Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate WP_012590055.1 MSIL_RS05250 O-succinylhomoserine sulfhydrylase
Query= SwissProt::P9WGB5 (406 letters) >NCBI__GCF_000021745.1:WP_012590055.1 Length = 406 Score = 420 bits (1080), Expect = e-122 Identities = 215/386 (55%), Positives = 280/386 (72%), Gaps = 4/386 (1%) Query: 20 ATVGVRGGMLRSGFEETAEAMYLTSGYVYGSAAVAEKSFAGELDHYVYSRYGNPTVSVFE 79 AT+ V GG +R+ F ET+EA++LT GYV+ S FAGE +VYSRYGNPTV++FE Sbjct: 14 ATLLVHGGGVRTPFGETSEALFLTQGYVFASMEACAARFAGEEPGFVYSRYGNPTVAMFE 73 Query: 80 ERLRLIEGAPAAFATASGMAAVFTSLGALLGAGDRLVAARSLFGSCFVVCSEILPRWGVQ 139 R+ L+EGA AA ATA+GMAAV S+ + + AGD +VAAR+LFG+C + + LPR+GV Sbjct: 74 GRMALLEGAEAARATATGMAAVTASVMSQVRAGDHVVAARALFGACRYIVEDHLPRYGVA 133 Query: 140 TVFVDGDDLSQWERALSVPTQAVFFETPSNPMQSLVDIAAVTELAHAAGAKVVLDNVFAT 199 + VDGDDL QW A+ + T+ F E+P+NP + DIAA+ ++AH AGA +V+DNVFAT Sbjct: 134 STLVDGDDLDQWRAAVRLETKVFFLESPTNPCLDVYDIAAIAKIAHDAGAILVVDNVFAT 193 Query: 200 PLLQQGFPLGVDVVVYSGTKHIDGQGRVLGGAILGDREYIDGPVQKLMRHTGPAMSAFNA 259 P+LQ+ LG D+VVYS TKHIDG GR LGG ILG + ++G +Q+ +R TGPA+S FNA Sbjct: 194 PMLQKPLTLGADLVVYSATKHIDGGGRCLGGVILGAKALVEGDLQQFLRQTGPALSPFNA 253 Query: 260 WVLLKGLETLAIRVQHSNASAQRIAEFLNGHPSVRWVRYPYLPSHPQYDLAKRQMSGGGT 319 WVLLK LETLAIRV+ SA RIA+FL+ P+V +VRYP HP D+A+RQMSGGGT Sbjct: 254 WVLLKALETLAIRVERQTKSAARIADFLSEQPAVAFVRYPGRADHPHADIARRQMSGGGT 313 Query: 320 VVTFALDCPEDVAKQRAFEVLDKMRLIDISNNLGDAKSLVTHPATTTHRAMGPEGRAAIG 379 +V F + K AF ++LI IS+NLGDAKSL+THPATTTH + PE RAA+G Sbjct: 314 LVAFEI----VGGKPAAFAFGRALKLIKISSNLGDAKSLITHPATTTHHRLPPEARAALG 369 Query: 380 LGDGVVRISVGLEDTDDLIADIDRAL 405 + +G+VR+SVGLED +DLI D+ AL Sbjct: 370 VSEGLVRLSVGLEDEEDLIDDLKAAL 395 Lambda K H 0.319 0.135 0.395 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: 507 Number of extensions: 17 Number of successful extensions: 2 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: 406 Length of database: 406 Length adjustment: 31 Effective length of query: 375 Effective length of database: 375 Effective search space: 140625 Effective search space used: 140625 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 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