GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Cupriavidus basilensis 4G11

Align ABC transporter (characterized, see rationale)
to candidate RR42_RS27800 RR42_RS27800 ABC transporter ATP-binding protein

Query= uniprot:A0A166QFW2
         (381 letters)



>FitnessBrowser__Cup4G11:RR42_RS27800
          Length = 357

 Score =  241 bits (614), Expect = 3e-68
 Identities = 146/338 (43%), Positives = 209/338 (61%), Gaps = 13/338 (3%)

Query: 15  GMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLD-SICGGDLLIDGRRVNDLEPR 73
           G   L+ + L+I AGE VV +GPSGCGK+T LR+IAGL+    GG ++     V  L   
Sbjct: 19  GTLALQPLDLDIGAGETVVLLGPSGCGKTTTLRIIAGLEFPDAGGVVMFGDNDVTPLPIE 78

Query: 74  ERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQILQLDKLLQRKPKE 133
           +RGVGMVFQSYAL+P+M+V +NI++GL++ + D  + R RV +   ++ L    +R+  +
Sbjct: 79  QRGVGMVFQSYALFPNMTVAENIAYGLRVRRIDAAARRRRVDEMLAMMHLGPFAERRIDQ 138

Query: 134 LSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHDRLGSTMIYVTHD 193
           LSGGQRQRVA+ RA+A +P +LL DEPL+ LDA LR  +R +I +L   L  T +YVTHD
Sbjct: 139 LSGGQRQRVALARAIAVQPRVLLLDEPLTALDAKLRDALRADINQLLRSLHITAVYVTHD 198

Query: 194 QVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMNFLSARLQTPGETS 253
           Q EAM L D+I+V++ GR+ Q G+P+++Y  PA+ FVA F+G+  MN L A L+      
Sbjct: 199 QAEAMALGDRIIVMDRGRIAQTGTPQQIYRAPANAFVADFIGT--MNRLPAVLEADAW-- 254

Query: 254 LVDTLVWGITSLPFDSSNLAAGTP--LSLGIRPEHVSLKAADGT--AGVVVTAVEYLGSE 309
               +  G+      +++LAA       L  RPE V+L  A+     G VVTA+ +LG+ 
Sbjct: 255 ---RVPGGLVPRHGTAASLAAAPSPRAELLFRPEDVALAQAEDAHLGGSVVTAL-FLGNY 310

Query: 310 TYVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNL 347
           T + ++ G   PL+       GW AGDRV L LD  +L
Sbjct: 311 TRLLVDVGAPAPLVVDTTRRDGWLAGDRVGLRLDTGHL 348


Lambda     K      H
   0.320    0.137    0.394 

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: 321
Number of extensions: 14
Number of successful extensions: 3
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: 381
Length of database: 357
Length adjustment: 30
Effective length of query: 351
Effective length of database: 327
Effective search space:   114777
Effective search space used:   114777
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 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