GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Acidovorax sp. GW101-3H11

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate Ac3H11_606 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_606
          Length = 337

 Score =  301 bits (771), Expect = 2e-86
 Identities = 163/333 (48%), Positives = 223/333 (66%), Gaps = 12/333 (3%)

Query: 13  KRRFRWPTGMPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALLAIG 72
           + R  WP     L+ L L+L+V+++    F  +  +DG L+GS IDILNRAAP+ L+++G
Sbjct: 3   RHRLAWP-----LITLALLLVVNTVFNSSFLHIEWRDGHLYGSLIDILNRAAPLVLVSLG 57

Query: 73  MTLVIATGGIDLSVGAVMAIAGATTAAM-------TVAGFSLPIVLLSALGTGILAGLWN 125
           MTLVIAT GID+SVGA +AIA A  A M       T + F LP+ +L A+G  +L GLWN
Sbjct: 58  MTLVIATRGIDISVGATVAIAAAVAAWMIGGSVSGTESRFPLPVAILGAIGVALLCGLWN 117

Query: 126 GILVAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPDLSWFGSGSLLFLPTPVIIA 185
           G+LVA + +QP +ATLILMVAGRG+AQLIT GQI+T       + G G L  LP  V + 
Sbjct: 118 GVLVAKVGMQPIIATLILMVAGRGIAQLITDGQIITIYYTPYFFLGGGYLAGLPFSVFVV 177

Query: 186 VLTLILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVA 245
               +  +L   +TALG+FI+AVGIN  AA+ AGV    +++  YV  G+CA IAG++++
Sbjct: 178 AAVFVALYLAITRTALGLFIQAVGINPTAARVAGVQAGRLIVAAYVFCGVCAGIAGLLIS 237

Query: 246 ADIRGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFP 305
           ++++ AD NNAG  LELDAILAV +GG +L GGRF+L+ SV+GALIIQ +   I   G P
Sbjct: 238 SNVKSADGNNAGQLLELDAILAVTLGGTALTGGRFSLVGSVIGALIIQTLTYAIYSLGVP 297

Query: 306 PEMNQVVKAVVVLCVLIVQSQRFISLIKGVRSR 338
           PE+N VVKAVVV  V+++QS  F + +  +  R
Sbjct: 298 PEINLVVKAVVVFIVMLLQSPEFRAQVGALARR 330


Lambda     K      H
   0.327    0.142    0.416 

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: 350
Number of extensions: 12
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: 341
Length of database: 337
Length adjustment: 28
Effective length of query: 313
Effective length of database: 309
Effective search space:    96717
Effective search space used:    96717
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 (21.7 bits)
S2: 49 (23.5 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