GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TT_C0328 in Phaeobacter inhibens BS107

Align Glucose-binding protein aka TT_C0328, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate GFF1918 PGA1_c19500 putative sugar-binding periplasmic protein

Query= TCDB::Q72KX2
         (414 letters)



>FitnessBrowser__Phaeo:GFF1918
          Length = 414

 Score =  143 bits (361), Expect = 8e-39
 Identities = 105/350 (30%), Positives = 166/350 (47%), Gaps = 19/350 (5%)

Query: 15  SALAQGGKLEIFSWWAGDEGPALEALIRLYKQKYP--GVEVINATVTGGAGVNARAVLKT 72
           +A A G + E+  WW    G A  A I+++   Y   G E I+  + GG    A+     
Sbjct: 19  AATADGIRAEVIHWWVS-AGEA--AAIKVFADAYTANGGEWIDNGIGGGG---AKTTFVN 72

Query: 73  RMLGGDPPDTFQVHAGMELIGTWVVANRMEDLSALFRQEGWLQAFPKGLIDLISYKGGIW 132
           R++GGD P   Q +   E     V A  +  L A      W   FP  + +++   G  +
Sbjct: 73  RLMGGDAPQVGQFNTSREFEEI-VDAGLLHSLDAEAEAGNWSALFPGIIDNVVKRDGSYY 131

Query: 133 SVPVNIHRSNVMWYLPAKLKEWGVNPPRTWDEFLATCQTLKQKGLEAPLAL-GENWTQQH 191
           +VPVNIH SN +W+    + + G++ P  WD F    +TLK+ G+  PLA+ GE W ++ 
Sbjct: 132 AVPVNIHGSNWLWHNNQVMADAGLDVPTDWDSFFEAAETLKEAGI-IPLAVGGEAWQERL 190

Query: 192 LWESVALAVLGPDDWNNLWNGK--LKFTDPKAVRAWEVFGRVLDCANK---DAAGLSWQQ 246
            + SV L+V G D +  L+  K     T  +    ++V+ R+     +    + G SW  
Sbjct: 191 TFNSVLLSVGGQDLYLRLFEEKDTTALTSDEMKEVFDVYSRLRTLVRETDPGSPGRSWND 250

Query: 247 AVDRVVQGKAAFNVMGDWAAGYMTTTLKLKPGTDFAWAPSPGTQGVFMMLSDSFGLPK-- 304
           A + V+ G+AA  +MGDWA G   +   + PG ++   P+      +M+  D F  PK  
Sbjct: 251 ATNMVITGQAAMQIMGDWAKGEFLSA-GMTPGVEYGCTPAVIAGSPYMISGDVFVFPKTG 309

Query: 305 GAKNRQNAINWLRLVGSKEGQDTFNPLKGSIAARLDSDPSKYNAYGQSAM 354
             ++R+        +   E Q  FN +KGSI  R D D S+ +  GQ A+
Sbjct: 310 NEEDREAQSLMATTMLDAEVQVAFNNIKGSIPVRPDVDTSQLDVCGQQAI 359


Lambda     K      H
   0.319    0.134    0.429 

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: 512
Number of extensions: 27
Number of successful extensions: 5
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: 414
Length of database: 414
Length adjustment: 31
Effective length of query: 383
Effective length of database: 383
Effective search space:   146689
Effective search space used:   146689
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: 50 (23.9 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