Align (R)-3-amino-2-methylpropionate-pyruvate transaminase (EC 2.6.1.40); alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate AO356_28705 AO356_28705 hypothetical protein
Query= BRENDA::Q64565 (512 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_28705 Length = 449 Score = 201 bits (511), Expect = 5e-56 Identities = 146/457 (31%), Positives = 220/457 (48%), Gaps = 51/457 (11%) Query: 61 YNHVLEIHKQHLSPVNT---AYFQKPLLLHQGHMEWLFDSEGNRYLDFFSGIVTVGVGHC 117 Y H K+ P+++ A K L++ +G ++ D EG+R LD G+ V VGH Sbjct: 2 YEHYKTAQKKFWHPMSSSAPANRSKTLIIARGDGNYITDIEGHRMLDGVGGLWNVNVGHN 61 Query: 118 HPKVTAVAKKQMDRL--WHTSSVFFHSPMHEYAERLSALLP-EPLKVIFLVNSGSEANDL 174 P V A Q+D L + T H + + AERL+++ E + + + GS+A + Sbjct: 62 RPSVKAAIAAQLDELAYYQTFDGIAHPRVFDLAERLTSMFAQENMARVLFSSGGSDAVET 121 Query: 175 AMVMARAY------SNHTDIISFRGAYHGCSPYTLGLTNVGIYKMKV-PSTIACQSTMCP 227 A+ MAR Y T +S R YHG + G+Y P C P Sbjct: 122 ALKMARQYWIASGEPGRTRFLSLRNGYHGVHVGGTSVGGNGVYHYNHGPLLAGCHLLDTP 181 Query: 228 DVFRGPWGGSHCRDSPVQTVRKCSCAPDGCQAKERYIEQFKDTLNTSVATSIAGFFAEPI 287 ++R PW CRD P + C I Q +D + +IA AEP+ Sbjct: 182 WLYRNPWD---CRD-PEELTAHC-------------IRQLEDQIALLGPQTIAALIAEPV 224 Query: 288 QGVNGVVQYPKEFLKEAFALVRERGGVCIADEVQTGFGR----LGSHFWGFQTHDTMPDI 343 QG GV+ P + K + G + IADEV TGFGR LGS WG PD+ Sbjct: 225 QGAGGVIVPPAHYWKRLREVCDRHGILLIADEVVTGFGRTGCMLGSRGWG-----VAPDV 279 Query: 344 VTMAKGIGNGF-PMAAVVTTPEIASSL------AKHLHHFSTFGGSPLACAIGSAVLEVI 396 + +AKGI G+ PM A V IA ++ + + H T+ G P ACA AVL+++ Sbjct: 280 LCLAKGITAGYIPMGATVFNQRIADAIENGPGFSSVIMHGYTYSGHPTACAAALAVLDIV 339 Query: 397 EEENLQRNSQEVGTYMLLKFAKLRDEFDIVGDVRGKGLMVGIEMVQDKISRQPLPKTE-- 454 E E+L N+ +VG +L + L + + +VG+VRGKGLM+ +++V DK++R+PL Sbjct: 340 EAEDLPGNAGKVGAQLLEQLQPLTERYAVVGEVRGKGLMIAVDLVADKVTREPLDPANGL 399 Query: 455 VNQIHEDCKDMGLLVGRGGNFSQTFRIAPPMRVTKLE 491 ++I E + G+LV GN ++PP+ +T E Sbjct: 400 ASRIAEQARRAGVLVRPIGN---KIVMSPPLTLTSDE 433 Lambda K H 0.322 0.136 0.419 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: 536 Number of extensions: 26 Number of successful extensions: 5 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: 512 Length of database: 449 Length adjustment: 34 Effective length of query: 478 Effective length of database: 415 Effective search space: 198370 Effective search space used: 198370 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 (21.9 bits) S2: 51 (24.3 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