GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Herbaspirillum seropedicae SmR1

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate HSERO_RS05255 HSERO_RS05255 ribose ABC transporter permease

Query= TCDB::P23200
         (336 letters)



>FitnessBrowser__HerbieS:HSERO_RS05255
          Length = 347

 Score =  184 bits (468), Expect = 2e-51
 Identities = 114/321 (35%), Positives = 170/321 (52%), Gaps = 18/321 (5%)

Query: 19  YVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAGRQVGL 78
           +  LL+++    F  P F+ + NL +IL  ++V  ++A+    +I+T G DLS G  +  
Sbjct: 40  FASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGTMMTF 99

Query: 79  AAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVTPFITT 138
            AV+A  +L +             MP+ L I      GA+ G I+G++IA L V PFI T
Sbjct: 100 CAVMAGVVLTNWG-----------MPLPLGIAAAIFFGALSGWISGMVIAKLKVPPFIAT 148

Query: 139 LGTMIIVYGINSLYYDFVGASPISGFDS-GFSTFAQGFVA---LGSFRLSYITFYALIAV 194
           LG M+++ G++ +     G  PI   D+ GFS  AQ  +    + S  +        +  
Sbjct: 149 LGMMMLLKGLSLV---ISGTRPIYFNDTEGFSAIAQDSLIGDLIPSLPIPNAVLILFLVA 205

Query: 195 AFVWVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAGRIG 254
               ++ NKT FG+  FA+G N EA ++SGV V    + +Y  SG      G++ A R+ 
Sbjct: 206 IGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRLN 265

Query: 255 SATNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPYWQY 314
           SA   LG  YELDAIAA V+GG S SGG GT++G + G  I +V+  GL  + V   WQ 
Sbjct: 266 SAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQT 325

Query: 315 IIKGAIIIFAVALDSLKYARK 335
           ++ G III AV LD L+  R+
Sbjct: 326 VVTGVIIILAVYLDILRRRRR 346


Lambda     K      H
   0.327    0.143    0.415 

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: 285
Number of extensions: 18
Number of successful extensions: 3
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: 336
Length of database: 347
Length adjustment: 29
Effective length of query: 307
Effective length of database: 318
Effective search space:    97626
Effective search space used:    97626
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.

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