Align Amino acid:proton symporter (characterized, see rationale)
to candidate BWI76_RS08460 BWI76_RS08460 dicarboxylate/amino acid:cation symporter
Query= uniprot:A0A0N9WTL5 (431 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS08460 BWI76_RS08460 dicarboxylate/amino acid:cation symporter Length = 435 Score = 393 bits (1009), Expect = e-114 Identities = 215/433 (49%), Positives = 297/433 (68%), Gaps = 8/433 (1%) Query: 1 MKKNKLPRRIAMGIALGVLVGWACHHFAGSEQSAKEIASYFSMVTDIFLRMIKMIIAPLV 60 MKK L + I +G+ LG++ G ++ A ++ +AK A S+ T IFLRM+KMIIAPLV Sbjct: 1 MKKISLTKMIILGLILGMIAGVIINNMASAD-TAKSYAQDISIFTTIFLRMVKMIIAPLV 59 Query: 61 FATLVGGIASMGNSRSVGRIGARAMAWFVTASVVSLLIGMGLVNLFQPGAGLNMDVAQHA 120 +TLV GIA MG+++++GRI ++ F+ AS++S+ +G+ +VNLFQPGAG+N V A Sbjct: 60 ISTLVVGIAKMGDAKTLGRIFSKTFFLFICASLLSIALGLVIVNLFQPGAGINF-VPHDA 118 Query: 121 TAAVPVNTGDFSLKAFIGHVFPRSIAEAMANNEILQIVVFSLFFGFALA--GVKRAGYTR 178 A V + F+LK FI H P SI +AMA NEILQIVVFS+F G +LA G K + Sbjct: 119 GAVAAVQSEPFTLKVFISHAVPTSIVDAMARNEILQIVVFSIFLGCSLAAIGEKAEPIVK 178 Query: 179 ITDSIEELAKVMFKITDYVMAFAPIGVFAAIASAITTQGLGLLVDYGKLIAEFYLGILIL 238 + DS L VM K+T YVM FAP+ VFAAI+ I +GLG++V G + EFYL + +L Sbjct: 179 VLDS---LVHVMLKLTGYVMLFAPLTVFAAISGLIAERGLGVMVSAGIFMGEFYLTLGML 235 Query: 239 WALLFGAGYLFLGRSVFHLGKLIREPILLAFSTASSESAYPKTIEALEKFGAPKRVSSFV 298 WA+L G + +G + L K I EP LLAF+T+SSE+A+P T++ LEKFG +++SFV Sbjct: 236 WAILIGLSTVIVGPCISRLTKAIFEPALLAFTTSSSEAAFPGTLDKLEKFGVSSKIASFV 295 Query: 299 LPLGYSFNLDGSMMYQAFAILFIAQAYNIDLSFTQQLLILLTLMITSKGMAGVARASVVV 358 LP+GYSFNL GSM Y +FA +FIAQA N+ LS +Q+ +LL LM+TSKGMAGV RAS+VV Sbjct: 296 LPIGYSFNLVGSMAYCSFATVFIAQACNVHLSMGEQITMLLILMLTSKGMAGVPRASMVV 355 Query: 359 VAATLPMFNLPEAGLLLIIGIDQFLDMARTATNVVGNSIATAVVAKSESHEEADEEEGEH 418 +AATL FN+PEAGL+L++G+D FLDM R+ATNV+ N++ A+V + E + G Sbjct: 356 IAATLNQFNIPEAGLILLMGVDPFLDMGRSATNVMSNAMGAAIVGRWEGEHYGEGCRGT- 414 Query: 419 APARSRSEPVPVA 431 AP + + P + Sbjct: 415 APVKKPEQDRPAS 427 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: 460 Number of extensions: 20 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: 431 Length of database: 435 Length adjustment: 32 Effective length of query: 399 Effective length of database: 403 Effective search space: 160797 Effective search space used: 160797 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