGLADKLEGRQ---IPAPNPDYLVYTRKEPIGVVAAITPWNSPLLLLSWKLAPALAAGC 173 Query: 181 AAILKPSELASVTCLELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSS 240 ++KPSE A V+ E+ ++ G P GV+N+VT E GA LA HP VDK++FTGS+ Sbjct: 174 TVVVKPSEHAPVSTPTFAELFEQAGFPPGVVNVVTSQSREVGAYLAGHPGVDKVAFTGST 233 Query: 241 ATGSKIMTTAAQLVKPVSLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRL 300 +TG + AA+ + VSLELGGKSP VVF+D DL A V G F GQ C A SRL Sbjct: 234 STGLAVARAAAENLTAVSLELGGKSPQVVFDDADLAAAANGVVAGVFAAAGQTCMAGSRL 293 Query: 301 IVHESIAVEFVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATIL 360 IVHES+ E V+++ A +I++ DP + +GPI ++ QY+KVL + A ++G + Sbjct: 294 IVHESVHDELVERVADRAASIRLGDPRDPATEMGPIANQPQYEKVLGYLRRATADGTLVA 353 Query: 361 TGGRRPEHLKKGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTEEEAINLANDTHYG 420 TGG E L G FV PT++T VT + REEVFGPVLAV +F+ EEEA+ LANDT YG Sbjct: 354 TGGAADEEL-GGLFVRPTVLTGVTPEDTVVREEVFGPVLAVYSFTDEEEAVRLANDTPYG 412 Query: 421 LGSAVMSNDLERCERLSKALQAGIVWINCAQPSFIQAPWGGIKRSGFGRELGEWGLENYL 480 L AV + D+ R R++ L+AG VWIN + P+GG +SG GRE G +E Y+ Sbjct: 413 LAGAVWTKDVHRAHRVAARLRAGTVWINAYRAVAPGVPFGGYGQSGLGRENGWEAIEQYI 472 Query: 481 SVKQV 485 K V Sbjct: 473 ENKAV 477 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: 627 Number of extensions: 30 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: 503 Length of database: 492 Length adjustment: 34 Effective length of query: 469 Effective length of database: 458 Effective search space: 214802 Effective search space used: 214802 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 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