GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Bacteroides thetaiotaomicron VPI-5482

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate 350819 BT1291 spermidine/putrescine transport ATP-binding protein (NCBI ptt file)

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__Btheta:350819
          Length = 463

 Score =  220 bits (561), Expect = 6e-62
 Identities = 133/346 (38%), Positives = 192/346 (55%), Gaps = 13/346 (3%)

Query: 13  YAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTLRIGGTVVNDLP 72
           + G    L  + L++  GEFV +LGPSGCGK+T+LR+IAG +  S G +RI G  +   P
Sbjct: 18  FFGDKTALDDVTLNVKKGEFVTILGPSGCGKTTLLRLIAGFQTASEGEIRISGKEITQTP 77

Query: 73  ARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAALLNLEALLERKP 132
             +R V  VFQ YAL+PH++VYDNIAFGL+  K P   I ++V+    ++ +     R  
Sbjct: 78  PHKRPVNTVFQKYALFPHLNVYDNIAFGLKLKKTPKQTIGKKVKAALKMVGMTDYEYRDV 137

Query: 133 RAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLHQRLRTTTVYVT 192
            ++SGGQQQR AIARAI+  P V L DEPL+ LD K+R  ++ ++K +H+ L  T VYVT
Sbjct: 138 DSLSGGQQQRVAIARAIVNEPEVLLLDEPLAALDLKMRKDMQMELKEMHKSLGITFVYVT 197

Query: 193 HDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMNFLSGTVQRQDG 252
           HDQ EA+TL+D +++M +G+I Q G+P ++Y  P N F A FIG    N L+GT+     
Sbjct: 198 HDQEEALTLSDTIVVMSEGKIQQIGTPIDIYNEPINSFVADFIG--ESNILNGTMIHDKL 255

Query: 253 QLFIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREPAASLTCPVSVELVEIL 312
             F  T    +    E F        V + +RP+ + I    E  A LT  V   + +  
Sbjct: 256 VRFCGT---EFECVDEGFG---ENTPVDVVIRPEDLYIFPVSE-MAQLTGVVQTSIFK-- 306

Query: 313 GADALLTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHVFDVE 358
           G    +T  CG      LV      + GA + L +   ++H+   E
Sbjct: 307 GVHYEMTVLCGGYEF--LVQDYHHFEVGAEVGLLVKPFDIHIMKKE 350


Lambda     K      H
   0.321    0.137    0.403 

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: 425
Number of extensions: 16
Number of successful extensions: 1
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: 406
Length of database: 463
Length adjustment: 32
Effective length of query: 374
Effective length of database: 431
Effective search space:   161194
Effective search space used:   161194
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: 51 (24.3 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