Align Homocysteine/cysteine synthase; O-acetylserine/O-acetylhomoserine sulfhydrylase; OAS-OAH SHLase; OAS-OAH sulfhydrylase; EC 2.5.1.47; EC 2.5.1.49 (characterized)
to candidate WP_050997204.1 FRAAL_RS21135 bifunctional o-acetylhomoserine/o-acetylserine sulfhydrylase
Query= SwissProt::P06106 (444 letters) >NCBI__GCF_000058485.1:WP_050997204.1 Length = 440 Score = 403 bits (1036), Expect = e-117 Identities = 211/432 (48%), Positives = 290/432 (67%), Gaps = 16/432 (3%) Query: 5 FDTVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQNPTS 64 F+T Q+HAG D A +RAVPIY TTS+VF++++H + LF L G+ Y+R NPTS Sbjct: 18 FETRQIHAGAAP--DAATGARAVPIYQTTSFVFDDTRHAADLFSLAEVGFTYTRVVNPTS 75 Query: 65 NVLEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKISFKR 124 + LE+R+A LEGG AALA +SGQAAQTLA+ LA G ++VS++ LYGGTY FK + Sbjct: 76 DALEQRVADLEGGVAALATASGQAAQTLAVLNLAGAGSHLVSSTSLYGGTYALFKHTLAE 135 Query: 125 FGIEARFVEG-DNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPVVVD 183 GI FV+ D+ + ++ T A+Y ETIGNP+ NV D + + H G+P++VD Sbjct: 136 LGITTTFVDDPDDLDAWQAAIRPNTVALYGETIGNPRGNVLDIAGVAEVGHAAGLPLIVD 195 Query: 184 NTFGAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQFSQP 243 NT A Y +P+++GADIV HSATK+IGGHGT+IGG+IVD G+F W + P+F+ P Sbjct: 196 NTL-ASPYLNRPLEHGADIVLHSATKFIGGHGTSIGGVIVDGGRFDWT--AGRHPRFTTP 252 Query: 244 AEGYHGTIYNEAYGNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHGENA 303 YHG +++EA+ A+IV R LLRDLGP ++P +FLLLQG+ETLSLR ERH NA Sbjct: 253 DPAYHGLVFHEAFAETAFIVRARARLLRDLGPALSPVNAFLLLQGLETLSLRMERHSANA 312 Query: 304 LKLAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETDPFK 363 ++A WL + P VSWV+YPGLA + A++YL G G VL+FG++ A Sbjct: 313 ARVAAWLAERPEVSWVAYPGLADSRWYPAAQRYLPRGAGAVLAFGIRGGAAA-------- 364 Query: 364 LSGAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVGIEF 423 G ++ L+L S+LANVGD ++L I P TTH QL E++ SGV+++L+R+SVGIE Sbjct: 365 --GRAFIEGLELHSHLANVGDVRSLAIHPASTTHAQLTPDEQVDSGVSEELVRLSVGIEG 422 Query: 424 IDDIIADFQQSF 435 I+DI+AD + F Sbjct: 423 IEDILADLDRGF 434 Lambda K H 0.317 0.136 0.402 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: 486 Number of extensions: 17 Number of successful extensions: 5 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: 444 Length of database: 440 Length adjustment: 32 Effective length of query: 412 Effective length of database: 408 Effective search space: 168096 Effective search space used: 168096 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 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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