GapMind for catabolism of small carbon sources

 

Aligments for a candidate for mglB 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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