Align O-acetylhomoserine sulfhydrylase protein; EC 2.3.1.31 (characterized, see rationale)
to candidate 7023700 Shewana3_0930 O-acetylhomoserine/O-acetylserine sulfhydrylase (RefSeq)
Query= uniprot:D8J1Y3_HERSS (413 letters) >lcl|FitnessBrowser__ANA3:7023700 Shewana3_0930 O-acetylhomoserine/O-acetylserine sulfhydrylase (RefSeq) Length = 430 Score = 234 bits (598), Expect = 3e-66 Identities = 142/403 (35%), Positives = 224/403 (55%), Gaps = 20/403 (4%) Query: 30 PIHTSVTFGYEDARQLAEVFQGKQPGYRYGRQGNPTVAALEDKITKMEDGKSTICFATGM 89 PI+ + ++ ++D + A++F K G Y R NPT + LE ++ +E G + A+GM Sbjct: 24 PIYQTTSYTFDDTQHGADLFDLKVAGNIYTRIMNPTSSVLEQRLAAIEGGIGALALASGM 83 Query: 90 AAIGAIVQGLLREGDHVVSSAFLFGNTNSLWM-TVGAQGAKVSMVDATDVKNVEAAITAN 148 AAI +Q L + GD++VS++ L+G T +L+ T+ QG +V M D + ++A I A Sbjct: 84 AAITYAIQALTQVGDNIVSTSQLYGGTYNLFAHTLPRQGVEVRMAAFDDFEELDALIDAK 143 Query: 149 TRLVFVETIANPRTQVADLKRIGELCRERGILYVVDNTMTSPYLFRPKTVGAGLVVNSLT 208 T+ +F E+I NP + DLKR+ E+ + G+ +VDNT+ +P L RP GA +V++SLT Sbjct: 144 TKALFCESIGNPAGNIVDLKRLAEIAHKHGVPLIVDNTVATPVLCRPFEHGADIVIHSLT 203 Query: 209 KSIGGHGNALGGALTDTGEFDW-TRYPHIAENYKKNPA-------PQWGMA----QIRAK 256 K IGGHG +GG + D+G+FDW A + +P+ +G A + R Sbjct: 204 KYIGGHGTTIGGVIIDSGKFDWVANKERFALLNQADPSYHGVVYTEAFGAAAFIGRCRVV 263 Query: 257 ALRDFGGSLGPEAAHHIAVGAETIALRQERECKNALALAQMLQADERVAAVYYPGLESHP 316 LR+ G +L P +A + G ET++LR ER C NALALA+ L V+ V Y L S P Sbjct: 264 PLRNTGAALSPHSAFLLLQGLETLSLRMERHCSNALALAEYLILHPSVSWVNYGALPSSP 323 Query: 317 -QHALSKALFRSFGSLMSFELKDG------IDCFDYLNRLRLAIPTSNLGDTRTLVIPVA 369 + K ++SF +K I +++ L++ + N+GD ++L A Sbjct: 324 YRENCQKITGGKASGIISFGIKAATPEEGKIAGGKFIDALQMILRLVNIGDAKSLACHPA 383 Query: 370 HTIFYEMGAERRASMGIAESLIRVSVGLEDTDDLVADFRQALD 412 T ++ A A G++E LIR+SVG+E DD++AD QAL+ Sbjct: 384 STTHRQLDANELARAGVSEDLIRISVGIEHIDDIIADVAQALE 426 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: 480 Number of extensions: 28 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: 430 Length adjustment: 32 Effective length of query: 381 Effective length of database: 398 Effective search space: 151638 Effective search space used: 151638 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