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_075385271.1 BK574_RS19235 serine hydroxymethyltransferase
Query= SwissProt::D3DKC4 (427 letters) >NCBI__GCF_002019605.1:WP_075385271.1 Length = 413 Score = 521 bits (1341), Expect = e-152 Identities = 257/413 (62%), Positives = 312/413 (75%) Query: 1 MRHLFNTDAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRY 60 M L N D ++YEAI E RQ +E+IASENF S AVM QGSV+TNKYAEG P +RY Sbjct: 1 METLKNQDPKVYEAIQLELGRQRDKIEMIASENFVSEAVMATQGSVLTNKYAEGYPGRRY 60 Query: 61 YGGCEFVDIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHG 120 YGGCE+VDI EDLA +RAK +F AE+ NVQPHSG QANMAVY +L+ GDT++GM+LSHG Sbjct: 61 YGGCEYVDIVEDLARDRAKEIFGAEYVNVQPHSGAQANMAVYFTILETGDTVLGMNLSHG 120 Query: 121 GHLTHGAKVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDW 180 GHLTHG+ VNFSG YN V YGV ET IDYD++ LAKEHKPKLIV GASAYPR ID+ Sbjct: 121 GHLTHGSPVNFSGVQYNFVEYGVDQETQTIDYDKVLELAKEHKPKLIVAGASAYPREIDF 180 Query: 181 AKLREIADSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKK 240 K R IAD VGAYLMVDMAH AGL+A G++P+PVP+AHFVT+TTHKTLRGPR G ILCK+ Sbjct: 181 EKFRSIADVVGAYLMVDMAHIAGLVAAGLHPSPVPHAHFVTTTTHKTLRGPRGGMILCKE 240 Query: 241 EFAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEG 300 EF K IDKS+FPGIQGGPLMHVIAAKAVAF EA+ EF YA +V NA+ L E+ EG Sbjct: 241 EFGKKIDKSIFPGIQGGPLMHVIAAKAVAFGEALQPEFNTYAENIVKNAKRLGEKLTSEG 300 Query: 301 FKVVSGGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGT 360 K+VSGGTD+H++LLDL LTG+ E AL + IT NKN +PFDP P TSGIR+GT Sbjct: 301 IKLVSGGTDNHLLLLDLTGLKLTGKVAEHALDEVGITTNKNTIPFDPESPFVTSGIRIGT 360 Query: 361 PAMTTRGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLYPEL 413 A+T+RG+ E M + +++ +KNI +E+ ++ V + ++FP+YP L Sbjct: 361 AAVTSRGLDEAAMDELGEIMALTLKNIDNEEKLKEASARVDALTKKFPMYPNL 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: 604 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: 413 Length adjustment: 32 Effective length of query: 395 Effective length of database: 381 Effective search space: 150495 Effective search space used: 150495 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