Align aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate AO353_19510 AO353_19510 aldehyde dehydrogenase
Query= BRENDA::Q83XU8 (485 letters) >FitnessBrowser__pseudo3_N2E3:AO353_19510 Length = 496 Score = 311 bits (796), Expect = 4e-89 Identities = 188/465 (40%), Positives = 256/465 (55%), Gaps = 10/465 (2%) Query: 24 SPLNNAVIAKVHEAGRAEVDAAVAAAQAALK-GAWGRMSLAQRVEVLYAVADGINRRFDD 82 +P V+ V +A +VD AV AA+ A AW R +R +L+ +AD + R + Sbjct: 39 NPATGEVLCVVPKATPDDVDRAVLAARNAFDDSAWTRTRPRERQNLLWKLADLMERDAEL 98 Query: 83 FLAAEVEDTGKPMSLARHVDIPRGAANFKIFADVVKNVPTEFFEMPTP--DGVGAINYAV 140 E + GK ++A+ +D+ + A + E+ P ++ Sbjct: 99 LAQLECLNNGKSAAVAQVMDVQLSIDFLRYMAGWATKIEGSSVEVSLPLMPDDQFHSFIR 158 Query: 141 RRPVGVVGVICPWNLPLLLMTWKVGPALACGNTVVVKPSEETPQTAALLGEVMNTAGVPP 200 R VGVVG I WN PLLL WK+GPALA G TVV+KP++ETP TA L E++ AG P Sbjct: 159 REAVGVVGAIVAWNFPLLLACWKLGPALATGCTVVLKPADETPLTALKLAELVLEAGYPS 218 Query: 201 GVYNVVHGFGPNSTGEFLTSHPDVNAITFTGETGTGEAIMKAAADGARPVSLELGGKNAA 260 GV+NVV G G S G LT +P V+ +TFTG T G+ I K A D V+LELGGK+ Sbjct: 219 GVFNVVTGTGI-SAGSALTHNPLVDKLTFTGSTAVGKQIGKIAMDSMTRVTLELGGKSPT 277 Query: 261 IVFADCDLDKAIEGTLRSCFANCGQVCLGTERVYVERPIFDRFVSRLKKGAEGMQLGRPE 320 IV AD DL A G + F N GQVC R+YV+R FD V+ + A M+LG Sbjct: 278 IVMADADLGSAAAGAASAIFFNQGQVCCAGSRLYVQRKHFDNVVADIAGIANAMKLGNGL 337 Query: 321 DLATGMGPLISQEHREKVLSYYKKAVEAGATVVTGGGVPEMPEALKGGAWVQPTIWTGLG 380 D + MGPLIS +E+V +Y + E+GAT+V GG E G +V+PT+ + Sbjct: 338 DPSVDMGPLISARQQERVYNYIEMGRESGATIVCGG------EQFGPGFFVKPTVIVDVD 391 Query: 381 DDSVVAREEIFGPCALVMPFDSEEEVIRRANDNDYGLARRIWTTNLSRAHRVAGAIEVGI 440 + +EEIFGP + +PFD E + +R AND+ YGL IW+ +L+ HR+ I+ G Sbjct: 392 QKHSLVQEEIFGPVLVAIPFDDEADALRMANDSPYGLGASIWSNDLAAVHRMIPRIKSGS 451 Query: 441 AWVNSWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELKNVCIKL 485 WVN D FGG K SG+GRE G ++E YTELK+V IKL Sbjct: 452 VWVNCHSALDPALPFGGYKMSGVGREMGYAAIEHYTELKSVLIKL 496 Lambda K H 0.318 0.135 0.406 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: 573 Number of extensions: 29 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: 485 Length of database: 496 Length adjustment: 34 Effective length of query: 451 Effective length of database: 462 Effective search space: 208362 Effective search space used: 208362 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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