GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Echinicola vietnamensis KMM 6221, DSM 17526

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate Echvi_1280 Echvi_1280 Ribose/xylose/arabinose/galactoside ABC-type transport systems, permease components

Query= uniprot:D8J112
         (347 letters)



>FitnessBrowser__Cola:Echvi_1280
          Length = 318

 Score =  223 bits (567), Expect = 7e-63
 Identities = 123/314 (39%), Positives = 188/314 (59%), Gaps = 18/314 (5%)

Query: 36  KLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGT 95
           K  +  +L+++ L  S  S  F+ + N  ++++  +VN  +++  T VI+T+GIDLSVG+
Sbjct: 6   KFQSLIALIILCLVLSLLSDRFLTLANGWNVMRQVSVNICISVGMTLVILTAGIDLSVGS 65

Query: 96  MMTFCAVMAGVVLTNW----GMPLPLGIAA------AIFFGALSGWISGMVIAKLKVPPF 145
           ++  C  +   ++ N     G+ L +G A        +  G   GW +G  I + KVPPF
Sbjct: 66  ILALCGAVTASLIKNGIAVEGLNLHIGFAPLGAVILGVGLGFGLGWFNGWTITRFKVPPF 125

Query: 146 IATLGMMMLLKGLSLVISGTRPIYFNDTEGFSAIAQDSLIGDLIPSLPIPNAVLILFLVA 205
           +ATL M+ + +GL+++ +G  PI     E F+ +     +G       IP  V I  ++ 
Sbjct: 126 VATLAMLTIARGLTMLWTGGFPIN-GLGEDFAFLGTGWFLG-------IPMPVWITAVIV 177

Query: 206 IGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRLN 265
             A ++  KT FGRY +A+G NE A RLSG+ +   K+ VY  +G +  + G+I+ SRL+
Sbjct: 178 ALAVLLTKKTKFGRYVYAIGGNERAARLSGINISRVKMTVYAIAGGLAAVGGMIVTSRLD 237

Query: 266 SAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQT 325
           SAQP  G  YELDAIAAVVIGGTSLSGG GTI+G ++G  I+ VL NGL +++V+  WQ 
Sbjct: 238 SAQPNAGISYELDAIAAVVIGGTSLSGGKGTIMGAVLGGIIIGVLNNGLVLLNVSPFWQQ 297

Query: 326 VVTGVIIILAVYLD 339
           VV G +I+LAV +D
Sbjct: 298 VVKGAVILLAVVID 311


Lambda     K      H
   0.326    0.139    0.398 

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: 250
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: 347
Length of database: 318
Length adjustment: 28
Effective length of query: 319
Effective length of database: 290
Effective search space:    92510
Effective search space used:    92510
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 (21.7 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