GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1750 in Phaeobacter inhibens BS107

Align TM1750, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate GFF668 PGA1_c06820 dipeptide transport ATP-binding protein DppF

Query= TCDB::Q9X272
         (328 letters)



>FitnessBrowser__Phaeo:GFF668
          Length = 321

 Score =  241 bits (615), Expect = 2e-68
 Identities = 131/297 (44%), Positives = 185/297 (62%), Gaps = 8/297 (2%)

Query: 27  KRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPDGGKIFFEGKDITNLND 86
           K  L AV  +S +IKE     LVGESG GKST+G+ ++ LL    G +   G D+    D
Sbjct: 30  KSHLTAVSDVSFDIKEKTVYSLVGESGSGKSTIGKMVVGLLENSSGAVKVSGVDLNRETD 89

Query: 87  K-EMKPYRKKMQIIFQDPLGSLNPQMTVGRIIEDPLIIHKIGTKKERRKRVEELLDMVGI 145
              +   R  +Q+IFQDP  S+NP+  V  II +P +  K G  KE  +R   LL+ VG+
Sbjct: 90  AVAITKARDAIQMIFQDPYASMNPRWRVRDIIAEP-VAAKGGETKELAER---LLEQVGL 145

Query: 146 GREFINSFPHEFSGGQQQRIGIARALALNPKFIVCDEPVSALDVSIQAQIIDLLEEIQQK 205
             E  + FPHEFSGGQ+QRI IAR+LA  P+ IVCDEP SALDVS+QAQ+++L+ +++  
Sbjct: 146 SAEDADKFPHEFSGGQRQRICIARSLASQPRLIVCDEPTSALDVSVQAQVLNLMSDLKDD 205

Query: 206 MGISYLFIAHNLAVVEHISHKVAVMYLGKIVEYGDVDKIFLNPIHPYTRALLKSVPKIPW 265
           +G++YLFI+H+L VV HIS ++ V+YLG++VE    D +F  P HPYT+ LL + PK+  
Sbjct: 206 LGLTYLFISHDLTVVRHISDRIGVLYLGRLVEEAAPDDLFEAPKHPYTQMLLAAAPKM-- 263

Query: 266 DGQKQRFYSLKGELPSPIDLPKGCRFQTRCTEKKAICFEKEPELTEVEKNHFVSCHL 322
           D   +     +GE+P PI+ P GC F  RC    A C +  P++  +  +  V+CHL
Sbjct: 264 DAFGREVEPPQGEIPDPINPPSGCAFHPRCPIATAQCSQVRPQMRNINGSR-VACHL 319


Lambda     K      H
   0.321    0.142    0.417 

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: 292
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: 328
Length of database: 321
Length adjustment: 28
Effective length of query: 300
Effective length of database: 293
Effective search space:    87900
Effective search space used:    87900
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