GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1746 in Paraburkholderia bryophila 376MFSha3.1

Align TM1746, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate H281DRAFT_03129 H281DRAFT_03129 oligopeptide transport system substrate-binding protein

Query= TCDB::Q9X268
         (642 letters)



>FitnessBrowser__Burk376:H281DRAFT_03129
          Length = 538

 Score =  161 bits (408), Expect = 6e-44
 Identities = 107/345 (31%), Positives = 174/345 (50%), Gaps = 18/345 (5%)

Query: 68  VVPAVCESYTVSEDGLTYTFYLRKDKRWSNGDPVTAYDFEFAWKRAASPETPTLPLWASP 127
           VVP V +S+T +    T+ F LR D RWSNG PVTA DF +AW+R   P+T +   +   
Sbjct: 80  VVPGVAQSWTRTGPD-TWVFKLRHDARWSNGQPVTAADFIYAWQRVLDPKTGSK--YTVL 136

Query: 128 VQYIKNVYDCKSGAKPLDELGVKALDDYTLQVTLSRPMPSFINMLVLGGAMPLHRKTVQE 187
           V+++KN     +G  PL  LG +A+D YT++VT   P   F  +  +    P++R  V  
Sbjct: 137 VEFVKNAKAILAGKAPLASLGARAVDPYTIEVTTEVPAAFFPQLAAMPTMAPVNRDVVAR 196

Query: 188 HPEDWWKPEYFVGNGPYVIESFTPNYEIVLVRNKYYVGDFPGNVDRIV---LKAGGLGLQ 244
              +W +P  FVGNGPY++  + PN  +V  ++K Y       + ++    ++     ++
Sbjct: 197 FGNEWTRPGNFVGNGPYMLADWQPNNRLVGAKSKTYWNASKVVITKVTYLPIENDETAMR 256

Query: 245 QYLAGEIDAVFITAVGDYVFALKNKQLSKELHEESGVQWVGYEIT-RSLSPVFDDIRIRK 303
            Y AG+ D  +    G  ++A  +KQ   EL  ++G+Q   Y  +  +  P+F D R+R+
Sbjct: 257 MYQAGQFDYTYSIPSG--IYAQVSKQFGPEL--KTGLQIATYYYSLNNEDPIFKDKRVRQ 312

Query: 304 ALAMAIDKKVLTDIVLGGMAIPTHAYCSPDSEIAEAVK----GIPYDP--EQAKKLLAEA 357
           AL+M +D+ +LT  +     +P +   S  ++ A   K    G P     + A+ LL  A
Sbjct: 313 ALSMVLDRDLLTQRLTADGELPMYGLISKGTQGAAVFKPDWAGWPMAKRVDYARNLLKSA 372

Query: 358 GYPNGKGFPKVKFYITG-ASDPVAEALVDQWKKVLGITFEIENIE 401
           GY + K       Y T      VA     +W+  LG+  ++EN+E
Sbjct: 373 GYSDAKPLTFTLTYNTNDLHKKVALFATSEWRTKLGVNTKLENVE 417


Lambda     K      H
   0.319    0.138    0.431 

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: 928
Number of extensions: 50
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 642
Length of database: 538
Length adjustment: 37
Effective length of query: 605
Effective length of database: 501
Effective search space:   303105
Effective search space used:   303105
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 (21.7 bits)
S2: 53 (25.0 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