Align O-acetylhomoserine sulfhydrylase protein; EC 2.3.1.31 (characterized, see rationale)
to candidate SMc01809 SMc01809 O-acetylhomoserine aminocarboxypropyltransferase
Query= uniprot:D8J1Y3_HERSS (413 letters) >FitnessBrowser__Smeli:SMc01809 Length = 426 Score = 254 bits (649), Expect = 3e-72 Identities = 151/423 (35%), Positives = 234/423 (55%), Gaps = 24/423 (5%) Query: 8 GFTTTILHSDRQKGIEHGSLHKPIHTSVTFGYEDARQLAEVFQGKQPGYRYGRQGNPTVA 67 GF+T +H+ Q G+ PI+ + +F + D A +F +Q G Y R NPT A Sbjct: 6 GFSTLAIHAGAQPDPTTGARATPIYQTTSFVFNDTDHAAALFGLQQFGNIYTRIMNPTQA 65 Query: 68 ALEDKITKMEDGKSTICFATGMAAIGAIVQGLLREGDHVVSSAFLFGNT-NSLWMTVGAQ 126 LE++I +E G + + ++G AA + ++R GD+ VS+ L+G + N A Sbjct: 66 VLEERIAALEGGTAGLAVSSGHAAQLLVFHTIMRPGDNFVSARQLYGGSANQFGHAFKAF 125 Query: 127 GAKVSMVDATDVKNVEAAITANTRLVFVETIANPRTQVADLKRIGELCRERGILYVVDNT 186 +V D+ + ++ +A I T+ +F+E++ANP D+ I ++ R G+ +VDNT Sbjct: 126 DWQVRWADSAEPESFDAQIDERTKAIFIESLANPGGTFVDIAAIADVARRHGLPLIVDNT 185 Query: 187 MTSPYLFRPKTVGAGLVVNSLTKSIGGHGNALGGALTDTGEFDWT---RYPHIAENYKKN 243 M +PYL RP GA +VV+SLTK IGGHGN++GG + D G FDW+ +YP ++E Sbjct: 186 MATPYLMRPLEHGADIVVHSLTKFIGGHGNSMGGIIVDGGTFDWSKSGKYPLLSE----- 240 Query: 244 PAPQWGMAQI-------------RAKALRDFGGSLGPEAAHHIAVGAETIALRQERECKN 290 P P++G + R LRDFG ++ P A I G ET+ LR +R C N Sbjct: 241 PRPEYGGVVLHQAFGNFAFAIAARVLGLRDFGPAISPFNAFLIQTGVETLPLRMQRHCDN 300 Query: 291 ALALAQMLQADERVAAVYYPGLESHPQHALSKALF-RSFGSLMSFELKDGIDCFD-YLNR 348 AL +A+ L+ E+V+ V Y GLE P HAL K + G++ +F L G + ++ Sbjct: 301 ALEVAKWLKGHEKVSWVRYSGLEDDPNHALQKRYSPKGAGAVFTFGLAGGYEAGKRFVEA 360 Query: 349 LRLAIPTSNLGDTRTLVIPVAHTIFYEMGAERRASMGIAESLIRVSVGLEDTDDLVADFR 408 L + +N+GDTR+LVI A T ++ E++ + G +IR+SVG+ED D++AD Sbjct: 361 LEMFSHLANIGDTRSLVIHPASTTHRQLTPEQQVAAGAGPDVIRLSVGIEDVADIIADLE 420 Query: 409 QAL 411 QAL Sbjct: 421 QAL 423 Lambda K H 0.319 0.134 0.391 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: 499 Number of extensions: 22 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: 413 Length of database: 426 Length adjustment: 32 Effective length of query: 381 Effective length of database: 394 Effective search space: 150114 Effective search space used: 150114 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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