GapMind for catabolism of small carbon sources

 

Alignments for a candidate for chvE in Phyllobacterium brassicacearum STM 196

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_106712329.1 CU102_RS17160 D-xylose ABC transporter substrate-binding protein

Query= TCDB::P25548
         (354 letters)



>NCBI__GCF_003010955.1:WP_106712329.1
          Length = 347

 Score =  169 bits (429), Expect = 8e-47
 Identities = 122/354 (34%), Positives = 183/354 (51%), Gaps = 25/354 (7%)

Query: 1   MKSIISLMAACAIGAASFAAPAFAQDKGSVGIAMPTKSSARWIDDGNNIVKQLQEAGYKT 60
           MK   + +A  A+ A S A PA A+DK  VG++       RW  D   I K L+  G K 
Sbjct: 1   MKKYATALAGAAVLAVSIAGPALAKDK-VVGVSWSNFQEERWKTDEAAIKKALEANGDKY 59

Query: 61  DLQYADDDIPNQLSQIENMVTKGVKVLVIASIDGTTLSDVLKQAGEQGIKVIAYDRLIRN 120
               A      QL+ +E+++++G   L+I + D   +   +++A  +GI V+ YDRLI N
Sbjct: 60  ISADAQSSASKQLTDVESLISQGANALIILAQDSGAIGPAVEKAVAEGIPVVGYDRLIEN 119

Query: 121 SGDVSYYATFDNFQVGVLQATSITDKLGLKDGKGPFNIELFGGSPDDNNAFFFYDGAMSV 180
               ++Y TFDN +VG +QA       G+   K   N     GS  D NA F + GA  V
Sbjct: 120 KD--AFYITFDNKEVGRMQAR------GVFAVKPEGNYVFIKGSSADPNADFLFSGAQEV 171

Query: 181 LKPYIDSGKLVVKSGQMGMDKVGTLRWDPATAQARMDNLLSAYYTDAKVDAVLSPYDGLS 240
           LK  IDSGK+        + +  T  W PA AQ  M+  L+A   D KVDAV++  DG +
Sbjct: 172 LKEAIDSGKI------KNVGEAYTDGWLPANAQKNMEQFLTA--NDNKVDAVVAANDGTA 223

Query: 241 IGIISSLKGVGYGTKDQPLPVVSGQDAEVPSVKSIIAGEQYSTIFKDTRELAKVTVNMVN 300
            G I++L+  G       +P VSGQDA+  ++  +  G Q  TI+KD+REL      + +
Sbjct: 224 GGAIAALQAQGLAGN---VP-VSGQDADFAALNRVALGTQTVTIWKDSRELGAQAAGIAS 279

Query: 301 AVMEGKE-PEVNDTKTYENGVKVVP--SYLLKPVAVTKENYKQVLVDGGYYKED 351
           A+ +GK+  E+ + + +  G   V   +  L PV VTK+N   V++D G+  +D
Sbjct: 280 ALADGKKMEEIPNVQKFAGGANKVEVNAVFLTPVPVTKDNL-DVVIDAGWVTKD 332


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: 320
Number of extensions: 20
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: 347
Length adjustment: 29
Effective length of query: 325
Effective length of database: 318
Effective search space:   103350
Effective search space used:   103350
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 24 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