GapMind for catabolism of small carbon sources

 

Alignments for a candidate for chvE in Pseudomonas fluorescens FW300-N2E2

Align CVE1 aka ChvE aka ATU2348 aka AGR_C_4267, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate Pf6N2E2_1455 Xylose ABC transporter, periplasmic xylose-binding protein XylF

Query= TCDB::P25548
         (354 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1455
          Length = 333

 Score =  158 bits (400), Expect = 2e-43
 Identities = 110/349 (31%), Positives = 179/349 (51%), Gaps = 22/349 (6%)

Query: 1   MKSIISLMAACAIGAASFAAPAFAQDKGSVGIAMPTKSSARWIDDGNNIVKQLQEAGYKT 60
           MK+    + A A+   S    A A     +G ++      RW  D +  V   ++   K 
Sbjct: 1   MKTFKRTLLAGALALLSLPVMADAAHP-KIGFSIDDLRLERWSRDRDYFVAAAEKLDAKV 59

Query: 61  DLQYADDDIPNQLSQIENMVTKGVKVLVIASIDGTTLSDVLKQAGEQGIKVIAYDRLIRN 120
            +Q AD +   Q+SQIEN++++GV V+VI   + T L++ + +A + GIKV++YDRLI N
Sbjct: 60  FVQSADANEQKQISQIENLISRGVDVIVIVPFNATVLTNAVAEAKKAGIKVVSYDRLILN 119

Query: 121 SGDVSYYATFDNFQVGVLQATSITDKLGLKDGKGPFNIELFGGSPDDNNAFFFYDGAMSV 180
           + D+  Y +FDN +VG +QA+      G+       N  L GG+P DNNA    +G M V
Sbjct: 120 A-DIDAYISFDNEKVGEMQAS------GVLKAAPKGNYFLLGGAPTDNNAKVLREGQMKV 172

Query: 181 LKPYIDSGKLVVKSGQMGMDKVGTLRWDPATAQARMDNLLSAYYTDAKVDAVLSPYDGLS 240
           L+P ID G + +   Q          W+P  A + ++N L+    + K+D +++  D  +
Sbjct: 173 LQPAIDKGDIKIVGQQW------VKEWNPTEALSIVENALTR--NNNKIDGIVASNDATA 224

Query: 241 IGIISSLKGVGYGTKDQPLPVVSGQDAEVPSVKSIIAGEQYSTIFKDTRELAKVTVNMVN 300
            G I +L       K   +P +SGQDA++ +VK +I G Q  T++K  + +A     +  
Sbjct: 225 GGAIQALAAQKMAGK---VP-ISGQDADLAAVKRVIDGTQTMTVYKPLKLIASEAAKLSV 280

Query: 301 AVMEGKEPEVNDTKTYENGVKVVPSYLLKPVAVTKENYKQVLVDGGYYK 349
            +   ++P    +  Y+NG K V + LL P  +TK+N   +  DG Y K
Sbjct: 281 QLARNEKPTF--SSQYDNGSKKVDTILLTPTPLTKDNIDLLEKDGFYTK 327


Lambda     K      H
   0.314    0.133    0.372 

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: 308
Number of extensions: 17
Number of successful extensions: 5
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: 354
Length of database: 333
Length adjustment: 29
Effective length of query: 325
Effective length of database: 304
Effective search space:    98800
Effective search space used:    98800
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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