GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Rhodobacter viridis JA737

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate WP_110804244.1 C8J30_RS03245 ABC transporter ATP-binding protein

Query= uniprot:D8IPI1
         (406 letters)



>NCBI__GCF_003217355.1:WP_110804244.1
          Length = 332

 Score =  300 bits (768), Expect = 4e-86
 Identities = 169/360 (46%), Positives = 220/360 (61%), Gaps = 31/360 (8%)

Query: 1   MADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGT 60
           M +I  + + K + G   V+ P+DL I DGEFVV +GPSGCGKST+LR+IAGLED+SGG 
Sbjct: 1   MGEIVLKGVTKRF-GDVEVIPPIDLAIHDGEFVVFVGPSGCGKSTLLRLIAGLEDVSGGK 59

Query: 61  LRIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAA 120
           + I G    +    +R +AMVFQ+YALYPHMSV  NIAF L+  K P AEI+ +V+  A 
Sbjct: 60  IEIDGKDATETAPSDRGLAMVFQSYALYPHMSVKKNIAFPLKMAKLPPAEIEAKVQAAAK 119

Query: 121 LLNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRL 180
           +LNL A L+RKP  +SGGQ+QR AI RAI+++P  FLFDEPLSNLDA LR  +R +I  L
Sbjct: 120 VLNLSAYLDRKPGQLSGGQRQRVAIGRAIVRSPEAFLFDEPLSNLDAALRVNMRLEISEL 179

Query: 181 HQRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAM 240
           H  L+TT +YVTHDQ+EAMT+AD+++++Q GRI Q GSP ELYR PRN F AGFIG+P M
Sbjct: 180 HHTLKTTMIYVTHDQVEAMTMADKIVVLQAGRIEQVGSPLELYRTPRNRFVAGFIGSPKM 239

Query: 241 NFLSGTVQRQDGQLFIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREPAASL 300
           NF+ G    + G                         A  + +RP+H+RI+   E     
Sbjct: 240 NFIEGAEAAKHG-------------------------AHAIGIRPEHIRIS-TTEGMWKG 273

Query: 301 TCPVSVELVEILGADALLTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHVFDVESG 360
           T  VS    E LG+D  L        L      +     G ++ L+ D  +LH FD E G
Sbjct: 274 TVGVS----EHLGSDTFLHVTTEHGLLNVRAGGEVDLHHGDSVFLSPDMAQLHRFDKEGG 329


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: 366
Number of extensions: 17
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: 406
Length of database: 332
Length adjustment: 30
Effective length of query: 376
Effective length of database: 302
Effective search space:   113552
Effective search space used:   113552
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: 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