GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Collimonas pratensis Ter91

Align Ribose ABC transport system, permease protein RbsC (characterized, see rationale)
to candidate WP_061938906.1 CPter91_RS07340 ABC transporter permease

Query= uniprot:A0A0C4Y7K0
         (337 letters)



>NCBI__GCF_001584185.1:WP_061938906.1
          Length = 343

 Score =  219 bits (558), Expect = 8e-62
 Identities = 132/338 (39%), Positives = 200/338 (59%), Gaps = 14/338 (4%)

Query: 4   SITRPAASTGAPLPAGTLGRLTTQERLRALGMLPVLVLLCIGFSVLTENFAGWQNLSIIA 63
           S  +P     A + A      T Q+ L    +L ++V     FS  + NF    NL  I 
Sbjct: 9   SQAQPGQGAFAAVKAKIFHPATRQKLLAFASLLALMVF----FSFASSNFLEIDNLVSIL 64

Query: 64  QQASINMVLAAGMTFVILTGGIDLSVGSILSISAVVA-MLVSLMPQLGMLSVPAALLCGL 122
           Q  ++N VLA   TFVI+T GIDLSVG++++  AV+A + ++ M     + + AA+  G 
Sbjct: 65  QSTAVNGVLAIACTFVIITAGIDLSVGTLMTFCAVMAGVFLTYMGLPIYIGIVAAVFFGA 124

Query: 123 LFGIVNGALVAFMKLPPFIVTLGTLTAVRGLARLVGNDSTIY-NPDIGFAFIGNGEVLG- 180
           L G V+G LVA +K+PPFI TLG +  ++GL+ ++     IY N   GF+ I    ++G 
Sbjct: 125 LCGWVSGVLVAKLKIPPFIATLGMMMLLKGLSLVISGTKPIYFNDTPGFSAISQDSLIGS 184

Query: 181 ------VPWLVIIAFAVVAVSWFVLRRTVLGLQIYAVGGNAEAARLSGIKVWVVLLFVYA 234
                 +P  V+I F V   +  +L +T+ G   +A+G N EA RLSG+ V    + +Y 
Sbjct: 185 LIPVLPIPNAVLILFLVAIGAGIILNKTIFGRYTFALGSNEEALRLSGVNVDFWKVAIYT 244

Query: 235 VSGLLAGLGGVMSSARLYAANGLQLGQSYELDAIAAVILGGTSFVGGTGSIVGTLVGALI 294
            SG + G+ G++ ++RL +A    LGQ YELDAIAAV++GGTS  GGTG+I+GT++GA I
Sbjct: 245 FSGAICGIAGLLIASRLNSAQPA-LGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFI 303

Query: 295 IAVLSNGLVLLGVSDIWQYIIKGLVIIGAVALDSYRRK 332
           ++VL NGL ++ V+  WQ ++ G++II AV +D  RR+
Sbjct: 304 MSVLINGLRMMSVAQEWQTVVTGVIIILAVYMDILRRR 341


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: 341
Number of extensions: 14
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: 343
Length adjustment: 28
Effective length of query: 309
Effective length of database: 315
Effective search space:    97335
Effective search space used:    97335
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