Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_024850420.1 N745_RS0101730 homoserine O-acetyltransferase
Query= SwissProt::D0L1T6 (403 letters) >NCBI__GCF_000526715.1:WP_024850420.1 Length = 386 Score = 511 bits (1316), Expect = e-149 Identities = 246/379 (64%), Positives = 294/379 (77%), Gaps = 6/379 (1%) Query: 16 SVGIVEPKTARFSEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGF 75 SVGIV +T S PL + CG LP Y+L +ETYG+LND+ SNA+LICHALSG H AGF Sbjct: 3 SVGIVHSQTLHISTPLNMVCGSVLPEYDLAFETYGELNDDHSNAILICHALSGHQHVAGF 62 Query: 76 HAETDRKPGWWDSAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPI 135 H E D+ GWWDS IGPGK IDTDRFFVVC NNLGGC GS+GP S++P +G+ YGPDFPI Sbjct: 63 H-EGDKDAGWWDSYIGPGKVIDTDRFFVVCSNNLGGCHGSSGPTSINPETGQVYGPDFPI 121 Query: 136 VTVKDWVHAQYRLMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSA 195 VT KDWV++Q L +YL + WAA+IGGS+GGMQV+QW+I YPD + HAVVIA+AP+LSA Sbjct: 122 VTCKDWVNSQNELRKYLKIEAWAAIIGGSMGGMQVMQWAIDYPDKIKHAVVIASAPKLSA 181 Query: 196 QNIAFNEVARQAIITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGREL 255 QNIAFNEVAR+AI+TDP+F GR+ + N P+RGL LARMLGH+TYLSDD M KFGREL Sbjct: 182 QNIAFNEVARRAIMTDPDFLDGRFIEKNTTPKRGLALARMLGHLTYLSDDLMGTKFGREL 241 Query: 256 RAGQVQYGFDVEFQVESYLRYQGTSFVDR--FDANTYLLMTKALDYFDPAQASNDDLVAA 313 R G++ Y ++VEFQVESYLRYQG F + FDANTYLLMTKALDYFDPA ++DL A Sbjct: 242 REGKLNYNYEVEFQVESYLRYQGEKFATKQNFDANTYLLMTKALDYFDPASEYDNDLTKA 301 Query: 314 LAEVKAHFLVVSFTSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYH 373 L+ KA FLV+SFT+DWRF+PERS EIV+ALL + VSYAEIES HGHDAFL+ P+Y Sbjct: 302 LSHAKAKFLVISFTTDWRFAPERSHEIVKALLDNDADVSYAEIESKHGHDAFLLPNPHYE 361 Query: 374 RVLAGYMANI---DFASTP 389 V Y+ + D A P Sbjct: 362 NVFRAYLNQVVCRDIAPVP 380 Lambda K H 0.320 0.135 0.412 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: 558 Number of extensions: 18 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: 403 Length of database: 386 Length adjustment: 31 Effective length of query: 372 Effective length of database: 355 Effective search space: 132060 Effective search space used: 132060 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