Align 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_079649158.1 B5X82_RS15880 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-20632 (478 letters) >NCBI__GCF_900167915.1:WP_079649158.1 Length = 478 Score = 563 bits (1451), Expect = e-165 Identities = 278/475 (58%), Positives = 350/475 (73%) Query: 1 MTDTLRHYIGGERVAADAPAESLNPSNTNDVVAKVPMGGQAEVDAAVDAARKAFPAWADA 60 MT L H +GGER+ A ES NPS+ +D+VA P G A +D A+ AA A P WA Sbjct: 1 MTIVLSHRVGGERIGGGAAIESRNPSDLSDLVATTPEGDAALLDRAIAAAAAAQPDWAAR 60 Query: 61 SPEVRSDLLDKVGSTIIARSADIGRLLAREEGKTLAEGIGETVRAGRIFKYFAGEALRRH 120 SPE R D+LD+ + ++ R+ ++G LL+REEGKTLAEG E +RA RI +YF GEALR H Sbjct: 61 SPEARGDILDRAAALLMERAGELGTLLSREEGKTLAEGKSEVMRAARILRYFGGEALRLH 120 Query: 121 GQNLESTRPGVEIQTYRQAVGVYGLITPWNFPIAIPAWKAAPALAFGNTVVIKPAGPTPA 180 G+ + S RPG+++ T ++ +G+ GLITPWNFPIAIPAWKAAPALAFGN VV+KPAG TPA Sbjct: 121 GRAMASVRPGIDVATRQEPLGIVGLITPWNFPIAIPAWKAAPALAFGNAVVLKPAGITPA 180 Query: 181 TANVLADIMAECGAPAGVFNMLFGRGSMGDALIKHKDVDGVSFTGSQGVGAQVAAAAVAR 240 A+ LAD++ E G P G+FN++F G++ + + V G+SFTGS GVG ++A AA A Sbjct: 181 IASALADVLEEAGLPPGLFNLVFVPGAVAGRMAEDARVAGLSFTGSTGVGRRLAVAAAAH 240 Query: 241 QARVQLEMGGKNPLIVLDDADLERAVAIALDGSFFATGQRCTASSRLIVQDGIHDKFVAL 300 R+QLEMGGKNPL+VLDDADL+RAVA+ALDGSFF +GQRCTASSRLIV DGIHD+FVA Sbjct: 241 GKRIQLEMGGKNPLVVLDDADLDRAVAVALDGSFFGSGQRCTASSRLIVTDGIHDRFVAA 300 Query: 301 LAEKVAALRVGDALDPNTQIGPAVSEDQMETSYRYIDIAASEGGRVVTGGDRIKLDNPGW 360 L +A LRVG ALDP+TQIGP SE+Q T Y+ IA +GG + GG+R++ G+ Sbjct: 301 LTAAMAKLRVGHALDPDTQIGPVASEEQRATIEAYLAIAVEQGGGLACGGERVRRATDGY 360 Query: 361 YVRPTLIADTQAGMRINNEEVFGPVASTIRVKSYEEALEIANGVEFGLSAGIATTSLKHA 420 ++ P LI T MR+N EE+FGPVAS +RV + A+ +ANG EFGLSAGI T+SL HA Sbjct: 361 FLAPALITGTSPEMRVNREEIFGPVASVVRVPDLDAAIAVANGSEFGLSAGIVTSSLAHA 420 Query: 421 RHFQRYARAGMTMVNLATAGVDYHVPFGGTKSSSYGAREQGFAAVEFFTQTKTSY 475 F+ A+AGM MVN TAGVDYHVPFGGTK+SS G REQGF+A EF+T+TKT Y Sbjct: 421 SRFKASAQAGMVMVNAPTAGVDYHVPFGGTKASSLGPREQGFSAHEFYTRTKTIY 475 Lambda K H 0.317 0.133 0.384 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: 711 Number of extensions: 33 Number of successful extensions: 2 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: 478 Length of database: 478 Length adjustment: 34 Effective length of query: 444 Effective length of database: 444 Effective search space: 197136 Effective search space used: 197136 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: 51 (24.3 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