Align C4-dicarboxylate TRAP transporter large permease protein DctM (characterized)
to candidate 3609368 Dshi_2753 TRAP dicarboxylate transporter, DctM subunit (RefSeq)
Query= SwissProt::Q9HU16 (427 letters) >lcl|FitnessBrowser__Dino:3609368 Dshi_2753 TRAP dicarboxylate transporter, DctM subunit (RefSeq) Length = 429 Score = 317 bits (813), Expect = 3e-91 Identities = 169/429 (39%), Positives = 268/429 (62%), Gaps = 5/429 (1%) Query: 3 ILFLFLLLFLLMFIGVPIAVSLGLSGALTILLFSPDSVRSLAI---KLFETSEHYTLLAI 59 +L FL LFLL F+ + + V GL A +LL+ R + + ++ + + L+AI Sbjct: 1 MLIWFLPLFLL-FLMIGLPVFFGLLAAPGLLLWLNGQERDITLLYRNVYNGMDSFPLMAI 59 Query: 60 PFFLLSGAFMTTGGVARRLIDFANACVGHIRGGLAIAAVLACMLFAALSGSSPATVAAVG 119 PFF+L+G M GG+ RL++FA A +GH RGGLA +L+ MLFA LSGS+ A +A+G Sbjct: 60 PFFMLAGELMNRGGITLRLVEFAQALMGHFRGGLAHVNILSSMLFAGLSGSAVADTSALG 119 Query: 120 SIAIAGMVRSGYPQAFGAGIVCNAGTLGILIPPSIVMVVYAAATETSVGKLFIAGVVPGL 179 S+ I M + GY + F A I + +G +IPPS +M++YA SV LF+AG+VPG+ Sbjct: 120 SMLIPAMEKQGYTRRFAAAITAASSVIGPIIPPSGIMIIYAYVMGESVAALFLAGIVPGI 179 Query: 180 LLGLILMVVIYIVARVKKLP-AMPRVSLREWLASARKALWGLLLMVIILGGIYSGAFTPT 238 L+G+ LM V+ ++A P A + + + ++ KA + L+ VIILGGI +G FTPT Sbjct: 180 LVGVGLMGVVKLMADKYDFPVASAKTTWGQRGQASLKAFFPLMTPVIILGGILAGVFTPT 239 Query: 239 EAAAVAAVYSAFVALFVYRDMRLSECPKVLLESGKLTIMLMFIIANAMLFAHVLTTEQIP 298 EAAAVA Y+ + FV R +++S+ P +L +G + +++ ++ AM F V++ P Sbjct: 240 EAAAVAVAYALIIGFFVMRTLKVSDLPDILGRAGITSAVVLLLVGAAMAFKTVVSLSYAP 299 Query: 299 QSIASWVTELGLSPWMFLLVVNIVLLIAGNFMEPSAIILILAPIFFPIAMELGIDPIHLG 358 Q +A ++ L +P + LL++N++L + G F++ I+IL PI PI ++LG+DPIH Sbjct: 300 QIMADFMLSLSENPLILLLLINLLLFVVGMFLDAGPAIIILGPILGPIFVDLGVDPIHFA 359 Query: 359 IIMVVNMEIGLITPPVGLNLFVTSAVTGMPLGATIRAALPWLMILLVFLIIVTYIPAVSL 418 IIM VN+ +GL TPP+GL LFV S+V+G + +A LP+L + ++ + ++TY PA+S+ Sbjct: 360 IIMSVNLTVGLATPPMGLVLFVASSVSGERVERIAKAILPFLAVEILVIFLITYFPAISM 419 Query: 419 ALPNWLGMS 427 +P G + Sbjct: 420 TIPRLTGFA 428 Lambda K H 0.330 0.144 0.425 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: 476 Number of extensions: 23 Number of successful extensions: 2 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: 427 Length of database: 429 Length adjustment: 32 Effective length of query: 395 Effective length of database: 397 Effective search space: 156815 Effective search space used: 156815 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 (21.9 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