Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate WP_010440535.1 G7G_RS0108790 aldehyde dehydrogenase
Query= metacyc::MONOMER-15108 (486 letters) >NCBI__GCF_000192475.1:WP_010440535.1 Length = 498 Score = 340 bits (871), Expect = 9e-98 Identities = 186/477 (38%), Positives = 285/477 (59%), Gaps = 14/477 (2%) Query: 14 FIDGKFVPSLDGKTFDNINPATEEKLGTVAEGGAAEIDLAVQAAKKALN-GPWKKMTANE 72 FIDG + P++ G+ F+ +NPAT L ++A G ++D AV+ A++A + G W KM ++ Sbjct: 23 FIDGGYRPAISGQVFETVNPATGALLTSIAACGVEDVDFAVEKAREAFDDGRWSKMHPSD 82 Query: 73 RIAVLRKVGDLILERKEELSVLESLDTGKPTWLSGSIDIPRAAYNFHFFSDYIRTITNEA 132 R VL ++ LI EL+V+ES+D+GK + ++D+P + + ++ I I ++ Sbjct: 83 RKDVLIRLCKLITRNARELAVMESIDSGKTIYDCETVDVPETIHCLKWHAEAIDKIYDQV 142 Query: 133 TQMDDVALNYAIRRPVGVIGLINPWNLPLLLMTWKLAPALAAGNTVVMKPAELTPMTATV 192 + D + +R P+GV+GL+ PWN PLL++ WK+ PALAAG +VV+KPA T +TA Sbjct: 143 SPASDDHIAMVVREPIGVVGLVLPWNFPLLMLAWKIGPALAAGCSVVVKPATETSLTALK 202 Query: 193 LAEICRDAGVPDGVVNLVHGFGPNSAGAALTEHPDVNAISFTGETTTGKIIMA-SAAKTL 251 +AE+ +AG+P GV+N+V G G G + H D++ +SFTG T TGK ++ SA Sbjct: 203 VAELASEAGLPRGVLNVVPG-GGAEVGEPIGRHMDIDMVSFTGSTVTGKKFLSYSAESNA 261 Query: 252 KRLSYELGGKNPNVIFADS-NLDEVIETTMKSSFINQGEVCLCGSRIYVERPAYEAFLEK 310 K + E+GGKNP ++ D+ NLD V + +F N GE C SR+ V + LE+ Sbjct: 262 KEVVLEMGGKNPAIVMDDAENLDRVAAHVVNGAFWNMGENCSASSRLIVHKDVKAELLER 321 Query: 311 FVAKTKELVVGDPFDAKTKVGALISDEHYERVTGYIKLAVEEGGTILTGGKRPEGLEKGY 370 K VG+P D +T++GAL+S+ HY +V GY+ E+ +L GGK +G Sbjct: 322 IAHHAKHWNVGEPLDPETRMGALVSEGHYNKVCGYL----EQAENVLIGGKAEKG----- 372 Query: 371 FLEPTIITGLTRDCRVVKEEIFGPVVTVIPFDTEEEVLEQINDTHYGLSASVWTNDLRRA 430 F+E T++ D + +EEIFGPV++VI +E + NDT YGL AS++ + +RA Sbjct: 373 FVEATVVEVPGNDATLAREEIFGPVLSVIEVSGFDEAISIANDTEYGLCASIFMANAKRA 432 Query: 431 HRVAGQIEAGIVWVNTWFLRDLRTPFGGMKQSGI-GREGGLHSFEFYSELTNICIKL 486 R A I AG V VN++ D+ TPFGG KQSG GR+ +H+ + Y++L I I L Sbjct: 433 IRGARAIRAGTVTVNSFGEGDITTPFGGYKQSGFGGRDNSVHAHDQYTQLKTIWIDL 489 Lambda K H 0.318 0.136 0.404 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: 633 Number of extensions: 31 Number of successful extensions: 6 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: 486 Length of database: 498 Length adjustment: 34 Effective length of query: 452 Effective length of database: 464 Effective search space: 209728 Effective search space used: 209728 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 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