Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate WP_004687625.1 BMI_RS15595 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= metacyc::MONOMER-15108 (486 letters) >NCBI__GCF_000022745.1:WP_004687625.1 Length = 504 Score = 405 bits (1041), Expect = e-117 Identities = 216/471 (45%), Positives = 289/471 (61%), Gaps = 3/471 (0%) Query: 12 LHFIDGKFVPSLDGKTFDNINPATEEKLGTVAEGGAAEIDLAVQAAKKALNGPWKKMTAN 71 L+ I G+ V + DG TF+ I+P + L TVA G AA+ID A +AAK A W M+ + Sbjct: 23 LNRIGGEDVAAADGATFETISPVDLKPLATVALGKAADIDRAARAAKAAFP-EWAAMSGD 81 Query: 72 ERIAVLRKVGDLILERKEELSVLESLDTGKPTWLSGSIDIPRAAYNFHFFSDYIRTITNE 131 R +L K+ D I+ R EE++ +E +DTG+ + R A NF FF+D + Sbjct: 82 ARKKLLHKIADAIVARAEEIAFVECMDTGQSLKFMAKAAL-RGAENFRFFADRAPEARDG 140 Query: 132 ATQMDDVALNYAIRRPVGVIGLINPWNLPLLLMTWKLAPALAAGNTVVMKPAELTPMTAT 191 T +N R P+G +G+I PWN P +L TWK+APALAAG TVV KPAE +P+TA Sbjct: 141 KTLRGPGQVNMTTRVPIGPVGVITPWNTPFMLSTWKIAPALAAGCTVVHKPAEFSPLTAR 200 Query: 192 VLAEICRDAGVPDGVVNLVHGFGPNSAGAALTEHPDVNAISFTGETTTGKIIMASAAKTL 251 +L EI +AG+P GV NLV+GFG + AG ALTEHPD+ AI F GE+ TG +IM A TL Sbjct: 201 LLVEIAEEAGLPKGVWNLVNGFGED-AGKALTEHPDIKAIGFVGESRTGSLIMKQGADTL 259 Query: 252 KRLSYELGGKNPNVIFADSNLDEVIETTMKSSFINQGEVCLCGSRIYVERPAYEAFLEKF 311 KR+ +ELGGKNP V+FAD++L+ ++ + + GE C SR+ VE YE F Sbjct: 260 KRVHFELGGKNPVVVFADADLERAVDAAVFMIYSLNGERCTSSSRLLVEASIYEKFTALV 319 Query: 312 VAKTKELVVGDPFDAKTKVGALISDEHYERVTGYIKLAVEEGGTILTGGKRPEGLEKGYF 371 K K + VG P D +T VG LI H ++V YI++ EG T+ GG + G G + Sbjct: 320 AEKAKRIKVGHPLDPETVVGPLIHPVHEKKVLEYIEIGRSEGATVAAGGAKFAGPGGGCY 379 Query: 372 LEPTIITGLTRDCRVVKEEIFGPVVTVIPFDTEEEVLEQINDTHYGLSASVWTNDLRRAH 431 + PT+ T R+ +EEIFGPV+T IPF E E L ND YGL+ +WTND+ RA Sbjct: 380 VSPTLFTAAHNGMRIAQEEIFGPVLTAIPFKDEAEALALANDVKYGLTGYLWTNDVTRAF 439 Query: 432 RVAGQIEAGIVWVNTWFLRDLRTPFGGMKQSGIGREGGLHSFEFYSELTNI 482 R +EAG++WVN+ +R L TPFGG+K SGIGR+GG SF+FY E NI Sbjct: 440 RFTDALEAGMIWVNSENVRHLPTPFGGVKNSGIGRDGGDWSFDFYMETKNI 490 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: 644 Number of extensions: 32 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: 486 Length of database: 504 Length adjustment: 34 Effective length of query: 452 Effective length of database: 470 Effective search space: 212440 Effective search space used: 212440 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