GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TT_C0327 in Ruegeria conchae TW15

Align Glucose transport system permease protein aka TT_C0327, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate WP_010438514.1 G7G_RS0103675 sugar ABC transporter permease

Query= TCDB::Q72KX3
         (369 letters)



>NCBI__GCF_000192475.1:WP_010438514.1
          Length = 290

 Score =  162 bits (411), Expect = 8e-45
 Identities = 118/358 (32%), Positives = 168/358 (46%), Gaps = 85/358 (23%)

Query: 9   LVLLPSVLAVGVFVYGFIGQNLWVSLTDWGKDPAQALALRPELRFVGLENYRELFTGFVD 68
           +VL PS +AV +FVYGFIG   WVSLT           L P+    G   Y  LF     
Sbjct: 12  VVLAPSFIAVLIFVYGFIGWTAWVSLT--------RSKLLPKYEIKGFIQYERLFDS--- 60

Query: 69  VRFRQSVVNLIFFTLFFMAGSLGLGLLLALAVDKAPRGEGFFRTVFLFPMALSFVVTGTI 128
            R+  ++ NL  F   F+  ++ LGLLLA+ +D+  R EG  RT++L+PMALS +VTGT 
Sbjct: 61  PRWDTAINNLYIFGALFIVIAMVLGLLLAILLDQKIRVEGAIRTIYLYPMALSMIVTGTA 120

Query: 129 WRWLLQPQGGVNVLPTLFGLPPLSFPWLATREQVLVFDWNRLPFYTALVVGLVLLYVAYT 188
           W+W+L P  G+  +   +G     F WL   +                       Y  YT
Sbjct: 121 WKWILNPGLGIESMVQGWGFANFEFDWLVNPD-----------------------YAIYT 157

Query: 189 AYREGERRRALWGLASAGVLLLWAFAFGQGLRLLPYPEVHGFSLALVGVILAAVWQMSGY 248
                    A+W                         +  GF +AL    LA +  + G 
Sbjct: 158 IV-----MAAIW-------------------------QSSGFVMAL---FLAGLRSVDG- 183

Query: 249 TMALYLAGLRGIPVEVLEAARVDGASEWQLFRRVIFPMLAPITLSAMIVLGHIALKIFDL 308
              +  A + GIP              W+++  +I P +API LSA IVL H+A+K FDL
Sbjct: 184 -EIIKAAQVDGIPT-------------WRIYTAIIIPSMAPIFLSAFIVLAHLAIKSFDL 229

Query: 309 VFAM--AGLDYAPTDVPAIYMYLLAFRGNQFAKGAAIGILLLLLVAVVVVPYLATQLR 364
           V A+   G  YA TD+PA YMY +AF      + A+  ++++L+V  +VVPYL ++LR
Sbjct: 230 VIALTGGGPGYA-TDLPATYMYAMAFSRGDIGQAASSAMIMMLVVFAIVVPYLYSELR 286


Lambda     K      H
   0.331    0.146    0.458 

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: 308
Number of extensions: 15
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 369
Length of database: 290
Length adjustment: 28
Effective length of query: 341
Effective length of database: 262
Effective search space:    89342
Effective search space used:    89342
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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