Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate H281DRAFT_03566 H281DRAFT_03566 alanine-glyoxylate transaminase / serine-glyoxylate transaminase / serine-pyruvate transaminase
Query= BRENDA::P74281 (384 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_03566 H281DRAFT_03566 alanine-glyoxylate transaminase / serine-glyoxylate transaminase / serine-pyruvate transaminase Length = 406 Score = 254 bits (649), Expect = 3e-72 Identities = 145/381 (38%), Positives = 223/381 (58%), Gaps = 9/381 (2%) Query: 4 KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSG 63 + L IPGP+PVP+++L AM+ I HR +F ++ ++ +K + +T++ V++ SG Sbjct: 11 RHFLQIPGPSPVPDRILRAMSYPTIDHRGPEFGELGLKVLDGIKKIFKTQHPVVIYPASG 70 Query: 64 TGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAE----WGKALDPND 119 TGA EA++ N LSPGD VL+ G F W K+A++ GL E + W + + P Sbjct: 71 TGAWEAALSNTLSPGDHVLMFETGHFATLWKKMAESLGLKPEFLGLPGIEGWRRGVQPQM 130 Query: 120 FKTLLEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGG-ALMIVDAVTSLGATPV 178 + L D+ +IKA+ + H+ETSTGV +D+AA+ A A G AL++VD ++ L Sbjct: 131 IEARLREDTQHSIKAVCVVHNETSTGVTSDIAAVRRAIDAAGHPALLLVDTISGLACADY 190 Query: 179 AIDDLGLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDS 238 D+ G+DV SGSQKG M+PPG+ F ++S KA A + A +PR + D + + Sbjct: 191 RHDEWGVDVTVSGSQKGLMLPPGISFNAISPKAVAASKHAKLPRSFWDWSEIVEMNKTGY 250 Query: 239 SPFTPPINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAA-SN 297 P+TP NL+YGL +L+M+ EGLD +F RH+R ATR A++A L + D A S Sbjct: 251 WPYTPNTNLLYGLHEALEMILGEGLDNVFARHERLAEATRRAVRAWGLEIQCADPAVYSP 310 Query: 298 AITAV-APLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGAL 356 +T V P GV+A+ +R + ++FD+++ G +KG++FRIGHLG D +L+ + Sbjct: 311 VLTGVMMPDGVDADAVRKLIYERFDMSLGTGLGKMKGRMFRIGHLGDCNDLMLLATLAGC 370 Query: 357 EATLIELGYEGVTPGSGVAAA 377 E L G GSG+ AA Sbjct: 371 EMGLRLAGVP--LKGSGLPAA 389 Lambda K H 0.317 0.134 0.386 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: 372 Number of extensions: 13 Number of successful extensions: 4 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: 384 Length of database: 406 Length adjustment: 31 Effective length of query: 353 Effective length of database: 375 Effective search space: 132375 Effective search space used: 132375 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 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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