Align Citrate-proton symporter; Citrate carrier protein; Citrate transporter; Citrate utilization determinant; Citrate utilization protein A (characterized)
to candidate GFF2854 PS417_14575 MFS transporter
Query= SwissProt::P0A2G3 (434 letters) >FitnessBrowser__WCS417:GFF2854 Length = 445 Score = 240 bits (613), Expect = 6e-68 Identities = 153/437 (35%), Positives = 229/437 (52%), Gaps = 11/437 (2%) Query: 3 QHTPATSRAGTFGAILRVTSGNFLEQFDFFLFGFYATYIARTFFPAESEFASLMLTFAVF 62 Q +P T R I+ GNF+E FDF ++GF AT IA+ FFP+ A+L+ TFAVF Sbjct: 8 QVSPQTLRK----VIIAAGIGNFVEWFDFAVYGFLATTIAQQFFPSGDASAALLKTFAVF 63 Query: 63 GSGFLMRPVGAIVLGAYIDRIGRRKGLMVTLAIMGCGTLLIALVPGYQTIGLAAPALVLL 122 F RP+G I G DRIGR++ L +T+ +M T LI L+P Y IG+AAP L+ L Sbjct: 64 AVAFAFRPLGGIFFGMLGDRIGRKRTLAMTILLMAGATTLIGLLPTYAAIGVAAPILLSL 123 Query: 123 GRLLQGFSAGVELGGVSVYLSEIATPGNKGFYTSWQSASQQVAIVVAALIGYSLNITLGH 182 R QGFSAG E G YL E A + +Y S+ S A AA++ Y+L +L Sbjct: 124 IRCAQGFSAGGEYAGACAYLMEHAPSDKRAWYGSFVPVSTFSAFAAAAVVAYALEASLSA 183 Query: 183 DAISEWGWRIPFFIGCMIIPLIFVLRRSLQETEAF--LQRKHRPDTREIFATIAKNWRII 240 +A+ WGWR+PF I + + LR L ET AF ++ +H + T+ + I Sbjct: 184 EAMGSWGWRLPFLIAAPLGLVGLYLRWKLDETPAFQAVKEEHTVAHSPLKETLRNHGAAI 243 Query: 241 TAGTLLVAMTTTTFYFITVYTPTYGRTVLNLSARDSLIVTMLVGVSNFIWLPIGGAISDR 300 + V++T +FY T Y TY + LS +L+V+++ + P+ G SDR Sbjct: 244 SCLGAFVSLTALSFYMFTTYFATYLQVAGGLSRAMALLVSLIALIFAAAICPLAGLYSDR 303 Query: 301 IGRRAVLMGITLLALITTWPVMQWLTAAPDFTRMTLVLLWFSFFFGMYNGAMVAA-LTEV 359 +GRRA +M +L ++ +P +L A+ ++V + + G + AA L+E Sbjct: 304 VGRRATVMTACVLLMVVVYP--SFLMASSGSFAASIVGVMLLAVGAVLCGVVTAALLSET 361 Query: 360 MPVYVRTVGFSLAFSLATAIFGGLTPAISTALVKLTGDKSSPGWWLMCAALCGLAATAML 419 P R ++ ++LA IFGG P ++T L+ TG SP ++L+ AL LA L Sbjct: 362 FPTRTRYTASAITYNLAYTIFGGTAPLMATWLISTTGSNLSPAFYLIAVALLALAGGLAL 421 Query: 420 --FVRLSRGYIAAENKA 434 R+S + AE+K+ Sbjct: 422 PETSRISLHDVGAEDKS 438 Lambda K H 0.329 0.140 0.432 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: 496 Number of extensions: 17 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: 434 Length of database: 445 Length adjustment: 32 Effective length of query: 402 Effective length of database: 413 Effective search space: 166026 Effective search space used: 166026 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 (21.8 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