GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deh in Dyella japonica UNC79MFTsu3.2

Align Acetate/haloacid transporter, Dehp2, with a possible atypical topology (characterized)
to candidate N515DRAFT_3073 N515DRAFT_3073 Arabinose efflux permease

Query= TCDB::F8SVK1
         (552 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3073
          Length = 551

 Score =  777 bits (2007), Expect = 0.0
 Identities = 377/534 (70%), Positives = 446/534 (83%), Gaps = 3/534 (0%)

Query: 18  KRVIFASSLGTVFEWYDFYLAGSLAAFISKSFFSGVNPTAAFIFTLLGFAAGFAVRPFGA 77
           +RVI ASSLGTVFEWYDFYL GSLA  I K FFSG+N T+AFIF LL FAAGFAVRPFGA
Sbjct: 16  RRVILASSLGTVFEWYDFYLYGSLAVLIGKHFFSGLNETSAFIFALLAFAAGFAVRPFGA 75

Query: 78  LVFGRLGDMVGRKYTFLITIVIMGLSTCVVGFLPGYAAIGMASPVIFIAMRLLQGLALGG 137
           +VFGRLGD+VGRKYTFLITI+IMGLST +VG LP Y+ +GM +PV+ I +RLLQGLALGG
Sbjct: 76  IVFGRLGDLVGRKYTFLITIIIMGLSTFLVGVLPSYSTVGMIAPVLLIVLRLLQGLALGG 135

Query: 138 EYGGAATYVAEHAPANRRGFYTAWIQTTATLGLFLSLLVILGVRTAMGEDAFGAWGWRIP 197
           EYGGAATYVAEHAP  +RG YT++IQ TAT GLFLSLLVILG R A+G+  F  WGWRIP
Sbjct: 136 EYGGAATYVAEHAPDGKRGLYTSFIQITATFGLFLSLLVILGTRMALGDKVFEDWGWRIP 195

Query: 198 FVASLVLLGISVWIRMQLHESPAFERIKAEGKTSKAPLSEAFGQWKNLKIVILALIGVTA 257
           F+ S VL+ +SV+IR+QL ESP F+++KAEGK SKAPL+EAFG WKNLK+VILAL+G TA
Sbjct: 196 FLISSVLVAVSVYIRLQLQESPVFQQMKAEGKHSKAPLTEAFGHWKNLKVVILALLGATA 255

Query: 258 GQAVVWYTGQFYALFFLTQTLKVDGASANILIAIALLIGTPFFLFFGSLSDRIGRKPIIL 317
           GQAVVWYTGQFYAL+FLTQ+LK+DG +AN+LIA AL+IGTPFF+FFG LSDRIGRK I+L
Sbjct: 256 GQAVVWYTGQFYALYFLTQSLKIDGTTANLLIAAALIIGTPFFVFFGWLSDRIGRKSIVL 315

Query: 318 AGCLIAALTYFPLFKALTHYANPALEAATQKSPIVVIANPDECSFQFNPVGTSKFTSSCD 377
           AGCL+AALTYFP+FK LTH+ NPA+E A   +P+ VIA+P+ CSFQF+PVG SKFTSSCD
Sbjct: 316 AGCLLAALTYFPIFKGLTHFGNPAIETAAASAPVTVIADPNACSFQFDPVGKSKFTSSCD 375

Query: 378 IAKSALSKAGLNYDNVAAPAGTLAQIKVGDTTIDTYDGKAADAKD---AGKAFDKNLGTA 434
           +AK+ L+K G+ Y N AAPAG +AQ+ +G  TI++++G   D+       KAF   +G A
Sbjct: 376 VAKTVLAKKGIPYRNEAAPAGAVAQVTIGTGTIESFEGGGLDSATFAAQSKAFGTKIGDA 435

Query: 435 LKAASYPPKADPSQLNWPMTVVILTILVIYVTMVYGPIAAMLVEMFPTRIRYTSMSLPYH 494
           LKAA YP KADP+Q N  M V++L ILV+YVTMVYGPIAA LVEMFPTRIRYTSMSLPYH
Sbjct: 436 LKAAGYPEKADPAQRNDVMLVILLAILVLYVTMVYGPIAAWLVEMFPTRIRYTSMSLPYH 495

Query: 495 IGNGWFGGFLPATAFAIVAAKGNIYSGLWYPIIIALATFVIGLLFVRETKDSNI 548
           IGNGWFGGF+P   F +VA KG+IY GLWYPII+A+ TF IGLLF++ETKD NI
Sbjct: 496 IGNGWFGGFVPTIGFMLVAWKGDIYYGLWYPIIVAVGTFFIGLLFLKETKDVNI 549


Lambda     K      H
   0.325    0.139    0.422 

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: 899
Number of extensions: 33
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: 552
Length of database: 551
Length adjustment: 36
Effective length of query: 516
Effective length of database: 515
Effective search space:   265740
Effective search space used:   265740
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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:

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