GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1749 in Phaeobacter inhibens BS107

Align TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate GFF3769 PGA1_262p01730 putative glutathione import ATP-binding protein

Query= TCDB::Q9X271
         (324 letters)



>FitnessBrowser__Phaeo:GFF3769
          Length = 325

 Score =  278 bits (712), Expect = 1e-79
 Identities = 148/322 (45%), Positives = 203/322 (63%), Gaps = 5/322 (1%)

Query: 3   ELLNVNNLKVEFHRVEGIVKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINRNG 62
           +LL +++L V++    G +KA+  IS+ +NKGE +GIVGESG GKS  + ++LRLI  N 
Sbjct: 4   KLLEIDDLSVDYETARGDLKALRSISFDVNKGEIVGIVGESGCGKSTLISAILRLIAPNT 63

Query: 63  RIVDGEAIFLGKDLLKLNKEELRNIRGKDISIIFQNPMTSLNPIIRVGIQVMEPIIWHRL 122
           R  +GE  F G+DLL  +   +R++RG DISI+FQ+PM + NP+I +G Q+++  I HR 
Sbjct: 64  RFRNGEVRFKGEDLLVASDRHIRDLRGDDISIVFQDPMQTHNPVISIGKQMVD--IQHRS 121

Query: 123 MKNE-EARERAIELLERVGIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLIADEP 181
             ++ E    A ++L  VGIP+   R   YP +FSGGMRQR+ IAMAL   P LLIADEP
Sbjct: 122 KASKAEKLATAAKMLGAVGIPDPEMRLKQYPHEFSGGMRQRIAIAMALMSEPDLLIADEP 181

Query: 182 TTALDVTIQAQIMELLQELKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEAPVEE 241
           TTALD T++ QI+E L+EL+ E+G +++FI+H L V    CDR++ MYAG +VE   V E
Sbjct: 182 TTALDATLEVQIIERLKELQSEFGCAILFISHHLGVIAELCDRVVVMYAGAVVESGTVRE 241

Query: 242 ILKTPLHPYTKGLLN-STLEIGSRGKKLVPIPGNPPNPTKHPSGCKFHPRCSFAMEICQR 300
           I   P HPYT+ L+      +  R + L  IPG  P+    P GC F  RC  AM+ C  
Sbjct: 242 IFHNPKHPYTRRLIECDPGHLKERARVLPTIPGEVPDLANLPEGCIFRDRCDQAMDRC-A 300

Query: 301 EEPPLVNISENHRVACHLIKGE 322
             PPL  +SE H  AC L   E
Sbjct: 301 SVPPLARLSEGHNAACWLNHAE 322


Lambda     K      H
   0.320    0.139    0.401 

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: 271
Number of extensions: 9
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: 324
Length of database: 325
Length adjustment: 28
Effective length of query: 296
Effective length of database: 297
Effective search space:    87912
Effective search space used:    87912
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: 48 (23.1 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