Align Putative TRAP dicarboxylate transporter, DctM subunit (characterized, see rationale)
to candidate 6938090 Sama_2211 C4-dicarboxylate transport protein (RefSeq)
Query= uniprot:Q88NP0 (426 letters) >lcl|FitnessBrowser__SB2B:6938090 Sama_2211 C4-dicarboxylate transport protein (RefSeq) Length = 466 Score = 261 bits (667), Expect = 3e-74 Identities = 156/450 (34%), Positives = 259/450 (57%), Gaps = 38/450 (8%) Query: 9 SFIVLILIGMPVAYALGLSALIGAW-WIDIPLQAMMIQVASGVNK-FSLLAIPFFVLAGA 66 + + +L+GMP+A ALG S+++ + + L ++ +++ ++ ++LLAIPFF+L+ A Sbjct: 9 TLFLCMLLGMPIAIALGFSSMLTILLFSNDSLASVALKLYEATSEHYTLLAIPFFILSSA 68 Query: 67 IMAEGGMSRRLVAFAGVLVGFVRGGLSLVNIMASTFFGAISGSSVADTASVGSVLIPEME 126 ++ GG++RR++ FA VG +RGGL++ ++MA F A+SGSS A A++GS++I M Sbjct: 69 FLSTGGVARRIIDFAMDSVGHIRGGLAMASVMACMLFAAVSGSSPATVAAIGSIVIVGMV 128 Query: 127 RKGYPREFSTAVTVSGSVQALLTPPSHNSVLYSLAAGGTVSIASLFMAGIMPGLLLSAVM 186 R GYP++F+ V + +L PPS ++Y AA VS A +FMAG++PGLL+ ++ Sbjct: 129 RAGYPQKFAAGVITTSGTLGILIPPSIVMLVY--AAATEVSAARMFMAGLIPGLLMGVLL 186 Query: 187 MGLCLIFAKKRNYPKGEVIPLREALKIAGEALWGLMAMVIILGGILSGVFTATESAAVAV 246 M I A+ +N P ++ + +A+ GL + I+LG I GV + TE+AAVA Sbjct: 187 MVAIYIVARIKNLPSRPFPGVKALSLSSAKAMGGLALIFIVLGSIYGGVASPTEAAAVAC 246 Query: 247 VWSFFVTMFIYRDY------KWRD---------LPKLMH------------------RTV 273 V+++ V +F YRD WR + L+H R Sbjct: 247 VYAYLVAVFGYRDIGPLKEVPWRKEGEAILAAIVRNLLHVGLGLIKTPTDKEIRNVVRDG 306 Query: 274 RTISIVMI-LIGFAASFGYVMTLMQIPSKITTAFLTLSDNRYVILMCINFMLMLLGTVMD 332 +SI+++ +I A F +V+T +IP I + + L+ +N +L+ G M+ Sbjct: 307 AKVSIMLLFIIANAMLFAHVLTTERIPHIIAETIVGWGLPPWGFLIIVNLLLLAAGNFME 366 Query: 333 MAPLILILTPILLPVITGIGVDPVHFGMIMLVNLGIGLITPPVGAVLFVGSAIGKVSIES 392 + ++LI+ PIL P+ +G+DP+H G+IM+VN+ IG++TPPVG LFV + I SI Sbjct: 367 PSAILLIMAPILFPIAVQLGIDPIHLGIIMVVNMEIGMLTPPVGLNLFVTAGITGRSIGW 426 Query: 393 TVKALMPFYLALFLVLMAVTYIPAISLWLP 422 + A +P+ L L L+ +TY+P ISL+LP Sbjct: 427 VIHACLPWLLLLLGFLVLITYVPQISLFLP 456 Lambda K H 0.329 0.142 0.418 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: 561 Number of extensions: 29 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: 426 Length of database: 466 Length adjustment: 32 Effective length of query: 394 Effective length of database: 434 Effective search space: 170996 Effective search space used: 170996 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 preprint 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