GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Rhizobium freirei PRF 81

Align Ribose ABC transport system, permease protein RbsC (characterized, see rationale)
to candidate WP_004124101.1 RHSP_RS23330 hypothetical protein

Query= uniprot:A0A0C4Y7K0
         (337 letters)



>NCBI__GCF_000359745.1:WP_004124101.1
          Length = 334

 Score =  233 bits (595), Expect = 4e-66
 Identities = 140/313 (44%), Positives = 189/313 (60%), Gaps = 10/313 (3%)

Query: 30  LRALGMLPVLVLLCIGFSVLTENFAGWQNLSIIAQQASINMVLAAGMTFVILTGGIDLSV 89
           ++  G+    +LL I  S   E F    N+S +  Q SIN VLA GMTFVILT GIDLSV
Sbjct: 22  IQEYGIFLAFLLLAIVLSFSNEYFLTAGNISNVLLQTSINGVLAIGMTFVILTRGIDLSV 81

Query: 90  GSILSISAVV-AMLVSLMPQLGMLSVP----AALLCGLLFGIVNGALVAFM----KLPPF 140
           GS+++++ +V A   +     G++  P     AL  GLL G+  GA+V  +     +P F
Sbjct: 82  GSVVALTGIVSASFATTSATAGIVGAPYPPYVALAVGLLVGVACGAVVGLIVSRFAVPAF 141

Query: 141 IVTLGTLTAVRGLARLVGNDSTIYNPDIGFAFIGNGEVLGVPWLVIIAFAVVAVSWFVLR 200
           + TLG L+A RG+  + G    +      F +IG G VL +P  VI+   V  V+W+VL 
Sbjct: 142 VATLGMLSAARGMTLIYGGGKPVPALTPDFRWIGTGSVLSIPMPVILLAIVFIVAWWVLN 201

Query: 201 RTVLGLQIYAVGGNAEAARLSGIKVWVVLLFVYAVSGLLAGLGGVMSSARLYAANGLQLG 260
           RT  G  IYAVGGN  AA  SGI V  +   VY +SG L+GL G++ +AR  +A   Q G
Sbjct: 202 RTRFGRYIYAVGGNPHAATTSGIDVSKLRFLVYVISGGLSGLAGMILAARTGSALP-QAG 260

Query: 261 QSYELDAIAAVILGGTSFVGGTGSIVGTLVGALIIAVLSNGLVLLGVSDIWQYIIKGLVI 320
            +YELDAIAAV++GGTS  GG G I GTL+GALII V++NGL L+G+   +Q ++KG +I
Sbjct: 261 IAYELDAIAAVVIGGTSLSGGVGRITGTLIGALIIGVMNNGLDLMGIQSYYQQVLKGTLI 320

Query: 321 IGAVALDSYRRKG 333
           +GAV LD  R  G
Sbjct: 321 VGAVMLDQKRNLG 333


Lambda     K      H
   0.325    0.141    0.409 

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: 414
Number of extensions: 25
Number of successful extensions: 4
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: 337
Length of database: 334
Length adjustment: 28
Effective length of query: 309
Effective length of database: 306
Effective search space:    94554
Effective search space used:    94554
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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