Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate WP_110207396.1 DNK54_RS13100 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-15108 (486 letters) >NCBI__GCF_003194585.1:WP_110207396.1 Length = 507 Score = 341 bits (875), Expect = 3e-98 Identities = 185/480 (38%), Positives = 285/480 (59%), Gaps = 12/480 (2%) Query: 13 HFIDGKFVPSLDGKTFDNINPATEEKLGTVAEGGAAEIDLAVQAAKKALNGPWKKMTANE 72 HFI G++V + G+ F+NI+P + +A G A +I+ AV AA A + W + + + Sbjct: 22 HFIGGQWVDPIKGQYFENISPVNGKPFTEIARGTAEDIEAAVDAAWAAADA-WGRTSTTD 80 Query: 73 RIAVLRKVGDLILERKEELSVLESLDTGKPTWLSGSIDIPRAAYNFHFFSDYIRTITNEA 132 R +L K+ D + ++L+V+E+ D GK + + D+P A +F +F+ +R Sbjct: 81 RSNILLKIADRMERHLDDLAVIETWDNGKAVRETLNADLPLAIDHFRYFAGALRGQEGGI 140 Query: 133 TQMDDVALNYAIRRPVGVIGLINPWNLPLLLMTWKLAPALAAGNTVVMKPAELTPMTATV 192 +++D+ + Y P+GV+G I PWN P+L+ WKLAPALAAGN VV+KPAE TP + Sbjct: 141 SEIDENTVAYHFHEPLGVVGQIIPWNFPILMAVWKLAPALAAGNCVVLKPAEQTPWSILK 200 Query: 193 LAEICRDAGVPDGVVNLVHGFGPNSAGAALTEHPDVNAISFTGETTTGKIIMASAAKTLK 252 L E+ D +P GV+N+V+GFG AG L P + I+FTGETTTG++IM A++ + Sbjct: 201 LVELVGDL-LPAGVLNVVNGFGV-EAGKPLASSPRIRKIAFTGETTTGRLIMQYASENII 258 Query: 253 RLSYELGGKNPNVIFAD--SNLDEVIETTMKS---SFINQGEVCLCGSRIYVERPAYEAF 307 ++ ELGGK+PN+ F D ++ D + ++ +NQGEVC C SR V++ Y F Sbjct: 259 PVTLELGGKSPNIFFDDVATSRDAFYDKALEGFTMFALNQGEVCTCPSRALVQQSMYADF 318 Query: 308 LEKFVAKTKELVVGDPFDAKTKVGALISDEHYERVTGYIKLAVEEGGTILTGGKRP--EG 365 + +A+ + + G+P D T +GA S++ E++ Y+++ +EG +LTGG+R EG Sbjct: 319 VPDAIARVEAIKQGNPLDVSTMMGAQASNDQLEKILSYLEIGKQEGAKVLTGGERNVLEG 378 Query: 366 -LEKGYFLEPTIITGLTRDCRVVKEEIFGPVVTVIPFDTEEEVLEQINDTHYGLSASVWT 424 L +GY+++PT+ G R+ +EEIFGPVV++ F E + L+ NDT YGL A +WT Sbjct: 379 DLAEGYYVQPTVFEG-NNAMRIFQEEIFGPVVSLTSFSDEADALQTANDTLYGLGAGLWT 437 Query: 425 NDLRRAHRVAGQIEAGIVWVNTWFLRDLRTPFGGMKQSGIGREGGLHSFEFYSELTNICI 484 D RA R+ I+AG VW N + FGG KQSGIGRE + Y + N+ + Sbjct: 438 RDGSRAFRMGKGIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHKMMLDHYQQTKNLLV 497 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: 617 Number of extensions: 31 Number of successful extensions: 7 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: 507 Length adjustment: 34 Effective length of query: 452 Effective length of database: 473 Effective search space: 213796 Effective search space used: 213796 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