Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate WP_053768122.1 BVI061214_RS09125 PLP-dependent transferase
Query= SwissProt::P55218 (403 letters) >NCBI__GCF_001280255.1:WP_053768122.1 Length = 412 Score = 245 bits (626), Expect = 1e-69 Identities = 158/405 (39%), Positives = 222/405 (54%), Gaps = 37/405 (9%) Query: 19 FDTLAVRAGQRRTPEGEHGEALFTTSSYVFRTAADAAARFA-GEVPGNVYSRYTNPTVRT 77 ++TLAV AG P G G ++ ++Y F+T + A RFA GE G VY+R +PT R Sbjct: 3 YETLAVHAGLPEDPHGALGLPIYAVAAYGFKTLEEGAERFATGE--GYVYARQKDPTARA 60 Query: 78 FEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSRSVFGSTISLFDKYFKRFG 137 EER+ ALEGA+ AVA ASG +A A +++L GD V+ +R +FG TI LF + G Sbjct: 61 LEERLKALEGADYAVALASGQAATFAALLALLRQGDEVVAARGLFGQTIGLFGQVLGLMG 120 Query: 138 IQVDY-PPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAALAEIAHAKGALLAVDNC 196 ++V Y P D A P+T+ FVE+ +NP + D+ LA +A KG L VDN Sbjct: 121 VRVRYVDPEPDRV--REALSPSTRAIFVETLANPALYIPDLEGLASLAEEKGVALIVDNT 178 Query: 197 F-CTPALQQPLKLGADVVIHSATKYIDGQGRGMGGVVAG-----------------RGEQ 238 F AL +PL+ GA VV+ S TK+ G G +GG V RG+ Sbjct: 179 FGAAGALCRPLRWGAHVVVQSLTKWASGHGSVLGGAVLSRDTALWARYPQFLEKDPRGQV 238 Query: 239 MKEVVG-----------FLRTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLE 287 E +G L G LSPF+A+L +GLET+ +R+ S +A LAE L+ Sbjct: 239 PWEALGGRCYPERVRTLGLSLLGMALSPFHAYLLFQGLETVALRVARMSETAHFLAERLQ 298 Query: 288 RQPGIERVYYAGLPSHPQHELARRQQSGFGAVVSFDVKGGRDAAWRFIDATRMVSITTNL 347 P ++ + Y GL P H AR+ S FG +++ D+ G ++AA RF+ A + NL Sbjct: 299 GHPKVKALRYPGLEGDPAHGRARKYLSAFGPMLTLDL-GSQEAASRFLRAIPLPK-AANL 356 Query: 348 GDTKTTIAHPATTSHGRLSPEDRARAGIGDSLIRVAVGLEDLDDL 392 GD +T + HP TT+H RL E R +AG+ L+RV+VGLE +DL Sbjct: 357 GDARTLLVHPWTTTHSRLPEEGRLQAGVTPGLVRVSVGLEAPEDL 401 Lambda K H 0.319 0.133 0.392 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: 413 Number of extensions: 22 Number of successful extensions: 6 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: 403 Length of database: 412 Length adjustment: 31 Effective length of query: 372 Effective length of database: 381 Effective search space: 141732 Effective search space used: 141732 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