GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ibpA in Chromobacterium vaccinii MWU205

Align Inositol ABC transporter, periplasmic inositol-binding protein IbpA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate WP_046158460.1 VL52_RS18725 ribose ABC transporter substrate-binding protein RbsB

Query= TCDB::B8H228
         (326 letters)



>NCBI__GCF_000971335.1:WP_046158460.1
          Length = 311

 Score =  151 bits (382), Expect = 2e-41
 Identities = 93/280 (33%), Positives = 161/280 (57%), Gaps = 8/280 (2%)

Query: 19  GLGTAALGLMTGCARGGAEAEVVVSFNDLSQPFFVAMRRELEDEAAKLGVKVQVLDAQNN 78
           G G+A  G  +  A  G +  V ++ + L+ PFFV +R     EA K GV +  +DAQ++
Sbjct: 24  GPGSAPAGDASAAAADG-KVTVGLAVSTLNNPFFVELRDGAAAEAKKQGVNLITVDAQDD 82

Query: 79  SSKQISDLQAAAVQGAKVVIVAPTDSKALAGAADDLVEQGVAVISVDRNIAGGKTAVPHV 138
            +KQ + ++    +   V+++ PTDS A+A    +   +G+ V+S+DR++ G + +  H+
Sbjct: 83  PAKQQASVEDLIQKKVSVILINPTDSSAVANVVKEATSKGIKVVSLDRSVNGAEVSA-HI 141

Query: 139 GADNVAGGRAMADWVVKTYPAGARVVVITNDPGSSSSIERVKGVHDGLAAGGPAFKIVTE 198
            +DN+AGG     +++       R+V +    GSS++ ER +G H  +       K++ +
Sbjct: 142 ASDNIAGGVMAGKYLLDKLGGKGRIVELEGIAGSSAARERGEGFHQ-VVDKKEGVKLLAK 200

Query: 199 QTANSKRDQALTVTQNILTSMRDTPPDVILCLNDDMAMGALEAVRAAGLDSAKVKVIGFD 258
           Q A+  R + L+V +NI+   +D     +   ND+MA+GA++A++AAGL +  V V+GFD
Sbjct: 201 QPADFDRAKGLSVMENIIQGNKDI--QGVFAHNDEMALGAVKAIQAAGLKN--VAVVGFD 256

Query: 259 AIPEALARIKAGEMVATVEQNPGLQIRTALRQAVDKIKSG 298
           A P+A+A +KAG + ATV+Q P L  +  + QA  K+  G
Sbjct: 257 ATPDAVAAVKAGALSATVQQQPALIGQYGV-QAAKKLADG 295


Lambda     K      H
   0.315    0.130    0.353 

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: 246
Number of extensions: 21
Number of successful extensions: 6
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: 326
Length of database: 311
Length adjustment: 27
Effective length of query: 299
Effective length of database: 284
Effective search space:    84916
Effective search space used:    84916
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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