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_011023436.1 MA_RS18395 bifunctional serine hydroxymethyltransferase/L-allo-threonine aldolase
Query= curated2:D3DKC4 (427 letters) >NCBI__GCF_000007345.1:WP_011023436.1 Length = 412 Score = 514 bits (1324), Expect = e-150 Identities = 252/411 (61%), Positives = 321/411 (78%), Gaps = 1/411 (0%) Query: 1 MRHLFNTDAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRY 60 M ++ D +++EAI KE +RQ + L LIASEN+ S AVMEAQGS+MTNKYAEG KRY Sbjct: 1 MSYIEKIDPDMFEAIQKEADRQEHKLNLIASENYASRAVMEAQGSIMTNKYAEGYSGKRY 60 Query: 61 YGGCEFVDIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHG 120 YGGC+FVDIAE+LAI RAK +F A++ NVQPHSG+ ANMAVY +VL+PGDTIM MDLSHG Sbjct: 61 YGGCDFVDIAENLAIARAKEIFGAKYVNVQPHSGSGANMAVYFSVLQPGDTIMSMDLSHG 120 Query: 121 GHLTHGAKVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDW 180 GHL+HG+ V+FSGK+YN V YGV ET +DYD+L ++AKE KPK+IV GASAYPRVID+ Sbjct: 121 GHLSHGSPVSFSGKLYNIVPYGVSKETEALDYDELMKMAKECKPKMIVCGASAYPRVIDF 180 Query: 181 AKLREIADSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCK- 239 K REIAD VGAYL+ D+AH AGL+ GV+P+PVPYA FVT+TTHKTLRGPR G I+ K Sbjct: 181 KKFREIADEVGAYLLADIAHIAGLVVSGVHPSPVPYADFVTTTTHKTLRGPRGGMIISKT 240 Query: 240 KEFAKDIDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKE 299 +E A ++K+VFPGIQGGPLMHVIAAKAVAFKEAM ++F++ Q V NA+VL ++ Sbjct: 241 EELAMGVNKAVFPGIQGGPLMHVIAAKAVAFKEAMDEKFRQDQAQTVKNAKVLCACLKEK 300 Query: 300 GFKVVSGGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLG 359 GF +VSGGTD+H++L++L + +TG++ E A+ KA I NKN VPF+ P TSG+RLG Sbjct: 301 GFDIVSGGTDNHLMLVNLNNMNITGKDAEAAMSKAGIIANKNTVPFETRSPFITSGVRLG 360 Query: 360 TPAMTTRGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410 TPA TTRGMKE +M +IA I IKN G++ ++ V +V ++C +FP+Y Sbjct: 361 TPACTTRGMKEKEMELIADYIETAIKNAGNDALLSEVSAKVRDLCSRFPVY 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: 549 Number of extensions: 24 Number of successful extensions: 2 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 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