Align Glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate WP_019894223.1 A377_RS0101085 serine hydroxymethyltransferase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_2685 (418 letters) >NCBI__GCF_000384235.1:WP_019894223.1 Length = 425 Score = 629 bits (1623), Expect = 0.0 Identities = 313/423 (73%), Positives = 355/423 (83%), Gaps = 6/423 (1%) Query: 1 MFSKHDQIKGYDDELLAAMNAEDARQEHHIELIASENYTSQRVMQAQGSGLTNKYAEGYP 60 MF I GYDDEL AM AE RQE HIELIASENYTS RVM+AQGS LTNKYAEGYP Sbjct: 1 MFEPTMTIAGYDDELATAMQAEATRQEDHIELIASENYTSPRVMEAQGSVLTNKYAEGYP 60 Query: 61 GKRYYGGCEHVDVVEQLAIDRARQLFGADYANVQPHSGSQANAAVYLALLQAGDTVLGMS 120 KRYYGGCEHVDVVEQLAIDRA++LFGADYANVQPHSGSQANA VY+AL++ G+TVLGMS Sbjct: 61 FKRYYGGCEHVDVVEQLAIDRAKELFGADYANVQPHSGSQANAPVYMALMKPGETVLGMS 120 Query: 121 LAHGGHLTHGAKVSFSGKLYNAVQYGIDTTTGLIDYDEVERLAVEHKPKMIIAGFSAYSK 180 LAHGGHLTHGA V+FSGK+Y AVQYG++ TG IDYDEV RLA EH+PKMI+AGFSAYS+ Sbjct: 121 LAHGGHLTHGAHVNFSGKIYKAVQYGLNPETGEIDYDEVARLAREHQPKMIVAGFSAYSQ 180 Query: 181 TLDFPRFRQIADKVGAYFFVDMAHVAGLVATGLYPNPLPYADVVTTTTHKTLRGPRGGLI 240 +D+ RFR+IAD+VGAY VDMAHVAGLVA G+YPNP+PYADVVTTTTHKTLRGPR GLI Sbjct: 181 VVDWGRFREIADEVGAYLLVDMAHVAGLVAAGIYPNPVPYADVVTTTTHKTLRGPRSGLI 240 Query: 241 LAKANPELEKKLNAAVFPGGQGGPLMHVIAAKAVCFKEALEPAFKTYQSQVIRNAQAMAQ 300 LAK+NPELEKKLN+A+FPG QGGPLMHVIAAKAV FKEA+EP FKTY V++NA+AMA+ Sbjct: 241 LAKSNPELEKKLNSAIFPGQQGGPLMHVIAAKAVAFKEAMEPEFKTYAENVVKNAKAMAK 300 Query: 301 VFIERGYDVVSGGTDNHLFLVSLIRQGLTGKDADAALGRAGITVNKNAVPNDPQSPFVTS 360 VF+ERGYDVVS GT+NHLFLVSLI QGLTGK DAALG A IT+NKN+VPNDP+SPFVTS Sbjct: 301 VFMERGYDVVSKGTENHLFLVSLIEQGLTGKLVDAALGAAHITINKNSVPNDPKSPFVTS 360 Query: 361 GLRIGTPAITSRGFKEAQSIALAGWICDIL------DHLGDADIEANVARQAAALCADFP 414 G+R+GT A T+RGF EA S LA W+CD++ + D + A V + ALCA P Sbjct: 361 GIRVGTAASTTRGFTEADSTDLAHWMCDVIAACDQENETWDEAVVAQVREKVTALCAQRP 420 Query: 415 VYR 417 VYR Sbjct: 421 VYR 423 Lambda K H 0.319 0.135 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: 649 Number of extensions: 22 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: 418 Length of database: 425 Length adjustment: 32 Effective length of query: 386 Effective length of database: 393 Effective search space: 151698 Effective search space used: 151698 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 (21.7 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