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_013554591.1 NITSA_RS08370 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_000186245.1:WP_013554591.1 Length = 416 Score = 465 bits (1197), Expect = e-135 Identities = 234/404 (57%), Positives = 301/404 (74%), Gaps = 2/404 (0%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D E+Y+AIV E +R+ HLE+IASENFT VMEA GSV TNKYAEG P KRYYGGCE+ Sbjct: 9 DPEVYQAIVDELKRETEHLEMIASENFTFPDVMEAMGSVFTNKYAEGYPAKRYYGGCEYA 68 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 D E LAI+R K LF E+ANVQPHSG+QAN AVY A++K GD I+GMDLSHGGHLTHG+ Sbjct: 69 DKVEQLAIDRCKELFGCEYANVQPHSGSQANGAVYAALIKAGDKILGMDLSHGGHLTHGS 128 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 KV+FSGK Y++ YGV + IDYD++ +AK +PK+IV GASAYPR ID+A+ REIA Sbjct: 129 KVSFSGKNYHSFTYGVELDGR-IDYDRVRDIAKIVQPKIIVCGASAYPREIDFARFREIA 187 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCK-KEFAKDI 246 D VGA L D+AH AGL+ G +P+P P+AH VT+TTHKTL GPR G I+ +E AK I Sbjct: 188 DEVGALLFADIAHIAGLVVAGEHPSPFPHAHVVTTTTHKTLAGPRGGAIMTNDEEIAKKI 247 Query: 247 DKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSG 306 + ++FPG+QGGPL+HV+AAKAV FK ++ E+KEYA+QV ANA+VLA+ +K G+ VVSG Sbjct: 248 NSAIFPGLQGGPLVHVVAAKAVGFKHNLAPEWKEYAKQVKANAKVLADVLMKRGYDVVSG 307 Query: 307 GTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTR 366 GTD+H+VL+ D +G++ + ALG+A ITVNKN VP + P TSGIR+G+PA+T R Sbjct: 308 GTDNHLVLVSFLDKEFSGKDADAALGRAGITVNKNTVPGETRSPFVTSGIRIGSPALTRR 367 Query: 367 GMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 GMKE + +IA I V+ I D + V++E+ E+ QF +Y Sbjct: 368 GMKEKEFELIANRICDVLDRIDDHEFQAKVKEEMKELALQFVIY 411 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: 640 Number of extensions: 23 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: 416 Length adjustment: 32 Effective length of query: 395 Effective length of database: 384 Effective search space: 151680 Effective search space used: 151680 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