Align Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate BWI76_RS14455 BWI76_RS14455 aspartate aminotransferase family protein
Query= SwissProt::Q940M2 (476 letters) >FitnessBrowser__Koxy:BWI76_RS14455 Length = 447 Score = 199 bits (505), Expect = 2e-55 Identities = 152/429 (35%), Positives = 218/429 (50%), Gaps = 37/429 (8%) Query: 78 PLNIVEGKMQYLYDESGRRYLDAFAGIVTVSCGHCHPDILNAITEQSKLLQHA-TTIYLH 136 P V + Y+ D SG+RYLDA G GH HPD+L A+ Q L +A T+ + Sbjct: 13 PAVAVSAQGAYITDASGQRYLDACGGAAVSCLGHAHPDVLAAMHRQIDRLAYAHTSFFTS 72 Query: 137 HAIGDFAEALAAKMPGNLKVVYFVNSGSEANELAMMMARLYTGSLEM------ISLRNAY 190 + AE L PG+L YFV+ GSEA E A+ +AR Y + I+ + +Y Sbjct: 73 DTVEQLAEQLVRTAPGSLNYAYFVSGGSEAVETALKLARQYFVEIGQPDRTLFIARKQSY 132 Query: 191 HGGSSNTIGLTAL--NTWKY----PLPQGEIHHVVNPDPYRG-VFGSDGSLYAKDVHDHI 243 HG NT+G A+ N W+ PL ++ V + YR G Y + + + Sbjct: 133 HG---NTLGALAVGGNEWRRRQFAPLLM-DVVRVSACNEYRDREAGESQQQYTERLLGEL 188 Query: 244 EYGTSG----KVAGFIAETIQGVG-GAVELAPGYLKSVYEIVRNAGGVCIADEVQTGFGR 298 E K+ GFIAET+ G GA+ PGYL+ V + G + IADEV G GR Sbjct: 189 EAAILDAGPEKIIGFIAETVVGATTGAMPPTPGYLQGVRRLCDKYGILYIADEVMCGMGR 248 Query: 299 TGSHYWGFQTQDVVPDIVTMAKGIGNGL-PLGAVVTTPEIASVL-ASKILF---NTFGGN 353 TG+ + F+ VVPDIVT+AKG+G G P+GAV+ + +I + L A +F +T+ + Sbjct: 249 TGTLH-AFEQDGVVPDIVTIAKGLGGGYQPIGAVLASEQIVAALQAGSGMFQHGHTYICH 307 Query: 354 PVCSAGGLAVLNVIDKEKRQEHCAEVGSHLIQRLKDVQKRHDIIGDVRGRGLMVGIELVS 413 P +A LAV VI++++ E + G++L Q L DV +GD RGRGL G+ELV Sbjct: 308 PTAAAAALAVQQVIERDRLLEQVQQQGAYLQQALHDVLGGLPYVGDTRGRGLFAGVELVC 367 Query: 414 DRKDKT---PAKAETSVLFEQLRELGILVGK-----GGLHGNVFRIKPPMCFTKDDADFL 465 D++ KT P + + Q G+LV G G+ I PP ++ + DF+ Sbjct: 368 DKERKTAFDPLLKLHAAIKAQCMGHGLLVYPMGGTIDGQRGDHILIAPPFIVSRSELDFV 427 Query: 466 VDALDYSIS 474 VD L IS Sbjct: 428 VDTLHKVIS 436 Lambda K H 0.320 0.138 0.412 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: 516 Number of extensions: 28 Number of successful extensions: 7 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: 476 Length of database: 447 Length adjustment: 33 Effective length of query: 443 Effective length of database: 414 Effective search space: 183402 Effective search space used: 183402 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 (21.8 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