Align glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate WP_011813701.1 HHAL_RS04615 serine hydroxymethyltransferase
Query= BRENDA::R9YJZ9 (417 letters) >NCBI__GCF_000015585.1:WP_011813701.1 Length = 416 Score = 643 bits (1658), Expect = 0.0 Identities = 309/417 (74%), Positives = 357/417 (85%), Gaps = 1/417 (0%) Query: 1 MLKKAMNIADYDPELFKAIEDETRRQEEHIELIASENYTSPRVMEAQGSQLTNKYAEGYP 60 M + M IA YDPEL AIEDE +RQE+HIELIASENY SPRVMEAQGS LTNKYAEGYP Sbjct: 1 MFSRDMTIAGYDPELAAAIEDERQRQEDHIELIASENYASPRVMEAQGSVLTNKYAEGYP 60 Query: 61 GKRYYGGCEYVDVVETLAIERAKQLFGATYANVQPHSGSQANSAVYMALLQPGDTVLGMN 120 GKRYYGGCE+VDV E LAI+RAKQLFGA YANVQPHSGSQAN+AV+ ALL+PGDT+LGM+ Sbjct: 61 GKRYYGGCEHVDVAEQLAIDRAKQLFGADYANVQPHSGSQANAAVFHALLKPGDTILGMS 120 Query: 121 LAHGGHLTHGSPVNFSGKLYNIIPYGIDESGKIDYSELETLALEHKPKMIIGGFSAYSGI 180 L HGGHLTHG+ VNFSGKL+N + YGI++ G+IDY E++ LA EH+PKM+IGGFSAYS + Sbjct: 121 LDHGGHLTHGAKVNFSGKLFNAVQYGINDDGQIDYDEIQRLATEHQPKMVIGGFSAYSQV 180 Query: 181 VDWAKLREIADKIGAYLFVDMAHVAGLIAAGVYPNPVPHAHVVTSTTHKTLAGPRGGVIL 240 VDWA+LR+IAD +GAYL VDMAH+AGL+AAGVYP+P+PHA VTSTTHKTL GPRGG+IL Sbjct: 181 VDWARLRQIADSVGAYLVVDMAHIAGLVAAGVYPSPIPHADAVTSTTHKTLRGPRGGIIL 240 Query: 241 SAADDEDLYKKLNSAVFPGGQGGPLMHVIAGKAVAFKEALEPEFKTYQQQVVNNAKAMVE 300 A + DL KK S VFPG QGGPLMH IAGKAVAFKEALEP+FK YQ+QVV NA+AM Sbjct: 241 -ARSNPDLEKKFQSLVFPGTQGGPLMHAIAGKAVAFKEALEPDFKQYQEQVVANARAMAR 299 Query: 301 VFLERGYKIVSGGTDNHLMLVDLIGRELTGKEADAALGRANITVNKNSVPNDPRSPFVTS 360 +ERGY +VSGGTDNHL L+DL + LTGK+ADAALGRANITVNKN+VPNDP+SPFVTS Sbjct: 300 RVIERGYNVVSGGTDNHLFLMDLTPKNLTGKDADAALGRANITVNKNTVPNDPQSPFVTS 359 Query: 361 GVRIGTPAITRRGFKEAEARELTGWICDVLDNAHDDAVIERVKSQVLELCARFPVYG 417 G+RIGTPAIT RGFKEAEA L WICDVLDN D++V+ERV+ +V ++C FPVYG Sbjct: 360 GLRIGTPAITTRGFKEAEATRLADWICDVLDNMGDESVVERVRGEVEQICREFPVYG 416 Lambda K H 0.316 0.135 0.393 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: 666 Number of extensions: 26 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: 417 Length of database: 416 Length adjustment: 31 Effective length of query: 386 Effective length of database: 385 Effective search space: 148610 Effective search space used: 148610 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: 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