Align Amino acid:proton symporter (characterized, see rationale)
to candidate Pf6N2E2_2249 Proton/glutamate symport protein @ Sodium/glutamate symport protein
Query= uniprot:A0A0N9WTL5 (431 letters) >lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_2249 Proton/glutamate symport protein @ Sodium/glutamate symport protein Length = 420 Score = 790 bits (2039), Expect = 0.0 Identities = 413/420 (98%), Positives = 415/420 (98%) Query: 12 MGIALGVLVGWACHHFAGSEQSAKEIASYFSMVTDIFLRMIKMIIAPLVFATLVGGIASM 71 MGIALGVLVGWACHHFAGSEQSAKEIASYFSMVTDIFLRMIKMIIAPLVFATLVGGIASM Sbjct: 1 MGIALGVLVGWACHHFAGSEQSAKEIASYFSMVTDIFLRMIKMIIAPLVFATLVGGIASM 60 Query: 72 GNSRSVGRIGARAMAWFVTASVVSLLIGMGLVNLFQPGAGLNMDVAQHATAAVPVNTGDF 131 GNSRSVGRIGARAMAWFVTASVVSLLIGMGLVNLFQPGAGLNMDVAQHATAAVPVNTGDF Sbjct: 61 GNSRSVGRIGARAMAWFVTASVVSLLIGMGLVNLFQPGAGLNMDVAQHATAAVPVNTGDF 120 Query: 132 SLKAFIGHVFPRSIAEAMANNEILQIVVFSLFFGFALAGVKRAGYTRITDSIEELAKVMF 191 SLKAFIGHVFPRSIAEAMANNEILQIVVFSLFFGFALAGVKRAGYTRITD IEELAKVMF Sbjct: 121 SLKAFIGHVFPRSIAEAMANNEILQIVVFSLFFGFALAGVKRAGYTRITDCIEELAKVMF 180 Query: 192 KITDYVMAFAPIGVFAAIASAITTQGLGLLVDYGKLIAEFYLGILILWALLFGAGYLFLG 251 KITDYVMAFAPIGVFAAIASAITTQGLGLLVDYGKLIAEFYLGILILWALLFGAGYLFLG Sbjct: 181 KITDYVMAFAPIGVFAAIASAITTQGLGLLVDYGKLIAEFYLGILILWALLFGAGYLFLG 240 Query: 252 RSVFHLGKLIREPILLAFSTASSESAYPKTIEALEKFGAPKRVSSFVLPLGYSFNLDGSM 311 RSVFHLGKLIREPILLAFSTASSESAYPKTIEALEKFGAPKRVSSFVLPLGYSFNLDGSM Sbjct: 241 RSVFHLGKLIREPILLAFSTASSESAYPKTIEALEKFGAPKRVSSFVLPLGYSFNLDGSM 300 Query: 312 MYQAFAILFIAQAYNIDLSFTQQLLILLTLMITSKGMAGVARASVVVVAATLPMFNLPEA 371 MYQAFAILFIAQAYNIDLSFTQQLLILLTLM+TSKGMAGVARASVVVVAATLPMFNLPEA Sbjct: 301 MYQAFAILFIAQAYNIDLSFTQQLLILLTLMVTSKGMAGVARASVVVVAATLPMFNLPEA 360 Query: 372 GLLLIIGIDQFLDMARTATNVVGNSIATAVVAKSESHEEADEEEGEHAPARSRSEPVPVA 431 GLLLIIGIDQFLDMARTATNVVGNSIATAVVAKSE HEEADE+EG AP RSRSEPVPVA Sbjct: 361 GLLLIIGIDQFLDMARTATNVVGNSIATAVVAKSEPHEEADEDEGAGAPVRSRSEPVPVA 420 Lambda K H 0.325 0.138 0.392 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: 690 Number of extensions: 16 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: 431 Length of database: 420 Length adjustment: 32 Effective length of query: 399 Effective length of database: 388 Effective search space: 154812 Effective search space used: 154812 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 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.
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