Align Serine hydroxymethyltransferase; SHMT; Serine methylase; L-threonine/L-allo-threonine aldolase; EC 2.1.2.1; EC 4.1.2.48 (characterized)
to candidate WP_011976226.1 SMED_RS10455 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_000017145.1:WP_011976226.1 Length = 425 Score = 397 bits (1021), Expect = e-115 Identities = 205/407 (50%), Positives = 279/407 (68%), Gaps = 4/407 (0%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D + +AI E +RQ +ELIASEN S AV++A G MTNK EG P R++GG +FV Sbjct: 17 DPLVAQAIDNERKRQQDQIELIASENIVSRAVLDALGHEMTNKTLEGYPGNRFHGGGQFV 76 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 D+ E AI+RAK LF +ANVQPHSGTQAN+AV+ +L PGD ++ +DL+ GGHL+HG Sbjct: 77 DVVEQAAIDRAKQLFGCAYANVQPHSGTQANLAVFFLLLTPGDKVLSLDLAAGGHLSHGM 136 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 K N SG+ + Y V+PET +IDYD+L R+A+E +P L++ G SAYPR +D+ ++ IA Sbjct: 137 KGNLSGRWFEPHNYNVNPETEVIDYDELERIAEEVRPTLLITGGSAYPRELDFERMGNIA 196 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKKE-FAKDI 246 VGA+ +VDMAH AGL+AGGV+P+P P+A VT TT KTLRGPR G IL E + K + Sbjct: 197 KKVGAWFLVDMAHIAGLVAGGVHPSPFPHADIVTCTTTKTLRGPRGGLILTNNEAWFKKL 256 Query: 247 DKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSG 306 +VFPG+QG +V+AAKA+ EA+ +FK YA QV NARVLA+ + G +VVSG Sbjct: 257 QSAVFPGVQGSLHSNVLAAKAICLGEALRDDFKVYAAQVKTNARVLADVLMARGVRVVSG 316 Query: 307 GTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTR 366 GTD+HIVL+DL GL G++ E+ L +ANIT NKN +P D P + G+RLG A TTR Sbjct: 317 GTDTHIVLVDLSSKGLIGKQAEDLLARANITANKNPIPNDSPRPPEWLGMRLGVSAATTR 376 Query: 367 GMKEDQMRIIARLISKVI--KNIGDEKV-IEYVRQEVIEMCEQFPLY 410 GMKED+ R + +I+ +I + G+ + +E + +V E+ FP+Y Sbjct: 377 GMKEDEFRTLGTIIADLIEAEAAGNADLSVEAAKTKVAELTAAFPVY 423 Lambda K H 0.319 0.136 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: 523 Number of extensions: 17 Number of successful extensions: 2 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: 427 Length of database: 425 Length adjustment: 32 Effective length of query: 395 Effective length of database: 393 Effective search space: 155235 Effective search space used: 155235 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: 51 (24.3 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