GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglB in Tistlia consotensis USBA 355

Align CVE1 aka ChvE aka ATU2348 aka AGR_C_4267, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate WP_085126171.1 B9O00_RS28470 multiple monosaccharide ABC transporter substrate-binding protein

Query= TCDB::P25548
         (354 letters)



>NCBI__GCF_900177295.1:WP_085126171.1
          Length = 360

 Score =  534 bits (1376), Expect = e-156
 Identities = 263/346 (76%), Positives = 304/346 (87%)

Query: 8   MAACAIGAASFAAPAFAQDKGSVGIAMPTKSSARWIDDGNNIVKQLQEAGYKTDLQYADD 67
           +AA A+   +F+  A A  KG +GIAMPTKSSARWI DG+++VKQ + AGYKTDLQYA+D
Sbjct: 13  LAAVALSTPAFSTGALAASKGYIGIAMPTKSSARWISDGSSMVKQFEAAGYKTDLQYAED 72

Query: 68  DIPNQLSQIENMVTKGVKVLVIASIDGTTLSDVLKQAGEQGIKVIAYDRLIRNSGDVSYY 127
           DIPNQLSQIENM+TKGV VLVIA+IDGTTLS+ L  A   GIKVIAYDRLIR+S +V YY
Sbjct: 73  DIPNQLSQIENMITKGVNVLVIAAIDGTTLSNALANAEAAGIKVIAYDRLIRDSANVDYY 132

Query: 128 ATFDNFQVGVLQATSITDKLGLKDGKGPFNIELFGGSPDDNNAFFFYDGAMSVLKPYIDS 187
           ATFDNF+VGVLQA SI D L L   KGPFNIELFGGSPDDNNA+FFY+GAMSVL+PYID 
Sbjct: 133 ATFDNFKVGVLQAQSIVDSLDLAHKKGPFNIELFGGSPDDNNAYFFYNGAMSVLQPYIDK 192

Query: 188 GKLVVKSGQMGMDKVGTLRWDPATAQARMDNLLSAYYTDAKVDAVLSPYDGLSIGIISSL 247
           G LVVKSGQMGMDKVGTLRWD + AQARMDNLLSAYYTDA+VDAVLSPYDGLSIGIISSL
Sbjct: 193 GVLVVKSGQMGMDKVGTLRWDGSVAQARMDNLLSAYYTDARVDAVLSPYDGLSIGIISSL 252

Query: 248 KGVGYGTKDQPLPVVSGQDAEVPSVKSIIAGEQYSTIFKDTRELAKVTVNMVNAVMEGKE 307
           KGVGYGTKDQP+PV++GQDAEVPSVK+I+ G+Q STIFKDTRELA+VTV MVNA++ G +
Sbjct: 253 KGVGYGTKDQPMPVITGQDAEVPSVKAILRGDQTSTIFKDTRELARVTVGMVNALIGGGK 312

Query: 308 PEVNDTKTYENGVKVVPSYLLKPVAVTKENYKQVLVDGGYYKEDQL 353
           PE+NDTKTY+NGVKVVPSYLL PV VT++N++++LV  GYYK+DQ+
Sbjct: 313 PEINDTKTYDNGVKVVPSYLLNPVLVTRDNWEKILVGSGYYKKDQI 358


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: 525
Number of extensions: 19
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: 360
Length adjustment: 29
Effective length of query: 325
Effective length of database: 331
Effective search space:   107575
Effective search space used:   107575
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 Apr 09 2024. 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