Align Amino acid transporter (characterized, see rationale)
to candidate WP_036259385.1 DL86_RS06255 amino acid permease
Query= uniprot:A0A0H3C3Q5 (483 letters) >NCBI__GCF_000746085.1:WP_036259385.1 Length = 498 Score = 344 bits (882), Expect = 5e-99 Identities = 193/494 (39%), Positives = 290/494 (58%), Gaps = 26/494 (5%) Query: 9 SFWTRR-------KAIDTITAGHADSHQLKKTLSWPHLVALGVGAIVGTGIYTLTG-VGA 60 + W R+ +A D +++ L +TLS ++ALG+G I+G GI+ LTG A Sbjct: 3 NIWARKSMAVLEAEANDAEFGAGSETAGLHRTLSLASVIALGIGCIIGAGIFVLTGHAAA 62 Query: 61 GLAGPGVILSFLIAGAVCACAALCYAELSTMIPASGSAYTYSYAAMGEPVAWFVGWSLIL 120 AGP V LSF++AG VCA A LCYAE+++ +P +GSAYTY+YA MGE +AW +GW LIL Sbjct: 63 SYAGPAVSLSFVLAGIVCAFAGLCYAEMASTVPVAGSAYTYAYATMGEFIAWIIGWDLIL 122 Query: 121 EYTLVCAAVAVGWSAHAHGLFKM--IGFPDALLAGP-----------HQGGLINMPAVFI 167 EY VA+GWS + K I P AL + P G L N+PA FI Sbjct: 123 EYAFGATTVAIGWSGYVTSFLKDFDITIPAALASAPLAYDPANGDWTSTGALFNIPAAFI 182 Query: 168 SMAVAGLLALGTRESATVNMVLVFVKIIALIVFVVLCLPAFNLAHF-TPFMPNGFQAHVP 226 + + LL +G RESA VN +V +K+ +++F+V + + + A++ T P+G A +P Sbjct: 183 IVLLTVLLVVGIRESARVNNAIVLIKLAIILLFIVAGVSSISAANWVTSTNPSG--AFIP 240 Query: 227 EGAA-ADAAKVGVMAAASLIFFAFYGFDAVSTAAEETKNPKRDLTIGIVGSMAVCTAIYM 285 G++ A+++FFA+ GFDAVSTAA+E KNP+RD+ +GI+GS+A+CT +Y+ Sbjct: 241 PNLGPGQYGWSGIIRGAAVVFFAYIGFDAVSTAAQEAKNPQRDMPLGILGSLAICTVLYV 300 Query: 286 IVAAVSIGASRTEVFSKSEAPLVFILESLNHGKIAQLVALAAVIALPTVILAFMYGQSRI 345 +V V G + + + P+ ++++ G ++ L+ A++ L +VIL + GQ RI Sbjct: 301 LVGVVITGVVPFDKLNVPD-PIALGVDAIGLGWLSFLIKFGAILGLSSVILVLLLGQPRI 359 Query: 346 FFVMARDGLLPRALSKVNAKTGTPVMMTLLTGVLAAVISGLLSLKDIAELANAGTLWAFI 405 F+ MARDGLLP + V+ + TP + T+LTG + A++SGLL + + EL + GTL+AF Sbjct: 360 FYSMARDGLLPPFAAMVHPRFRTPYVTTILTGAIVAILSGLLPIGLVGELVSIGTLFAFT 419 Query: 406 AVGASVILLRLREPNRPRVFSTPLWPIVAPAGILGCLYLFLSLPGKTQLYFLYAHLIGAV 465 V V++LR+ P R F TP +VAP G ++L LP T L +IG Sbjct: 420 VVCLGVLVLRITHPEIRRPFKTPFVFVVAPLGAASAIFLMFGLPSDTWLRLGIWLVIGLA 479 Query: 466 VYLAYGMRKSVLAQ 479 +Y YG + S LA+ Sbjct: 480 IYFFYGRQHSHLAR 493 Lambda K H 0.326 0.138 0.415 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: 736 Number of extensions: 38 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: 483 Length of database: 498 Length adjustment: 34 Effective length of query: 449 Effective length of database: 464 Effective search space: 208336 Effective search space used: 208336 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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:
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