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_069664047.1 BCR25_RS13185 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_001730305.1:WP_069664047.1 Length = 412 Score = 495 bits (1275), Expect = e-145 Identities = 247/405 (60%), Positives = 310/405 (76%), Gaps = 2/405 (0%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D ++++AI KE +RQ +LELIASEN S VM AQGS++TNKYAEG P KRYYGGCEF+ Sbjct: 7 DPDLWDAIAKENDRQENNLELIASENVVSEGVMAAQGSILTNKYAEGYPGKRYYGGCEFI 66 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 DI EDLAI+RAK LF A+ ANVQPHSG+QAN A Y+++++PGDT++GMDLS GGHLTHG+ Sbjct: 67 DIVEDLAIDRAKELFGAKFANVQPHSGSQANTAAYLSLIEPGDTVLGMDLSAGGHLTHGS 126 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 VNFSGK YN V YGV P T +IDY+ + LA+EH+PKLIV GASAY R ID+ K REIA Sbjct: 127 PVNFSGKTYNFVSYGVDPTTEVIDYNVVRILAREHQPKLIVAGASAYSRTIDFEKFREIA 186 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCK-KEFAKDI 246 D VGA LMVDMAH AGL+A G++PNPVPYA TSTTHKTLRGPR G IL +E AK I Sbjct: 187 DEVGAKLMVDMAHIAGLVAAGLHPNPVPYADITTSTTHKTLRGPRGGLILTNDEELAKKI 246 Query: 247 DKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIK-EGFKVVS 305 + ++FPGIQGGPL HVIA KAVAFKEA+ FKEY+ QV+ NA+ + + F + ++VS Sbjct: 247 NSNIFPGIQGGPLEHVIAGKAVAFKEALDISFKEYSEQVIENAKAMTKVFNQTPESRLVS 306 Query: 306 GGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTT 365 G TD+H++L+D+ GL G+E E L NIT NKN++PF+ L P KTSGIR+GTPA+TT Sbjct: 307 GSTDNHLLLIDVSGFGLNGKEAEAILDNVNITANKNSIPFEQLSPFKTSGIRIGTPAITT 366 Query: 366 RGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 RG KED +A+LI KV+K+ +E + VR V E+ +++PLY Sbjct: 367 RGFKEDDCVEVAKLIVKVLKDHENETTLSEVRAAVSELTKKYPLY 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: 558 Number of extensions: 21 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: 412 Length adjustment: 32 Effective length of query: 395 Effective length of database: 380 Effective search space: 150100 Effective search space used: 150100 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 26 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