Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_108402347.1 B9Z44_RS09990 aldehyde dehydrogenase family protein
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_003063475.1:WP_108402347.1 Length = 485 Score = 281 bits (718), Expect = 5e-80 Identities = 166/482 (34%), Positives = 263/482 (54%), Gaps = 22/482 (4%) Query: 12 IDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDWSAASG 71 ID EW+ + ++NP+ +IG A+ D + A+ AA+RA R DW A S Sbjct: 9 IDNEWQPAQSGQFEDSVNPADGRVIGRYAASDGADAEAAIAAARRAFERP---DW-AQSP 64 Query: 72 SLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEALADLDDVVACFEYYAGLAEELDSK 131 LR + A +++ DEL L +++ GK L ++ ++ ++ YYAGL Sbjct: 65 RLRQMVMLKWADRLEAHADELAHLLTLENGKVLAQSRGEMAGAISEIRYYAGLTR----- 119 Query: 132 QKAPISLPMDTFK------SYILKEPIGVVALITPWNYPFLMATWKIAPALAAGCAAILK 185 +P F+ S +LKEP GV +I PWN P ++ I PALAAGC ++K Sbjct: 120 -----FIPGHVFEVEPGAYSTLLKEPAGVAGIIVPWNAPVVLLIRSITPALAAGCTTVIK 174 Query: 186 PS-ELASVTCLELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGS 244 P+ + A +T L ++ LPRGVLN+V+ GH +L + DVD ISFTGS+ATG Sbjct: 175 PAPQTALITAAVLADLQAVAELPRGVLNLVSECGHAVAQALTTSADVDVISFTGSNATGQ 234 Query: 245 KIMTTAAQLVKPVSLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRLIVHE 304 +IM AA +K +SLELGGKS +VF+DVD+ ++A +GQ C+A R++VH Sbjct: 235 RIMAAAAPTMKKLSLELGGKSCCLVFDDVDVSRIAPQLAAAATIISGQQCTAARRVLVHA 294 Query: 305 SIAVEFVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGGR 364 S E L + + + ++ L G +LGP++ +++V I+ A ++ G Sbjct: 295 SRYDEMKVALSQALQALVVAPGLAAGAQLGPLIDAPSHQRVSQAIAQATDLADEVILRGG 354 Query: 365 RPEHLK-KGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTEEEAINLANDTHYGLGS 423 RP+ L G+F+ PT++ TS ++E+FGP + ++ F E++A+ AN + YGL + Sbjct: 355 RPDGLSASGHFMTPTLVAHRDTSAFFVQDEIFGPFVVLEKFEDEQDAVKRANHSDYGLSA 414 Query: 424 AVMSNDLERCERLSKALQAGIVWINCAQPSFIQAPWGGIKRSGFGRELGEWGLENYLSVK 483 +V + D R R+++AL+ G VW+N F +A GG +RSG GR G L +++ +K Sbjct: 415 SVWTQDGARQMRVARALRNGTVWLNEHNKLFAEAETGGYRRSGLGRLHGYDALIDFMEIK 474 Query: 484 QV 485 + Sbjct: 475 HI 476 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: 490 Number of extensions: 14 Number of successful extensions: 5 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: 485 Length adjustment: 34 Effective length of query: 469 Effective length of database: 451 Effective search space: 211519 Effective search space used: 211519 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