GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpF in Dyadobacter tibetensis Y620-1

Align Glycerol uptake facilitator protein 3 (characterized)
to candidate WP_025762849.1 X939_RS0108570 aquaporin family protein

Query= SwissProt::F9UTW9
         (240 letters)



>NCBI__GCF_000566685.1:WP_025762849.1
          Length = 246

 Score =  259 bits (661), Expect = 4e-74
 Identities = 129/238 (54%), Positives = 164/238 (68%), Gaps = 11/238 (4%)

Query: 11  LGEFLGTFILILLGDGVVAGVTLNKSKAQNAGWVAITLGWGFAVTMGVY-ASSFMSP-AH 68
           LGE +GT +LILLG+GVVA V LNK+K QN GW+ IT GW FAV  GV+ A++  SP AH
Sbjct: 7   LGELIGTMVLILLGNGVVANVVLNKTKGQNGGWIVITAGWAFAVMAGVFTATALGSPGAH 66

Query: 69  LNPAVSLGMAVAGKFPWAYVIPYSAAQIAGGVIGGLVVWLHYYPHWQATKDAGAILGIFA 128
           LNPAV++G A   +  ++ +  +  AQI GG++G  +VW+ YYPHW  T D GA L  FA
Sbjct: 67  LNPAVTIGFAFLQQ-DFSLITTFIPAQILGGILGATIVWIQYYPHWAVTDDPGAKLACFA 125

Query: 129 TGPGIRRYFWNFISEVIGTFVLVFGLLAF--------TKGQFTAGLNPIVVGILIIAIGL 180
           TGP IR    NF+SE I T +L+ G++A          +G     L P +VG+L+ +IGL
Sbjct: 126 TGPAIRATIPNFLSEFIATGMLILGIVAIGYSNVIGAAQGGIPPALGPYLVGMLVWSIGL 185

Query: 181 SLGGTTGYAINPARDLGPRIAHAVLPIANKGTSDWAYSWVPIAGPLVGGALGALLFNV 238
           SLGGTTGYAINPARDLGPRIAH +LPIANKGTSDW Y W+PI  PL+G A+  L+  +
Sbjct: 186 SLGGTTGYAINPARDLGPRIAHTILPIANKGTSDWGYGWIPIVAPLLGAAIFGLVLRL 243



 Score = 26.6 bits (57), Expect = 5e-04
 Identities = 34/110 (30%), Positives = 49/110 (44%), Gaps = 27/110 (24%)

Query: 140 FISEVIGTFVLVF---GLLA-----FTKGQ------FTAGLNPIVVGILIIAIGLSLGGT 185
           F+ E+IGT VL+    G++A      TKGQ       TAG    V+  +  A  L   G+
Sbjct: 6   FLGELIGTMVLILLGNGVVANVVLNKTKGQNGGWIVITAGWAFAVMAGVFTATAL---GS 62

Query: 186 TGYAINPARDLGPRIAHAVLPIANKGTSDWAYSWVPIAGPLVGGALGALL 235
            G  +NPA  +G     A L        D++     I   ++GG LGA +
Sbjct: 63  PGAHLNPAVTIG----FAFL------QQDFSLITTFIPAQILGGILGATI 102


Lambda     K      H
   0.325    0.143    0.459 

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: 298
Number of extensions: 20
Number of successful extensions: 5
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: 240
Length of database: 246
Length adjustment: 23
Effective length of query: 217
Effective length of database: 223
Effective search space:    48391
Effective search space used:    48391
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: 46 (22.3 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