GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoP in Bacteroides fluxus YIT 12057

Align 2-Deoxy-D-ribose porter, DeoP (characterized)
to candidate WP_009124055.1 HMPREF9446_RS03580 L-fucose:H+ symporter permease

Query= TCDB::Q8XEV7
         (438 letters)



>NCBI__GCF_000195635.1:WP_009124055.1
          Length = 439

 Score =  206 bits (524), Expect = 1e-57
 Identities = 130/419 (31%), Positives = 221/419 (52%), Gaps = 24/419 (5%)

Query: 19  LFQFILLSCLFPLWGCAAALNDILITQFKSVFSLSNFASALVQSAFYGGYFLIAIPASLV 78
           L  FIL++  F LWG A  + + ++  F  +F +S    ALVQ AFYGGYF +A PA++ 
Sbjct: 18  LIPFILITSCFALWGFANDITNPMVKAFSKIFRMSVTDGALVQVAFYGGYFAMAFPAAMF 77

Query: 79  IKKTSYKVAILIGLTLYIVGCTLFFPASHMATYTMFLAAIFAIAIGLSFLETAANTYSSM 138
           I+K SYK  +L+GL LY +G  LFFPA    +Y  FL A F +  GLSFLET++N Y   
Sbjct: 78  IRKYSYKAGVLLGLGLYALGAFLFFPAMLTGSYYPFLIAYFVLTCGLSFLETSSNPYILS 137

Query: 139 IGPKAYATLRLNISQTFYPIGAAAGILLGKYLVFSEGESLE----KQMAGMNAEQVHNFK 194
           +G +  AT RLN++Q+F P+G+  G+ +    + +    ++     Q+A  + E V +  
Sbjct: 138 MGTEETATRRLNLAQSFNPMGSLLGMYVAMNFIQNRLNPMDTVERSQLAAADFEAVRDSD 197

Query: 195 VLMLENTLEPYKYMIMVLVVVMVLFLLTRFPTCKVAQTASHKRPSALDTLRYLASNARFR 254
           + +L        Y+++ ++V+++LFL+      K A   SH+      TL+ +     +R
Sbjct: 198 LSVLIG-----PYLVIGIIVLLMLFLIRMVKMPKNAD-QSHE-IDFFPTLKRIFRIKHYR 250

Query: 255 RGIVAQFLYVGMQVAVWSFTIRLA--LELGDINERDAS-----TFMVYSFACFFIGKFIA 307
            G++AQF YVG Q+  W+F I+    L + D  E  A+      + + +   F   +FI 
Sbjct: 251 EGVIAQFFYVGAQIMCWTFIIQYGTRLFMADGMEEKAAEVLSQEYNIIAMIIFCCSRFIC 310

Query: 308 NILMTRFNPEKVLILYSVIGALFLAYVALAPSFSAVYVAVLVSVLFGPCWATIYAGTLDT 367
             ++   +P  +L + +++  L    V    +   +Y  V VS      + TIY   L  
Sbjct: 311 TFILRYLSPGLLLKVLAIVACLLTGGVIGFQNIWGMYCLVGVSACMSLMFPTIYGIALQG 370

Query: 368 VDNEHTEMAGAVIVMAIVGAAVVPAIQGYVADM-----FHSLQLSFLVSMLCFVYVGVY 421
           + ++  +   A ++MAI+G +V+P +Q  + D        ++ LSF++ ++CFV + +Y
Sbjct: 371 LGDD-AKFGAAGLIMAILGGSVLPPLQASIIDQHTLLGMPAVNLSFILPLICFVVITIY 428


Lambda     K      H
   0.329    0.139    0.412 

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: 454
Number of extensions: 22
Number of successful extensions: 3
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: 438
Length of database: 439
Length adjustment: 32
Effective length of query: 406
Effective length of database: 407
Effective search space:   165242
Effective search space used:   165242
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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