Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_090271786.1 BLU11_RS01865 aldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_900105005.1:WP_090271786.1 Length = 506 Score = 325 bits (833), Expect = 2e-93 Identities = 184/480 (38%), Positives = 276/480 (57%), Gaps = 16/480 (3%) Query: 7 INGE-LVSGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVRAE 65 I GE +V +GE +P TG+V+ E + A +D A+ AA AA WG+T+P+ RA Sbjct: 23 IGGEFMVPADGEYFTNTSPVTGEVIAEFPRSKAADIDKALDAAHAAADAWGKTSPQDRAL 82 Query: 66 CLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAGE 125 LLK+AD IE N ++ A ++ + GK + N ++P D FR+FAG R G AA E Sbjct: 83 VLLKIADRIEANLEMLAVADTWDNGKAIRETLNADVPLAADHFRYFAGCIRAQEGSAA-E 141 Query: 126 YLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKLA 185 E + +PLGVV I PWN+PL+MAAWKLAPALAAGNCVVLKP+E TPL+ A Sbjct: 142 INEHTVAYHFHEPLGVVGQIIPWNFPLLMAAWKLAPALAAGNCVVLKPAEQTPLSMSLFA 201 Query: 186 ELAKDIFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKRTHM 245 EL D+ P GV+NI+ G GK G+ L ++ ++ TGS G HI+ A +I + + Sbjct: 202 ELVGDLLPPGVLNIVQGFGKEAGEALATSTRIAKIAFTGSTPVGAHIMHCAAENIIPSTV 261 Query: 246 ELGGKAPVIVFDD------ADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEK 299 ELGGK+P I F+D IE EG+ G++N G+ CT R Q+ I++ + + Sbjct: 262 ELGGKSPNIFFEDIMSAEPEFIEKAAEGL-VLGFFNQGEVCTCPSRALVQESIFEPFMNE 320 Query: 300 LGAAVATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRK----- 354 + + +K G P D T +G +S E++ ++ A+ G +V+TGGE K Sbjct: 321 VMKKIKKIKRGDPLDTETMVGAQASEQQFEKILSYLDIAQEEG-AQVLTGGEAEKLEGGL 379 Query: 355 GNGYYYAPTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKD 414 +GYY PTLL G + Q+E+FGPV+ VT F +E + + AND+++GL + +WT+D Sbjct: 380 ASGYYIQPTLLKGD-NSMRVFQEEIFGPVIGVTTFKDEAEALEVANDTEFGLGAGLWTRD 438 Query: 415 VGRAHRVSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVMVKH 474 + RA+R+ ++ G W N + + + GG K SG G++ L+ Y ++++V + Sbjct: 439 MNRAYRMGRGIKAGRVWTNCYHLYPAHAAFGGYKKSGVGRENHKMMLDHYQQTKNLLVSY 498 Lambda K H 0.317 0.134 0.397 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: 572 Number of extensions: 26 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: 474 Length of database: 506 Length adjustment: 34 Effective length of query: 440 Effective length of database: 472 Effective search space: 207680 Effective search space used: 207680 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 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