Align Serine hydroxymethyltransferase; SHMT; Serine methylase; EC 2.1.2.1; L-threonine/L-allo-threonine aldolase; EC 4.1.2.48 (uncharacterized)
to candidate WP_013449931.1 SULKU_RS13440 serine hydroxymethyltransferase
Query= curated2:D3DKC4 (427 letters) >NCBI__GCF_000183725.1:WP_013449931.1 Length = 420 Score = 436 bits (1121), Expect = e-127 Identities = 222/404 (54%), Positives = 291/404 (72%), Gaps = 2/404 (0%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D E++ I E+ERQ HLE+IASENFTS AVMEA GS+ TNKYAEG P+KRYYGGC+F Sbjct: 13 DTEVFAIIQNEFERQSTHLEMIASENFTSPAVMEAMGSIFTNKYAEGYPNKRYYGGCQFA 72 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 D E LA +R +F ++ANVQPHSG+QAN AVY A+L+ GD I+GMDL HGGHLTHGA Sbjct: 73 DQVEQLAKDRLCKIFGCDYANVQPHSGSQANGAVYAALLQAGDKILGMDLRHGGHLTHGA 132 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 K +FSGK Y++ YGV + + DY+++ ++A+ KPK+IV GASAY R ID+ K R IA Sbjct: 133 KPSFSGKNYHSFTYGVEADGRM-DYEKIAQIAEIVKPKIIVCGASAYTREIDFKKFRTIA 191 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILC-KKEFAKDI 246 + VGA L D+AH AGL+A G + NP PYA VTSTTHKTLRGPR G I+ +E AK I Sbjct: 192 ERVGAILFADIAHIAGLVAAGEHMNPFPYADVVTSTTHKTLRGPRGGVIMTNNEEIAKKI 251 Query: 247 DKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSG 306 D ++FPGIQGGPL+HVIAAKAVAF E + +KEYA+ V +NA++L E + GF+++SG Sbjct: 252 DSAIFPGIQGGPLVHVIAAKAVAFGEVLHPSWKEYAKAVKSNAKLLGEIMNQRGFQLISG 311 Query: 307 GTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTR 366 GTD+H++L+ L D +G E AL A ITVNKN++P DP P TSGIR+G+ A+TT Sbjct: 312 GTDNHMILISLMDKEFSGEEASVALENAGITVNKNSIPSDPRPASSTSGIRIGSAALTTL 371 Query: 367 GMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 GMKE + +IA IS V+ +I + + ++ E+ + + F +Y Sbjct: 372 GMKEKEFTLIAHRISDVLDDIQNIPLQMEIKAELETLLKGFRVY 415 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: 553 Number of extensions: 17 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: 427 Length of database: 420 Length adjustment: 32 Effective length of query: 395 Effective length of database: 388 Effective search space: 153260 Effective search space used: 153260 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 Apr 09 2024. The underlying query database was built on Sep 17 2021.
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