GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araUsh in Sinorhizobium meliloti 1021

Align Periplasmic binding protein/LacI transcriptional regulator (characterized, see rationale)
to candidate SM_b21587 SM_b21587 sugar uptake ABC transporter substrate-binding protein precursor

Query= uniprot:A0KWY4
         (313 letters)



>FitnessBrowser__Smeli:SM_b21587
          Length = 320

 Score =  352 bits (903), Expect = e-102
 Identities = 179/316 (56%), Positives = 235/316 (74%), Gaps = 10/316 (3%)

Query: 5   KIITALGLWAVSATCAYATT------VGFSQVGSESGWRTSFSEAVKAEAKQRGIDLKFA 58
           KI+ AL    + A C + +       VGFSQ+GSESGWR + +   K +A++RGIDLKFA
Sbjct: 2   KIVKALASATILAACTFGSASAAELVVGFSQIGSESGWRAAETTLTKQQAEERGIDLKFA 61

Query: 59  DAQQKQENQIKAVRSFIAQGVDAIIIAPVVETGWKPVLKEAKRAKIPVVIVDRNIKVDDD 118
           DAQQKQENQIKA+RSFIAQGV+AI++APVV TGW  VL+EAK A+IPV+++DR +   DD
Sbjct: 62  DAQQKQENQIKAIRSFIAQGVNAILLAPVVATGWDEVLEEAKDAEIPVILLDRTVDASDD 121

Query: 119 SLFLTRIASDFSEEGRKIGQWLMDKTQGN-CDIAELQGTVGATAAIDRAAGFNQVIANYP 177
            L+LT + SD   EG   G+WL+D   G  C++ ELQGT G++ AIDR  GF Q ++   
Sbjct: 122 -LYLTAVTSDLVHEGSVAGKWLVDTVAGKPCNVVELQGTTGSSPAIDRKKGFEQALSGND 180

Query: 178 NAKIVRSQTGEFTRAKGKEVMEGFLKAQN-GQPLCAVWSHNDEMALGAVQAIKEAGLKPG 236
           N KIVRSQTG+FTR KGKEVME FLKA++ G+ +CA+++HND+MA+GA+QAIKEAGLKPG
Sbjct: 181 NLKIVRSQTGDFTRTKGKEVMESFLKAEDGGKNICALYAHNDDMAVGAIQAIKEAGLKPG 240

Query: 237 KDILIVSVDGVPDYFKAMADGDVNATVELSPYLGGPAFDAIDAYLKGNKDQAKLISTTGD 296
           KDIL+VS+D VPD F+AMA G+ NATVEL+P + GPAFDA+ A+LK  K+  K I T   
Sbjct: 241 KDILVVSIDAVPDIFQAMAAGEANATVELTPNMAGPAFDALAAFLKDGKEPPKWIQTESK 300

Query: 297 VFTQ-ETAAAEYEKRR 311
           ++TQ +     YE+++
Sbjct: 301 LYTQADDPMKVYEEKK 316


Lambda     K      H
   0.316    0.131    0.376 

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: 337
Number of extensions: 12
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: 313
Length of database: 320
Length adjustment: 27
Effective length of query: 286
Effective length of database: 293
Effective search space:    83798
Effective search space used:    83798
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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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