Align RhaT, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized)
to candidate H281DRAFT_03380 H281DRAFT_03380 monosaccharide ABC transporter ATP-binding protein, CUT2 family
Query= TCDB::Q7BSH4 (512 letters) >FitnessBrowser__Burk376:H281DRAFT_03380 Length = 515 Score = 409 bits (1050), Expect = e-118 Identities = 218/501 (43%), Positives = 323/501 (64%), Gaps = 6/501 (1%) Query: 16 DAPA---ILEMRGISQIFPGVKALDNVSIALHPGTVTALIGENGAGKSTLVKILTGIYRP 72 D PA IL+++G+S+ FPGV ALD + + L G V A+ GENGAGKSTL+KI++G Y Sbjct: 15 DVPAPREILQLKGVSKRFPGVVALDGIDLDLRSGEVHAVCGENGAGKSTLMKIISGQYHA 74 Query: 73 NEGEILVDGRPTTFASAQAAIDAGVTAIHQETVLFDELTVAENIFLGHAPRTRFRTIDWQ 132 ++G I +G+P FAS A AG+ IHQE L L+VAENI+L P+ R +D++ Sbjct: 75 DDGVICYEGKPVQFASTSDAQAAGIAIIHQELNLVPHLSVAENIYLAREPK-RGPFVDYR 133 Query: 133 TMNSRSKALLTALESNIDPTIRLKDLSIAQRHLVAIARALSIEARIVIMDEPTAALSRKE 192 T+N+ ++ L + N+ PT + LSIAQ+ +V IA+ALS++AR++IMDEPT++L+ E Sbjct: 134 TLNANAQRCLQRIGLNVSPTTLVGALSIAQQQMVEIAKALSLDARVLIMDEPTSSLTESE 193 Query: 193 IDDLFRIVRGLKEQGKAILFISHKFDELYEIADDFVVFPRRSRRPVRGVSRKTPQDEIVR 252 LFRI+R L+ G AIL+ISH+ DE+ EI D V R R T +EIV Sbjct: 194 TVQLFRIIRELRADGVAILYISHRLDEMAEIVDRVTVL-RDGRHIATSDFASTTINEIVA 252 Query: 253 MMVGRDVENVFP-KIDVAIGGPVLEIRNYSHRTEFRDISFTLRKGEILGVYGLIGAGRSE 311 MVGR +++ +P + V ++ +R+ F +SF LRKGEILG GL+GAGR+E Sbjct: 253 RMVGRALDDAYPPRESVPTEQVLMRVRDLQRTDTFGPLSFDLRKGEILGFAGLMGAGRTE 312 Query: 312 LSQSLFGITKPLSGKMVLEGQEITIHSPQDAIRAGIVYVPEERGRHGLALPMPIFQNMTL 371 +++++FG + SG + L +TI SP++AIR GI Y+ E+R + GLAL MP+ N+TL Sbjct: 313 VARAIFGAERLDSGSIQLGDTPVTIRSPREAIRHGIAYLSEDRKKDGLALSMPVAANITL 372 Query: 372 PSLARTSRRGFLRAANEFALARKYAERLDLRAAALSVPVGTLSGGNQQKVVIGKWLATAP 431 ++ S RGFLR + E A+A +Y L +R + LSGGNQQK+VI KWL Sbjct: 373 SNVRAISSRGFLRFSEETAIAERYVRELAIRTPTVKQIARNLSGGNQQKIVISKWLYRGS 432 Query: 432 KVIILDEPTKGIDIGSKAAVHGFISELAAEGLSIIMVSSELPEIIGMSDRVLVMKEGLSA 491 +++ DEPT+GID+G+K A++ + LAA+G+ ++++SSELPE++GM+DR+ V EGL Sbjct: 433 RILFFDEPTRGIDVGAKYAIYKLMDRLAADGVGVVLISSELPELLGMTDRIAVFHEGLIT 492 Query: 492 GIFERAELSPEALVRAATGNA 512 + E + S E ++ A+G + Sbjct: 493 AVLETRQTSQEEILHYASGRS 513 Lambda K H 0.320 0.137 0.382 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: 614 Number of extensions: 31 Number of successful extensions: 8 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: 512 Length of database: 515 Length adjustment: 35 Effective length of query: 477 Effective length of database: 480 Effective search space: 228960 Effective search space used: 228960 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 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