Align Na(+)-malate symporter; Sodium-dependent malate transporter (characterized)
to candidate BWI76_RS04430 BWI76_RS04430 citrate carrier protein
Query= SwissProt::O05256 (448 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS04430 BWI76_RS04430 citrate carrier protein Length = 446 Score = 262 bits (669), Expect = 2e-74 Identities = 149/438 (34%), Positives = 243/438 (55%), Gaps = 11/438 (2%) Query: 14 QKDSQEKNLFQKIWSWEIGVIPLPLYTVLAVIIILAAYYNELPANMLGGFAIIMILGVFL 73 Q S EK I ++I +PLPLY + ++L+ +YN LP +++GGFAI+ I+G Sbjct: 6 QAPSAEKKGVSDILGFKIFGMPLPLYAFALITLLLSHFYNALPTDIVGGFAIMFIIGAVF 65 Query: 74 GDIGQRIPIL-KDIGGPAILSLFVPSFLVFYNVLNSTSLDAVTNLMKTSNFLYFYIACLV 132 G+IG+R+PI K IGG ++ V ++ V+ + ++A+TN+M SNFL +IA L+ Sbjct: 66 GEIGKRLPIFNKYIGGAPVMIFLVAAYFVYAGIFTQKEIEAITNVMDKSNFLNLFIAVLI 125 Query: 133 VGSILGMNRIVLIQGFIRMFVPLVAGTIAAVAAGILVGFIFGYSAYDSFFFVVVPIIAGG 192 G+IL +NR +L++ + ++ G + A GIL+G FG S V+PI+ GG Sbjct: 126 TGAILSVNRKLLLKSLLGYIPTILMGILGASIFGILIGLCFGISVDRIMMLYVLPIMGGG 185 Query: 193 IGEGILPLSIAYSQILGSSADVFVSQLVPAAIIGNVFAIICAALMKKLGDKRPDLNGNGR 252 G G +PLS Y + G S + + S + I N+FAI+ AAL+ +G K L+G G Sbjct: 186 NGAGAVPLSEIYHSVTGRSREEYYSTAIAILTIANIFAIVFAALLDIIGKKHTWLSGEGE 245 Query: 253 LVKSKKANEIFNQKEAEAKIDFKLMGAGVLLACTFFIFGGLLEKFIF--IPGAIL----- 305 LV +KA+ E +I + G++LA T F+ ++ K I I G + Sbjct: 246 LV--RKASFKVEDDEKAGQITHRETAVGLVLATTCFLLAYVIAKKILPSIGGVSIHYFAW 303 Query: 306 MIISAAAVKYANILPKKMEEGAYQLYKFISSSFTWPLMVGLGILFIPLDDVASVISIPFV 365 M++ AA+ + + +++ GA +L F S W LMVG+G+ + L ++ I+ V Sbjct: 304 MVLIVAALNASGLCSPEIKAGAKRLSDFFSKQLLWVLMVGVGVCYTDLQEIIDAITFANV 363 Query: 366 IICISVVIAMIGSGYFVGKLMNMYPVESAIVT-CCHSGLGGTGDVAILSASGRMGLMPFA 424 +I +V+ + G L+ +P+ESAI C + GG+GD+ +LSA RM L+ +A Sbjct: 364 VIAAVIVVGAVVGAAVGGWLIGFFPIESAITAGLCMANRGGSGDLEVLSACNRMNLISYA 423 Query: 425 QISTRLGGAGTVICATVL 442 QIS+RLGG ++ A+++ Sbjct: 424 QISSRLGGGIVLVIASIV 441 Lambda K H 0.328 0.145 0.427 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: 627 Number of extensions: 35 Number of successful extensions: 4 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: 448 Length of database: 446 Length adjustment: 33 Effective length of query: 415 Effective length of database: 413 Effective search space: 171395 Effective search space used: 171395 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: 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