Align Alr3027 protein, component of The 2-oxo monocarboxylate transporter (Pernil et al., 2010). Transports pyruvate which is inhibited by various 2-ketoacids (characterized)
to candidate 3607284 Dshi_0699 TRAP C4-dicarboxylate transport system permease DctM subunit (RefSeq)
Query= TCDB::Q8YSQ7 (445 letters) >FitnessBrowser__Dino:3607284 Length = 437 Score = 239 bits (611), Expect = 1e-67 Identities = 149/436 (34%), Positives = 230/436 (52%), Gaps = 11/436 (2%) Query: 12 MFAGALV-LLSSGYPVAFSLGGVAILFGLLGIGLGVFDPIFLTAMPQRIFGIMANYTLLA 70 + GA+V L++ G PVA + + +LG + + + + G + Y L+ Sbjct: 9 LLLGAIVALMALGMPVALAF----LAANILGAWVFMGGERGIVQLLNNGLGALTTYALVP 64 Query: 71 IPYFIFMGAMLEKSGIAERLLETMGILLGRLRGGLALAVVLVGALLAATTGVVAATVVAM 130 IP F+ MG + +G+ R+ + LLGRL G L+ VL G + +G + + Sbjct: 65 IPLFLLMGEIFFHTGLGGRMFTAIDRLLGRLPGRLSYVTVLGGTGFSTLSGSSMGSTALL 124 Query: 131 GLISLPIMLRYGYNKELATGVIAASGTLGQIIPPSVVLVVLGDQLGISVGDLFIGSVIPG 190 G + +P M GY ++ G I +G L IIPPS + V+L I VG L I VIPG Sbjct: 125 GSLMVPEMNARGYKSHMSIGPILGTGGLAIIIPPSALAVLLATLAQIDVGALLIAGVIPG 184 Query: 191 LMMASAFALHVLIVAFIRPDVAPALPAQVREIGGKALGKRVIQVMIPPLILILLVLGSIF 250 LM+A + + I P APA +G K LG +++ ++P + ++++++ + Sbjct: 185 LMLAGFYIATIWIQTRRDPSAAPAYEVAEVSLGAK-LGL-LLRDVVPMVGVMVVIVSLMI 242 Query: 251 FGFATPTEAGAVGCAGAIALAAANGQFTLESLRQVCDTTLRITSMVVFILIGSTAFS--L 308 FG TP+EA A G G I LAAA T+E+LR+ L++T M I+ GS FS L Sbjct: 243 FGIVTPSEAAAFGALGVIILAAAFRCLTVEALRRSVVGALKVTLMAYMIVFGSATFSQLL 302 Query: 309 VFRGLNGDQFMFDVLANLPGGKIGFLFVSMTTVFLLGFFIDFFEIAFIVIPLFVPVAQKL 368 F G +G + +L I L + +LG F++ I + +P+F P+AQ L Sbjct: 303 AFSGASGGLIGWATGFDLD--PIWMLLAMFGVLLVLGMFMEQISIMLLTVPIFFPLAQSL 360 Query: 369 GIDLVWYGVILGANLQTSFLTPPFGFALFYLRGVAPPEVTTSDIYRGVIPFILLQLLVLL 428 G DL+W+ +I+ L+ SF TPPFG LF ++GVAPP T +IY IPFI LL++ Sbjct: 361 GFDLIWFALIMLLALEISFTTPPFGLLLFVMKGVAPPSTTMREIYLAAIPFIACSLLLVA 420 Query: 429 LIIIFPGIVSFLPSLG 444 L+I+FP + ++LP LG Sbjct: 421 LLILFPPLATWLPGLG 436 Lambda K H 0.331 0.149 0.437 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: 536 Number of extensions: 32 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: 445 Length of database: 437 Length adjustment: 32 Effective length of query: 413 Effective length of database: 405 Effective search space: 167265 Effective search space used: 167265 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.8 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