Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_092345255.1 BLU87_RS04830 homoserine O-acetyltransferase
Query= SwissProt::A0A0I9QGZ7 (379 letters) >NCBI__GCF_900107645.1:WP_092345255.1 Length = 370 Score = 327 bits (837), Expect = 4e-94 Identities = 161/371 (43%), Positives = 241/371 (64%), Gaps = 2/371 (0%) Query: 4 NTSVGIVTPQKIPFEMPLVLENGKTLPRFDLMIETYGELNAEKNNAVLICHALSGNHHVA 63 N SVGIVT + F++ L LE+G+ L L ETYGELNA+ +N +L+ HA +GN H A Sbjct: 2 NNSVGIVTTKYAEFDVELRLESGRLLGPLTLAYETYGELNADASNVILVTHAWTGNAHAA 61 Query: 64 GKHSAEDKYTGWWDNMVGPGKPIDTERFFVVGLNNLGGCDGSSGPLSINPETGREYGADF 123 G+HS ED+ GWWDNM+GPGK +DT R+F++ N +G C GS+GP SINP T + Y F Sbjct: 62 GRHSEEDRKPGWWDNMIGPGKVLDTNRYFILSSNTIGSCKGSTGPTSINPRTRKPYRLSF 121 Query: 124 PMVTVKDWVKSQAALADYLGIEQWAAVVGGSLGGMQALQWAISYPERVRHALVIASAPKL 183 P++ ++D V++Q L D+LGI AA+VGGS+G MQA++WAI YP+ VR + IA K Sbjct: 122 PVIMIRDMVRAQKLLLDHLGITSLAAIVGGSMGAMQAIEWAIHYPDMVRAIVPIAGTGKT 181 Query: 184 STQNIAFNDVARQAILTDPDFNEGHYRSHNTVPARGLRIARMMGHITYLAEDGLGKKFGR 243 + IA N +ARQAI DP + +G+Y+ + PA G +AR +GHI++L++ + KF R Sbjct: 182 APMAIALNALARQAIFNDPLWKKGNYQPEHP-PADGFSLARAVGHISFLSDISMQLKFER 240 Query: 244 DLRSNGYQYGYSVEFEVESYLRYQGDKFVGRFDANTYLLMTKALDYFDPAADFGNSLTRA 303 + + +FEVE YL Y G FV +FD N++L + KALD +D A +F +SL+ A Sbjct: 241 RFSVRDGMFDFFGKFEVERYLDYNGKNFVDQFDPNSFLYLAKALDLYDVAWNF-DSLSEA 299 Query: 304 VQDVQAKFFVASFSTDWRFAPERSHELVKALIAAQKSVQYIEVKSAHGHDAFLMEDEAYM 363 ++ VQ +F++DW + +++ ELV+ L K+V Y + S +GHD+FL+E E Y+ Sbjct: 300 LERVQCPSIWFAFNSDWLYPAQQTEELVEELQRLNKTVDYHLIDSDYGHDSFLVEPEKYI 359 Query: 364 RAVTAYMNNVD 374 + +++ ++ Sbjct: 360 PLLKEFLDQLN 370 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: 401 Number of extensions: 26 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: 370 Length adjustment: 30 Effective length of query: 349 Effective length of database: 340 Effective search space: 118660 Effective search space used: 118660 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