GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Pseudomonas fluorescens FW300-N2E3

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate AO353_25130 AO353_25130 ABC transporter

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_25130
          Length = 381

 Score =  297 bits (760), Expect = 4e-85
 Identities = 167/360 (46%), Positives = 216/360 (60%), Gaps = 6/360 (1%)

Query: 15  GGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTLRIGGTVVNDLPAR 74
           GG  +L  + L I  GEFVV +GPSGCGKST+LR+IAGL+ I  G L I    VNDL  R
Sbjct: 14  GGVRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICAGDLLIDERRVNDLEPR 73

Query: 75  ERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAALLNLEALLERKPRA 134
           ER V MVFQ+YALYPHMSVYDNI+FGL+  K   + +  RV   A +L L+ LL+RKP+ 
Sbjct: 74  ERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKSSLRERVLRTAQILQLDKLLQRKPKE 133

Query: 135 MSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLHQRLRTTTVYVTHD 194
           +SGGQ+QR A+ RA+ + P + LFDEPLSNLDA LR Q+R +I RLH RL +T +YVTHD
Sbjct: 134 LSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHARLGSTMIYVTHD 193

Query: 195 QLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMNFLSGTVQRQDGQL 254
           Q+EAMTLAD+++++  GR+ Q GSP ELY  P + F AGF+G+P MNFL+  +       
Sbjct: 194 QVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMNFLAARLHAPGETS 253

Query: 255 FIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRIAGEREPAASLTCPVSVELVEILGA 314
            ++T            S L     + L VRP+HV +      AA  T  V V  VE LG+
Sbjct: 254 LVDTPVLGMTSLPFDSSNLAADTPLSLGVRPEHVSL-----KAADGTVGVIVTGVEYLGS 308

Query: 315 DALLTTRCG-DQTLTALVPADRLPQPGATLTLALDQHELHVFDVESGENLSLPDAALTAP 373
           +  +    G D  L      +   Q G  + L LD   LH+FD +       P A  T P
Sbjct: 309 ETYVHLDTGQDDPLICRCEVNAGWQVGDRVELQLDIGNLHLFDADGTALRRPPQAIETLP 368


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: 422
Number of extensions: 18
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: 381
Length adjustment: 31
Effective length of query: 375
Effective length of database: 350
Effective search space:   131250
Effective search space used:   131250
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