GapMind for catabolism of small carbon sources

 

Alignments for a candidate for chvE in Herbaspirillum seropedicae SmR1

Align CVE1 aka ChvE aka ATU2348 aka AGR_C_4267, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate HSERO_RS22460 HSERO_RS22460 xylose ABC transporter substrate-binding protein

Query= TCDB::P25548
         (354 letters)



>FitnessBrowser__HerbieS:HSERO_RS22460
          Length = 338

 Score =  201 bits (511), Expect = 2e-56
 Identities = 127/352 (36%), Positives = 198/352 (56%), Gaps = 23/352 (6%)

Query: 2   KSIISLMAACAIGAASFAAPAFAQDKGSVGIAMPTKSSARWIDDGNNIVKQLQEAGYKTD 61
           K++++LM    +   + +A A A++   +G ++      RW  D +      ++ G K  
Sbjct: 7   KTVLALMTVTTLSMVAGSAMADAKNP-KIGFSIDDLRVERWARDRDFFTAAAEKLGAKVY 65

Query: 62  LQYADDDIPNQLSQIENMVTKGVKVLVIASIDGTTLSDVLKQAGEQGIKVIAYDRLIRNS 121
           +Q AD     Q+SQIEN++++GV V+VI   + T L++ +K+A + GIKV++YDRLI N+
Sbjct: 66  VQSADASEQRQISQIENLISRGVDVIVIVPFNATVLTNTIKEAKKAGIKVLSYDRLILNA 125

Query: 122 GDVSYYATFDNFQVGVLQATSITDKLGLKDGKGPFNIELFGGSPDDNNAFFFYDGAMSVL 181
            DV  Y +FDN +VG +QA       G+   K   N  L GGSP DNNA  F +G M  L
Sbjct: 126 -DVDAYISFDNEKVGEMQAE------GILKVKNKGNFFLLGGSPTDNNAKMFREGQMKAL 178

Query: 182 KPYIDSGKLVVKSGQMGMDKVGTLRWDPATAQARMDNLLSAYYTDAKVDAVLSPYDGLSI 241
           KPYID G + +   Q          W+P  A + ++N L+A   + K+DA+++  DG + 
Sbjct: 179 KPYIDKGDIKIVGQQW------VKEWNPTEALSIVENALTA--NNNKIDAIVASNDGTAG 230

Query: 242 GIISSLKGVGYGTKDQPLPVVSGQDAEVPSVKSIIAGEQYSTIFKDTRELAKVTVNMVNA 301
           G I +L       K   +P VSGQDA++ +VK ++AG Q  T++K  +++A     +   
Sbjct: 231 GAIQALAAQKLAGK---VP-VSGQDADLAAVKRVVAGTQTMTVYKPLKQIATEAAKLSVE 286

Query: 302 VMEGKEPEVNDTKTYENGVKVVPSYLLKPVAVTKENYKQVLVDGGYYKEDQL 353
           +   ++P  N    Y+NG K V S LLKP+ +TKEN K VLVD G+Y + Q+
Sbjct: 287 LARNEKPTYN--AQYDNGFKKVDSLLLKPILLTKENVK-VLVDDGFYTQAQI 335


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: 338
Number of extensions: 24
Number of successful extensions: 6
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: 338
Length adjustment: 29
Effective length of query: 325
Effective length of database: 309
Effective search space:   100425
Effective search space used:   100425
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