GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manZ in Megamonas funiformis YIT 11815

Align PTS system, mannose/fructose/sorbose family, IID component, component of The primary glucose /mannose uptake transporter, ManLMN (characterized)
to candidate WP_008539788.1 HMPREF9454_RS10755 PTS system mannose/fructose/sorbose family transporter subunit IID

Query= TCDB::E1UCI2
         (303 letters)



>NCBI__GCF_000245775.1:WP_008539788.1
          Length = 278

 Score =  147 bits (372), Expect = 2e-40
 Identities = 88/279 (31%), Positives = 147/279 (52%), Gaps = 36/279 (12%)

Query: 26  WNYERMQNGGWAFSMIPAIKKLYKTKEDRSSALKRHLEFFNTHPYIASPILGVTLALEEE 85
           ++ E MQ  G+  +M+P I++LYKTKE++  A++ +  FFNT P + S ++G+T +LEE 
Sbjct: 25  FSQEHMQTFGYLCAMLPIIEELYKTKEEQKKAMQTYTAFFNTEPQVGSVVVGITASLEEA 84

Query: 86  RANGAE-VDDVAIQGVKVGMMGPLAGVGDPVFWFTIRPMLGALGASLALSGNILGPILFF 144
           +ANGA+ ++   I G++ G+MGPLAG+GD +   T+ P+L  +   L+  G+ +G I + 
Sbjct: 85  KANGADDINAETINGLRAGLMGPLAGIGDSLVVGTLIPILLGIAMGLSTGGSPIGAIFYI 144

Query: 145 VAWN-VIRWGFMWYTQEFGYKAGSKITDDLSGGLLQDITKGASILGMFVLAALVQRWVNI 203
           + WN +I WG M +    GY+ G K  D L G     I +   +LG  V+ A+   W+NI
Sbjct: 145 IVWNLLITWG-MRFLYFKGYELGGKAIDFLVGERATAIRESIVMLGTIVIGAVAGTWINI 203

Query: 204 QFAPIISKVKLDEGAYIDWSHLPQGAQGIKTALEQQQAGLALSEIKVTTLQNNLDNLIPG 263
           +                  +     A+G              ++     LQ+ L+ + P 
Sbjct: 204 R------------------TGFTMTAEG--------------ADKPFLVLQDTLNGVFPN 231

Query: 264 LAAVALTFLCMWLL-KKKISPIIIILGLFVVGIVGHLIG 301
           + +      C +LL K+ +SPI ++L L V+  VG L+G
Sbjct: 232 ILSAVFVIFCWYLLTKRNMSPIYVMLLLVVIAFVGVLVG 270


Lambda     K      H
   0.323    0.140    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: 216
Number of extensions: 11
Number of successful extensions: 2
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: 303
Length of database: 278
Length adjustment: 26
Effective length of query: 277
Effective length of database: 252
Effective search space:    69804
Effective search space used:    69804
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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