Align O-acetylhomoserine sulfhydrylase (EC:2.5.1.49) (characterized)
to candidate H281DRAFT_06059 H281DRAFT_06059 O-succinylhomoserine sulfhydrylase
Query= reanno::Korea:Ga0059261_3194 (402 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_06059 H281DRAFT_06059 O-succinylhomoserine sulfhydrylase Length = 396 Score = 379 bits (972), Expect = e-109 Identities = 194/386 (50%), Positives = 261/386 (67%), Gaps = 7/386 (1%) Query: 19 TQAIRGGTARSEWGETSEALFLTSGYAYDCAGDAAARFSGDQQGMTYSRLQNPTVEMLEQ 78 T A+R GT RS++ E SEA+FLTS + + A DAA RF + TYSR NPTV M + Sbjct: 9 TLAVRSGTVRSDFNEHSEAIFLTSSFVFASAADAAERFKNSEDYYTYSRFTNPTVSMFQD 68 Query: 79 RIALLEGAEACRATASGMAAMTAALLCQLSAGDHLIGGRAAFGSCRWLTDTQLPKFGIET 138 R+A LEG EAC ATASGMAA+ + ++ L AGDHL+ +A FGS + KFGI T Sbjct: 69 RLAALEGGEACMATASGMAAIMSVVMSTLQAGDHLVSSQALFGSTLGMFSQIFSKFGITT 128 Query: 139 TVVDARDPQQFIDAIRPNTKVFFFETPANPTMDVVDLKAVCAIARERGIVTVVDNAFATP 198 T VD + + +A+RP TK+FF ETP+NP +V D++A+ IA+ + VVDN F +P Sbjct: 129 TFVDPTNLDAWKNAVRPETKMFFLETPSNPLTEVADIEAISKIAKAANALFVVDNCFCSP 188 Query: 199 ALQRPMDFGADVVAYSATKMMDGQGRVLAGAVCGTEEFINNTLLPFHRNTGPTLSPFNAW 258 ALQ+P+ GADVV +SATK +DGQGRVL GA+ G+++FI + PF R+ GPTLS FNAW Sbjct: 189 ALQQPLKLGADVVMHSATKFLDGQGRVLGGALVGSKKFIMEKVFPFVRSAGPTLSAFNAW 248 Query: 259 VVLKGLETLDLRIQRQSENALKVARFLEGR--VPRVNFPGLPSHPQHNLAMSQMAAAGPI 316 V+LKG+ETL LR+++QS NAL++AR+L+ V RV +PGL SHPQH LAM Q A G I Sbjct: 249 VLLKGMETLSLRVEKQSANALEIARWLDDHPSVKRVFYPGLESHPQHALAMRQQKAGGAI 308 Query: 317 FSIELDGG-----RTQAHGLLDALGLIDISNNIGDSRSLMTHPASTTHSGVAEDQRLLMG 371 S EL G R A ++D+ + I+ N+GD+R+ +THPA+TTH V + R G Sbjct: 309 VSFELKGDTPEQMRANAWRVIDSTKICSITGNLGDTRTTITHPATTTHGRVTPEARAAAG 368 Query: 372 VGEGMLRLNVGLEDPEDLIADLDQAL 397 + EG++RL VGLE+ D+ ADL++ L Sbjct: 369 ITEGLIRLAVGLENAADIRADLERGL 394 Lambda K H 0.319 0.134 0.396 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: 426 Number of extensions: 12 Number of successful extensions: 3 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: 402 Length of database: 396 Length adjustment: 31 Effective length of query: 371 Effective length of database: 365 Effective search space: 135415 Effective search space used: 135415 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