Align 2-aminomuconate semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate WP_085216991.1 B9N75_RS00315 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-13349 (490 letters) >NCBI__GCF_900177405.1:WP_085216991.1 Length = 479 Score = 219 bits (558), Expect = 2e-61 Identities = 160/492 (32%), Positives = 226/492 (45%), Gaps = 37/492 (7%) Query: 6 NYINGEWVESARRFDDVNPV------------DGTVVAQVHEADREAVDSAIRAGHAAVR 53 ++I G E A F NP D +VA+V +A R+AV++ AG Sbjct: 9 HHIAGNRREGAAAFAQDNPARADDLHVEGPEADAALVAEVVDAARQAVEALAAAG----- 63 Query: 54 GAWGRTTVAERAAILCRIADEIDRRYDDFLAAEIADTGKPVAMASTIDIPRGAANFRVFA 113 + RA L RI + D +TGK + S ++ R A F FA Sbjct: 64 -------IEARADALARIGRTLGAEADRIALLIARETGKTLG-DSKGEVMRAARLFDFFA 115 Query: 114 DILKTAPLDTFQTDLPDGARALNYAVRKPLGVVGVISPWNLPLLLLTWKIAPALACGNAV 173 + F + P +++ P+GVV I+PWN P+ + WKIAPALA GNAV Sbjct: 116 GETLRNAGERFASTRPGAIVEVDHV---PVGVVAAITPWNFPIAIPAWKIAPALAYGNAV 172 Query: 174 VAKPSEETPGTATLLAEVMHTVGVPPGVFNLVHGFGPDSAGEFITTNDDIDAITFTGESR 233 + KPSE TA L V+ G+P G N++ G G AG I D +DA++FTG Sbjct: 173 LWKPSEIASATADALMAVIAGAGLPDGSVNMLLGMG--DAGRAIVEADGVDAVSFTGSVA 230 Query: 234 TGSAIMRAAATHVKPVSFELGGKNAAIIFADCDFEKMIDGMMRAVFLHSGQVCLCAERVY 293 TG+ + AAA V E+GG N I+ AD D + +D + F +GQ C R+ Sbjct: 231 TGARVRAAAAERGARVQLEMGGVNGLIVMADADLDNAVDCAVNGAFFAAGQRCTATSRMI 290 Query: 294 VERPIYNRFLDAFVERVKALKLGWPQDGTTGMGPLISAEHRDKVLSYFKLAREEGAQVLV 353 V I +RF+DA ERV ALK+G P D T +GPL + ++ + GA+ + Sbjct: 291 VGDAIADRFIDAVRERVAALKIGDPTDAATQVGPLAAPHQKETIARQVAAVEASGAKPVF 350 Query: 354 GGGVPKFGDARDAGFWVEPTIITGLPQTARCIKEEVFGPICHVSPFDTEAEAIALANDTK 413 GG G A + F+ PT+ +EE+FGP+ V EA+ + N + Sbjct: 351 GGS----GAAMEQCFYA-PTLFDCAAPEGTLGQEEIFGPVAGVFRVSGFDEAMTVLNGNR 405 Query: 414 YGLSATTWTGNLNRGHRVSEAMRVGLSWVNSWFLR-DLRTPFGGVGLSGIG-REGGMHSL 471 +GLSA T +L R G+ VN D PFGGV S G RE G + Sbjct: 406 FGLSAGICTRSLLHAEEFKRRARAGMKMVNLPTAGVDYHAPFGGVADSSYGPREQGRAAR 465 Query: 472 NFYSELTNVCVR 483 FY+ +T V+ Sbjct: 466 AFYTNMTTSYVK 477 Lambda K H 0.321 0.137 0.420 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: 575 Number of extensions: 27 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: 490 Length of database: 479 Length adjustment: 34 Effective length of query: 456 Effective length of database: 445 Effective search space: 202920 Effective search space used: 202920 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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