Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate Pf1N1B4_4502 Aldehyde dehydrogenase (EC 1.2.1.3)
Query= metacyc::MONOMER-15108 (486 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4502 Length = 506 Score = 353 bits (905), Expect = e-101 Identities = 195/480 (40%), Positives = 283/480 (58%), Gaps = 12/480 (2%) Query: 13 HFIDGKFVPSLDGKTFDNINPATEEKLGTVAEGGAAEIDLAVQAAKKALNGPWKKMTANE 72 +FI G+FV ++G+ F N +P T E + AA+I+ A+ AA A + W K +A + Sbjct: 21 NFIGGEFVAPINGEYFTNTSPVTGEVIAEFPRSSAADIEKALDAAHAAADA-WGKTSAQD 79 Query: 73 RIAVLRKVGDLILERKEELSVLESLDTGKPTWLSGSIDIPRAAYNFHFFSDYIRTITNEA 132 R VL K+ D I + E L+V E+ D GK + + D+P AA +F +F+ IR A Sbjct: 80 RSLVLLKIADRIEQNLEILAVTETWDNGKAVRETLNADVPLAADHFRYFAGCIRAQEGGA 139 Query: 133 TQMDDVALNYAIRRPVGVIGLINPWNLPLLLMTWKLAPALAAGNTVVMKPAELTPMTATV 192 +++++ Y P+GV+G I PWN PLL+ WKLAPALAAGN +V+KPAE TP++ V Sbjct: 140 AEINELTTAYHFHEPLGVVGQIIPWNFPLLMAAWKLAPALAAGNCIVLKPAEQTPLSIMV 199 Query: 193 LAEICRDAGVPDGVVNLVHGFGPNSAGAALTEHPDVNAISFTGETTTGKIIMASAAKTLK 252 AE+ D +P GV+N+V GFG AG AL + I+FTG T G IM AA+ + Sbjct: 200 FAELIADL-LPAGVLNIVQGFG-REAGEALATSKRIAKIAFTGSTPIGAHIMHCAAENII 257 Query: 253 RLSYELGGKNPNVIF-----ADSNLDEVIETTMKSSFINQGEVCLCGSRIYVERPAYEAF 307 + ELGGK+PN+ F A+ E + +F NQGEVC C SR V+ YE F Sbjct: 258 PSTVELGGKSPNIFFEDIMNAEPQFIEKAAEGLVLAFFNQGEVCTCPSRALVQESIYEPF 317 Query: 308 LEKFVAKTKELVVGDPFDAKTKVGALISDEHYERVTGYIKLAVEEGGTILTGG--KRPEG 365 + + + K ++ G+P D +T VGA S++ Y+++ Y+K+A EEG +LTGG +R EG Sbjct: 318 MAEVMKKIVKIKRGNPLDTETMVGAQASEQQYDKILSYLKIAQEEGAELLTGGAAERLEG 377 Query: 366 -LEKGYFLEPTIITGLTRDCRVVKEEIFGPVVTVIPFDTEEEVLEQINDTHYGLSASVWT 424 L GY+++PT++ G + RV +EEIFGPVV + F E E L ND+ +GL A +WT Sbjct: 378 DLSSGYYIQPTLLKGHNK-MRVFQEEIFGPVVGITTFKDEAEALAIANDSEFGLGAGLWT 436 Query: 425 NDLRRAHRVAGQIEAGIVWVNTWFLRDLRTPFGGMKQSGIGREGGLHSFEFYSELTNICI 484 D+ RA+R+ I+AG VW N + L FGG K+SG+GRE + Y + N+ + Sbjct: 437 RDINRAYRMGRAIKAGRVWTNCYHLYPAHAAFGGYKKSGVGRENHKMMLDHYQQTKNLLV 496 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: 605 Number of extensions: 29 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: 506 Length adjustment: 34 Effective length of query: 452 Effective length of database: 472 Effective search space: 213344 Effective search space used: 213344 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 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:
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