Align 2-aminomuconate semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate WP_023432018.1 N177_RS09120 aldehyde dehydrogenase
Query= metacyc::MONOMER-13349 (490 letters) >NCBI__GCF_000496075.1:WP_023432018.1 Length = 492 Score = 301 bits (771), Expect = 3e-86 Identities = 172/487 (35%), Positives = 260/487 (53%), Gaps = 9/487 (1%) Query: 3 QYRNYINGEWV--ESARRFDDVNPVDGTVVAQVHEADREAVDSAIRAGHAAVRGAWGRTT 60 +Y+ I GEW + R D VNP V A + +A V AI H W Sbjct: 4 EYQMLIGGEWTGGSGSERLDSVNPYTQEVWATLPQAGDADVARAIEIAHDTYVSVWRGVN 63 Query: 61 VAERAAILCRIADEIDRRYDDFLAAEIADTGKPVAMASTIDIPRGAANFRVFADILKTAP 120 +RA +L R+AD +++ D + D GK + + + A N+R FA + Sbjct: 64 GRDRALMLNRLADLVEQNGPDLARIDTTDNGKVIRETGS-QMKFAARNYRYFAGLADKLQ 122 Query: 121 LDTFQTDLPDGARALNYAVRKPLGVVGVISPWNLPLLLLTWKIAPALACGNAVVAKPSEE 180 +T D L+Y + +PLGV +I+ WN PL LL K+APALA GN VV KPSE Sbjct: 123 GNTIPLD---NGEMLDYTIVEPLGVAVLITAWNSPLPLLANKLAPALAAGNTVVIKPSEH 179 Query: 181 TPGTATLLAEVMHTVGVPPGVFNLVHGFGPDSAGEFITTNDDIDAITFTGESRTGSAIMR 240 + ++ G P GV N+V G G G +TT+ + I+FTG T I+ Sbjct: 180 ASISTLAFGRLIAEAGFPDGVVNIVTGDG--RIGPALTTHKRVKKISFTGGLPTARRILE 237 Query: 241 AAATHVKPVSFELGGKNAAIIFADCDFEKMIDGMMRAVFLHSGQVCLCAERVYVERPIYN 300 AAA + PV+ ELGGK+ IIF D D + ++G + +F SGQ C+ R+ V+ IY+ Sbjct: 238 AAARRLVPVTTELGGKSPNIIFEDADLKAAVNGAVAGIFGASGQTCIAGSRLLVQSSIYD 297 Query: 301 RFLDAFVERVKALKLGWPQDGTTGMGPLISAEHRDKVLSYFKLAREEGAQVLVGGGVPKF 360 D +E+V+ ++LG P D T MGP+ + D++LS A EGA++ +GG Sbjct: 298 EVCDRVLEKVRGIRLGNPLDPATEMGPVANRAQFDRILSLIAQAENEGAKLALGGRQAT- 356 Query: 361 GDARDAGFWVEPTIITGLPQTARCIKEEVFGPICHVSPFDTEAEAIALANDTKYGLSATT 420 G + GF++EPT++ + + ++EVFGP+ + F+ EA+A+ +AND+ YGL+A Sbjct: 357 GPGLERGFFIEPTVLKDVEPSLTIARDEVFGPVLCILRFEDEADAVRIANDSDYGLAAGV 416 Query: 421 WTGNLNRGHRVSEAMRVGLSWVNSWFLRDLRTPFGGVGLSGIGREGGMHSLNFYSELTNV 480 WT ++ R HR++ + GL WVN++ + PFGG LSG GRE H+L Y+++ NV Sbjct: 417 WTNDVRRAHRMAREIEAGLVWVNTYRASYVGAPFGGTKLSGHGRERSWHTLMEYTQVKNV 476 Query: 481 CVRIDQE 487 + + E Sbjct: 477 MLDLSGE 483 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: 654 Number of extensions: 25 Number of successful extensions: 4 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: 492 Length adjustment: 34 Effective length of query: 456 Effective length of database: 458 Effective search space: 208848 Effective search space used: 208848 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