GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ngcF in Desulfovibrio vulgaris Miyazaki F

Align NgcF, component of N-Acetylglucosamine/N,N'-diacetyl chitobiose porter (NgcK (C) not identified) (characterized)
to candidate 8499892 DvMF_0657 binding-protein-dependent transport systems inner membrane component (RefSeq)

Query= TCDB::Q8RJU9
         (308 letters)



>FitnessBrowser__Miya:8499892
          Length = 297

 Score =  145 bits (365), Expect = 1e-39
 Identities = 95/297 (31%), Positives = 155/297 (52%), Gaps = 26/297 (8%)

Query: 3   HGKYRFIVGFLAV--PLGLYALLVVWPFIQSIYYSF-TDWTGLSPDFKTVGFDNYERMLD 59
           H   R I  +L +   L   A    +P + +  +SF  D  G +P  + VG ++Y+ +L+
Sbjct: 8   HATMRTIHAWLLLLPALAFIAAFTHYPAVNTFIHSFFLDGRGGAPA-QFVGLEHYQYLLE 66

Query: 60  DDIFWKSLQHSLLFALLLPVVTIGLALFFAFMINVGGRRRRGGPVITGVRGSGFYKIVYF 119
           D++F K+L ++LLFA     ++IGLA+  AF++N G            + G    ++ YF
Sbjct: 67  DEVFRKALVNNLLFASGTIPLSIGLAMTMAFLVNAG------------LAGQSVLRLCYF 114

Query: 120 FPQVLSIAIVALLFAFAYNPDSGAINSLLRGIGLGDVQPVWLGDPDLALWCVMAVIVWST 179
            P VL +  VA ++ F Y P+ G +  +   +GL  V   WLG    AL CV+AV VW  
Sbjct: 115 VPTVLPMIAVANIWLFFYTPEYGLLEQIRGALGLAGVN--WLGSESTALPCVIAVAVWKD 172

Query: 180 VGFFVVLFSAGMASIPADIYEAALLDGANRVTTFFRITLPLLWDTVQSGWVYMGILALGA 239
            GFF++ + A +  IP  + EAA+L+GA+R+  + R+ +PLL  T     V   I A   
Sbjct: 173 AGFFMIFYLAALQQIPPSLGEAAMLEGASRLYYYRRVVIPLLMPTTLFVLVNATINAFR- 231

Query: 240 ESFAVVHIMTTGPGGPDYSTTVMVLYVYQKAFRDGQAAYATTIGVALLIVTLAFAAV 296
               V H+     GGP+ ++++++ Y+Y+ +F+     Y    G AL +V L F A+
Sbjct: 232 ---MVDHLFVLTQGGPNNASSLLLYYIYEVSFKYWDTGY----GAALTMVLLGFLAL 281


Lambda     K      H
   0.330    0.145    0.458 

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: 272
Number of extensions: 19
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: 308
Length of database: 297
Length adjustment: 27
Effective length of query: 281
Effective length of database: 270
Effective search space:    75870
Effective search space used:    75870
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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