Align Amino acid transporter (characterized, see rationale)
to candidate WP_012589784.1 MSIL_RS03830 amino acid permease
Query= uniprot:A0A0H3C3Q5 (483 letters) >NCBI__GCF_000021745.1:WP_012589784.1 Length = 494 Score = 349 bits (895), Expect = e-100 Identities = 191/492 (38%), Positives = 293/492 (59%), Gaps = 24/492 (4%) Query: 9 SFWTRRKAIDTITAGH-----ADSHQLKKTLSWPHLVALGVGAIVGTGIYTLTG-VGAGL 62 S W+ + H +++ L++TLS L++LG+G I+G GI+ LTG A Sbjct: 3 SIWSTKSIASLKAEAHEAEFGSETPNLRRTLSLASLISLGIGCIIGAGIFVLTGHAAAAY 62 Query: 63 AGPGVILSFLIAGAVCACAALCYAELSTMIPASGSAYTYSYAAMGEPVAWFVGWSLILEY 122 AGP + LSF++AG VCA A LCYAE+++ +P +GSAYTY+YA +GE +AW +GW L+LEY Sbjct: 63 AGPAISLSFVLAGLVCALAGLCYAEMASTVPVAGSAYTYAYATLGEFIAWIIGWDLLLEY 122 Query: 123 TLVCAAVAVGWSAHAHGLFK--MIGFPDALLAGP-----------HQGGLINMPAVFISM 169 VA+GWS + + IG P AL P H G L+N PAV I + Sbjct: 123 AFGATTVAIGWSGYVVSFLRDFHIGIPAALAGAPFAFDPASGAWTHTGALVNAPAVAIVL 182 Query: 170 AVAGLLALGTRESATVNMVLVFVKIIALIVFVVLCLPAFNLAHF-TPFMPNGFQAHVPEG 228 A+ LL +G ESA VN ++V +K+ ++VF++ L + + A++ T P+G A +P Sbjct: 183 ALTALLVVGVNESAKVNNIIVAIKLAIIVVFILAGLSSVSTANWVTSANPDG--AFIPPN 240 Query: 229 AA-ADAAKVGVMAAASLIFFAFYGFDAVSTAAEETKNPKRDLTIGIVGSMAVCTAIYMIV 287 A + G++ A+++FFA+ GFDAVSTAA+E KNP+RD+ +GI+GS+ +CT +Y++V Sbjct: 241 AGPGEYGWSGILRGAAVVFFAYIGFDAVSTAAQEAKNPQRDMPLGILGSLVICTVLYVLV 300 Query: 288 AAVSIGASRTEVFSKSEAPLVFILESLNHGKIAQLVALAAVIALPTVILAFMYGQSRIFF 347 + V G + S + P+ ++ + ++ +V L A++ L +V+L + GQ+R+ + Sbjct: 301 SIVITGIVPFDRLSVPD-PIALGVDVIGLRWLSTVVKLGAILGLSSVVLVLLLGQTRVLY 359 Query: 348 VMARDGLLPRALSKVNAKTGTPVMMTLLTGVLAAVISGLLSLKDIAELANAGTLWAFIAV 407 +ARDGLLP +KV+ + TP + T+ TG++ AV++G+L + + EL + GTL+AF V Sbjct: 360 SIARDGLLPPIAAKVHPRFRTPYLTTIGTGLIVAVMAGVLPIGLVGELVSIGTLFAFAIV 419 Query: 408 GASVILLRLREPNRPRVFSTPLWPIVAPAGILGCLYLFLSLPGKTQLYFLYAHLIGAVVY 467 A V+ LR P R F PL IVAP G + L L LP T + F IG ++Y Sbjct: 420 CAGVLFLRYTHPQIHRPFRAPLIAIVAPLGAAAAVVLMLGLPRDTWIRFAIWLAIGLILY 479 Query: 468 LAYGMRKSVLAQ 479 YG R S LA+ Sbjct: 480 FTYGRRHSRLAR 491 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: 733 Number of extensions: 54 Number of successful extensions: 6 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: 494 Length adjustment: 34 Effective length of query: 449 Effective length of database: 460 Effective search space: 206540 Effective search space used: 206540 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