GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Sinorhizobium meliloti 1021

Align CVE1 aka ChvE aka ATU2348 aka AGR_C_4267, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate SM_b20895 SM_b20895 sugar uptake ABC transporter substrate-binding protein precursor

Query= TCDB::P25548
         (354 letters)



>FitnessBrowser__Smeli:SM_b20895
          Length = 355

 Score =  547 bits (1409), Expect = e-160
 Identities = 272/353 (77%), Positives = 307/353 (86%)

Query: 1   MKSIISLMAACAIGAASFAAPAFAQDKGSVGIAMPTKSSARWIDDGNNIVKQLQEAGYKT 60
           MK   SL+AA AI  A FAAPA AQ+KG VGI+MPTK+S RWI DG  + K  +EAGY  
Sbjct: 1   MKFFTSLLAAAAITVAGFAAPAVAQEKGMVGISMPTKTSTRWISDGETMEKLFKEAGYTP 60

Query: 61  DLQYADDDIPNQLSQIENMVTKGVKVLVIASIDGTTLSDVLKQAGEQGIKVIAYDRLIRN 120
           DLQ+ADDDIPNQL+QIENMVTKG KVLVI +IDGTTLSD+L++A + G+KVIAYDRLIR+
Sbjct: 61  DLQFADDDIPNQLAQIENMVTKGAKVLVIGAIDGTTLSDILQKAADAGVKVIAYDRLIRD 120

Query: 121 SGDVSYYATFDNFQVGVLQATSITDKLGLKDGKGPFNIELFGGSPDDNNAFFFYDGAMSV 180
           SG+V YYATFDNFQVGVLQATS+ + L L     P N+ELFGGSPDDNNAFFFYDGAMSV
Sbjct: 121 SGNVDYYATFDNFQVGVLQATSLVEGLKLDSATEPKNVELFGGSPDDNNAFFFYDGAMSV 180

Query: 181 LKPYIDSGKLVVKSGQMGMDKVGTLRWDPATAQARMDNLLSAYYTDAKVDAVLSPYDGLS 240
           L+P IDSGK+VVKSGQMGMD+VGTLRWD A AQARM+NLLS+ YTDAKVD VLSPYDGLS
Sbjct: 181 LQPLIDSGKIVVKSGQMGMDQVGTLRWDGAVAQARMENLLSSAYTDAKVDGVLSPYDGLS 240

Query: 241 IGIISSLKGVGYGTKDQPLPVVSGQDAEVPSVKSIIAGEQYSTIFKDTRELAKVTVNMVN 300
           IGIIS+LKGVGYG+ D P+P+V+GQDAE+PSVKSI+AGEQYST+FKDTRELAKVTVNMVN
Sbjct: 241 IGIISALKGVGYGSGDMPMPIVTGQDAELPSVKSILAGEQYSTVFKDTRELAKVTVNMVN 300

Query: 301 AVMEGKEPEVNDTKTYENGVKVVPSYLLKPVAVTKENYKQVLVDGGYYKEDQL 353
           A+M+GKEPEVNDTKTYENGVKVVPSYLLKPV+V K N K VLV  GYY EDQL
Sbjct: 301 AIMDGKEPEVNDTKTYENGVKVVPSYLLKPVSVDKSNAKDVLVGSGYYTEDQL 353


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: 554
Number of extensions: 24
Number of successful extensions: 1
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: 355
Length adjustment: 29
Effective length of query: 325
Effective length of database: 326
Effective search space:   105950
Effective search space used:   105950
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