GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpF in Echinicola vietnamensis KMM 6221, DSM 17526

Align Hg2+-inhibitable aquaporin, AqpM (transports both water and glycerol as well as CO2) (Kozono et al., 2003; Araya-Secchi et al., 2011). Its 3-d structure has been determined to 1.7 Å. In AqpM, isoleucine replaces a key histidine residue found in the lumen of water channels, which becomes a glycine residue in aquaglyceroporins. As a result of this and other side-chain substituents in the walls of the channel, the channel is intermediate in size and exhibits differentially tuned electrostatics when compared with the other subfamilies (characterized)
to candidate Echvi_3097 Echvi_3097 MIP family channel proteins

Query= TCDB::Q9C4Z5
         (246 letters)



>FitnessBrowser__Cola:Echvi_3097
          Length = 227

 Score =  145 bits (365), Expect = 9e-40
 Identities = 90/247 (36%), Positives = 131/247 (53%), Gaps = 28/247 (11%)

Query: 6   KRCIAEFIGTFILVFFGAGSAAVTLMIASGGTSPNPFNIGIGLLGGLGDWVAIGLAFGFA 65
           K+ IAEFIGTF LV  G GSA +               +GIG  G       + LAFG  
Sbjct: 2   KKLIAEFIGTFWLVLGGCGSAVLAAAFPE---------LGIGFAG-------VALAFGLT 45

Query: 66  IAASIYALGNISGCHINPAVTIGLWSVKKFPGREVVPYIIAQLLGAAFGSFIFLQCAG-- 123
           +    YA+G++SGCH+NPAV+IGLW+  +F  +E++PYI+AQ+LG    + +    A   
Sbjct: 46  VLTMAYAIGHVSGCHLNPAVSIGLWAGGRFEAKELLPYILAQVLGGLVAAAVLYVIASDN 105

Query: 124 ----IGAATVGGLGATAPFPGISYWQAMLAEVVGTFLLMITIMGIAVDERAPKGFAGIII 179
               +G     G G  +P  G     A++ EVV TF  +  I+G A   +AP+G AG+ I
Sbjct: 106 PAFELGGFAANGYGEHSP-GGYGMTAALVTEVVMTFAFLFVILG-ATHSKAPQGLAGVAI 163

Query: 180 GLTVAGIITTLGNISGSSLNPARTFGPYLNDMIFAGTDLWNYYSIYVIGPIVGAVLAALT 239
           GL +  I      ++ +S+NPAR+     +  IF G        ++ + PIVGA+LA   
Sbjct: 164 GLCLTLIHLISIPVTNTSVNPARS----TSQAIFVGDWALGQLWLFWVAPIVGAILAGWV 219

Query: 240 YQYLTSE 246
           Y+YL+ E
Sbjct: 220 YKYLSPE 226


Lambda     K      H
   0.326    0.144    0.441 

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: 203
Number of extensions: 17
Number of successful extensions: 7
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: 246
Length of database: 227
Length adjustment: 23
Effective length of query: 223
Effective length of database: 204
Effective search space:    45492
Effective search space used:    45492
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 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