GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Dyella japonica UNC79MFTsu3.2

Align D-xylose ABC transporter, periplasmic D-xylose-binding protein (characterized)
to candidate N515DRAFT_3231 N515DRAFT_3231 xylose-binding protein

Query= CharProtDB::CH_003787
         (330 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3231
          Length = 341

 Score =  394 bits (1012), Expect = e-114
 Identities = 194/337 (57%), Positives = 255/337 (75%), Gaps = 9/337 (2%)

Query: 3   IKNILLTLCTSLLLTNVAAHA---------KEVKIGMAIDDLRLERWQKDRDIFVKKAES 53
           +K +   +  +L+ T +A  A          + KIG +IDD+RLERW +DRD FV  AE 
Sbjct: 1   MKRLFARVLLALVATGLAVAALTACSGKASDQPKIGFSIDDMRLERWTRDRDYFVAAAEK 60

Query: 54  LGAKVFVQSANGNEETQMSQIENMINRGVDVLVIIPYNGQVLSNVVKEAKQEGIKVLAYD 113
           LGAKV+VQSA+GNE+ Q+ Q+EN+I+RGV+VLVI+P+N +VL NV+ EAK+ GIKV++YD
Sbjct: 61  LGAKVYVQSADGNEQRQVQQLENLISRGVNVLVIVPFNSKVLDNVIAEAKRNGIKVISYD 120

Query: 114 RMINDADIDFYISFDNEKVGELQAKALVDIVPQGNYFLMGGSPVDNNAKLFRAGQMKVLK 173
           R+I  AD+D YISFDNEKVGELQA+ ++D VP+GNYFL+GGSP DNNAK+ R GQ+KVL+
Sbjct: 121 RLILGADVDAYISFDNEKVGELQAQGVLDAVPKGNYFLLGGSPTDNNAKILREGQLKVLQ 180

Query: 174 PYVDSGKIKVVGDQWVDGWLPENALKIMENALTANNNKIDAVVASNDATAGGAIQALSAQ 233
           P +D G +K+VG QW   W    AL+I+E+ALTAN+N I  +VASNDATAGGAIQAL+AQ
Sbjct: 181 PAIDRGDVKIVGQQWTPEWDASKALRIVEDALTANHNDIQGIVASNDATAGGAIQALAAQ 240

Query: 234 GLSGKVAISGQDADLAGIKRIAAGTQTMTVYKPITLLANTAAEIAVELGNGQEPKADTTL 293
            L+GKVA+SGQDADLAG++R+  GTQ MTVYKP+  +A TAAE+AV+L  G+ P     +
Sbjct: 241 QLAGKVAVSGQDADLAGVRRVVDGTQAMTVYKPLKTIATTAAELAVKLAKGEAPTYTGKM 300

Query: 294 NNGLKDVPSRLLTPIDVNKNNIKDTVIKDGFHKESEL 330
           NNG KDV S LL P  + K+ + DTVIKDGF+   ++
Sbjct: 301 NNGKKDVDSVLLQPTLLTKDKVDDTVIKDGFYTREQI 337


Lambda     K      H
   0.314    0.132    0.366 

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: 387
Number of extensions: 12
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: 330
Length of database: 341
Length adjustment: 28
Effective length of query: 302
Effective length of database: 313
Effective search space:    94526
Effective search space used:    94526
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 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