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_013450717.1 CALNI_RS02960 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_000183405.1:WP_013450717.1 Length = 418 Score = 569 bits (1466), Expect = e-167 Identities = 275/403 (68%), Positives = 335/403 (83%) Query: 8 DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67 D EIY+A+ KE ERQ H+ELIASENF S AV+EAQGS+MTNKYAEG P KRYYGGCEFV Sbjct: 11 DPEIYDALKKEIERQETHIELIASENFVSPAVLEAQGSIMTNKYAEGYPAKRYYGGCEFV 70 Query: 68 DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127 DIAE+LAI+RAK LF AEHANVQ HSG+QANMAVY AVLKPGDTIMGM+LSHGGHLTHG+ Sbjct: 71 DIAEELAIKRAKELFGAEHANVQAHSGSQANMAVYFAVLKPGDTIMGMNLSHGGHLTHGS 130 Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187 VNFSGK++N + YGV+ ET IDYD+ +LA EHKPKLI+ GASAYPR ID+ K REIA Sbjct: 131 PVNFSGKLFNVISYGVNKETETIDYDEAEKLATEHKPKLIMVGASAYPRTIDFKKFREIA 190 Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKKEFAKDID 247 D VGA L+VDMAH AGL+A G +P+PVPYA FVT+TTHKTLRGPR G ILCK+E+AK ++ Sbjct: 191 DKVGAVLVVDMAHIAGLVAAGAHPSPVPYADFVTTTTHKTLRGPRGGLILCKEEYAKTLN 250 Query: 248 KSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSGG 307 +FPGIQGGPLMHVIAAKAVA KEAMS++FK Y Q+V NA+ L+E +K GFK+VSGG Sbjct: 251 SQIFPGIQGGPLMHVIAAKAVALKEAMSEDFKVYQHQIVKNAKRLSERLMKHGFKLVSGG 310 Query: 308 TDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTRG 367 TD+H++L++L ++ +TG+E EEALG+ANITVNKN VPF+ P TSG+R+GTPA+TTRG Sbjct: 311 TDNHLMLINLSNSEITGKEAEEALGRANITVNKNTVPFETRSPFVTSGVRIGTPAVTTRG 370 Query: 368 MKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 MKE +M I LI++V+ +I + I V+ +V+E+C+QFPLY Sbjct: 371 MKESEMDFIGDLIAQVLSDIKSDLNINDVKSKVLELCKQFPLY 413 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: 622 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: 418 Length adjustment: 32 Effective length of query: 395 Effective length of database: 386 Effective search space: 152470 Effective search space used: 152470 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