GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaQ in Rhodobacter viridis JA737

Align RhaQ (characterized, see rationale)
to candidate WP_110804518.1 C8J30_RS04455 sugar ABC transporter permease

Query= uniprot:Q7BSH2
         (337 letters)



>NCBI__GCF_003217355.1:WP_110804518.1
          Length = 429

 Score = 80.5 bits (197), Expect = 7e-20
 Identities = 56/174 (32%), Positives = 91/174 (52%), Gaps = 13/174 (7%)

Query: 31  LLFAVAVLIFVFNSLASPYFLDAWNLSDATFNFTEKAMIAFAMALLVISGEIDLSVAAII 90
           ++ A  V+  VFN +    FL   N+ + +      A++A  M  ++++  IDLSV A++
Sbjct: 28  MIGAFVVICLVFNVITDGRFLTPRNIFNLSIQTVSVAIMATGMVFVIVTRHIDLSVGAVL 87

Query: 91  ALASTAMGAA-VQI-----GIGTPGL----VLIGIGTGLACGVFNGVLVSVLKLPSIVVT 140
           A+ S+ MG   VQ+     GIG P +    VL G+ TG A G  NG LV   ++P+ +VT
Sbjct: 88  AICSSVMGVMQVQLLPQLFGIGHPLVMPLTVLAGLLTGAAIGALNGWLVGYQRIPAFIVT 147

Query: 141 IGTMSLFRGISYIVLGDQAYGKYPADFAYFG--QGYVVWVFSFEF-VLFIVLAV 191
           +G + ++R + + +   Q  G     F  FG  +G V    S+   ++F VLAV
Sbjct: 148 LGGLLIWRNVGWYLTDGQTVGPLDQTFMLFGGVEGTVGSALSWGLAIVFSVLAV 201



 Score = 70.5 bits (171), Expect = 7e-17
 Identities = 47/200 (23%), Positives = 95/200 (47%), Gaps = 4/200 (2%)

Query: 132 LKLPSIVVTIGTMSLFRGISYIVLGDQAYGKYPADFAYFGQGYVVWV-FSFEFVLFIVLA 190
           L   S+   +G +++    SY +   +   ++ +      +GYV +       ++ +V+ 
Sbjct: 227 LMATSVAAILGFVAILN--SYAIPVGRLKREFESRGEVMPEGYVDYFGLPISVLMLVVIV 284

Query: 191 VLFAILLHATNFGRQVYAIGNNDFAARFSGIPVERVKSILFLLTGIMSGIAAVCLTSRLG 250
           V+  ++   T  GR ++A G N  AA  SGI    +   +F L G++  I+A+   +RL 
Sbjct: 285 VVMTLVARKTRLGRYIFAAGGNPDAAELSGINTRMLTVKIFTLMGVLCAISAMVAQARLA 344

Query: 251 STRPSIAQGWELEVVTMVVLGGISILGGFRHDRGVFVIAAFVMGLVTFGLGLLNLPGIVM 310
           +    I    EL V+   V+GG ++ GG     G  V+ A +M  +  G+ ++ +     
Sbjct: 345 NHTNDIGSLDELRVIAAAVIGGTALAGGIGTIYGA-VLGAVIMQSLQSGMAMVGVDAPFQ 403

Query: 311 SIFIGLLIIVTIAIPIIARR 330
           +I +G ++++ + I I  R+
Sbjct: 404 NIVVGGVLVLAVWIDIQYRK 423


Lambda     K      H
   0.330    0.145    0.423 

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: 377
Number of extensions: 20
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 337
Length of database: 429
Length adjustment: 30
Effective length of query: 307
Effective length of database: 399
Effective search space:   122493
Effective search space used:   122493
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 50 (23.9 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