Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_055435763.1 ASC41_RS05615 aldehyde dehydrogenase
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_001418085.1:WP_055435763.1 Length = 478 Score = 343 bits (879), Expect = 1e-98 Identities = 192/478 (40%), Positives = 273/478 (57%), Gaps = 12/478 (2%) Query: 11 FIDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDWSAAS 70 +I+G ++ PI + I N NPS + G IP ++KEDV+ A AAK A WS S Sbjct: 6 YINGTFQNPIQDNWIDNYNPSNGEVYGQIPNSSKEDVENAYKAAKSAFP-----SWSKTS 60 Query: 71 GSLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEALA-DLDDVVACFEYYAGLAEELD 129 R+R L I+ ++ + ES D GKP+ A A D+ + F ++ + Sbjct: 61 IEERSRILIKISELLEANLQRFAEAESKDNGKPISLAKAVDIPRAASNFRFFGNAITQFA 120 Query: 130 SKQKAPISLPMDTFKSYILKEPIGVVALITPWNYPFLMATWKIAPALAAGCAAILKPSEL 189 S+ I ++ Y L++PIGVVA I+PWN P + TWKIAPA+AAG + KPSE+ Sbjct: 121 SESHESIGQAIN----YTLRQPIGVVACISPWNLPLYLFTWKIAPAIAAGNCVVAKPSEV 176 Query: 190 ASVTCLELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGSKIMTT 249 +T LGEIC E GLP+GVLNIV GLG G ++ H D+ ISFTG +ATG+ I Sbjct: 177 TPMTAYLLGEICNEAGLPKGVLNIVHGLGGSTGQAIIEHEDIKAISFTGGTATGAHIAKV 236 Query: 250 AAQLVKPVSLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRLIVHESIAVE 309 AA L K +SLELGGK+P ++F D D D + + TV F GQIC SR+ V SI + Sbjct: 237 AAPLFKKLSLELGGKNPNIIFADCDYDDMLDTTVRSSFANQGQICLCGSRIFVETSIYEK 296 Query: 310 FVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGGRR--PE 367 F V + +K+ P E +G +VS+ +KV I+ AK+E TIL GG + Sbjct: 297 FKKDFVAKVKALKVGHPSEASTNIGALVSKPHIEKVKEYINIAKAENGTILCGGNEVTVK 356 Query: 368 HLKKGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTEEEAINLANDTHYGLGSAVMS 427 + GY++EPT+I ++ +EE+FGPV+ + F+TE+E + +AN YGL + + + Sbjct: 357 GYENGYYLEPTVIEVPNDECRVNQEEIFGPVVTIMPFTTEDEVLKMANKVKYGLSATLWT 416 Query: 428 NDLERCERLSKALQAGIVWINCAQPSFIQAPWGGIKRSGFGRELGEWGLENYLSVKQV 485 N+L+R ++S LQAGIVW+N ++ P+GGIK SG GRE G L + K V Sbjct: 417 NNLKRTMKMSNELQAGIVWVNTWMMRDLRTPFGGIKASGVGREGGFEALRFFTEAKNV 474 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: 585 Number of extensions: 31 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 503 Length of database: 478 Length adjustment: 34 Effective length of query: 469 Effective length of database: 444 Effective search space: 208236 Effective search space used: 208236 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