Align NADH-dependent phenylglyoxylate dehydrogenase subunit epsilon; Phenylglyoxylate:NAD oxidoreductase; Phenylglyoxylate:acceptor oxidoreductase; EC 1.2.1.58 (characterized)
to candidate WP_043744649.1 AMB_RS14715 NAD(P)/FAD-dependent oxidoreductase
Query= SwissProt::Q8L3B0 (421 letters) >lcl|NCBI__GCF_000009985.1:WP_043744649.1 AMB_RS14715 NAD(P)/FAD-dependent oxidoreductase Length = 421 Score = 165 bits (418), Expect = 2e-45 Identities = 122/409 (29%), Positives = 194/409 (47%), Gaps = 13/409 (3%) Query: 10 YLIAGSSHAALEAINAIRMHDAEGPITVVTRDAHLPYSPTVLPYVVSGKSAPERIFLRDD 69 +LI G+ A + A IR + IT+V + PYS +PY++ GK + +LR Sbjct: 3 HLIVGAGPAGVTAAEIIRELEPGATITLVGDEPEPPYSRMAIPYMLVGKVGEDGTYLRKG 62 Query: 70 -DFFARNKVAYRPKAALKALHADRNTAELADGSSVVYEKLLLATGASPAIPPIPGIDTVS 128 + + R + P + L L G ++ Y++LLLA GA P P I G+D Sbjct: 63 PNHYERLGITLMPGRRMSGLDPAARRIVLDGGETLAYDRLLLALGARPLRPDIEGLDLPG 122 Query: 129 YHVLRTLDDALKLRGAIAESKQAVVLGAGLVGMHAAENLVKAGATVTIVEMSEQLTSGYF 188 H TL DA K+ V++GAG VG E L ++T+VEM +++ Sbjct: 123 IHTCWTLADARKIAAQAIPGSHVVLMGAGFVGTIVLEALALRQVSLTVVEMGDRMVPRMM 182 Query: 189 DKVAADMIEQAFRDAGGKIMTGSRVVRLEPTAAGAK------LTLENGTTLEADLLLVAT 242 D+ A M+++ G +++TG+ + R+ A A + L +GT+L A L++V+ Sbjct: 183 DETAGGMLKRWCEAKGVRVLTGTGIRRITQAQAAADTRDSLVVELSDGTSLPAHLVVVSA 242 Query: 243 GVKPEMDYLNGSGVEHAQGILVDDRMQTTAENVWAAA-TAQARGFFTGTKVMNAILPDAT 301 GV+ + + SG+ GILVDD M+T+ +V+AA AQ R F +G ++AI A Sbjct: 243 GVRSNTEAVAASGIALGNGILVDDHMRTSLPDVFAAGDVAQGRDFMSGEAHVHAIQITAA 302 Query: 302 IQGRVAGMAMAGDPGVKDYAGAVPLNTYHFFGRHAISVGSSTVPEGGEVVTRFDEKTGRY 361 GR+A M G+ + Y G++ +N G S G S GG+ DE RY Sbjct: 303 AHGRIAAYNMTGND--QAYHGSLNMNVLDTLGLITCSFG-SWQGNGGDCARLVDEAGFRY 359 Query: 362 LKAIF-AADGPLTGIFGVNEFFDGGVMAQLILRRTDL-TPLRSRFVANP 408 L+ F + G V G + LI + L T ++ + +A+P Sbjct: 360 LRLEFDGTSDVVIGAQAVGTTDHVGALRGLIQSKRRLGTAVKEQMMADP 408 Lambda K H 0.318 0.134 0.382 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: 405 Number of extensions: 19 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: 421 Length of database: 421 Length adjustment: 32 Effective length of query: 389 Effective length of database: 389 Effective search space: 151321 Effective search space used: 151321 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 (21.7 bits) S2: 50 (23.9 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 preprint 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