Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate WP_012973881.1 AZL_RS06685 O-succinylhomoserine sulfhydrylase
Query= SwissProt::P9WGB5 (406 letters) >NCBI__GCF_000010725.1:WP_012973881.1 Length = 402 Score = 413 bits (1062), Expect = e-120 Identities = 210/384 (54%), Positives = 278/384 (72%), Gaps = 5/384 (1%) Query: 24 VRGGMLRSGFEETAEAMYLTSGYVYGSAAVAEKSFAGELDHYVYSRYGNPTVSVFEERLR 83 V GG+ RS F+ET EA+Y TSG+VYGSA AE +FA + +VYSR+ NPT ++FE+RL Sbjct: 21 VHGGIRRSQFDETCEALYQTSGFVYGSAEEAEHAFANDGARHVYSRFRNPTSAMFEDRLA 80 Query: 84 LIEGAPAAFATASGMAAVFTSLGALLGAGDRLVAARSLFGSCFVVCSEILPRWGVQTVFV 143 EGA A+ATASGMAAV +L + L GDR+VA R+LF SC+ + ++ R+G++TVFV Sbjct: 81 EYEGAEWAYATASGMAAVHGALMSGLRTGDRVVAPRALFISCYWILKDLCSRYGIETVFV 140 Query: 144 DGDDLSQWERALSVPTQAVFFETPSNPMQSLVDIAAVTELAHAAGAKVVLDNVFATPLLQ 203 DG +L++WE ALS PT+AVF ETPSNP +VD+ AV LAH AGA VV DN FATP+LQ Sbjct: 141 DGTNLAEWEEALSTPTKAVFLETPSNPGLEVVDLEAVCALAHKAGAVVVADNAFATPVLQ 200 Query: 204 QGFPLGVDVVVYSGTKHIDGQGRVLGGAILG-DREYIDGPVQKLMRHTGPAMSAFNAWVL 262 + F G DVV+YS TKHIDGQGR LGG IL D++Y + +R+TGP +S FN+W+L Sbjct: 201 RPFEFGADVVIYSATKHIDGQGRCLGGVILAKDKKYAAEVIHPFLRNTGPTISPFNSWLL 260 Query: 263 LKGLETLAIRVQHSNASAQRIAEFLNGHPSVRWVRYPYLPSHPQYDLAKRQMSGGGTVVT 322 LKG+ETL +RV +A+ ++AEFL HP V V YP LPSHPQYDL ++QM+GGG +++ Sbjct: 261 LKGMETLELRVHAQSAAGLQVAEFLESHPKVAQVLYPLLPSHPQYDLVRKQMTGGGNMLS 320 Query: 323 FALDCPEDVAKQRAFEVLDKMRLIDISNNLGDAKSLVTHPATTTHRAMGPEGRAAIGLGD 382 L K AF L+ +R++ ISNNLGD+KSL+THPAT+TH + E +AA + Sbjct: 321 VFL----KGGKAEAFNTLNALRMVMISNNLGDSKSLITHPATSTHSKLTDEEKAAARIEP 376 Query: 383 GVVRISVGLEDTDDLIADIDRALS 406 G++R+SVGLED D+I D+DRAL+ Sbjct: 377 GLLRLSVGLEDPQDIIEDLDRALA 400 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: 503 Number of extensions: 15 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: 406 Length of database: 402 Length adjustment: 31 Effective length of query: 375 Effective length of database: 371 Effective search space: 139125 Effective search space used: 139125 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