Align glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate WP_014027034.1 PYRFU_RS07375 serine hydroxymethyltransferase
Query= BRENDA::Q9UWT5 (433 letters) >NCBI__GCF_000223395.1:WP_014027034.1 Length = 441 Score = 580 bits (1494), Expect = e-170 Identities = 283/419 (67%), Positives = 344/419 (82%), Gaps = 6/419 (1%) Query: 3 LPKELEKVLEITKAQNVWRRTQTLNLIASENVMSPLAESVYMSDFMSRYAEGKPYKRYYQ 62 LP E+ +V+E T+A N WRR +T+NLIASENVMSPLAE+ Y++D M RYAEGKP KRYYQ Sbjct: 11 LPSEVREVIETTRAHNRWRR-ETINLIASENVMSPLAEAAYLNDMMHRYAEGKPRKRYYQ 69 Query: 63 GTKYTDEIETLTMELMNEITNSKDCDLRPTSGTIANAAVFRVLA-----EPGDKALIAPV 117 G +Y D +E L M+ M E+ + RP SGTIANA VFR LA E KALIAPV Sbjct: 70 GLRYVDVVEELVMKYMGELLGGAFIEPRPVSGTIANATVFRALASCPSSEGRPKALIAPV 129 Query: 118 QAGAHVSHTKFGTLGALGIQHIEMPFDEENINVDVDKAIKMIEEVKPKFVVLGGSLYLFP 177 QAGAHVSHTKFGTLGAL I+HIE+P+D +N+NVDVDKA+KMIE+VKP FVVLGGSLYLFP Sbjct: 130 QAGAHVSHTKFGTLGALCIEHIELPYDPDNLNVDVDKAVKMIEDVKPVFVVLGGSLYLFP 189 Query: 178 HPTKELAQHVHAVGAKLVYDAAHVYGLIEGKVWSNPLKDGADIMTVSTHKTFPGPQGGAI 237 HP +E+A+ H+VGAKLVYDAAHV GLI GK W NPL GADIMT STHKTFPGPQGG I Sbjct: 190 HPVREIAEAAHSVGAKLVYDAAHVLGLIVGKRWRNPLDHGADIMTASTHKTFPGPQGGII 249 Query: 238 FSDGSEVFKQVSKTIFPWFVSNHHLHRLPATAVTAIEMKYFGESYANQILRNSKALAEAL 297 + +++K VS+ +FP+FVSNHHLHRLPA A+TA+EMKY+GE+YA+Q++RN+KALAEAL Sbjct: 250 ATRQEDLYKAVSRIVFPYFVSNHHLHRLPALAITALEMKYYGEAYADQVVRNAKALAEAL 309 Query: 298 AERGFKVIGENLGYTKSHQVAVDVRQFGGGNKIAKLLEDANIIVNKNLLPYDKPEDVSDP 357 A GFKV+GE+LGYT+SHQVAVDVR++GGG K A+LLE+ANIIVNKNLLPYD P+ + +P Sbjct: 310 AAEGFKVLGEHLGYTRSHQVAVDVREYGGGAKAAQLLEEANIIVNKNLLPYDPPDAIKNP 369 Query: 358 SGLRIGVQEMTRYGMKEGEMEEIAELFKKVIIDKKDVNEVKKEVIEMRRNFLEVKYTFD 416 SGLR+GVQEMTR+GMKE +M EIA ++V+ID +D +V+KEV+E RRNF +V Y FD Sbjct: 370 SGLRLGVQEMTRWGMKEDDMREIARFMRRVVIDGEDPAKVRKEVVEFRRNFQKVHYAFD 428 Lambda K H 0.316 0.134 0.379 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: 614 Number of extensions: 19 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: 433 Length of database: 441 Length adjustment: 32 Effective length of query: 401 Effective length of database: 409 Effective search space: 164009 Effective search space used: 164009 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 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