GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Phaeobacter inhibens BS107

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate GFF667 PGA1_c06810 putative dipeptide transport ATP-binding protein DppD

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Phaeo:GFF667
          Length = 326

 Score =  197 bits (501), Expect = 3e-55
 Identities = 116/303 (38%), Positives = 176/303 (58%), Gaps = 12/303 (3%)

Query: 24  AVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPLTLVDGKIFLRVNGEFVELSS 83
           A D +S++I   E++GVVGESG GK+   N +   +  P  +  G+I  R+NG+ ++  +
Sbjct: 24  ATDKVSYDIAPGEILGVVGESGAGKSMAGNAVIGLLNPPARITGGEI--RLNGQRID--N 79

Query: 84  MTRDEVKRKFWGKEITIIPQAAMNALMPTIRM-EKYVRHLAESHGIDEEELLDKARRRFE 142
           + R++++R   GKEI +I Q  + +L P +R+ ++    + E   + + E   +A    E
Sbjct: 80  LPREKMRR-LRGKEIGMIFQDPLTSLNPLLRIGDQLTETMMEHLELTKPEARARAIAALE 138

Query: 143 EVGLDPLW--IKRYPFELSGGMRQRAVIAIATILNPSLLIADEPTSALDVVNQKVLLKVL 200
           EVG+      I  YP E SGGMRQR VIA+A    PSL+IADEPT+ALDV  Q  ++ +L
Sbjct: 139 EVGIPAASERIDSYPHEFSGGMRQRVVIALALCAEPSLIIADEPTTALDVSVQAQIIALL 198

Query: 201 MQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKIVEFAPVESLLEKPLHPYTQGLFN 260
            ++ R+    +++ ITHD+  + + ADR+ +MYAG++ E   V  ++ +P HPYT GL  
Sbjct: 199 KRLCRER-GTAVMLITHDMGVIAEAADRVAVMYAGRMAEIGDVRDVVTRPRHPYTDGLMG 257

Query: 261 SVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPRCPHAMDVCKEKEPPLTEIEPGRRV 320
           S  TP     +  +  IPGA P L + P GC F PRC  A + C+   PP  E + GR  
Sbjct: 258 S--TPSASAGQHRLRQIPGAMPRLHSLPPGCAFSPRCERANERCRNSPPPTLEADNGRS- 314

Query: 321 ACW 323
           ACW
Sbjct: 315 ACW 317


Lambda     K      H
   0.321    0.138    0.405 

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: 310
Number of extensions: 16
Number of successful extensions: 4
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: 330
Length of database: 326
Length adjustment: 28
Effective length of query: 302
Effective length of database: 298
Effective search space:    89996
Effective search space used:    89996
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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