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_012991487.1 THAL_RS02215 serine hydroxymethyltransferase
Query= curated2:D3DKC4 (427 letters) >NCBI__GCF_000025605.1:WP_012991487.1 Length = 428 Score = 738 bits (1905), Expect = 0.0 Identities = 362/426 (84%), Positives = 394/426 (92%) Query: 1 MRHLFNTDAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRY 60 M HL TD EIY I+KEYERQFYHLELIASENFTSLAVMEAQGS++TNKYAEGLP KRY Sbjct: 1 MDHLKRTDPEIYHVILKEYERQFYHLELIASENFTSLAVMEAQGSLLTNKYAEGLPGKRY 60 Query: 61 YGGCEFVDIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHG 120 YGGCE+VD+AE LAIERAK LF AEHANVQPHSG+QANMAVYMAVL+PGDT++GMDL+HG Sbjct: 61 YGGCEWVDVAETLAIERAKKLFGAEHANVQPHSGSQANMAVYMAVLQPGDTLLGMDLAHG 120 Query: 121 GHLTHGAKVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDW 180 GHLTHGAKVNFSGKIYNAVYYGV P T LIDYDQLYRLAKEHKPKLIVGGASAYPR+IDW Sbjct: 121 GHLTHGAKVNFSGKIYNAVYYGVDPNTELIDYDQLYRLAKEHKPKLIVGGASAYPRIIDW 180 Query: 181 AKLREIADSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKK 240 AKLREIAD VGA LMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCK Sbjct: 181 AKLREIADEVGALLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKS 240 Query: 241 EFAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEG 300 +FAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAM++EFK YARQVVANA+ LAEE KEG Sbjct: 241 QFAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMTEEFKVYARQVVANAKALAEELTKEG 300 Query: 301 FKVVSGGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGT 360 F++V+GGTDSHIVL+DLR TGLTG+EVE ALG+A+ITVNKNAVPFDPLPP KTSGIRLGT Sbjct: 301 FRIVTGGTDSHIVLVDLRGTGLTGKEVEAALGRAHITVNKNAVPFDPLPPTKTSGIRLGT 360 Query: 361 PAMTTRGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLYPELREEINHL 420 PAMTTRGM+ED+MR IA+LIS VIKNI DEKVIE VR EV+E+CEQFPLYPE+RE ++ L Sbjct: 361 PAMTTRGMREDEMRRIAKLISTVIKNISDEKVIERVRGEVMELCEQFPLYPEMRERLHEL 420 Query: 421 AKIKAT 426 + +AT Sbjct: 421 SDSQAT 426 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: 736 Number of extensions: 23 Number of successful extensions: 1 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: 428 Length adjustment: 32 Effective length of query: 395 Effective length of database: 396 Effective search space: 156420 Effective search space used: 156420 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