Align 2-aminomuconate semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate WP_008506742.1 BIBO1_RS10835 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-13349 (490 letters) >NCBI__GCF_000182725.1:WP_008506742.1 Length = 505 Score = 355 bits (911), Expect = e-102 Identities = 201/489 (41%), Positives = 291/489 (59%), Gaps = 17/489 (3%) Query: 2 KQYRNYINGEWVE--SARRFDDVNPVDGTVVAQVHEADREAVDSAIRAGHAAVRGAWGRT 59 K+Y N+I G+WVE S R F++ +PV+G V+ +V +D V++A+ A HAA + WGRT Sbjct: 16 KRYGNFIGGKWVEPRSGRYFENTSPVNGQVLCEVARSDAADVEAALDAAHAA-KELWGRT 74 Query: 60 TVAERAAILCRIADEIDRRYDDFLAAEIADTGKPVAMASTIDIPRGAANFRVFADILKTA 119 +VAERA IL RIAD I+ AAE D GKP+ + D+P +FR FA +++ Sbjct: 75 SVAERALILNRIADRIEENLPALAAAETWDNGKPIRETTNADLPLAVDHFRYFAGVIRAQ 134 Query: 120 PLDTFQTDLPDGARALNYAVRKPLGVVGVISPWNLPLLLLTWKIAPALACGNAVVAKPSE 179 + D A Y +PLGVVG I PWN PLL+ TWK+APALA GN VV KP+E Sbjct: 135 EGGISEIDHDTVA----YHFHEPLGVVGQIIPWNFPLLMATWKLAPALAAGNCVVLKPAE 190 Query: 180 ETPGTATLLAEVMHTVGVPPGVFNLVHGFGPDSAGEFITTNDDIDAITFTGESRTGSAIM 239 +TP + +L E++ + +PPGV N+V+GFG + AG+ + ++ I I FTGE+ TG IM Sbjct: 191 QTPASILVLMELIADI-LPPGVVNIVNGFGLE-AGKPLASSPRIAKIAFTGETTTGRLIM 248 Query: 240 RAAATHVKPVSFELGGKNAAIIFADC-----DF-EKMIDGMMRAVFLHSGQVCLCAERVY 293 + A+ ++ PV+ ELGGK+ I F D DF +K I+G + L+ G+VC C R Sbjct: 249 QYASQNLIPVTLELGGKSPNIFFKDVAAEDDDFLDKAIEGFVMFA-LNQGEVCTCPSRAL 307 Query: 294 VERPIYNRFLDAFVERVKALKLGWPQDGTTGMGPLISAEHRDKVLSYFKLAREEGAQVLV 353 ++ IY+RF++ ++RV+A+ G P D T +G S+E +K+LSY + R+EGA+VL Sbjct: 308 IQESIYDRFMEKALKRVEAIVQGDPLDPATMIGAQASSEQLEKILSYLDIGRQEGAEVLA 367 Query: 354 GGGVPKFGDARDAGFWVEPTIITGLPQTARCIKEEVFGPICHVSPFDTEAEAIALANDTK 413 GG G++V+PT+ G R +EE+FGP+ V+ F +AEA+++ANDT Sbjct: 368 GGERNMLPGDLAGGYYVKPTVFKG-HNKMRIFQEEIFGPVVSVATFKDDAEALSIANDTL 426 Query: 414 YGLSATTWTGNLNRGHRVSEAMRVGLSWVNSWFLRDLRTPFGGVGLSGIGREGGMHSLNF 473 YGL A WT + R +R A++ G W N + FGG SGIGRE + L+ Sbjct: 427 YGLGAGIWTRDGTRAYRFGRAIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHLKMLDH 486 Query: 474 YSELTNVCV 482 Y N+ V Sbjct: 487 YQNTKNMLV 495 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: 589 Number of extensions: 37 Number of successful extensions: 8 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: 505 Length adjustment: 34 Effective length of query: 456 Effective length of database: 471 Effective search space: 214776 Effective search space used: 214776 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