GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Desulfovibrio vulgaris Hildenborough

Align Trehalose import ATP-binding protein SugC; EC 7.5.2.- (characterized)
to candidate 209225 DVU0291 ABC transporter, ATP-binding protein

Query= SwissProt::P9WQI3
         (393 letters)



>MicrobesOnline__882:209225
          Length = 354

 Score =  174 bits (441), Expect = 4e-48
 Identities = 116/332 (34%), Positives = 168/332 (50%), Gaps = 19/332 (5%)

Query: 16  GHTAVRDLNLTIADGEFLILVGPSGCGKTTTLNMIAGLEDISSGELRIAGERVNEKAPKD 75
           G   + D+NLT A GE + LVGPSG GKTT L  IAGL+    G +R+   + +      
Sbjct: 14  GREVLHDVNLTAAAGEVVCLVGPSGVGKTTLLRCIAGLDAPDEGTIRVTPPQGHGGG--- 70

Query: 76  RDIAMVFQSYALYPHMTVRQNIAFPLTLAKMRKADIAQKVSETAKIL-----DLTNLLDR 130
             + +VFQ Y L+PH++V +N+AF      +R A + ++V    +       DL ++  R
Sbjct: 71  --VVLVFQDYLLFPHLSVFENVAFGPRARGVRGAALKERVHTMLRAFRLDTDDLAHMASR 128

Query: 131 KPSQLSGGQRQRVAMGRAIVRHPKAFLMDEPLSNLDAKLRVQMRGEIAQLQRRLGTTTVY 190
            P+QLS GQRQRVA+ RA+V  P   L+DEP +NLD  LR +M   +  + RR G  TV 
Sbjct: 129 YPAQLSAGQRQRVALARALVCDPAVLLLDEPFANLDRGLRGEMAAFVRDVVRRFGVATVT 188

Query: 191 VTHDQTEAMTLGDRVVVMYGGIAQQIGTPEELYERPANLFVAGFIGSPAMNFFPARLTAI 250
           VTHD  EA  +GDR+ VM GG   Q+  P ++Y  PA+   A F+G   +     R T  
Sbjct: 189 VTHDLEEAFAIGDRLGVMLGGTLAQLAPPLDVYRHPADEATARFLGPVTVLDETTRRTLG 248

Query: 251 GLTLPFGEVTLAPEVQGVIAAHPKPENVIVGVRPEHIQDAALIDAYQRIRALTFQVKVNL 310
             T P      A  +QG+    P+     + VRP     A L+ A       T QV   L
Sbjct: 249 IDTPPAAATACADTMQGLRLYRPE----ALAVRPWADGPAVLVSA-----RFTGQVMQLL 299

Query: 311 VESLGADKYLYFTTESPAVHSVQLDELAEVEG 342
           ++  G +  ++   ++P   +     L E+ G
Sbjct: 300 LDVEGQELLVHTLDDAPPTGTRLCVSLREIPG 331


Lambda     K      H
   0.319    0.135    0.377 

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: 347
Number of extensions: 18
Number of successful extensions: 3
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: 393
Length of database: 354
Length adjustment: 30
Effective length of query: 363
Effective length of database: 324
Effective search space:   117612
Effective search space used:   117612
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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