GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Rhodobacter johrii JA192

Align Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate WP_108223269.1 C8J29_RS11820 ABC transporter permease

Query= TCDB::G4FGN4
         (313 letters)



>NCBI__GCF_003046325.1:WP_108223269.1
          Length = 363

 Score =  191 bits (486), Expect = 2e-53
 Identities = 108/315 (34%), Positives = 183/315 (58%), Gaps = 18/315 (5%)

Query: 13  IFLILIAIVVFLGVTTREFLTVENIFTVILNVSFIAIMSFGMTMVIITSGIDLSVGSILG 72
           + ++++++ +F  +  ++F +   +  ++  V+ + I+    T+V++T+GIDLSVG+I+ 
Sbjct: 48  LIVLVVSVSIFGALLGQKFFSAFTLTLILQQVAIVGIVGAAQTLVVLTAGIDLSVGAIMV 107

Query: 73  AASVVMGLLMDEKGLSPFLSVVIGLAVGVGFGLANGLLITKARLAPFISTLGMLSVGRGL 132
            +SV+MG      G+   LSV+ GLA G G G  NG L+ + +L PFI TLGM  +    
Sbjct: 108 LSSVIMGQFTFRYGIPAPLSVLCGLAAGAGIGFVNGTLVARMKLPPFIVTLGMWQIVLAA 167

Query: 133 AYVMSGGWPISP------------FPESFTVH----GQGMVGPVPVPVIYMAVIGVIAHI 176
            ++ S    I              F  +F +     G+G        V+ + ++ VIA++
Sbjct: 168 NFLYSANETIRSQDISAQAPILQFFGNTFRLGADEAGRGGAVFTYGAVLLILLVLVIAYV 227

Query: 177 FLKYTVTGRRIYAIGGNMEASKLVGIKTDRILILVYTINGFLAAFAGFLLTAWLGVAQPN 236
            L+ T  GR +YA+G + +A++L G++T  +L+ VYT++G + A AG+++   LG   P 
Sbjct: 228 -LRQTAWGRHVYAVGDDPDAAELAGVQTRNVLVTVYTLSGLICALAGWVMIGRLGSVSPT 286

Query: 237 AGQGYELDVIAATVIGGTSLSGGEGTILGAFLGAVIMGVLRNGMILLGVSSFWQQVVIGI 296
           AGQ   ++ I A VIGG SL GG G++LG   GA+I+GV   G+ L+G    W  ++IG+
Sbjct: 287 AGQFANIESITAVVIGGISLFGGRGSVLGMLFGALIVGVFSLGLKLMGTDPQWTYLLIGM 346

Query: 297 VIIIAIAIDQ-IRRA 310
           +II A+A+DQ IR+A
Sbjct: 347 LIIAAVAVDQWIRKA 361


Lambda     K      H
   0.328    0.145    0.421 

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: 302
Number of extensions: 13
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: 313
Length of database: 363
Length adjustment: 28
Effective length of query: 285
Effective length of database: 335
Effective search space:    95475
Effective search space used:    95475
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 (21.7 bits)
S2: 49 (23.5 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