GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpF in Shewanella sp. ANA-3

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 7025915 Shewana3_3064 aquaporin Z (RefSeq)

Query= TCDB::Q9C4Z5
         (246 letters)



>FitnessBrowser__ANA3:7025915
          Length = 231

 Score =  153 bits (387), Expect = 3e-42
 Identities = 96/248 (38%), Positives = 138/248 (55%), Gaps = 29/248 (11%)

Query: 2   VSLTKRCIAEFIGTFILVFFGAGSAAVTLMIASGGTSPNPFNIGIGLLGGLGDWVAIGLA 61
           ++++++  AEF+GT  LV  G GSA +               +GIGLLG       + LA
Sbjct: 1   MNMSQKMAAEFLGTLWLVLGGCGSAVLAAAFPE---------VGIGLLG-------VALA 44

Query: 62  FGFAIAASIYALGNISGCHINPAVTIGLWSVKKFPGREVVPYIIAQLLGAAFGSFIFLQC 121
           FG  +    +A+G+ISGCH+NPAV+ GLW+  +FP  E++PYIIAQ+ G   G+ +    
Sbjct: 45  FGLTVLTMAFAIGHISGCHLNPAVSFGLWAGGRFPASELLPYIIAQVAGGIVGAGVLYAI 104

Query: 122 A----GIGAA---TVGGLGATAPFPGISYWQAMLAEVVGTFLLMITIMGIAVDERAPKGF 174
           A    G   A      G G  +P  G S    ++ E+V T   ++ I+G A DERAPKGF
Sbjct: 105 ASGQEGFSLAAGFASNGFGEHSP-GGYSMMSVLICEIVMTLFFLLVILG-ATDERAPKGF 162

Query: 175 AGIIIGLTVAGIITTLGNISGSSLNPARTFGPYLNDMIFAGTDLWNYYSIYVIGPIVGAV 234
           A I IGL +  I      +S +S+NPAR+ GP L    +A + LW    I+ + PIVGA+
Sbjct: 163 APIAIGLCLTLIHLISIPVSNTSVNPARSTGPALFVGDWAVSQLW----IFWVAPIVGAI 218

Query: 235 LAALTYQY 242
           LA + Y+Y
Sbjct: 219 LAGMIYRY 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: 223
Number of extensions: 18
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 246
Length of database: 231
Length adjustment: 23
Effective length of query: 223
Effective length of database: 208
Effective search space:    46384
Effective search space used:    46384
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.

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