Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate PP_2487 PP_2487 putative aldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >FitnessBrowser__Putida:PP_2487 Length = 503 Score = 351 bits (900), Expect = e-101 Identities = 193/474 (40%), Positives = 284/474 (59%), Gaps = 9/474 (1%) Query: 5 LLINGELVSGE-GEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVR 63 L I+ + V+ E GE + NPA G +L I A+A VD AV+AA AF W T+P R Sbjct: 23 LFIDNQWVTAEYGETLDIINPANGKILTNIPNATAADVDRAVQAAQRAFVTWRTTSPAER 82 Query: 64 AECLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAA 123 A LLK+AD++E + FA LE+ + GKP+ + + +IP +D FR+FAG R + A Sbjct: 83 ANALLKIADLLEADADRFAVLETLDVGKPIRESRSVDIPLAIDHFRYFAGVIRSQSDEAV 142 Query: 124 GEYLEGHT-SMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTAL 182 L+ T S+ +PLGVV + PWN+PL+MAAWK+APA+AAGN VV+KPSE+TP+T L Sbjct: 143 --MLDEQTLSIALSEPLGVVGQVIPWNFPLLMAAWKIAPAIAAGNTVVIKPSELTPVTIL 200 Query: 183 KLAELAKDIFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKR 242 +LA++ + PAGV+NI+ G G TVG L HP +R ++ TGS GE + + A I Sbjct: 201 ELAKIFAKVLPAGVVNIVTGLGTTVGQALLDHPDLRKLAFTGSTRVGELVANAAAKKIIP 260 Query: 243 THMELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLGA 302 +ELGGK+ IVF DA+ + VEG +N GQ C + R++ + IY+ + +L Sbjct: 261 ATLELGGKSANIVFPDANWDKAVEGAVLAILWNQGQVCESGARLFVHESIYERFLAELKH 320 Query: 303 AVATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKG----NGY 358 ++ G P + T +G S +ER+ V+ AK G +V+ GG + G G+ Sbjct: 321 KFEAVRVGDPLNPDTMMGAQVSKTQMERILGYVDIAKEEG-AEVLIGGGRLTGADYDAGF 379 Query: 359 YYAPTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRA 418 + PT+L G D + +E+FGPV+ V PF +E +V+ ANDS+YGLA +VWT+D+ RA Sbjct: 380 FIQPTILVGVRNDMRVAYEEIFGPVLCVIPFKDEAEVIAMANDSEYGLAGAVWTQDINRA 439 Query: 419 HRVSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVMV 472 RV+ ++ G WVNT+ + + P GG K SG G++ LE Y+ +++ V Sbjct: 440 LRVARAVETGRMWVNTYHEIPAHAPFGGYKKSGLGRETHKSMLEAYSQKKNIYV 493 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: 532 Number of extensions: 19 Number of successful extensions: 3 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: 503 Length adjustment: 34 Effective length of query: 440 Effective length of database: 469 Effective search space: 206360 Effective search space used: 206360 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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