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_007472829.1 CMTB2_RS00200 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_000170735.1:WP_007472829.1 Length = 415 Score = 477 bits (1228), Expect = e-139 Identities = 238/404 (58%), Positives = 309/404 (76%), Gaps = 1/404 (0%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D ++Y + KE +RQ HLE+IASENFT VMEAQGSV TNKYAEG P+KRYYGGCE+ Sbjct: 7 DIDVYSILEKELKRQTDHLEMIASENFTLPEVMEAQGSVFTNKYAEGYPNKRYYGGCEYA 66 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 D+ E LAI+RAK LF E ANVQPHSG+QAN AVY+A+LKP D ++GMDLS+GGHLTHGA Sbjct: 67 DLVEQLAIDRAKELFGCEFANVQPHSGSQANGAVYVALLKPYDKLLGMDLSNGGHLTHGA 126 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 KVNFSGK Y++ YG+ +T IDYD++ +AK KPK+IV GASAYPR ID+AK +EIA Sbjct: 127 KVNFSGKHYHSFSYGIDEKTGRIDYDRVKDIAKIVKPKMIVCGASAYPREIDFAKFKEIA 186 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILC-KKEFAKDI 246 D VGA LM D+AH AGL+ +P+P P+ VT+TTHKTLRGPR G IL +E+AK I Sbjct: 187 DEVGAILMADVAHIAGLVVANEHPHPFPHCDVVTTTTHKTLRGPRGGLILTNNEEYAKKI 246 Query: 247 DKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSG 306 + ++FPGIQGGPL+HVIAAKAV FK ++ +KEYA+QV ANARVLAE ++ G+ +VSG Sbjct: 247 NSAIFPGIQGGPLVHVIAAKAVGFKMNLAPSWKEYAKQVKANARVLAEVLLERGYDLVSG 306 Query: 307 GTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTR 366 GTD+H+VL+ + +G+E EEALG+A ITVNKN VP + P TSGIR+G+PA+T R Sbjct: 307 GTDNHLVLVSFLNKEFSGKEAEEALGRAGITVNKNTVPGEKRSPFVTSGIRIGSPALTAR 366 Query: 367 GMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 GMKE++ R IA I+ V+ +I + ++ + V++E+ E+ +F +Y Sbjct: 367 GMKEEEFRFIANKIADVLDDIYNLELQDKVKEELKELASKFVIY 410 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: 629 Number of extensions: 27 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: 415 Length adjustment: 32 Effective length of query: 395 Effective length of database: 383 Effective search space: 151285 Effective search space used: 151285 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