Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate WP_050806487.1 G7G_RS0121155 aldehyde dehydrogenase
Query= BRENDA::Q1XGK8 (486 letters) >NCBI__GCF_000192475.1:WP_050806487.1 Length = 494 Score = 314 bits (805), Expect = 4e-90 Identities = 178/484 (36%), Positives = 271/484 (55%), Gaps = 11/484 (2%) Query: 6 HFINGAFVGSASGRTFEDINPSNGQVIGHVHEAGRAEVDAAVKAARAALK-GPWGKLSVA 64 HFI+G + S GRT + ++P +GQV+ + E ++DAA+ +ARAA + G W + + + Sbjct: 19 HFIDGCTIPSNEGRTHDVLSPIDGQVLTQIAEGTPCDMDAAIASARAAFEDGRWARRAPS 78 Query: 65 ERAEILHRVADGITARFDEFLEAECLDTGKPKSLASHIDIPRGAANFKVFADLLKNVANE 124 ER +IL ++AD I E D G ++A + A F+ +A+ + V Sbjct: 79 ERKKILLKLADLIEKHALELAVLGVRDNGTEITMAMKAEPMSAAGTFRYYAEAIDKV--- 135 Query: 125 AFEMATPDGAGAINYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPSEETP 184 + P + P GV+G I PWN+P+++ WK+ PALA GN+VV+KP+E Sbjct: 136 -YGQIAPTAENVLGLIHHAPVGVVGAIVPWNMPMMIGAWKLAPALAAGNSVVLKPAESAS 194 Query: 185 LTATLLGEVMQAAGVPAGVYNVVHGFGGDSAGAFLTEHPDVDAYTFTGETGTGEVIMRAA 244 LT L E+ AG+P GV NVV G G G L DVD FTG TG ++ + Sbjct: 195 LTLLKLAELAVEAGIPEGVLNVVTG-SGRVVGETLALSMDVDILVFTGSGATGRKLLEYS 253 Query: 245 AKG-VRQVSLELGGKNAGIVFADC-DMDKAIEGTLRSAFANCGQVCLGTERVYVERPIFD 302 A+ +++ LELGGK+ IVF D D+ +A + + F N GQ+C+ R+ V+ I D Sbjct: 254 ARSNLKRCYLELGGKSPNIVFKDVTDLAQAAKVSAAGIFRNSGQICVAASRLLVQADIHD 313 Query: 303 EFVARLKAGAESLMIGPPDDASSNFGPLVSLKHREKVLSYYQQAVDDGGSVITGGGVPDM 362 +FVA L AE++ +G P D +++ G + SL + L + ++A +G + GG D Sbjct: 314 DFVAELVENAEAMQVGDPLDLNNHIGAVHSLSELDANLEFVKKAQVEGAELQLGG---DQ 370 Query: 363 PAHLAGGAWVQPTIWTGLSDDSAVVTEEIFGPCCHIRPFDTEEEAIELANSLPYGLASAI 422 GG ++ PT+ TG+ + E+FGP + PF+TEEEAI+LANS YGL++ + Sbjct: 371 ILKDTGGYYMAPTVMTGVRSTDTLFRNEVFGPVLAVTPFETEEEAIQLANSTEYGLSAGV 430 Query: 423 WTENGSRAHRVAGQIEAGIVWVNSWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELKNI 482 WT N SRAHR+ I +G+V VN++ DL GG KQSG G + +H+LE Y++LK Sbjct: 431 WTSNLSRAHRMVAGIRSGVVHVNTYGGSDLTVPLGGVKQSGNGHDKSLHALEKYSDLKTA 490 Query: 483 CVKL 486 ++L Sbjct: 491 WIQL 494 Lambda K H 0.318 0.136 0.411 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: 629 Number of extensions: 33 Number of successful extensions: 9 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: 494 Length adjustment: 34 Effective length of query: 452 Effective length of database: 460 Effective search space: 207920 Effective search space used: 207920 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