GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TRIC in Escherichia coli BW25113

Align putative transporter, required for glycine and L-alanine utilization (characterized)
to candidate 14303 b0157 conserved inner membrane protein (NCBI)

Query= reanno::ANA3:7023996
         (213 letters)



>FitnessBrowser__Keio:14303
          Length = 207

 Score =  139 bits (351), Expect = 3e-38
 Identities = 78/203 (38%), Positives = 120/203 (59%), Gaps = 10/203 (4%)

Query: 12  LIGILAEAMTGALAAGRKQMDLFGVVIIGCATAIGGGTLRDMLLGNYPLIWVENVHYLLA 71
           ++G    A++G L AG+ +MD FGV+++G  TA+GGGT+RDM L + P+ WV++   L+ 
Sbjct: 8   IVGTAVFAISGVLLAGKLRMDPFGVLVLGVVTAVGGGTIRDMALDHGPVFWVKDPTDLVV 67

Query: 72  IAFASLLTVAIAPVMRYLSKLFL-AIDALGLAVFSIVGAQKTLMLGFSPTIAVVMGLVTG 130
               S+LT+ +    R L K  L  +DA+GLAVF  +G  K       P IAV MG++TG
Sbjct: 68  AMVTSMLTIVLVRQPRRLPKWMLPVLDAVGLAVFVGIGVNKAFNAEAGPLIAVCMGVITG 127

Query: 131 VFGGVIRDILCNQVPLIFKKELYA----VISLFTAGLYITLNA-YQLAEWINLVVCLTLG 185
           V GG+IRD+L  ++P+I + E+YA    +  +  A  Y T +   + A  + +VV L   
Sbjct: 128 VGGGIIRDVLAREIPMILRTEIYATACIIGGIVHATAYYTFSVPLETASMMGMVVTLL-- 185

Query: 186 FSLRMLALRYHWSMPTFDYQANG 208
             +R+ A+R+H  +PTF    NG
Sbjct: 186 --IRLAAIRWHLKLPTFALDENG 206



 Score = 42.4 bits (98), Expect = 6e-09
 Identities = 28/84 (33%), Positives = 46/84 (54%), Gaps = 3/84 (3%)

Query: 96  IDALGLAVFSIVGAQKTLMLGFSPTIAVVMGLVTGVFGGVIRDILCNQVPLIFKKE-LYA 154
           +D +G AVF+I G      L   P   +V+G+VT V GG IRD+  +  P+ + K+    
Sbjct: 6   LDIVGTAVFAISGVLLAGKLRMDPFGVLVLGVVTAVGGGTIRDMALDHGPVFWVKDPTDL 65

Query: 155 VISLFTAGLYITL--NAYQLAEWI 176
           V+++ T+ L I L     +L +W+
Sbjct: 66  VVAMVTSMLTIVLVRQPRRLPKWM 89


Lambda     K      H
   0.330    0.143    0.438 

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: 151
Number of extensions: 11
Number of successful extensions: 6
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: 213
Length of database: 207
Length adjustment: 21
Effective length of query: 192
Effective length of database: 186
Effective search space:    35712
Effective search space used:    35712
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 (21.8 bits)
S2: 45 (21.9 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