Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_004511679.1 GMET_RS13945 homoserine O-acetyltransferase
Query= SwissProt::A0A0I9QGZ7 (379 letters) >NCBI__GCF_000012925.1:WP_004511679.1 Length = 369 Score = 339 bits (870), Expect = 6e-98 Identities = 167/370 (45%), Positives = 247/370 (66%), Gaps = 4/370 (1%) Query: 6 SVGIVTPQKIPFEMPLVLENGKTLPRFDLMIETYGELNAEKNNAVLICHALSGNHHVAGK 65 SVGIV Q + F+ L LE+G+ L L ETYGELNA+++NA+L+ HA +GN H+AGK Sbjct: 2 SVGIVQEQSVTFDTELRLESGRILGPITLAYETYGELNADRSNAILVAHAWTGNAHLAGK 61 Query: 66 HSAEDKYTGWWDNMVGPGKPIDTERFFVVGLNNLGGCDGSSGPLSINPETGREYGADFPM 125 +S ED GWWD +VGPG+ +DT+R FV+ N +G C GS+GP SINP+TG+ Y FP+ Sbjct: 62 NSEEDTKPGWWDAIVGPGRLLDTDRCFVICSNVIGSCYGSTGPASINPKTGKRYNLTFPV 121 Query: 126 VTVKDWVKSQAALADYLGIEQWAAVVGGSLGGMQALQWAISYPERVRHALVIASAPKLST 185 +TV+D V++QA L D+LGI++ V+GGS+GGMQAL+WA +P+R+R A+ +A+ + S Sbjct: 122 ITVRDMVRAQALLLDHLGIDRLLTVLGGSMGGMQALEWATQFPDRIRSAIALATTSRPSP 181 Query: 186 QNIAFNDVARQAILTDPDFNEGHYRSHNTVPARGLRIARMMGHITYLAEDGLGKKFGRDL 245 Q I+ N VAR AI DP + +G YR + P GL +AR +GHIT+L+++ + +KFGR Sbjct: 182 QAISLNAVARWAIFNDPTWKKGEYRKN---PKDGLALARGIGHITFLSDESMWQKFGRRF 238 Query: 246 RSNGYQYGYSVEFEVESYLRYQGDKFVGRFDANTYLLMTKALDYFDPAADFGNSLTRAVQ 305 + + + +FEVE YL Y G FV RFD N++L + KALD +D A + SL A Sbjct: 239 NARDGLFDFFGQFEVERYLSYNGYNFVDRFDTNSFLYLAKALDLYDTAWGY-ESLEEAFS 297 Query: 306 DVQAKFFVASFSTDWRFAPERSHELVKALIAAQKSVQYIEVKSAHGHDAFLMEDEAYMRA 365 V+A +F++DW + P ++ E+ L + K V+Y ++SA+GHDAFL+E E + Sbjct: 298 RVKAPIQFFAFTSDWLYPPYQTEEMATILRSLGKPVEYHLIESAYGHDAFLLEHETFAPM 357 Query: 366 VTAYMNNVDK 375 V +++ V++ Sbjct: 358 VREFLDKVER 367 Lambda K H 0.319 0.135 0.408 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: 404 Number of extensions: 13 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: 379 Length of database: 369 Length adjustment: 30 Effective length of query: 349 Effective length of database: 339 Effective search space: 118311 Effective search space used: 118311 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