Align TRAP transporter, subunit DctM (characterized, see rationale)
to candidate Ac3H11_163 TRAP-type C4-dicarboxylate transport system, large permease component
Query= uniprot:I7DRS6 (467 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_163 Length = 425 Score = 298 bits (762), Expect = 3e-85 Identities = 174/459 (37%), Positives = 265/459 (57%), Gaps = 37/459 (8%) Query: 1 MDVVLLFSMVIGLLLIGVPIAVALGLSSTLFLLIYSDSSLASVAGTLFEAFEGHFTLLAI 60 M V++ +MV+ L + +AV++GL+S L + + + L SV A F L AI Sbjct: 1 MSAVMISTMVLCFALT-ISVAVSIGLASILGIQASNANMLISVKEMF--ASINKFPLAAI 57 Query: 61 PFFILASSFMTTGGVARRIIRFSIACVGHLPGGLAIAGVFACMLFAALSGSSPATVVAIG 120 PFFILA + M TGG++RR++ F+ + VG + GGL + V CM+FAA+SGSS AT AIG Sbjct: 58 PFFILAGNLMETGGISRRLVEFAKSIVGGVQGGLPMTCVLTCMIFAAVSGSSVATTFAIG 117 Query: 121 SIVIAGMRQVGYSKEFAAGVICNAGTLGILIPPSIVMVVYAAAVEVSVGRMFLAGVIPGL 180 +I+I + + GY +AA + + LG++IPPSI M++Y + EVS+G +F+AG PGL Sbjct: 118 AILIPALIKHGYPTSYAAALQATSAELGVIIPPSIPMILYGVSAEVSIGELFIAGFGPGL 177 Query: 181 MAGLMLMVTIYVMAKVKNLPKGEWLGWGEVAASAANASVGLLLIGIILGGIYGGIFTPTE 240 + LM+ ++ K K K + G + A LL+ IILGGIYGG+FTPTE Sbjct: 178 LISGALMLFVWAYCKYKGWGKNDGDGRMPFGKATLQAGWALLMPVIILGGIYGGVFTPTE 237 Query: 241 AAAVASVYAFFVATFVYRDMGPLKSAPKPKDMGQFLTMLPKMLGQTVVYFIPSFFHADTR 300 A+AVA YA V +YR++ K +D+ Y I Sbjct: 238 ASAVAVFYALLVGVVIYREI-------KLRDL----------------YAI--------- 265 Query: 301 HALFEAGKLTVTLLFVIANALILKHVLTDEQVPQQIATAMLSAGFGPVMFLIVVNVILLI 360 L ++ + ++F+IANA + ++T VP I + + P +FL+ VN L + Sbjct: 266 --LRKSAISSAVIMFIIANAGLFAFLITRAGVPDAIGRWLEAVLQSPALFLLGVNAALFV 323 Query: 361 GGQFMEPSGLLVIVAPLVFPIAIELGIDPIHLGIIMVVNMEIGMITPPVGLNLFVTSGVA 420 G F+E S ++++AP++ P+A+ GIDP+H G+IMVVN+ +GMITPP G+NLF VA Sbjct: 324 IGMFIETSAAIIVLAPILAPVAMHFGIDPVHFGLIMVVNLALGMITPPFGVNLFAACTVA 383 Query: 421 GMPMMAVVRAALPFLAVLFVFLIMITYIPWISTVLPNAV 459 + + +++ LPF+ V+ V L++ITY+P IS L + V Sbjct: 384 KISLDRIIKHLLPFVCVILVCLLVITYVPSISLALRDLV 422 Lambda K H 0.329 0.144 0.421 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: 557 Number of extensions: 33 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: 467 Length of database: 425 Length adjustment: 32 Effective length of query: 435 Effective length of database: 393 Effective search space: 170955 Effective search space used: 170955 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