Align Uncharacterized protein (characterized, see rationale)
to candidate Ga0059261_0201 Ga0059261_0201 Na+/H+-dicarboxylate symporters
Query= uniprot:A0A0C4Y5S4 (436 letters) >FitnessBrowser__Korea:Ga0059261_0201 Length = 455 Score = 442 bits (1137), Expect = e-128 Identities = 227/432 (52%), Positives = 305/432 (70%), Gaps = 11/432 (2%) Query: 5 RLPTLIFIAMLLGVLAGTAAHH-----YAPDPAAA----KSIADHLSILTDVFLRMIKMI 55 +L T I IA++ G + G H+ + D A A K++A + SI+T +FLR+IKMI Sbjct: 4 KLTTFILIALVAGAIVGLGLHYGIHNSFGADSAGAEAELKTVAGYFSIVTTIFLRLIKMI 63 Query: 56 IGPLVFATLVSGIASMGDGKAVGRIGMKAMAWFIAASITSLLLGLLMANLLRPGDGMNLA 115 I PLVFATLV+GIA MGD A+GR+G +A+AWFI AS+ SL LGL++ NL +PG G+N Sbjct: 64 IAPLVFATLVAGIAHMGDTAALGRVGGRAVAWFICASLVSLTLGLILVNLFQPGVGLNFP 123 Query: 116 LPAADAASNLKTGALNLREFIAHMFPKSFVEAMATNEILQIVVFSLFFGFALGTLKDGIG 175 LP DA S ++ A NL++F H+FP S +EAMA NEILQIV+FSLF G A+ + + Sbjct: 124 LPPVDATSGVEKAAFNLKDFFTHVFPASGIEAMAKNEILQIVIFSLFIGVAITAVGEK-A 182 Query: 176 KPVLAGIEGLSHVMLKITNYVMAFAPVGVFGAVAAVITAEGLGVLVVYAKLLGAVYLSLA 235 KP+++ +E L HVML++TNYVM FAP+ VF AVA + G ++ A +G Y+++ Sbjct: 183 KPLVSAVEALVHVMLQVTNYVMRFAPIAVFAAVAGTLAERGPAIIGNLAYFMGTFYIAMF 242 Query: 236 LLWVALIAGGYFFLGRDVFRLLKMVRAPLMIGFATASSESAYPKVIEQLGRFGVKERITG 295 LW LI Y +G+ L++ +R PL++ F+TASSE+AYP+ +E L RFGV RI Sbjct: 243 TLWALLIGVCYLIVGKRTGLLVRYIRDPLLLAFSTASSEAAYPRTLEALDRFGVPPRIAS 302 Query: 296 FVLPLGYSFNLDGSIMYTSFAALFVAQVYGIHLSLSQQVTMLLVLLVTSKGIAGVPRASL 355 FVLPLGYSFNLDGS++Y +FA +F+AQ YGI L+L Q++TMLLVL++TSKGIAGVPRASL Sbjct: 303 FVLPLGYSFNLDGSMIYMTFATIFIAQAYGIDLTLGQEITMLLVLMITSKGIAGVPRASL 362 Query: 356 VVVAAVLPMFGLPEAGILLVLGIDHVLDMGRTVTNVLGNAIATTVVAKSEGAIGAPV-PE 414 VV+AA L F +PEAG+LL+LGIDH LDMGR+ TNV+GNA+A+ VVAK EG P+ P Sbjct: 363 VVIAATLGFFDIPEAGLLLILGIDHFLDMGRSATNVVGNAVASAVVAKWEGGRLDPIEPA 422 Query: 415 EADDPAADGNRG 426 + + P A G Sbjct: 423 DIEPPHAPTGGG 434 Lambda K H 0.325 0.141 0.401 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: 488 Number of extensions: 16 Number of successful extensions: 3 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: 436 Length of database: 455 Length adjustment: 32 Effective length of query: 404 Effective length of database: 423 Effective search space: 170892 Effective search space used: 170892 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