Align Glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate GFF502 HP15_489 glycine hydroxymethyltransferase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_2685 (418 letters) >FitnessBrowser__Marino:GFF502 Length = 417 Score = 661 bits (1705), Expect = 0.0 Identities = 323/416 (77%), Positives = 369/416 (88%) Query: 1 MFSKHDQIKGYDDELLAAMNAEDARQEHHIELIASENYTSQRVMQAQGSGLTNKYAEGYP 60 MF++ +I G+DDEL AM AE+ RQE HIELIASENYTS RVM+AQGS LTNKYAEGYP Sbjct: 1 MFNREMKIAGFDDELWNAMQAEEKRQEAHIELIASENYTSPRVMEAQGSVLTNKYAEGYP 60 Query: 61 GKRYYGGCEHVDVVEQLAIDRARQLFGADYANVQPHSGSQANAAVYLALLQAGDTVLGMS 120 GKRYYGGCE VD+ E+LAI+RA++LFGA YANVQPHSGSQAN+AV++ALL+ GDTVLGMS Sbjct: 61 GKRYYGGCEFVDIAEELAIERAKELFGAAYANVQPHSGSQANSAVFMALLKPGDTVLGMS 120 Query: 121 LAHGGHLTHGAKVSFSGKLYNAVQYGIDTTTGLIDYDEVERLAVEHKPKMIIAGFSAYSK 180 LAHGGHLTHGA V+FSGK+YNAVQYGI+T TGL+DYDE+E LA+EHKPKMIIAGFSAYS+ Sbjct: 121 LAHGGHLTHGASVNFSGKIYNAVQYGINTDTGLLDYDEIESLALEHKPKMIIAGFSAYSQ 180 Query: 181 TLDFPRFRQIADKVGAYFFVDMAHVAGLVATGLYPNPLPYADVVTTTTHKTLRGPRGGLI 240 LDF RFR+IADKVGAY FVDMAHVAGLVA G+YP+P+P+A VV TTTHKTLRGPRGGLI Sbjct: 181 ELDFARFREIADKVGAYLFVDMAHVAGLVAAGVYPDPVPHAHVVATTTHKTLRGPRGGLI 240 Query: 241 LAKANPELEKKLNAAVFPGGQGGPLMHVIAAKAVCFKEALEPAFKTYQSQVIRNAQAMAQ 300 LA + +L+KKLN+AVFPGGQGGPLMHVIAAKAVCFKEA+ FKTYQ QV++NA AMAQ Sbjct: 241 LACDDADLQKKLNSAVFPGGQGGPLMHVIAAKAVCFKEAMSDDFKTYQQQVVKNASAMAQ 300 Query: 301 VFIERGYDVVSGGTDNHLFLVSLIRQGLTGKDADAALGRAGITVNKNAVPNDPQSPFVTS 360 VF++RGYDVVSGGT NHLFLVSLI+Q +TGKDADAALGRA ITVNKNAVPNDP+SPFVTS Sbjct: 301 VFVDRGYDVVSGGTKNHLFLVSLIKQDITGKDADAALGRAHITVNKNAVPNDPRSPFVTS 360 Query: 361 GLRIGTPAITSRGFKEAQSIALAGWICDILDHLGDADIEANVARQAAALCADFPVY 416 GLRIGTPAIT+RGF E++ LAGWICDILD+L D + + V Q +ALCA FPVY Sbjct: 361 GLRIGTPAITTRGFGESECRDLAGWICDILDNLDDEAVNSRVREQVSALCARFPVY 416 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: 659 Number of extensions: 17 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: 418 Length of database: 417 Length adjustment: 32 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 ( 7.4 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 Apr 09 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